Low levels of vitamin D may decrease the risk of death from all causes by 26 per cent, suggests a study with 13,000 initially healthy men and women.
The study, published in the Archives of Internal Medicine, highlights the importance of maintaining healthy vitamin D levels.
“Further observational studies are needed to confirm these findings and establish the mechanisms underlying these observations. If confirmed, randomized clinical trials will be needed to determine whether vitamin D supplementation at higher doses could have any potential benefit in reducing future mortality risk in those with 25(OH)D deficiency,” wrote lead author Michal Melamed from the Albert Einstein College of Medicine.
The vitamin is produced in the body on exposure to sunlight, but increasing vitamin D levels via sunlight or supplements has been a source of ongoing debate.
In the US, where over 1.5 million people are diagnosed with skin cancer every year, experts are pushing supplements, claiming recommendations for sun exposure are "highly irresponsible".
Another push for supplements comes from the fact that intakes are low from dietary sources coupled with a lack of sunshine in northern climates, has led to estimates that as much as 60 per cent of northern populations may be vitamin D deficient.
In adults, vitamin D deficiency may precipitate or exacerbate osteopenia, osteoporosis, muscle weakness, fractures, common cancers, autoimmune diseases, infectious diseases and cardiovascular diseases.
Vitamin D refers to two biologically inactive precursors - D3, also known as cholecalciferol, and D2, also known as ergocalciferol. Both D3 and D2 precursors are hydroxylated in the liver and kidneys to form 25- hydroxyvitamin D (25(OH)D), the non-active 'storage' form, and 1,25-dihydroxyvitamin D (1,25(OH)2D), the biologically active form that is tightly controlled by the body.
Study details
Melamind and co-workers from John Hopkins University used data from the Third National Health and Nutritional Examination Survey (NHANES III). Vitamin D levels were analysed in 13,331 healthy men and women
According previous results from the same nationwide survey, the optimum blood level of 25[OH]D is 30 nanograms per millilitre (ng/ml) or higher. However, about 41 per cent of American men and 53 per cent of American women have levels lower than 28 ng/ml. An unhealthy deficiency is considered blood levels of 17.8 ng/ml or lower.
Over the course of 8.7 years of follow-up, the researchers documented 1,806 deaths. Of these, nearly 700 deaths were associated with some form of heart disease, with 400 of these being deficient in vitamin D.
When the researchers compared people with the lowest and highest average 25(OH)D levels, they found that low levels were associated with a 26 per cent decreased rate of death from any cause.
No significant associations were found when the researchers assessed vitamin D levels and risk of death from cardiovascular disease or cancer alone.
"Our results make it much more clear that all men and women concerned about their overall health should more closely monitor their blood levels of vitamin D, and make sure they have enough," said study researcher Erin Michos.
"We think we have additional evidence to consider adding vitamin D deficiency as a distinct and separate risk factor for death from cardiovascular disease, putting it alongside much better known and understood risk factors, such as age, gender, family history, smoking, high blood cholesterol levels, high blood pressure, lack of exercise, obesity and diabetes," she added.
Considerations
“This is the first study, to our knowledge, to explore the association between 25(OH)D levels and mortality in the general population,” wrote the authors.
They note, however, several limitations to the study, most importantly that it is an observational study and therefore cannot prove if the role of vitamin D is causal.
“Several lines of evidence suggest that vitamin D deficiency may be a risk factor for cardiovascular, cancer, and all-cause mortality,” they added.
“Ecological studies reveal that CVD events are higher in the winter when vitamin D levels are lower and that cancer survival is better if the cancer is diagnosed in the summer when vitamin D levels are higher.”
Source: Archives of Internal Medicine Volume 168, Issue 15, Pages 1629-1637 “25-Hydroxyvitamin D Levels and the Risk of Mortality in the General Population” Authors: M.L. Melamed, E.D. Michos, W. Post, B. Astor
A MECHANISM OF BLOOD DAMAGE Clifford E Carnicom Dec 14 2009
I am not offering any medical advice or diagnosis with the presentation of this information. I am acting solely as an independent researcher providing the results of extended observation and analysis of unusual biological conditions that are evident.
An organism and a method that damages the condition of the blood has now been identified and it has been directly observed. The blood variations reported here are in direct association with the existence of and the severity of the so-called "Morgellons" condition.
The degradation occurs, at least in part, as a result of the existence of a chlamydia-likeorganism that has been repeatedly called to attention within the research during the past several years. This organism, along with a pleomorphic form tentatively identified as a mycoplasma variation, as well as certain filamentous forms, have been identified as common denominators in past and active biological and environmental examinations.
It will be recalled from earlier studies that essentially all individuals observed thus far display the presence of these blood anomalies to varying degree; statistically it would certainly appear as though the general population is subject to these forms. It has also been stated that the severity of the damage to the blood appears to occur in direct correlation with the manifestation of symptoms of the Morgellon's condition.
It is commonly perceived that skin anomalies and lesions (eruptions) are the major indicators as to the presence of the Morgellons "condition." It is asserted by this researcher that this criteria is completely and totally inadequate to establish the existence of the condition. A more comprehensive assessment appears to be that the presence of certain filamentous forms internal to the body and the presence of the chlamydia-like organism within the blood more positively establishes the existence of the condition. The presence of skin lesions (eruptions) and or filaments appears to be simply an outward manifestation by a subset of the population of the underlying biological changes that have occurred within the body. Thus far, all individuals studied show these changes within the body to varying degree.
The specific organisms (four specific forms in total, thus far) involved still require positive identification, as they have for several years now. I do not claim any medical or biological expertise at the level that is required. The size of the organisms alone is beyond conventional microscopy and they have been identified only with custom microscopic developments. Chlamydia-like and mycoplasma-like identifications must only be regarded as tentative and they are based primarily upon observation, research and deduction.
One of the dominant characteristics of the Chlamydia genus is that its members are metabolically incomplete, and that they require the energy of the host to thrive; this is one reason why they exist as intracellular (within the cell) within the host. In addition, intracellular organisms present a series of challenges to the immune system for detection and eradication, as recognition of a pathogen becomes much more difficult internal to the cell.
One of the dominant characteristics of the Mycoplama genus is that the species lack a cell wall, and hence the ability to assume various forms, i.e, pleomorphic.
Regardless of the eventual identifications that are to take place, the involvement of unconventional biology and genetic modification appears to affirmed by the unusual characteristics, enclosure and transport of these particular organisms under study.
The importance of this paper is that a specific organism and method of blood degradation that is in association with the Morgellons condition has been identified by function and has been observed and recorded, and that this same specific organism has been under study from several different vantage points for several years now. This chlamydia-like organism remains a focal point of investigation with respect to both the Aerosol Operations and the Morgellons issue; from the current studies it is expected to remain so for some time. The ubiquity and importance of this specific, (but still unidentified by species), organism will become even more apparent in future writings. In general, it would appear that the chlamydia-like and the mycoplasma-like intrusions set the stage for broader systematic degradation, immune suppression and additional pleomorphic manifestations upon sufficient invasion. In addition, genetic modification and transformation of the infective agents as well as the hosts are to be considered as very real possibilities.
The specific method of blood damage referred to in this paper is as follows:
1. The chlamydia-like organism appears to frequently exist in large numbers within the blood, i.e, the serum. The erythrocytes (red blood cells) can appear to be in good form even with the presence of the chlamydia-like organism in the serum external to the cells.
2. The chlamydia-like organism does appear to be attracted to the outer wall of the erythrocytes.
3. In the early stages of intrusion, the chlamydia like structures can surround and bind to the outer wall of the erthryocyte, with no damage to the cell wall necessarily apparent.
4. Upon increased intrusion of the cell, the chlamydia-like organism will be seen to have been incorporated within the cell wall. It is at this point that a breakdown of the integrity of the cell wall can often be observed.
5. Upon further intrusion, the chlamydia-like organism can exist in relatively large numbers within the erythrocyte. Further damage to the integrity of the cell occurs.
6. In extreme cases observed thus far, the integrity of the cell wall is radically compromised, along with the general structure of the red blood cells. Existence of the chlamydia-like organism can be rampant within the blood. The functioning of the blood would appear to be seriously impaired at this point and this is expected to have a major impact upon the health of an individual. The pleomorphic organism under study (i.e., mycoplasma-like) is also commonly observed under these conditions. Skin lesions (eruptions) and anomalies, such as filaments, may also be more common at this stage of the condition.
PHOTOGRAPHS:
Control photograph of human red blood cell (erythrocyte). Integrity and uniformity of cell is apparent. No visible damage from any external structures or organisms. This same individual has exhibited seriously compromised erthryocytic form in the past several years. No obvious or major external manifestations (skin) of the Morgellons condition have been exhibited by this same individual during that same time period. Certain protocols being followed during that same period may have influenced the improvement of erythrocytic form. This image is a result of improved microscopy developments over recent months. Approx. magnification is 15,000x..
The condition of the blood of the same individual as reported on to the left, but approximately two years ago. This observation was reported in the paper entitled "Morgellons : A 5th, 6th & 7th Match", dated January 21, 2008. It may be worthwhile to revisit that paper, as it describes numerous similarities of form between different sample types, both biological and environmental. One significant aspect of this photograph is the exposed presence of large numbers of the chlamydia-like organisms INTERNAL to the red blood cells. This was accomplished with the Gram stain process.. The result of the testing procedure was Gram-negative and this is one of many factors that established chlamydia-like organisms as a prime candidate for identification. Please note that it is EXPECTED that the erythrocytes (red blood cells) are to be damaged from this testing process, and the integrity of the red blood cells is not relevant in this particular photograph. The importance of this photograph is the revelation of the chlamydia like organisms in large numbers internal to the cells, and the numerous sample types (environmental and biological) in which this particular organism was observed. Magnification approx. 7000x.
A critical photograph of discovery. This photograph is the result of the improved microscopy techniques developed over the past several months. The photograph reveals, for the first time, that even if the erythrocytes are intact and of good form, the chlamydia-like organisms can exist in large numbers external to the cell, or IN THE BLOOD SERUM. This fact was discovered only because of minor variations in focusing of an improved and modified camera A human blood cell is on the order of 6-8 microns in diameter; the chlamydia-like structures are sub-micron (estimated 0.3 - 0.8 microns) and can easily escape detection with conventional microscopy. This observation establishes that the intracellular presence of the chlamydia-like organism is not a sufficient basis upon which to assess the health of the blood. The presence of the organism within the blood, i.e, serum or cells, provides a more comprehensive assessment of factors that may affect the health of the individual. In addition, previous papers clearly present evidence that the presence of this particular organism is not restricted to the blood. Please see the paper referred to, along with others on this site, to review the ubiquity of the organism and related forms. Magnification approx. 10,000x.
Digital magnification focusing on the chlamydia-like organism external to the erthyrocyte (red blood cell) wall. Approx. size is 0.5 microns; this size range represents the transition range between bacteria and viruses. Indeed, chlamydia species, upon discovery, were first categorized as vriuses. Camera techniques and equipment are critical factors in making the presence of this organism visible. Magnification (digital enhancement) approx. 30,000x.
Another critical photograph in the discovery process. It has become apparent now through observation how cellular damage to the erythrocyte occurs. All indications are that the chlamydia-like organism is attracted to the cell wall of the ertyhroycyte. This photograph shows clearly the alignment of the organisms on the outside wall of the red blood cells. The linkage between the presence of the organism external to the cell (in the serum) and its attachment to the cell itself is a critical mechanism of discovery that is reported here. Furthermore, this photograph also shows the ensuing damage of the cell wall that occurs with the sustained presence of the organism in contact with the cell. This photograph comes from observation of a separate individual than that reported on in the above four photographs. This individual also does not manifest any external skin symptoms of the so-called "Morgellons" condition; the failure of skin anomalies as a suitable criteria to establish the existence of the condition has been extensively asserted by this researcher within numerous prior papers. Magnification approx. 10,000x.
An additional important photograph of discovery. This set of photographs are of the same individual as reported on in the top set of four photographs., APPROXIMATELY THREE WEEKS LATER in time. This photograph shows that dramatic changes in the condition of the blood, at least with respect to this particular organism, can occur within a period of only three weeks.. This also has since been shown to occur in reverse (again, within approximately a three week period), with a corresponding improvement in health that may or may not correspond to certain protocols under investigation. In this case, however, the existence of the organism external to the cell appears to be a resident condition, regardless of the resistance level of the cells to internal invasion. The life cycle of a red blood cell is approximately three months.
It is to be considered only as anecdotal information, but it is a fact that this individual encountered a significant onset of illness in the midst of this same time interval. The symptoms of illness did have a certain level of correspondence with those that are associated with Chlamydia pnuemonia. It is also to be considered as anecdotal information, but aerosol operations of significance were conducted during the earlier portion of this same three week interval and the week preceding. No conclusions regarding direct association with a particular illness or atmospheric conditions are being made at this time. Magnification approx. 10,000x.
Further evidence of incorporation of the chlamyida-like organism into the external wall of the erthrocytes. This can be considered as an earlier stage of the invasive process. Cellular deformation is also apparent, as is commonly observed as an impact from the organism. Upon severe invasion, the integrity of the erythrocytes is radically compromised and the organism occurs frequently within the cell (i.e., intracellular) in addition to causing exterior wall damage. Magnification approx. 10,000x.
An additional photograph which demonstrates the effect of the chlamydia-like organism upon the erthryocytes and the mechanisms of damage. Magnification approx. 10,000x.
An additional photograph which demonstrates the effect of the chlamydia-like organism upon an erthryocyte and the mechanisms of damage. Magnification approx. 10,000x.
Additional Note : The term "eruptions" vs. "lesions" has been introduced into this paper due to discussions with an individual of medical background. This individual has studied and observed the dynamics of certain skin anomalies in detail. It has been suggested that this term may be more accurate in describing the specifics of presentation, and it is correspondingly offered to the readership for consideration. Appreciation is extended to this individual for the discernment that has been provided.
U.S. hospitals and long-term care facilities annually flush millions of pounds of unused pharmaceuticals down the drain, pumping contaminants into America's drinking water, according to an ongoing Associated Press investigation.
These discarded medications are expired, spoiled, over-prescribed or unneeded. Some are simply unused because patients refuse to take them, can't tolerate them or die with nearly full 90-day supplies of multiple prescriptions on their nightstands.
Few of the country's 5,700 hospitals and 45,000 long-term care homes keep data on the pharmaceutical waste they generate. Based on a small sample, though, the AP was able to project an annual national estimate of at least 250 million pounds of pharmaceuticals and contaminated packaging, with no way to separate out the drug volume.
One thing is clear: The massive amount of pharmaceuticals being flushed by the health services industry is aggravating an emerging problem documented by a series of AP investigative stories — the commonplace presence of minute concentrations of pharmaceuticals in the nation's drinking water supplies, affecting at least 46 million Americans.
Researchers are finding evidence that even extremely diluted concentrations of pharmaceutical residues harm fish, frogs and other aquatic species in the wild. Also, researchers report that human cells fail to grow normally in the laboratory when exposed to trace concentrations of certain drugs.
The original AP series in March prompted federal and local legislative hearings, brought about calls for mandatory testing and disclosure, and led officials in more than two dozen additional metropolitan areas to analyze their drinking water.
And while most pharmaceutical waste is unmetabolized medicine that is flushed into sewers and waterways through human excretion, the AP examined institutional drug disposal and its dangers because unused drugs add another substantial dimension to the problem.
"Obviously, we're flushing them — which is not ideal," acknowledges Mary Ludlow at White Oak Pharmacy, a Spartanburg, S.C., firm that serves 15 nursing homes and assisted-living residences in the Carolinas.
Such facilities, along with hospitals and hospices, pose distinct challenges because they handle large quantities of powerful and toxic drugs — often more powerful and more toxic than the medications people use at home. Tests of sewage from several hospitals in Paris and Oslo uncovered hormones, antibiotics, heart and skin medicines and pain relievers.
Hospital waste is particularly laden with both germs and antibiotics, says microbiologist Thomas Schwartz at Karlsruhe Research Center in Germany.
The mix is a scary one.
In tests of wastewater retrieved near other European hospitals and one in Davis County, Utah, scientists were able to link drug dumping to virulent antibiotic-resistant germs and genetic mutations that may promote cancers, according to scientific studies reviewed by the AP.
Researchers have focused on cell-poisoning anticancer drugs and fluoroquinolone class antibiotics, like anthrax fighter ciprofloxacin.
At the University of Rouen Medical Center in France, 31 of 38 wastewater samples showed the ability to mutate genes. A Swiss study of hospital wastewater suggested that fluoroquinolone antibiotics also can disfigure bacterial DNA, raising the question of whether such drug concoctions can heighten the risk of cancer in humans.
Pharmacist Boris Jolibois, one of the French researchers at Compiegne Medical Center, believes hospitals should act quickly, even before the effects are well understood. "Something should be done now," he said. "It's just common sense."
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Some contaminated packaging and drug waste are incinerated; more is sent to landfills. But it is believed that most unused pharmaceuticals from health care facilities are dumped down sinks or toilets, usually without violating state or federal regulations.
The Environmental Protection Agency told assembled water experts last year that it believes nursing homes and other long-term care facilities use sewer systems to dispose of most of their unused drugs. A water utility surveyed 45 long-term care facilities in 2006 and calculated that two-thirds of their unused drugs were scrapped this way, according to the National Association of Clean Water Agencies.
An internal EPA memo last year included pharmaceuticals on a list of "major pollutants of concern" at health care businesses. Still, few medical centers keep comprehensive records of drugs they cast down toilets or into landfills. When data are kept, drugs and tainted packaging are combined in the same totals.
In an attempt to quantify the problem, the AP examined records in Minnesota, where state regulators have pushed hospital administrators to keep closer track than elsewhere. Fourteen facilities were surveyed, in a range of settings from rural to urban. The AP projected those annual totals onto the national patient population for hospitals and adjusted for the relatively lower pharmaceutical use of Minnesotans. Since long-term care facilities generate more drug waste than hospitals, the AP conservatively doubled the number.
That calculation produced an estimate of at least 250 million pounds of annual drug waste from hospitals and long-term care centers, further complicated by the fact experts say drugs might account for only up to half of pharmaceutical waste, while the rest is packaging.
The AP estimate excludes many other sources of health industry drug waste, from doctors' to veterinary offices. Smaller medical offices typically dispose of expired samples and unwanted drugs like ordinary consumers — with little forethought.
Alan Davidner, president of Vestara of Irvine, Calif., which sells systems to manage drug waste, says his limited sampling suggests the health care industry's contribution could even be higher.
Plus, untold amounts of pills and tablets are being thrown away each year at federal and state correctional institutions.
At a state prison in Oak Park Heights, Minn., nurse Linda Peterson says the hospital unit serving inmates statewide has been throwing away up to 12,000 pills a year. She says some heart medicines and antibiotics are simply chucked into the trash. Tightly regulated narcotics susceptible to abuse go down the toilet.
"We flush it and flush it and flush it — until we can't see any more pills," she says.
She notes the presence of nursing homes, a hospital and another prison in the same area. "So what are all these facilities doing, if we're throwing away about 700 to 1,000 pills a month?"
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The EPA is considering whether to impose the first national standard for how much drug waste may be released into waterways by the medical services industry, but Ben Grumbles, the EPA's top water administrator, says a decision won't be made until next year, at the earliest.
So far, regulators have done little more than politely ask the medical care industry to stop pouring drugs into the wastewater system. "Treating the toilet as a trash can isn't a good option," says Grumbles.
Some think it's time to do more than ask. "It's strange that we have rules about the oil from your car; you're not allowed to simply flush it down the sewer," says U.S. Rep. Tim Murphy, R-Pa. "So why do we let these drugs, without any kind of regulation, continue to be flushed away in the water supply?"
Landfills are one alternative. At least they don't empty directly, and immediately, into waterways like some sewage.
Marjorie E. Powell, a lawyer for the Pharmaceutical Research and Manufacturers of America, says landfills are "more environmentally friendly," while EPA spokeswoman Roxanne Smith contends that landfilling of hazardous pharmaceutical waste "poses little threat to the public."
Still, Grumbles acknowledges that landfills, while safer, are not a permanent solution. That's because pharmaceuticals can eventually reach waterways from landfills through leaks or intentional releases of treated seepage known as leachate.
An agency staffer wrote in a memo last year: "EPA recognizes that residuals in the leachate could contaminate groundwater supplies and ultimately reach water treatment plants, but disposal into the trash is currently considered a BMP" — or best management practice.
Already, researchers have detected trace concentrations of drugs — including the pain reliever ibuprofen and seizure medicine carbamazepine — in seepage or groundwater near landfills.
Environmental professionals outside government are reaching a consensus that incinerators are the best disposal method.
"That's the best practice for today because we don't really know what the hell to do with the stuff," says industrial engineer Laura Brannen, an executive at Waste Management Healthcare Solutions, of Houston. She says burning destroys more drug waste than all other methods, though some contaminants may escape in smoke and ash.
On a recent day at Abbott Northwestern Hospital in Minneapolis, Mary Kuch was getting ready to squirt leftovers from a syringe of hydromorphone, a powerful morphine derivative, into a sink. When she started out in nursing 18 years ago, "I took it for granted, because I was a young nurse, and that's what other nurses did," she says. "But I did find it strange."
These days, only four gallons — drugs with high potential for abuse — go down the hospital's drains each year. Nearly all leftover medicine and contaminated packaging are instead tossed into black bins and rolled to a hospital storage room crammed with scores of 55-gallon drums.
There, waste-company employee Bryant Sears — dressed in a Teflon suit, rubber gloves and goggles — conducts a sorting operation. Pills, blister packs and liquid medicines collected in vials, along with syringes and IV bags, are separated out according to differing disposal standards and methods. Occasionally, he glances at a wall-sized placard with details on which drug goes where — hazardous waste in one barrel, nonhazardous in another. A roll of "hazardous waste" stickers hangs from a pole on the wall.
Sears points to some epinephrine, a heart drug, saying, "Now that it's past its expiration date, it's waste."
These leftovers and discards ultimately will be incinerated.
EPA's Smith says even municipal burners unapproved for hazardous waste "will destroy all but a minute fraction" of organic compounds — the kind found in pharmaceuticals.
But Stephen DiZio, a manager with the California Department of Toxic Substances Control, says not so fast. "I don't think we're encouraging incineration of anything. The public outcry would be so great."
The push for incineration hides an irony. Several decades ago, drug waste was routinely chucked into the trash and burned in hospital or city incinerators.
Then came a national campaign against air pollution. Most hospitals shut down their burners, and city incinerator managers became pickier about what they'd accept. With options restricted, hospitals began shipping more drug waste to landfills — and dumping more into toilets and sinks.
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A few choices are expanding. Some states have passed laws to make it easier to contribute unused drugs to charity pharmacies that supply low-income patients.
Also, a small share of unused drugs is shipped back to manufacturers for credit — and incineration, waste consultants say. But the drugs are supposed to be sent back in original packaging — sometimes impractical because the packaging is discarded or damaged.
Several long-term care residences want to deploy automatic drug-dispensing machines that suppliers would refill often to reduce waste.
While not yet practical, there are several experimental technologies, such as destroying trace drugs with an electrical arc, microwaves, or caustic chemicals.
Increasingly, some bureaucrats and health professionals are suggesting that drug makers help pay costs of managing drug waste. But the pharmaceutical industry says there's insufficient evidence of environmental harm to warrant the expense.
But impatience is mounting. Even the EPA has begun to take such suggestions seriously. Grumbles says drug makers "should do more for product stewardship and meds retrieval now." He says it would be unwise to wait for all the proof.
For now, many health facilities, especially small ones, are put off by the cost of proper handling. Drugs deemed hazardous by the EPA — about 5 percent of the market — might cost up to $2 a pound to incinerate in a certified hazardous waste incinerator, says Vestara's Davidner. A pound might cost 35 cents to burn in a regular trash incinerator.
Tom Clark, an executive at the American Society of Consultant Pharmacists, wonders: "When you can flush it down the toilet for free, why would you want to pay — unless there's some significant penalties?"
___
The AP National Investigative Team can be reached at investigate (at) ap.org
Several years ago, I had a man seeking asparagus for a friend who had cancer. He gave me a photocopied copy of an article, entitled, `Asparagus for cancer' printed in Cancer News Journal, December 1979.
I will share it here, just as it was shared with me: 'I am a biochemist, and have specialized in the relation of diet to health for over 50 years.
Several years ago, I learned of the discovery of Richard R. Vensal, D.D.S. that asparagus might cure cancer. Since then, I have worked with him on his project. We have accumulated a number of favorable case histories.
Here are a few examples:
Case No. 1: A man with an almost hopeless case of Hodgkin's disease (cancer of the lymph glands) who was completely incapacitated. Within 1 year of starting the asparagus therapy, his doctors were unable to detect any signs of cancer, and he was back on a schedule of strenuous exercise.
Case No. 2: A successful businessman 68 years old who suffered from cancer of the bladder for 16 years. After years of medical treatments, including radiation without improvement, he went on asparagus. Within 3 months, examinations revealed that his bladder tumor had disappeared and that his kidneys were normal.
Case No. 3: a man who had lung cancer. On March 5th 1971, he was put on the operating table where they found lung cancer so widely spread that it was inoperable. The surgeon sewed him up and declared his case hopeless. On April 5th he heard about the asparagus therapy and immediately started taking it. By August, x-ray pictures revealed that all signs of the cancer had disappeared. He is back at his regular business routine.
Case No. 4: A woman who was troubled for a number of years with skin cancer. She finally developed different skin cancers which were diagnosed by asking specialist as advanced. Within 3 months after starting on asparagus, her skin specialist said that her skin looked fine and no more skin lesions. This woman reported that the asparagus therapy also cured her kidney disease, which started in 1949. She had over 10 operations for kidney stones, and was receiving government disability payments for an inoperable, terminal, kidney condition. She attributes the cure of this kidney trouble entirely to the asparagus.
I was not surprised at this result, as `The elements of Materia Medica', edited in 1854 by a Professor at the University of Pennsylvania, and stated that asparagus was used as a popular remedy for kidney stones. He even referred to experiments, in 1739, on the power of asparagus in dissolving stones.
We would have other case histories but the medical establishment has interfered with our=2 0obtaining some of the records. I am therefore appealing to readers to spread this good news and help us to gather a large number of case histories that will overwhelm the medical skeptics about this unbelievably simple and natural remedy. For the treatment, asparagus should be cooked before using, and therefore canned asparagus is just as good as fresh.
I have corresponded with the two leading canners of asparagus, Giant and Stokely, and I am satisfied that these brands contain no pesticides or preservatives.
PROCEDURE: 1) Place the cooked asparagus in a blender and liquefy to make a puree, and store in the refrigerator.
2) Give the patient 4 full tablespoons twice daily, morning and evening.
Patients usually show some improvement in from 2-4 weeks. It can be diluted with water and used as a cold or hot drink. This suggested dosage is based on present experience, but certainly larger amounts can do no harm and may be needed in some cases.
As a biochemist I am convinced of the old saying that `what cures can prevent'. Based on this theory, my wife and I have been using asparagus puree as a beverage with our meals.
We take 2 tablespoons diluted in water to suit our taste with breakfast and with dinner. I take mine hot and my wife prefers hers cold.
For years we have made it a practice to have blood surveys taken as part of our regular checkups.
The last blood survey, taken by a=2 0medical doctor who specializes in the nutritional approach to health, showed substantial improvements in all categories over the last one, and we can attribute these improvements to nothing but the asparagus drink...
As a biochemist, I have made an extensive study of all aspects of cancer, and all of the proposed cures. As a result, I am convinced that asparagus fits in better with the latest theories about cancer. Asparagus contains a good supply of protein called histones, which are believed to be active in controlling cell growth. For that reason, I believe asparagus can be said to contain a substance that I call cell growth normalizer. That accounts for its action on cancer and enacting as a general body tonic. In any event, regardless of theory, asparagus used as we suggest, is a harmless substance.
The FDA cannot prevent you from using it and it may do you much good.. It has been reported by the US National Cancer Institute, that asparagus is the highest tested food containing glutathione, which is considered one of the body's most potent anticarcinogens and antioxidants.
(Copy of Email sent to all Arizona State Senate and House members) From Dick Fojut in Tucson, AZ 9-19-9
In a one-sided "frenzy," our Major Corporate "news" Media are trying to convince us we MUST all get the SWINE FLU VACCINE, declaring the vaccine totally safe!
But NOT ONE medical expert who disagrees (Blaylock, Mercola, Horowitz, Moulden, etc.), has been reported! We should all be suspicious...
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Avoid ALL VACCINATIONS warns Dr. Andrew Moulden
The public - and most medical doctors - do not understand HOW (all) vaccinations damage our bodies.
Dr. Andew Moulden explains that repeated VACCINATIONS (even aside from whatever ingredients the vaccines contain) produce additive ISCHEMIC "STROKES" in the 60,000 miles of microscopic blood vessels.
When the Immune System is OVER-stimulated responding to fight any foreign substance vaccine poison injected, the blood vessels (especially the tiniest ones) become CLOGGED with "armies" of white blood cells - the "soldiers" sent to combat the vaccine poison.
Result: Ischemic "strokes" from clogged blood vessels. Blood flow is impaired, preventing sufficient oxygen from reaching the brain, heart and other tissues. Removal of waste products and toxins is also impaired.
All vaccines have been causing "burns" to body and brain. The damage is additive.
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One medical expert the major media are NOT interviewing is Dr. Andrew Moulden who WARNS we should AVOID ALL VACCINATIONS - and explains WHY in the following article...
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Excerpts only from following VACTRUTH article...
ALL VACCINATIONS ARE CAUSING IMPAIRED BLOOD FLOW (Ischemia), CHRONIC ILLNESS, DISEASE AND DEATH FOR US ALLSPROVENSsee for yourself (at web site).
ALL vaccines are causing immediate and delayed, acute and chronic, waxing and waning, impairments to blood flow, throughout the brain and body. This IS causing us all to become chronically ill, sick, and causing brain damages along a continuum of clinically silent to death. This is causing ischemic "strokes". In some respects, this is also "aging." Since the damages are microscopic, we cannot see them as they occur. However, we can now see the neurological aftermath of these damages - within hours and days of vaccination - all vaccinations.
M.A.S.S. is an acronym for many chronic illnesses and diseases that impair blood flow - "Moulden Anoxia Spectrum
Syndromes."
In essence, we are creating disease and chronic illness by an over-zealous activation of a natural set of healing mechanisms in human physiology - a component phase of the MASS physiological response.
Remarkably, it is not so much the specific "germs and toxins" that are causing death and disease. It is the response of the body and blood to foreign substances entering the blood and tissues that causes pathology.
The cellular and tissue damages are additive with each exposure.
All vaccines have been causing "burns" to body and brain.
Once the blood vessels are damaged, to a critical point, the pathological process can take on a self-perpetuating life of its own - from infants to teenagers to adults, to companion pets alike.
When microscopic end blood vessels are destroyed (closed off), as blood flow diminishes and starts to "sludge", this impairs healing, cellular functioning, and promotes build-up of toxins, heavy metals, and pathogens in circumscribed tissue areas.
ALL VACCINATIONS ARE CAUSING IMPAIRED BLOOD FLOW (Ischemia), CHRONIC ILLNESS, DISEASE AND DEATH FOR US ALLSPROVENSsee for yourself.
By Andrew Moulden MD, PhD
www.BrainGuardMD.com
Medical & Neurobehavioral Therapies Director
www.Therapies4Kids.com
www.BrightStepsForward.org
Former Leader - www.CanadianActionParty.ca
Dr. Moulden has joined and supports the Christian Heritage Party of Canada
This is a stern, yet humble, warning to all citizens of the globe. It is now proven that we are all being harmed by repeat vaccinations. This evidence must be circulated broadly in light of the imminent Fall, 2009 plan to turn North American schools into MASS vaccine centers to institute triple flu vaccine to us all. Children will be the first to be injected with experimental flu vaccines. The entire vaccine industry, as it turns out, has been experimental. We did not know that we were causing damages - for us all.
In case you are wondering what will happen, the answers are contained in this article. The same thing will happen as has been happening with all vaccines. Clinically silent ischemic brain and body damages will happen. The only difference is that you can now see these damages, with your own eyes, in the here and now, in real time, and in your family photos going back fifty or more years if you have to.
ALL vaccines are causing immediate and delayed, acute and chronic, waxing and waning, impairments to blood flow, throughout the brain and body. This IS causing us all to become chronically ill, sick, and causing brain damages along a continuum of clinically silent to death. This is causing ischemic "strokes". In some respects, this is also "aging." Since the damages are microscopic, we cannot see them as they occur. However, we can now see the neurological aftermath of these damages - within hours and days of vaccination - all vaccinations.
[View with PicLens on web page]
In Revelations 18:4 by the epistle of Saint John we are told: "And I heard another voice from Heaven saying "Come out of her my people that ye be not partakers of her sins and that ye receive not of her plagues." All vaccinations, as you can now clearly see, are causing chronic illness and mass disorders on mass scales. The global health consequences clearly amount to plaques.
As a medically trained Doctor, a PhD trained neuroscientist/neuropsychologist, with a Masters degree in Child/language neurodevelopment, I have been trained to follow clinical observations to empirical assessment couched within the scientific model we rely upon to answer questions of: What is normal and what is not? What is cause? What is coincidence? What is factual? What is fancy? What is reproducible? What is random? What is measurable? What is predictable? What is truth? What is consequence? What is "going on"?
Science is only a man made truth-seeking tool. It is fallible. It is a statistical, probabilistic mathematical model. It has limitations. Wielded for profit - truth can become lost.
Scientific methods, design, and analyses can just as soon hide the truth as they can discover truth, or create 'truth" de-novo.
Science cannot replace God-given tools of common sense and observation we all have. You do not need statistical probabilistic mathematical models, wielded by experts, to deny what you can see with your very own eyes.
If you place your hand on a hot stove element, you will be burned. If you do not experience pain and you cannot see the burn, then you will not learn that touching hot stove elements is harmful.
All vaccines have been causing "burns" to body and brain. The brain has no pain receptors. You will not feel the pain. You can, however, see the footprints of these "burns" immediate and delayed, from each vaccination. The evidence was before our eyes all along. We simply did not appreciate what these "burns" meant let alone that they were emerging, after each vaccination. The "burns" are largely to internal organ systems. We can ALL now see the damaging effects of these "burns" with our own eyes.
As a physician, it is my sworn duty to cause no harm. As a human being, it is my duty to watch over my fellow beings. As an educator, it is my responsibility to teach awareness and understanding. As a scientist, it is my duty to separate cause from coincidence. As a Christian, it is my value to do unto others, as I would have others do unto myself. As a man, it is my responsibility to stand up to power, with truth and understanding, when those that wield power are in error.
My statements are not the words of a zealot. These are the words of integrity, couched with understanding, that has the potential to reside in every one of you.
Seek, and you shall find. Knock, and the door shall be opened unto you. I have sought. I have knocked. The door has been opened. I have found the truths I was seeking. The answers have not come from my own understandings. The answers are simply self-evident - res ipsa loquitur - the thing speaks for itself.
All vaccinations cause brain damage, disease, chronic illness, aging, and death - res veritas loquitur - the truth speaks for itself. If you do not seek, if you do not knock, if you do not look, if you trust your own understandings, then caveat emptor - buyer beware.
We have answers. We have solutions - www.Therapies4Kids.com . We cannot provide solutions or treatments to a medical system and model that denies it is sick.
My training has taught me how to translate anecdotal clinical observations into empirically sound clinical measurements in medicine, neurodevelopment, and human physiology. This is especially so in dealing with functions of the human brain and behavior.
The pictorial evidence attached to this article represents a small sample of the data I have now collected from thousands. The truth about all vaccinations causing harm is now available for your understanding.
The truth is frightening, disheartening, alarming, and now self-evident.
We have made a global medical mistake based on a lack of knowledge and understanding. We have translated forest fires for 1% of the population into chronic brush fires for the entire population. The brush fires are chronic illness and disease, least of which are the neurodevelopmental disorders.
12-IMAM Brain Damage measurement system
The measurement system I have created is based on the 12 cranial nerves and the clinical skills Doctors are supposed to use to assess brain function and integrity. I have called the measurement system the 12 "Eye" M.A.S.S. Anoxia Measures (12-IMAM).
[View with PicLens on web page]
M.A.S.S. is an acronym for many chronic illnesses and diseases that impair blood flow - "Moulden Anoxia Spectrum Syndromes." One-size-fits-all global vaccination schemes have created M.A.S.S. disorders on MASS scales. MASS disorders, from infectious diseases to vaccinations, have a common sequence of injuries which includes impaired blood flow, oxygenation, blood carrying capacity, and non-specific immune hyper-stimulation.
In essence, we are creating disease and chronic illness by an over-zealous activation of a natural set of healing mechanisms in human physiology - a component phase of the MASS physiological response.
Remarkably, it is not so much the specific "germs and toxins" that are causing death and disease. It is the response of the body and blood to foreign substances entering the blood and tissues that causes pathology. The state of the blood, the nature of the triggers, the state of the immune system relative to repeat antigenic challenges, conspires to effect damages along a continuum of harm - all organ systems can be affected.
The cellular and tissue damages are additive with each exposure. Direct vaccination is no longer necessary to be vaccine injured. Vaccinations are not the only trigger to pathology. Serial (repeat) vaccinations aggravate the core problems. Once the blood vessels are damaged, to a critical point, the pathological process can take on a self-perpetuating life of its own - from infants to teenagers to adults, to companion pets alike.
Four features of the 12-IMAM measurement system that you can now see, include the eye turning in, the eye turning out, the smile becoming asymmetrical, and the eye blinks coming out of sync. These are strokes, from ischemia, throughout the brain and body, for all. Repeat vaccination is the primary culprit, however, vaccination is not the only cause of this MASS problem in human physiology.
WHITE BLOOD CELL IMMUNE RESPONSE - CAUSING DISEASE
If you repetitively dump a million rubber duckies at the mouth of the Mississippi river, where they become lodged downstream will vary from truckload to truckload. Repeat vaccination, by its effects on the non-specific immune system, is like dumping the triggers which call for repetitive "dumping" of millions of rubber duckies (white blood cells) at the head of the Mississippi river. Once the "triggers" are sequestered in various bottleneck end tributary river branches, they continuously attract more "rubber duckies" to these areas. This impairs blood flow and leads to a net loss of tissue by acute or slow strangulation.
It is the act and magnitude of the "rubber duckies" being called to these end vascular areas that causes congestion, impaired blood flow, lack of oxygen, glucose and nutrients to the affected tissue areas. Without oxygen or nutrients, he cells lining the walls of capillaries self-cauterize (clamp shut). This is a healing mechanism that must be instituted in order to prevent leakage of plasma and or blood into tissues.
With MASS impairs blood flow and oxygenation to the tiny blood vessels in the eye, we sometimes see "retinal hemorrhages." When MASS occurs in the brain, we call it intracerebral bleeding. When MASS occurs to the bones, we call it brittle bones. Collectively, we label this "shaken baby syndrome."
A HORSE BY SEVERAL NAMES
When the blood sludging MASS process happens to brainstem areas controlling automatic respiration, the central drive for respiration is lost. We call this sudden infant death or sudden death.
When M.A.S.S. happens to the descending motor tracts in the brain, we call this paralysis, Guillain-Barré Syndrome, infantile paralysis, seizures, encephalopathy.
CBS News has found that since 1988, the vaccine court has awarded money judgments, often in the millions of dollars, to thirteen hundred and twenty two families whose children suffered brain damage from vaccines. All of these children will show the same IMAM-12 ischemic brain damages as children who have been rendered autistic, learning disabled or dead after vaccinations. The process that causes brain damages from vaccination is also the same MASS process that causes all damages after vaccination - all vaccinations. It is not the vaccines doing this. It is "M.A.S.S." ischemia. Vaccines have been inadvertently concocted to induce MASS.
When M.A.S.S. happens to internal organs or connective tissue, we call it colitis, irritable bowel, fibromyalgia, chronic fatigue, post-concussion syndrome, a psychiatric disorder.
When M.A.S.S. happens in infants, and children, we call it autism-spectrum disorders, specific learning disabilities, attention deficit disorders, Aspergers syndrome, global developmental delay, and some childhood cancers. Sometimes M.A.S.S. causes or compounds cerebral palsy - both conditions result from impaired oxygenation and blood flow to the brain.
Sometimes we call M.A.S.S. "Kawasaki" syndrome, "Moyamoya", 'aseptic meningitis", "encephalopathy", "Meningitis", hypsarrythmia, infantile spasms, West syndrome, or febrile seizures. It is all simply M.A.S.S. ischemia.
Autism and schizophrenia are the same ailment, in physiology, albeit the triggering pathways for schizophrenia (loss of immunological tolerance) has a different trajectory than acquired autism-spectrum disorders. Nonetheless, a similar mechanism is at work for both ailments - MASS ischemia from derailed blood flow.
When MASS happens in teen girls after Gardasil vaccination, it creates death, disease, illness, clouded thinking, and paralysis. Remarkably, the Gardasil shots are simply completing the silent ischemic vascular damages, to body and brain that were caused from each childhood vaccination the girl received. Sudden death is due to loss of central drive for respiration in the same manner that vaccinations are causing many cases of sudden infant death. Sometimes seizures may also occur. The course can be waxing and waning. All vaccines are causing these problems - silently, in an additive manner over each vaccination, for all of us. No one is spared.
When MASS happens in military and armed services personnel, this causes "Gulf war Syndrome."
When MASS happens to schizophrenia patients being treated with powerful psychotropic drugs that de-rail white blood cell functions, sudden "unexplained" death can occur by the same MASS sudden death sequence that vaccinations sometimes induce in infants and teen girls.
When MASS happens in the elderly, it causes a slow, step-wise deterioration in cognitive functions - we call this dementia. This is slow strangulation of brain tissue from ischemia at the microscopic level.
Febrile seizures are not caused by "fever". The fever expands the diameter of the tiny blood vessels so that more white blood cell infection fighting "soldiers" can traverse down the 'roads." When the blood vessel roads become jammed, by too many white blood cells, and altered fluid dynamics, there is ischemia. Ischemia causes a lack of oxygen to the brain.
No oxygen to electrically active cells causes depolarization. In the heart, ischemia causes arrhythmia - a seizure to the heart. In the brain, ischemia causes seizures - arrhythmia to the brain. Seizures are a symptom of impaired blood flow and oxygenation just like vaccine induced autism-spectrum is a symptom of the same process.
You can have autism without seizures. You can have seizures without autism. You can have brain damages with or without autism or seizures. This is all ischemia - immediate and delayed, from instability of blood flow dynamics.
I can make these statements of fact, and so can you, since the photographs you can now see, before and after vaccination, show we are all having ischemic microvascular strokes - silently. Some of these damages are called "bulbar palsies" and they are the exact same damages we saw from wild polio exposure as we now see from vaccinations. Remarkably, no one ever told you that wild polio and other infectious diseases, were inducing the body to cause ischemic strokes to the brain. Vaccinations induce the same process - albeit in an attenuated and chronic form.
[View with PicLens go to web page]
The ischemic brain damages, after vaccination, from infants to adults, cut across all symptom based medical diagnostic end points.
Type 1 insulin dependent diabetes mellitus is a MASS disorder, as is Parkinson Disease, Tourette's syndrome, Multiple Sclerosis, and several other neuropsychiatric disorders.
Aphasia and loss of expressive speech functions with vaccinations is called "isolation of speech syndrome" or "transcortical motor aphasia." This is caused by ischemia to end blood vessel watershed vascular territories in the brain - period.
Silent MASS ischemic strokes is how the body caused paralysis and respiratory failure from wild polio virus exposure. This is how death occurred from Smallpox. This is how swine flu vaccine caused paralysis and Guillain-Barré syndrome. This is how thalidomide caused infants to be born with no arms and legs. This is how a series of anthrax vaccines causes military veterans to give birth to children with no arms and legs 18 months after receiving the vaccine series. This is how Vioxx caused heart attack and stroke. This is how pre-natal German measles caused autism-spectrum and organ damages. This is how a systemic drop in maternal blood pressure, during gestation, causes Mobius syndrome (and autism-spectrum). This is how repeat vaccination is causing dementia.
M.A.S.S. is how vaccinations are causing a multitude of chronic illnesses and disease. It is not the germs causing this problem. It is the response of the body to de-railed and unbalanced immune challenges.
THE ROADS TO ROME ARE LOST
When microscopic end blood vessels are destroyed (closed off), as blood flow diminishes and starts to "sludge", this impairs healing, cellular functioning, and promotes build-up of toxins, heavy metals, and pathogens in circumscribed tissue areas. The ischemia causes disease, autoimmunity, and some cancers if the cells are forced to function in a low energy, low oxygen state. It is not so much "Rome" that is being damaged as it is the roads to and from Rome that are being damaged first. The "fall of Rome" follows as the Romans are starved, strangulated, and forced to live in a "City" that can neither bring supplies in to repair damages, nor can it remove waste from within its central territory by efficient means to meet supply and demand. This is an example of too many Roman Centurions (white blood cells) called to Rome to protect the City. The Centurions, by magnitude and response, block the roads to Rome by virtue of a chronic "Call to Arms."
There is a better way to prevent disease. Vaccination only masks the cause of disease, it does nothing to address the core problem in physiology - the non-specific M.A.S.S. response and colloidal stability of blood flow dynamics. There are alternative solutions to controlling infectious diseases in populations that do not require injecting foreign substances into your body.
Doctors, pathologists, and coroners cannot see what is right before their very eyes. The cause of sudden infant death, and dementia, in life, is impaired microscopic blood flow. In death, there is no blood flow. Medical science cannot find cause of death and disease, in life, from looking at dead tissue, when the dead tissue exhibits the same cause of death during life - no microscopic end vascular blood flow.
ELECTRODYNAMICS OF BODY FLUIDS - CAUSING DISEASE
A 300 foot Giant Redwood can transport water (nutrients and oxygen) against gravity from the ground to the very top of the tree. The redwood has no moving parts or pump. This transpiration feat is accomplished by the electrodynamics nature of water.
Human blood is 95% water. The human body is 75% water by weight. In physiology, when the electrodynamics quality of water is de-railed by heavy metals, infectious diseases, vaccinations, and other adverse influences, the water which carries oxygen, nutrients, glucose, and healing cells cannot traverse tiny blood vessels to deliver their life sustaining cargoes. This is especially true in end vascular "pipes" that are uniquely oriented against gravity. Blood flow is a function of the colloidal stability of the blood and its products.
The human blood is a colloidal suspension. Proteins. Amino acids, heavy metals etc.. are carried in suspension within the blood as a function of the net negative charge within the system. Drop the net negative charge, flow pressures in tiny end blood vessel "pipes" will start to sludge, agglomerate, and increase viscosity of blood in circumscribed microscopic vascular areas. Medical science has no live imaging tool powerful enough to see this process as it is happening.
By analogy, coffee cream remains in a fluid state when it is moving. If the cream remains stagnant in your coffee cup for several days, it will phase change into a gel. Stagnant blood also turns to sludge and "gel" when it stops moving in a spiral column. Stagnation causes an increase in mass as blood products "come together" to form various degrees of sludge and "gel".
Agglomerates of sludged blood products cannot traverse microscopic blood vessels designed to carry oxygen transporting red blood cells, in single file.Capillary blood vessels oriented against gravity are uniquely susceptible. Forward blood flow momentum is a function of the negative charge and "spin" in fluid dynamics which keeps particles with mass separated from one another.
Newtonian laws of physics govern how objects with mass move in our universe . The "Big G" is Newton's Universal Law that Force equals Acceleration x MASS. Increasing MASS (as in sludged blood) with no net increase in Force causes deceleration and no forward flow. No forward flow translates into no oxygen or fuel delivery. For the brain, and body, this causes hypoxia (low oxygen), anoxia (no oxygen) and ischemia (impaired blood flow).
In terms of vaccine damages, impaired forward blood flow in end vascular territories creates brain and organ damages - in us all. These damages have been clinically silent - for millennia. This ischemic process, from germs, toxins, to vaccinations, is the cause of much human disease, pain, and suffering. All vaccines are causing chronic disease, in our attempts to prevent acute disease. We never got rid of the problem, as we did not know what the problem was - until now.
There are some common "end vascular" blood vessels in the human brain, irrespective of age. It is for this reason that we see the exact same measurable signs of brain damage, immediate and delayed, from all vaccinations, for us all in the same manner we saw identical damages from the wild polio virus in the 1950's. Some of these damages are called bulbar palsies (paralyses) from impaired blood flow through the brain and brainstem. They were present from deadly infectious diseases as much as they are now present from vaccinations. This is slow death, for us all, rather than a fast death, for the few.
When there is impaired blood flow there is impaired oxygen delivery to tissue. Vaccines cause impaired blood flow in an immediate, delayed, waxing and waning pattern. This impairs oxygen delivery throughout the 60,000 miles of microscopic end blood vessel networks in the brain and body. Microscopic brain tissue regions can only survive 4 minutes in an absolute oxygen deprivation state.
Cerebral Vascular Network
Whenever you impair "flow" in any riverbed system, the first areas to "dry up" downstream are the weakest trickling streams furthest from the flow source. These areas are called "end vascular networks." If an area of tissue is served by a singular blood vessel branch, these areas are called "watershed vascular territories." These tissue areas are most susceptible to damages when blood flow is partly or completely impaired upstream. For example, the finger-tips, toe-tips, nose-tips, and ear-tips are most susceptible to frost bite as they are end vascular, watershed areas in the human body.
The evidence you can now see, represents the beginning of the end of a flawed medical model and system that has caused the greatest harm, by man-kind to man-kind, in the history of recorded history. Remarkably, we managed to perpetrate these acts under the guise of the greater good, for handsome profit, endorsed by political leaders, corporate merchants, public health officials, and medical professionals alike - they don't know what they don't know - a part of the problem.
WHERE HAVE WE BEEN
Debates over the safety, efficacy, and utility of the one-size-fits-all global vaccination programs has reached a fervent pitch. According to the World Health Organization there are 43 million vaccinations administered globally, on any given day. As citizens, we are told "leave the science to scientists." If you do not have a medical or advanced science degree, your input is irrelevant." You are told children can handle ten thousand vaccinations safely as they are all attenuated, killed germs, or weakened."
The problem is that medical science has not known what to measure in order to ensure safety - for all. Now that we have the hard, clinically reproducible, see for yourself measures of neurological damages, we can now see that ALL vaccinations, just like the wild viruses in the pre-vaccine era, are causing tissue, organ, and brain damages. These damages exist along a continuum of harm. The damages are additive with each vaccination received - you can now see this. The clinically silent adverse effects include derailments of all organ systems, to death. We call these adversities by a plethora of clinical labels that are seemingly unrelated to the causal event - repeat vaccinations.
Remarkably, I can now make these bold statements as we can all now see, with our own eyes, the ischemic brain damages, for us all, across ALL vaccinations, from infancy to adulthood, immediately and delayed, irrespective of the end organ damages or clinical diagnostic labels that emerge.
We are selling you vaccines, for profit, which are causing illnesses and death. We then sell you symptom based pharmaceutical products, for profit, to treat the damages and disorders we have caused.
Remarkably, I can now say that the vaccine damages extend to the realm of cancers in addition to varied autoimmune and neurodevelopment disorders.
1-877-NOW-I-CAN
Determining the cause of a particular disease or disorder, in medical physiology, is the first "Bright Step Forward" towards providing rational, targeted, therapeutic interventions to recover from the damages by which a particular disease and disorder state emerged.
All vaccinations are causing "silent" brain and organ damages in exactly the same way that wild polio virus caused paralysis and respiratory failure and how other infectious "plaques" of days gone by, have crippled, maimed, paralyzed, and killed. This is now proven. The damages are additive and summative with each vaccination given. The organ, tissue, and brain damages have been clinically silent, - until now.
You may now see, with your own eyes and understanding, amongst your own family and loved ones,. Evidence now before the United States federal Circuit Courts on vaccine injuries proves that we have ALL been harmed, and are being harmed, by this universal one-size-fits-all vaccination program. Some of this evidence is compiled in an educational 3 disk, 6 hour DVD series entitled: "Tolerance Lost - Volumes 1 to 3.
The Tolerance Lost DVD series, a USA vaccine legal exemption guidebook, and a evidence of harm materials are available at www.BrainGuardMD.com, , or by calling 1-877-NOW-I-CAN.
For answers, solutions, assessment, and help - please contact us directly at 1-877-NOW-I-CAN. www.Therapies4Kids.com, www.BrightStepsForward.org.
There are ways to address the MASS problem and to enable healing to occur even for those that have been damaged. This does not require placing foreign substances or synthetic drugs in the human body - MASS FLO2 LIFE is where the answers must start.
God heals, and the doctor collects the fee. We have reached a time, in history, that we must return to paying fees to the master physician as the medical sciences, in dogma and discourse, has clearly led us a stray.
"Be the change we must see in the worldSone Bright Step Forward at a time."
NEXT EDITION OF SPECTRUM MAGAZINE
The global vaccination program is an evil deed, perpetrated by mankind against mankind, for profit, based on a fallible man made tool ('scientific method") that can just as soon convince you that the what you see with your own eyes is not true as it can be wielded to "prove" the non-existence of G-D.
These vaccines, as it turns out, are like a maddening wine, which political leaders and "Kings" of the earth have enabled merchants of the planet to grow rich from, at the expense of our collective health and wellness.
The next issue of Spectrum magazine will contain more of the empirical, see for yourself, data and science to explain how this has happened, why it is happening, and what we must now do to help us all.
Matthew 13:41 "The Son of man shall send forth his Angels and they shall gather out of his kingdom all things that offend them which do iniquity.
These autism children are Angels. These vaccines are iniquity. The evidence now before you beckons your spirit, body, mind, and soul to "come out of her my people" as you see God's desire and character more clearly. Mystery, Babylon the Great.
Without Faith, without hope, we are lost. Faith and hope can be found. 1-877-NOW-I-CAN
Dr Andrew Moulden MD, PhD
BrainGuardMD.com "12-IMAM"
Therapies4Kids.com ; BrightStepsForward.org
1-877-NOW-I-CAN for assessment and help
VacTRUTH Author's Note:
Other articles and media concerning Dr. Andrew Moulden:
1. Interview with Dr. Andrew Moulden
2. Video interview with Dr. Andrew Moulden
3. See how the 1976 Swine Flu Vaccine caused the same general response in the body in which Dr. Andrew Moulden is referring to in this article.
COPYRIGHT 2009
Copyright Vaccine Research Project. All Rights Reserved.
In a stunning and unexpected 6-3 ruling the right-leaning Supreme Court went against the wishes of the last president, took the wind out of the sails of health care reform of the current president, sent irresponsible Big Pharma a major wake up call, and bluntly told the arrogant FDA that they are indeed not above the rule of law. It is a major victory for every American citizen
Central to the issue is a power a struggle between the federal government and states, which in this situation meant the federal government authority to pre-empt your state rights to sue if you are injured by a drug. The FDA, acting on behalf of the Bush administration and on the side of Big Pharma, has helped tie up thousands of drug injury lawsuits across the country. The FDA, who is supposed to be protecting consumers from drug injury and ensuring a correct risk/safety picture for any person taking a drug, was instead trying to shirk their responsibility and simply claim that Americans had no right to sue. This convoluted attempt by the FDA to undermine consumer safety was one of the main themes in my 2006 book, Fight for Your Health: Exposing the FDA’s Betrayal of America. The Bush Administration had intentionally appointed anti-safety people in high positions within the FDA, starting with its Chief Counsel, Daniel Troy (and continued as a legal philosophy after Troy was forced out for his Big Pharma connections). Troy set in motion the legal problem the Supreme Court just decided. During the final years of the Bush administration cancer industry insider Andrew von Eschenbach, MD, was appointed to run the FDA, and Wall Street insider, Scott Gottlieb, MD, was second in command. These individuals sought to fully implement the FDA label as senior to any rights of citizens. Their intention was to make sure that new biotech drugs would be protected from lawsuits, as the FDA wanted to speed new and even more dangerous drugs onto the market so as to foster the development of the biotech industry. In essence, the FDA management wanted to turn the American public into one large clinical experiment, with no right of recourse when injured. This was occurring against a backdrop wherein the FDA couldn’t even name all the drugs currently on the market, had failed to demand required aftermarket follow up safety testing on drugs, and had intentionally withheld safety information on existing drugs from the public. The current situation with drugs is that almost no drug, even blockbusters and those in use for decades have an accurate risk/benefit profile. Americans who use medications are already taking risks of unknown magnitude, which is a main reason over 100,000 Americans are killed every year and over 3 million are injured so seriously they need hospital care (ironically, over half those injuries occur while already in the hospital). The FDA knows full well that when a drug is approved for the market the full extent of the side effects won’t be known for years. History shows us time and again that Big Pharma actively hides risk data from the FDA and pays for “science” that distorts reality. This irresponsible behavior goes along with closed-door negotiations with the FDA, and has resulted in numerous drug disasters like Vioxx. FDA managers oftentimes go against the wishes of their own safety scientists and then move on to six figure salaries in the industry they regulate. Doctors are not apprised of the actual risks and consumers are in the dark. Currently, there are 450,000 additional new cases of heart failure every year in Americans over 65, a fact that parallels the increased use of heart-weakening statins in this older group. It is only a matter of time before the shoe drops on the 20-billion-dollar-a-year statin industry. The FDA insistence that a drug label, based on what is known at the time of approval, should supersede citizen’s states rights to sue if they were injured, has almost nothing to do with consumer safety. Rather, it is a federal power grab that is in the best financial interests of Big Pharma and Big Biotech, industries that do not have consumer safety as their top priority. By the way, don’t think President Obama is on the side of the citizens. In the health care section of the stimulus bill, there is specific pre-emption language. If the federal government is in charge of health care it will be named in future lawsuits when patients are injured from the care it doles out or doesn’t allow. The current Supreme Court ruling will undermine any system of federal health care wherein the drugs being used are injuring people. Experts believe this system is so badly broken, due to gross FDA management incompetence, that it will take 10 years of studies and many billions of dollars just to understand the actual risks of the drugs Americans are already taking. In writing for the majority, Justice John Paul Stevens put Big Pharma on notice. The defendant in this case, Wyeth, had argued that it could not comply with both federal and state law. Stevens told them they had a fundamental misunderstanding of regulation and were trying to hide behind the FDA, going on to say that it is a central premise of federal drug regulation that the manufacturer bears responsibility for the content of its label at all times. That is not the news Big Pharma wanted to hear. Stevens went on to write that there was no merit in the argument that the FDA’s labeling decisions could supersede state law, saying that this argument was “an untenable interpretation of congressional intent and an overbroad view of an agency’s power to pre-empt state law.” He pointed out that the FDA tried to push this on the public without any opportunity for comment from the public or from states, all done against a backdrop wherein the FDA is not able to keep up with safety issues in the first place, meaning that the FDA position lacked “thoroughness, consistency and persuasiveness.” Stevens stated that under such lacking standards the Bush position “is entitled to no weight.” This is a major victory for all Americans and for states. While the case itself is on the topic of Big Pharma and the FDA, the ruling is sweeping in nature and will extend far beyond prescription drugs. States have just been handed a major legal ruling against the ever-growing incursion of federal power.
In a back room of New Scientist's offices in London, I sit down at a table with the Russian biochemist Mikhail Shchepinov. In front of us are two teaspoons and a brown glass bottle. Shchepinov opens the bottle, pours out a teaspoon of clear liquid and drinks it down. He smiles. It's my turn.
I put a spoonful of the liquid in my mouth and swallow. It tastes slightly sweet, which is a surprise. I was expecting it to be exactly like water since that, in fact, is what it is - heavy water to be precise, chemical formula D2O. The D stands for deuterium, an isotope of hydrogen with an atomic mass of 2 instead of 1. Deuterium is what puts the heavy in heavy water. An ice cube made out of it would sink in normal water.
My sip of heavy water is the culmination of a long journey trying to get to the bottom of a remarkable claim that Shchepinov first made around 18 months ago. He believes he has discovered an elixir of youth, a way to drink (or more likely eat) your way to a longer life.
Many anti-aging medications are based on supplementing your body's own defenses with antioxidant compounds such as vitamin C and beta-carotene, though there is scant evidence that this does any good.
Shchepinov realized there was another way to defeat free radicals. While he was familiarizing himself with research on aging, his day job involved a well-established - if slightly obscure - bit of chemistry called the isotope effect. On Christmas day 2006, it dawned on him that putting the two together could lead to a new way of postponing the ravages of time.
The basic concept of the isotope effect is that the presence of heavy isotopes in a molecule can slow down its chemical reactions.
All of this is conventional chemistry: the isotope effect was discovered back in the 1930s and its mechanism explained in the 1940s. The effect has a long pedigree as a research tool in basic chemistry for probing the mechanisms of complex reactions.
Shchepinov, however, is the first researcher to link the effect with aging. It dawned on him that if aging is caused by free radicals trashing covalent bonds, and if those same bonds can be strengthened using the isotope effect, why not use it to make vulnerable biomolecules more resistant to attack? All you would have to do is judiciously place deuterium or carbon-13 in the bonds that are most vulnerable to attack, and chemistry should take care of the rest.
Found in markets under the brand names NutraSweet, Equal, E951, Canderel, and Benevia, aspartame (“APM”) has been sold for many years now as a safer sweetener than sugar or saccharin. And since aspartame is made of two amino acids that naturally occur in many foods, it is easy to convince consumers that this “natural” product is safe. Too many years have gone by since aspartame was approved by the Food and Drug Administration (“FDA”) for use as a sweetener, despite convincing evidence presented that this artificial product posed serious safety risks. New awareness of these risks, however, is bringing the curtain down on this charade.
The Risks Were Known at the Time
Listen in on the Senate Congressional Hearing on aspartame recorded in the Congressional Record of May 7, 1985, where Senator Howard Metzenbaum, an outspoken critic of aspartame, said, “G.D. Searle Company has not demonstrated to a reasonable certainty that the use of aspartame in soft drinks will not adversely affect human health as a result of the changes such use is likely to cause in the brain chemistry. The extensive deficiencies in the stability studies conducted by Searle render those studies inadequate and unreliable.”
In earlier submissions in 1983 to the FDA, the National Soft Drink Association (“NSDA”), representing American soda makers, emphatically objected to any government approval of the deadly chemical with an extensive, detailed written testimony, including these statements: ”Aspartame is inherently, markedly and uniquely unstable in aqueous media. In a liquid, such as a soft drink, APM will degrade as a function of temperature and pH. Higher temperatures and more acidic liquids increase the rate of degradation. . . . The inability to account for as much as thirty-nine (39) percent of APMs decomposition products is significant. With such a high unknown factor, judgments about the safety of APM in soft drinks cannot be made confidently.” (1983, 1985; see http://www.gene.ch/gentech/1998/May-Jul/msg00127.html
Aspartame’s Metabolic Offspring
What were these unnamed “decomposition products” referred to in the NSDA’s objection? They were:
Methyl Alcohol: Class-A carcinogen, cumulative poison, narcotic. One ounce is fatal.
Formaldehyde: Embalming fluid, kills all living things.
Formic Acid: Fire-ant poison, toxic even in minute quantities.
Diketopiperazine: Promotes brain tumors.
Amino Acids
There are twenty amino acids in our foods, which buffer each other and are metabolically selected competitively for protein construction. But some are toxic when isolated and unaccompanied by the others. Aspartame contains two synthetic ones that are toxic when isolated.
Aspartic Acid (40% of APM): Like MSG, aspartic acid is an excitotoxin. It can excite neurons to fire at an accelerated rate until they exhaust and die, and it destroys brain cells.
Phenylalanine (50% of APM): Deadly, phenylalanine lowers the seizure threshold and depletes serotonin, triggering psychiatric and behavioral problems. Extremely harmful to the unborn, phenylalanine is neurotoxic, causing abortions, birth defects and mental deficiency, as well as manifold neurological damage.
Professor of Pediatrics and Director of the Division of Medical Genetics at Emory University in Atlanta, Georgia, Dr. Louis J. Elsas, said in Congressional testimony: “I have spent 25 years in biomedical sciences trying to prevent birth defects caused by excess phenylalanine. Therein lies my basic concern, that aspartame is in fact a well known neurotoxin and teratogen [causes birth defects] which in some as yet undefined dose will …. irreversibly in the developing child or fetal brain produce adverse effects” [November 8, 1987]
Earlier, in a letter submitted by Dr. Elsas to the Committee of Labor and Human Resources on the subject "Nutrasweet: Health and Safety Concerns," dated November 3, 1987 (http://www.dorway.com/dr-elsas.txt), he observed:
“In the developing fetus such a rise in maternal blood phenylalanine could be magnified four to six fold by the concentrative efforts of the placenta and fetal blood brain barrier. Thus a maternal phenylalanine of 150 µM could reach 900 µM in the developing fetal brain cell and this concentration kills such cells in tissue culture. The effect of such an increased fetal brain concentrations in vivo would probably be much more subtle and expressed as mental retardation, microcephaly or potential certain birth defects.
In the rapidly-growing post-natal brain (children of 0-12 months) irreversible brain damage could occur by the same mechanism.”
Show Time and No Refunds
Presented with adversarial testimony and scientific evidence of APM toxicity, the FDA at first denied approval. G. D. Searle Company was desperate but politically savvy, so the company hired Donald Rumsfeld as its CEO. It is said that he then called in his markers and Arthur Hayes was appointed as FDA Commissioner, who approved aspartame over the objections of FDA’s own Public Board of Inquiry. The Aspartame Follies Show was on the road!
But an avalanche of spontaneous consumer complaints soon embarrassed the FDA for approving the introduction of a toxin into thousands of foods that are wreaking havoc on the national health. What to do? FDA simply slammed shut the complaint window, and for these last twelve-plus years has denied such a list ever existed. Complain about aspartame and you might just as well report a mugging to the Mafia. Evidently your welfare is less important than the profits of chemical companies whose fees pay a great deal of the FDA’s income. The customer is King at FDA.
The Seven Dwarfs Reborn
Remember the “Seven Dwarfs,” those seven tobacco presidents swearing to Congress that nicotine is safe? It’s harmless like candy or coffee, they testified, and cannot be addictive. Not one of these murderers spent a day in prison regardless of the cemeteries filling up with their victims. Even the chairman of the American Medical Association Board/Trustees, Dr. Lonnie Bristow, challenged them to walk with him through hospital wards to see the dying lung-cancer patients and pulmonary cripples. No takers.
FDA aspartame stooges are their present-day clones, mouthing identical lies: Aspartame is harmless, not addictive, and methyl alcohol is as safe as fruit. Yet not only the FDA but other agencies such as the Centers for Disease Control prattle on about aspartame safety with full knowledge of the carnage they are permitting. “It’s the most tested product in history,” they claim. I’ll say. In a study conducted on seven infant monkeys fed aspartame, five had grand mal seizures and one died. You’re the monkey now!
Obesity, Diabetes, and More
The FDA’s “Seal of Approval” and the economic incentive of using cheaper aspartame instead of sugar, and advertising “sugar free” slogans, APM spread like bacteria into thousands of foods and drinks. Specifically targeted are healthcare professionals and the weight-control industry for their blitzkrieg of propaganda. In reality, aspartame has caused an epidemic of obesity. Sharon Fowler’s study at the University of Texas reported in 2005 used eight years of data and linked diet drinks to obesity. Again, in February 2008, a Purdue study found artificial sweeteners linked to weight gain. Even in the May l985 Senate Congressional Record, Dr. Richard Wurtman’s affidavit was quoted wherein he attested that aspartame makes users crave carbohydrates so that they actually gain weight.
Unfortunately, doctors treating diabetics advise it for their patients. Dentists recommend NutraSweet gum & desserts to cut cavities. Dietitians pour it over school lunches. Professional organizations such as the American Diabetes Association and the American Dietetic Association continually run aspartame ads in their magazines and strangle the truth.
The fact of the matter is that aspartame can precipitate diabetes, simulate and aggravate diabetic retinopathy and neuropathy, destroy the optic nerve, cause diabetics to go into convulsions, and even interact negatively with insulin. This is discussed at length in the 1000-page medical text, Aspartame Disease: An Ignored Epidemic, by H. J. Roberts, M.D.
The sweetener also binds to calcium as proven in a Norwegian study and is particularly deadly in gum. Because it is really an excito-neurotoxic drug, it works like nitroglycerin under the tongue, goes through saliva like Hitler through France and straight into the brain. Abby Cormack in New Zealand almost died on Wrigley’s aspartame gum and made World news last Summer. Today, there is a petition to ban aspartame in New Zealand being circulated by the Safe Food Campaign.
APM’s atrocities exceed tobacco’s. At least nicotine is voluntary, not mixed into children’s sweets and soda pop and thousands of processed foods, even vaccines and pediatric medicines. Aspartame has poisoned the World’s food supply! Corporate-neutral research shows the extreme danger presented to our children and us. But when you are as rich as Saudi Arabia you buy universities, doctors, medical journals, and any print or electronic billboard you can get. But it is not working anymore.
Aspartame’s 2006 European Obituary
In a market wire dated March 30, 2006, it was announced that the Holland Sweetener Company (HSC) was going to exit from the aspartame business and will terminate its aspartame activities by the end of 2006. “The global aspartame markets are facing structural oversupply,” the wire reported, “which has caused worldwide strong price erosion over the last 5 years. This has resulted in a persistently unprofitable business position for HSC. No significant improvements are expected in the near or foreseeable future.” (emphasis added) HSC was the largest aspartame producer in Europe. (http://sys-con.com/read/200579_p.htm)
Another company, Merisant, based in the United States but with sales in over 90 different countries, accounts for more than one-third of the estimated $1.2 billion global tabletop sweetener market. Over half of Merisant sales are outside of the United States. Yet even Merisant has lost $50 million a year, dropped a third of its North American sales in 3 years, and is upside down, owing $100 million more than its worth. The aspartame biz isn’t sweet any more.
Adding to aspartame’s woes in 2006, some 47 Members of Parliament signed on to ban Aspartame! “That this House expresses deep concern over the numerous independent toxicological studies and thousands of subjective reports attesting to the toxic effects of the artificial sweetener aspartame on human health; notes that aspartame, once patented as a biochemical warfare agent, is the synthetically produced methyl ester of a dipeptide which is readily broken down in the gut to release methanol; further notes that in naturally occurring foodstuff methanol is either not released into the body or present together with natural defense mechanisms that mitigate its toxic effects; recognizes that methanol is a well known poison and is further converted into formaldehyde, a class A carcinogen according to the World Health Organization’s International Agency for Research on Cancer; accepts that severe health concerns occur from the gradual accumulation of formaldehyde in the body which cannot be excreted and that further research has shown that long term low level exposure to formaldehyde induces leukemia and nasopharyngeal cancer in humans; acknowledges that of the 166 studies conducted on aspartame's safety deemed relevant to humans, 92 per cent of independently sponsored studies identified one or more problems with aspartame's safety whereas industry-sponsored studies found unanimously in favor of aspartame's safety; and urges the Government to abide by the precautionary principle and make use of Statutes 13 and 16 of the 1990 Food Safety Act to remove aspartame from the permitted list of additives on the UK market.”
More Bad News for the Poison
Continued independent scientific studies flow in with the bad news. On February 5, 2008, the New York Times reported in an article entitled “Symptoms: Metabolic Syndrome Is Tied to Diet Soda” that, “Researchers have found a correlation between drinking diet soda and metabolic syndrome – the collection of risk factors for cardiovascular disease and diabetes that include abdominal obesity, high cholesterol and blood glucose levels and elevated blood pressure.” We have known that for years. All one had to do is pick up Dr. H. J. Roberts medical text, and it is all explained. It also goes into drug interaction – the fact the formaldehyde converted from the free-methyl alcohol embalms living tissue and damages DNA as proven by the Trocho Study, and even how this poison causes sudden death! Dr. Maria Alemany, who did the Trocho Study, wrote on February 12, 2008, “I am very sorry the health of so many people depends on a product that should not be available for human consumption, that is harmful and which long time effects have not been established nor even investigated.”
Dr. Russell Blaylock, a board-certified neurosurgeon, wrote in Health & Nutrition Secrets To Save Your Life, “So in the case of diet drinks in aluminum cans, the very toxic brain aluminum fluoride compound co-exists with multiple toxins found in aspartame, thus creating the most powerful government-approved toxic soup imaginable. With the strong association between aluminum, excitotoxins, aluminum fluoride complexes and Alzheimer’s disease, it would be completely irresponsible to encourage people to consume this toxic mixture.” Dr. Blaylock is also the author of Excitotoxins: The Taste That Kills. Both aspartame experts can be seen in the 2004 aspartame documentary Sweet Misery: A Poisoned World.
Around the World consumers demand that aspartame be removed from the planet. Last year the battle to ban aspartame was in New Mexico, mostly fighting those pro-aspartame lobbyists who just wouldn’t tell the truth. Just recently, there was another such battle with Hawaii’s bills to ban the poison. In fact, many Hawaiians keep saying, “We want this poison gone.” Nobody will stop until Rumsfeld’s Plague has been obliterated. Death and disability are simply not acceptable costs of doing business.
There are current efforts to ban aspartame in Hawaii. Two bills were deferred by House and Senate committees but because of the public outcry over the deferments two resolutions were drafted. One by Representative Josh Green, M.D., Chairman of the House Committee on Health, will require either warning labels or a total aspartame ban. It was passed by one House committee and has been submitted to another.
In Senate Resolution 191, it asks the Department of Health and the National Academy of Sciences to review all aspartame studies including independent ones done without funding by the aspartame industry. It requests that the FDA rescind approval of aspartame in U.S. markets, phasing it out in 6-to-12 months. This resolution is by the courageous Senator Suzanne Chun-Oakland. There is such a thunder of moaning and groaning Worldwide by aspartame victims that the manufacturers surely see the writing on the wall. Victims in other States are striving to get similar bills introduced to protect people from this poison.
The two Ramazzini Studies reported in 2005 and 2007 prove aspartame to be a multipotential carcinogen, even in small amounts; and that if a child survives exposure, then cancer may still result. These are two of the most impeccable studies ever done and confirm aspartame is a carcinogen as reported by FDA toxicologist Dr. Adrian Gross over 30 years ago! Aspartame as a poison even causes chemical hypersensitization. There is no use for it at all except as a killer. Jan Kinnard, an informant who was formerly hired as a professional temp to shred aspartame studies, supports these views. She reported on February 24, 2008, about these and other records on aspartame: “They were the lab results from the tested rats and other animals. The results were outrageous. This stuff killed everything it touched.”
To add more grist to the mill, the FDA has ignored over 100 independent, scientific peer-reviewed studies showing aspartame toxicity, a petition for ban over 6 years ago, a current amendment based on an imminent health hazard, as well as a letter from 12 toxicologists demanding that the Agency ban the product. Over 30 years ago, FDA toxicologist Dr. Jacqueline Verrett, who also testified to Congress that aspartame has never been proven safe, wrote the book Eating May Be Hazardous To Your Health: The Case Against Food Additives. Even then she summed up by saying, “What can be done to restore to consumers their right to safe food regardless of economic and political interests? . . . Probably the best solution, as some members of Congress have suggested, is to abolish the FDA and start over with a completely new agency free of some of the political pressures. . . . When science and the public interest win out, it is invariably only after the government has been pushed to the wall by consumer advocates and other public pressure.”
Worldwide consumer action, alert physicians, and conscientious officials – plus competition – are turning the tide and the aspartame marketplace is drying up.
(NewsTarget) Pharmaceutical Research and Manufacturers of America (PhRMA) -- a drug industry lobbying group -- held a meeting in Washington, D.C. last month following midterm elections to draft a plan of action to retain political sway in the Democrat-controlled U.S. Congress. PhRMA president Billy Tauzin and other members of the organization met with a number of Democratic senators and representatives, urging them to seek positions as chairs of influential subcommittees with authority over Medicare and drug industry regulations. Tauzin also met with a number of Democrats who have supported legislation on issues such as allowing imports of cheaper brand-name drugs from Canada, authorizing Medicare to negotiate cheaper prescription drug prices with manufacturers and restricting direct-to-consumer drug advertising. Major drug companies have also hired a number of former aides to influential Democrats to assist in lobbying campaigns. For example, Merck recently hired a former aide to liberal House Democrat Jim McDermott (D-Wash.), while Cephalon hired a former health policy aide to Nebraska Democrat Ben Nelson. The biotechnology industry has also mobilized its lobbyists after resounding victories for Congressional Democrats last month. The Biotechnology Industry Organization recently signed on Paul T. Kim, a former aide to both Senator Edward M. Kennedy (D-Mass.) and Rep. Henry A. Waxman (D-Calif.). "It's all hands on deck," said Ken Johnson, senior vice president of PhRMA. "It's like a hurricane warning flag. You don't know where it will hit. You don't know who will be affected. But everybody has to be prepared." Drug and biotech companies face serious profit cuts if Democrats pass legislation that allows Medicare price negotiations. Democrats -- set to head a number of influential subcommittees, including the Senate Finance Committee and the Committee on Health, Education, Labor and Pensions -- plan to push for stricter drug safety regulations, as well as the development of low-cost generic alternatives to brand-name drugs.
Guidelines for Determining the Development of Electromagnetic Hypersensitivity (EH)
Adapted from Electric UFOs: Fireballs, Electromagnetics and Abnormal States by Albert Budden (London: Blandford, 1998)
1. Do you frequently get severe shocks from door handles, car bodywork, and other surfaces?
2. Do you feel uncomfortable in synthetic materials, such as acrylic, polyester, or nylon?
3. Are you sensitive to perfumed products, aerosols, cigarette smoke, gasoline, natural gas, make-up, aftershave, and similar substances.?
4. Does electrical equipment go wrong or behave oddly in your presence?
5. Are there any foods or drinks that you either avoid or consume large amounts of? Do you have food allergies, for example, to chocolate, coffee, milk, orange juice, food with artificial coloring or flavors, or wheat products?
6. Did you have a happy childhood? If no, give reason(s) briefly.
7. Do you ever have hairs on your body stand on end, feel suddenly cold or overheated, or experience tingling or numbness?
8. Do you ever get a metallic taste in your mouth?
9. Do you get deja vu strongly and often?
10. Do you ever get the overwhelming sensation that someone is in the room with you, watching, although you cannot see anyone?
11. Are you very sensitive to light? (Sunlight? Flickering light? Do you wear tinted glasses?)
12. Are you sensitive to medications, especially antibiotics?
13. Do you have what could be called psychic experiences, such as ghostly encounters or out-of-body-experiences (OBEs)?
14. Do you find that objects in your home go missing or sometimes seem to behave oddly in any way?
15. Do light bulbs or batteries seem to last for a very short period of time in your home?
16. Have you ever been close to a lightning strike or suffered major electrocution? Or defibrillation? Or electroconvulsive therapy (ECT)?
17. Do you ever see small lights darting about the room?
18. Does fluorescent light bother you at all?
19. Do you ever have periods where you lose all concentration, feel over-heated, see light flashes, lose muscle power in your legs, or feel tingly and heavy?
20. Are there any of the following features near your home: a quarry, radio mast, power lines, reservoir, hill, military base, TV or radio station, radio ham?
21. Does time ever seem to slow down or pass in a flash?
22. Have you ever had periods of time for which you cannot account?
23. As an activity, do you write very much?
24. Have you ever had the experience of everything going very still, timeless, and silent?
25. Do you ever get painful electrical rippling sensations under the skin?
Psychic Phenomena and the EM Hypothesis
by William Patrick Bourne
With development of the experimental understanding of electromagnetic
(EM) energy during the nineteenth century, it was natural that
parapsychology researchers would entertain the notion that some
psychic phenomena, for example telepathy, might be a manifestation of
direct brain-to-brain communication using EM carrier waves of some
sort.
EM waves are used today for a variety of purposes, including radio
and television communication. It has also been demonstrated that the
human body and nervous system produce EM energy of various
frequencies.
Although EM signals of some type between people might be significant
over short distances, they cannot explain the great accumulated body
of evidence in the parapsychology literature.
The total electrical power emitted by the human brain is very weak,
less than 0.000001 watts. We know that the strength of an
electromagnetic signal drops off very quickly as it travels, and yet
long range telepathy and PK experiments have been performed which
indicate that psychic prowess does not seem to diminish with distance.
Furthermore, successful telepathic reception of target information
has been achieved while the subject was enclosed within an
electromagnetically shielded chamber called a Faraday cage. Although
extremely low frequencies (ELF) may still penetrate such a chamber,
the information-carrying capacity of these long wavelengths seems to
be too low to account for the quality of the psychic signal in, for
example, remote-viewing experiments.
Physicist Z.V. Harvalik published an interesting series of papers
during the 1970s in American Dowser Quarterly Digest. Working with
expert dowser Wilhelm De Boer, he showed that the subject reacted
with great sensitivity to changes in a magnetic field. By placing
strips of magnetic-shielding material on the dowser's body, Harvalik
determined that biological dowsing sensors seem to be located at the
kidneys as well as in the vicinity of the pineal gland within the
brain. When one of these two areas was shielded the dowsing signal
was completely extinguished, but when both areas were shielded the
dowser's sensitivity returned and even seemed enhanced. This would
seem to indicate that a non-EM sensory system was available to take
over.
The evidence is strong that signals with unknown characteristics,
certainly unlike electromagnetic waves, exist within Nature.
Further reading:
Harvalik, Z. V. (1973-1976). American Dowser Quarterly Digest
(Danville, Vermont).
Krippner, Stanley (Ed.) (1987). Advances in Parapsychological
Research, Vol. 5. North Carolina: McFarland & Co. (See pages 112-
116.)
Targ, Russell, & Harold Puthoff. (1977). Mind Reach. New York: Dell
WASHINGTON - A mixture of six bacteria-killing viruses can be safely sprayed on meat and poultry to combat common microbes that kill hundreds of people a year, federal health officials said Friday.
The mixture of special viruses, called bacteriophages, would target strains of Listeria monocytogenes, the Food and Drug Administration said in declaring it is safe to use. The viruses are designed to be sprayed on ready-to-eat meat and poultry products just before they are packaged.
The bacterium they target can cause a serious infection called listeriosis, primarily in pregnant women, newborns and adults with weakened immune systems. In the United States, an estimated 2,500 persons become seriously ill with listeriosis each year, according to the Centers for Disease Control and Prevention. Of those, 500 die.
The preparation of bacteriophages � the name is Greek for "bacteria- eater" � infects only various strains of the Listeria bacterium and not human or plant cells, the FDA said.
People normally come into contact with phages through food, water and the environment, and they are found in our digestive tracts, the FDA said.
The viral preparation is made by Intralytix Inc. The Baltimore company first petitioned the FDA in 2002 to allow the viruses to be used as a food additive.
Messages left with the company and the FDA were not immediately returned Friday.
The viruses are grown in a preparation of the very bacteria they kill, and then purified. The FDA had concerns that the virus preparation potentially could contain toxic residues associated with the bacteria. However, testing did not reveal the presence of such residues, which likely wouldn't cause health problems anyway, the FDA said.
Scientists have long studied bacteriophages as a bacteria-fighting alternative to antibiotics
August 2009 Last Temptation An interview with Wendell Potter
The former mouthpiece for insurance giant Cigna divulges his role in misleading the public, the emotional day that led to his whistle-blowing, and what should really scare you.
potter300.jpgIn June 2007, Wendell Potter was head of corporate communications at Cigna, one of the largest health insurance companies in America, when he attended the U.S. premier of Michael Moore’s Sicko. Potter was part of the team charged with discrediting Moore’s film, which advance word said was highly critical of the health insurance industry. Potter “sat quietly in the back and took notes,” but soon realized he had a problem. “When I saw the movie, I’ll be honest: I thought it was a real good documentary. I knew from my own studies of other healthcare systems that it was an accurate portrayal of those systems and how they are able to provide universal coverage.” Yet he was being paid by Cigna to tell people the opposite, that the film was full of lies.
Just a few weeks later, Potter, who is from Tennessee, read in a local paper about a free healthcare expedition being held in Wise County, Virginia. He decided to check it out. Walking through the fairground gates, Potter saw hundreds of people waiting in the rain while physicians attended to patients in animal stalls or on gurneys lying on the rain-soaked pavement. Tents had been pitched across the fairground lawns, creating a scene “like something that could’ve been happening on a battlefield or in a war-torn country.” Tears mixed with the rain to cloud Potter’s vision. “What I thought was: ‘Is this the United States?’ It was so remote from my reality. It just seemed impossible.”
In months and years prior, Potter had grown increasingly skeptical about his job as chief spokesman for Cigna. Though he insists he never intentionally lied to a reporter, he began to spout what he thought were either misleading or less than honest statements. Moreover, his job required him to hype new programs he felt were not in the best interest of patients or the U.S. healthcare system—particularly when it came to high-deductible, or “consumer driven” plans. He came to feel he was on the wrong side of the healthcare debate and would catch himself gazing into a mirror, wondering, “Who is this? How did this happen to me?” After Sicko and Wise County, he resigned.
Since then, Potter has become an outspoken advocate for healthcare reform. Why reform? Because of statistics like these: The U.S. healthcare system is the most expensive in the world, with each person spending more than twice as much on care than people in other industrialized nations. Yet our system ranks 29th in infant mortality, 28th in healthy life expectancy, and 37th overall. In June, Potter testified before the Senate on the devastating effects that Wall Street has on our healthcare system. The overwhelming demand to satisfy investors, Potter told the committee, is what causes insurance companies to “confuse their customers and dump the sick.”
With twenty years of industry experience—he was head of corporate communications with Humana before moving on to Cigna—Potter is an important voice in the healthcare debate. As a former insider, he is uniquely positioned to reveal the industry’s secrets, like its obsession with the medical-loss ratio—the difference between what health insurance companies pay out in claims and what it has left over—which, Potter says, causes otherwise good people in the industry to allow patients to die in order to increase profits. Yet in another sense, Potter is not so unique. We’ve seen them before, former insiders who reap huge financial benefits from an industry or system only to publicly denigrate it years later. If things were so bad, we’re left wondering, why didn’t Potter say something earlier? I recently spoke with Potter by phone.
—Jake Whitney for Guernica
Guernica: During your time in the industry, you created health insurance front groups to mislead the public. Can you give me an example of one of these front groups?
Wendell Potter: When the Clinton plan collapsed [in 1994], there was an effort to pass legislation that would give enrollees in managed care more protections. The industry saw this as anti-managed care legislation, so they established a group called the Health Benefits Coalition. The Health Benefits Coalition, with the funding it got from the insurance industry, killed off the effort to get a Patient’s Bill of Rights passed. A more recent example of a front group I was involved with was trying to blunt the effect of [Michael Moore’s documentary] Sicko. Through a PR firm, the industry created a front group to disseminate misleading information about the healthcare systems featured in Sicko—particularly in Canada, the U.K., and France. This front group was set up specifically to try to counter [Moore’s positive depiction of them].
Guernica: What were your duties with these front groups?
Wendell Potter: To help form messaging and develop strategy with public relations firms. PR firms help create the front groups and serve as the back offices to get the work done. The insurance industry contributes advice and counsel and feedback, but the real work gets done by the PR firms that the insurance industry hires.
Guernica: Was it difficult for you to discredit a movie you felt was accurate?
Wendell Potter: It was very difficult. I was beginning to hate my job. I’d look in the mirror and say, “Who is this? How did this happen to you?” But I had a job to do and was being paid quite a bit, so I soldiered on. I wouldn’t have stayed as long as I did if I didn’t believe that the company I worked for was honest and trying to meet the needs of people. I believed I was making some kind of positive contribution. As I was climbing up the corporate ladder, I got to understand more about how the companies make money and how they are so beholden to Wall Street—both investors and Wall Street analysts—and the things that they do to meet Wall Street’s expectations.
Guernica: You worked in the industry for twenty years. It doesn’t seem like it should have taken so long.
Wendell Potter: You don’t really focus on it or understand the significance of it. I’ll admit I knew that Wall Street looked at the medical-loss ratio. I knew it was an important measure. I didn’t know until, frankly, very recently how important it was. As recently as fifteen years ago, the medical-loss ratio in this country was 95 percent. Since then, there’s been great industry consolidation to the point that now there are seven companies that dominate. They’re all for-profit. During the time that this consolidation, this shift to for-profit occurred, the medical-loss ratio has continued to drop. Now it’s around 80 percent. That means twenty cents of every dollar goes to something other than paying medical claims. Just fifteen years ago, ninety-five cents of every dollar went to paying medical claims. This trend is due to pressure from Wall Street. If a company misses Wall Street’s expectations—if the medical-loss ratio starts to inch up—the company will suffer. I’ve seen companies lose 20 percent of their stock value in one day by disappointing Wall Street with their medical-loss ratio.
Our current reality is far scarier than the fear-mongering. What people have now is a corporate bureaucrat who stands between a person and his or her doctor.
Guernica: So are you saying our healthcare system would be better off if medical insurance companies weren’t publicly traded?
Wendell Potter: We would not have the same problems. Just look at what’s happened since 1993, the beginning of the conversion to for-profit status. The two biggest companies now are Wellpoint and United. In 1993, they were very small. They’ve grown to their size and influence through very aggressive acquisition strategies. In Wellpoint’s case, they bought up many non-profit Blue Cross and Blue Shield plans around the country, which have since converted to for-profit status. United has had a similar strategy. Aetna and Cigna are third and fourth in size, and they, too, have grown largely by acquisition. The fixation that Wall Street has with the medical-loss ratio has created huge problems because investors look at that measure even more than they look at earnings-per-share, which is the primary measure that investors look at in most industries.
Guernica: Shifting to President Obama’s plan: critics often say that Obama’s healthcare plan would be detrimental to care because it would take decisions away from doctors and patients and put them in the hands of a government bureaucrat. Is this a legitimate concern?
Wendell Potter: No. But it is one of those talking points the industry repeats every time we have a debate about reform. They said it in 1993. They say it whenever the industry is under threat of increased government involvement. What I’m telling people is that our current reality is far scarier than the fear-mongering. What people have now is a corporate bureaucrat who stands between a person and his or her doctor. That’s much scarier than the specter of more government. In any event, there is nothing in any healthcare plan that is being proposed that would put a government bureaucrat between a person and his or her doctor.
Guernica: Why is a corporate bureaucrat scarier?
Wendell Potter: Because every person who works for a for-profit company knows that the company has to meet Wall Street’s expectations. Every manager of the company has to pull his or her weight to make sure he and his team are doing all that they can to help the company meet that objective. That includes medical directors. Same with the nurses. They know what the company has to do to meet Wall Street’s expectations and to stay in the good graces of investors.
Guernica: So in other words, corporate bureaucrats have a profit incentive to deny care to people who are enrolled in their plans.
Wendell Potter: Absolutely. It doesn’t have to be stated directly to them that you will be paid a particular bonus if you deny X number of claims; it’s known, and it’s part of the culture.
Guernica: You said you’re familiar with the healthcare systems featured in Sicko and believe them to be superior to the U.S. system.
Wendell Potter: They’re better in many regards. No system is perfect. Every system has flaws and challenges.
Guernica: What about the long wait times we’re warned about, and that government-run healthcare would be one step on the path to socialism? Is there any legitimacy to these claims?
Wendell Potter: No. In fact, we can look at the wait times in this country as more horrific than anything you’ll see in the Canadian system, for example. For elective procedures in many of these countries, yes, you might wait longer for some elective procedure. You might wait longer for an MRI than you would in this country because, on a per capita basis, there are often more machines here than in some of those other systems. But life expectancy in almost every one of these other countries is greater than ours. People do not have to wait long for urgent or necessary care. In fact, in many countries it’s more likely that you would be able to get a same-day appointment with a doctor than here.
Guernica: How do you know?
Wendell Potter: I’ve traveled abroad a lot and I’ve studied them. I’ve been a student of statistics of these other systems, so I do know this, and yes, I have been there.
Guernica: Much was made during the Democratic primaries of health insurance contributions to Democrats. I believe Hillary Clinton raked in a record amount from healthcare companies. Do you think these donations have helped stall legislation?
Wendell Potter: Oh, absolutely. Every step of the way. Let me tell you a story. I am a great admirer of Hillary Clinton’s. I think she’s done terrific things for this country and is a great public servant. But money talks and relationships make a difference. These [insurance] companies contribute more to Democrats than they used to, and they’ve begun hiring lobbyists from the Democratic side of the aisle. They look for the best-connected lobbyists. The CEO of Cigna [H. Edward Hanway] wanted to spend a few minutes with Hillary when she was running for president. One of the lobbyists that Cigna hired was known to be very close to the Clintons, and Hillary Clinton, in particular. Lo and behold, she was able to arrange a meeting for [Hanway] to come to Washington and spend a few minutes with Hillary. I don’t think that [Hanway] necessarily persuaded her to see things from his point of view. She’s not a huge fan of insurance companies. But he was able to get in the door and spend a few minutes with her. And that’s what I’m talking about. It’s the influence insurance companies have been able to buy through hiring people who are well-connected, often former members of Congress or former staff members.
Guernica: Then there are the Blue Dog Democrats and their role in holding up legislation. What’s their motivation?
Wendell Potter: The industry has contributed so heavily to the Republicans over the years that they are pretty much assured that every single Republican in Congress will vote exactly the way they want on any issue pertaining to healthcare. This has not occurred just with campaign contributions. It’s also ideology. The industry has been very determined to carve out its niche on the right side of the political spectrum and, along with the business community, be advocates of a free-market approach to any aspect of our economy—and make sure that there is minimal regulation of any economic sector. So there is a great ideological kinship between the insurance industry and the Republican Party. And this is close to the ideology of the Blue Dog Democrats, who tend to be in border states of the south or where there are more Republicans. Industry has been feeding the Blue Dogs talking points and working overtime to make sure they see things from their philosophical and business perspectives.
Guernica: It was reported late last month [July 29] that a tentative agreement was reached with the Blue Dogs in the House that would omit the “public option.” Do you think that’s a good thing?
Wendell Potter: There have been some compromises that have been made to the Blue Dogs. But Nancy Pelosi said today that the public option is not being sacrificed. I think the leadership in the House and Senate will be fierce defenders of the public option. The Blue Dogs are insurers’ best hope of gutting healthcare reform and removing the public option from legislation. So they are very, very important to the industry, which is why you’re hearing so much about them right now.
Guernica: Do you think the public option is important?
The reason I started speaking out is I knew the insurance industry would come out with guns blazing to kill reform. It’s the same old playbook. I know it because I essentially helped write it.
Wendell Potter: It’s essential. Reform without the public option would be far less meaningful and effective. The public option may not go as far as people would like in some ways, but we need a mechanism that controls costs and makes healthcare more available to citizens. It would go a long way toward keeping the insurance industry more honest, as the president has said.
Guernica: Conservatives’ opposition to the public option is confusing. Shouldn’t conservatives welcome a system that gives more choices to the consumer, which is supposed to be a tenet of conservatism?
Wendell Potter: It doesn’t make a lot of sense. On the one hand, they’re saying that [a public option] would put the private sector at an unfair disadvantage, while they’re also saying that the private sector can operate more efficiently. They are trying to have it both ways. But the reality is that the free-market simply does not work in the healthcare sector as it might in other sectors. A public insurance plan wouldn’t need to have the sales, marketing, and underwriting expenses—and would certainly not need to pay executives exorbitant salaries, and would not need to set aside a significant chunk of every premium dollar to pay shareholders—that private plans do.
Guernica: The [July 30] New York Times had a story that said this: “Obama’s ability to shape the healthcare debate appears to be waning as opponents portray the effort as a government takeover.” Apparently conservative messaging is working.
The industry knows through many years of focus group testing what messages scare people. “Government takeover,” is one of those terms.
Wendell Potter: The reason I started speaking out is I knew the insurance industry would come out with guns blazing to kill reform. I knew the tactics they’d be using and buzzwords they’d be repeating—especially through their shills in Congress, media and business. It’s the same old playbook. I know it because I essentially helped write it. I knew that when the time came, they’d be unleashing that crap. And I knew that it would have the impact it’s having on people and Congress. It’s basically a political contest. At first, it seemed like Obama was just going to walk into office and transformative healthcare legislation would get passed. But I knew it would be a contentious fight—that the industry would be throwing everything conceivable to keep significant reform from happening. Because we’re talking about billions and billions of dollars at stake for those companies and investors. But it’s not a lost cause. Over the next few weeks, we will see one hell of a battle in the districts and over airwaves as proponents and opponents of change spend tons of money on TV and radio advertisements. We’ll be hearing fear mongering like we’ve never heard before, but also be hearing, I hope, effective advertising from the proponents of reform.
Guernica: The Times story really attests to the power of opponents of healthcare reform; don’t most Americans favor reform and some type of universal coverage?
Wendell Potter: They are in favor of it, yes. But the industry knows through many years of focus group testing what messages scare people. And the term you mentioned a few minutes ago, “government takeover,” is one of those terms that they’ve tested and know will scare the bejesus out of people. They know that in the past, people have been so afraid of anything that approaches socialism that you’ll hear that comparison all the time; that if we go with reform, we will have a government takeover of healthcare; that we’ll be on the slippery slope toward socialism.
Guernica: But what about programs like Medicare and the Veteran’s Administration? These are large, extremely effective, government-run programs that have been around a long time, despite the slippery slope rhetoric.
Wendell Potter: The health insurance industry knows this. That is why they’re so careful with language. Medicare is far more popular than almost any private health insurance program in the country. And people in other programs you mentioned are certainly very grateful. But many of them don’t know that it’s a public program.
Guernica: But we’ve heard this exact same talk of socialism decades ago during the battles over Medicare, Social Security, Medicaid, etc. And I don’t think very many people want to lose these programs now.
Wendell Potter: Conservatives are so bound to ideology they refuse to take a serious, open-minded look at how for-profit insurance companies have wrecked our healthcare. They don’t want to take the blinders off. What gives me hope is that despite all the lies and all the disinformation that opponents of reform have spread over the years, real reform has nevertheless been enacted. Like the Medicare program during the Johnson years; like the Medicaid program that is such an essential safety net for so many of our people; the Veteran’s program you mentioned. We have plenty of examples of government programs that work great and have done so much for so many billions of people over many years.
Guernica: You’ve mentioned that when you worked for Cigna, you liked your co-workers. You’ve said that you respected your bosses and still do. Have you had contact with them? Are they aware of what side you’re on these days?
Wendell Potter: Oh, there’s no doubt they know what side I’m on. I have not had contact with my former boss or CEO. My former boss was the company’s general counsel [Carol Ann Petren]. She reports to the CEO [Hanway]. I worked and served [Hanway] throughout my career, knew him very well, and like him personally. But he’s one of those people who we just talked about who are committed to privatizing all aspects of the economy. And he’s benefited enormously—earning many millions of dollars in compensation [According to Forbes, Hanway earned over $30 million in 2007]. So has my former boss, also one of the most highly compensated employees [Petren made $2.18 million in 2008]. She is of the same philosophy. I respect their right to have those opinions. But they’re dead wrong.
Guernica: This is an industry that allows people to die so it can increase profits. I would think that it would be difficult to respect people who remain in that industry.
Wendell Potter: When you’re in an executive office in a skyscraper, and you’ve got people bringing your lunch, who take you home in a company-owned limousine with a driver on the company payroll, you get a very skewed understanding of America. You are removed from the reality of how most people live. And the number—46.7 million people without insurance—remains just a number when you’re in that environment. It’s only when you let yourself be around people who are without insurance, who are underinsured, who wait in line... [long pause]
Guernica: Hello?
Wendell Potter: [Choked up] Yes, I’m here.
Guernica: Sounds like this is very emotional for you.
Wendell Potter: Yes. It’s crazy but I still get choked up when I remember the Wise County experience. Talking about it brings back the vision of all those people standing in line in the rain to get care in animal stalls.
Guernica: Did you ever express your concerns with colleagues at Cigna?
The tragic thing about these town hall meetings is how some of these angry citizens are being manipulated.
Wendell Potter: I talked to friends, but I didn’t muster the courage to [talk to co-workers]. When I decided to quit, I thought I’d just kind of go quietly. I announced it as a retirement, but I could have made a lot more money had I stayed. But I was okay with that. I wasn’t ready to go fishing, but I was ready to take a break. At one point, I thought I might have a chance to change things inside the company and the industry. But I realized very quickly that that was just wishful thinking. The industry is controlled by Wall Street investors. These companies are for-profit. Their first rule is to enhance shareholder value. That is what’s important. If what I said hindered a company’s profitability, I was not going to be listened to, plain and simple.
Guernica: What I’m getting at is this: You’ve become a significant voice in the healthcare debate. But there’s a portion of the public that looks at you skeptically. We’ve seen this before—Scott McClellan is a recent example—someone who is in an industry or system, they make a lot of money, they get out and that’s when they start crying corruption. They write a book and make a little more money. Some are left wondering; “If it was such a bad industry, why didn’t you speak up earlier?” Maybe you could have made a difference in the nineteen nineties.
Wendell Potter: I understand that completely. Looking back, I wish there had been a moment when I could’ve spoken up. On the other hand, I needed to spend time in the industry to gain the perspective I have. I bought into the industry and what it was doing for many years. The company treated me very well for fifteen years, and I didn’t want to be fired; I had to think about the needs of my family. So there was a lot I had to think about as I was sorting through everything. But I can’t help people from thinking that. To those that question my motives, I’d just like to say that I’m doing this because I think it’s the right thing to do. And the timing was something that… I don’t know if it would have been better had I done this earlier. Maybe so; I don’t know. But the way it’s turned out may be just as effective. Right now, the debate is at its peak.
Guernica: Let’s talk about these contentious town hall meetings. What role, if any, does the industry play in causing the disruptive, or what Senator Claire McCaskill called “rude” behavior?
Wendell Potter: One of the big PR firms [for] the insurance industry is APCO Worldwide. They’ve represented the industry for quite a long time. They’re skilled at setting up front groups to spread disinformation to challenge proposals. So they will get talking points into the hands of conservative radio talk show hosts and editorial writers at conservative publications. It all comes from the health insurance industry, but they spread this stuff in such a way that their fingerprints are not directly on it. A guy named Bill Pierce works for APCO; he is an executive there. He used to work as a spokesman for Blue Cross Blue Shield and the Bush Administration. So if you called the number for Healthcare America, you would be connected with Bill Pierce’s office at APCO... The tragic thing about these town hall meetings is how some of these angry citizens are being manipulated. When you see these stories about the meetings and how the participants are so concerned about government takeover of our healthcare system, they use the very words that were fed to them by the health insurance industry, not realizing that that’s where they came from, not realizing that they are unwitting pawns of the industry. Because they hear that stuff from people they believe are credible, like Rush Limbaugh or Glenn Beck. Guernica: What are the chances that the industry is actually busing people in to disrupt the meetings?
I am very aware of the efforts the [healthcare] industry goes to to bus people to Washington. It’s one of the most sophisticated grass-roots operations you will find in any industry.
Wendell Potter: I think indirectly they are. APCO and other PR firms do stuff like that. It would be hard to trace it directly because they go through a lot of trouble to funnel the money in ways that it’s not directly traceable to them. When I say money, of course we’re talking about insurance premiums that people pay, and it’s being used for these purposes.
Guernica: So you’re saying these PR firms could potentially be sticking people on buses and sending them to these town hall meetings in order to disrupt them?
Wendell Potter: Yeah, they know where to go, what kind of organizations to turn to to get that kind of stuff done. There’s no doubt about it. On the other hand, I’m sure there are individuals who show up at these meetings who show up on their own and feel like they need to make sure their voices are heard... But other people there are very orchestrated.
Guernica: When you were with Cigna, did you have any first-hand knowledge of these kinds of tactics?
Wendell Potter: I am very aware of the efforts the industry goes to to bus people to Washington. It’s one of the most sophisticated grass-roots operations you will find in any industry. They have a long list of senior citizens, for example, who are enrolled in the Medicare Advantage plan. Insurance companies will pay for these people to fly to Washington for a day of citizen lobbying. [The senior citizens] will give the impression that they are there speaking on their own, but it’s completely orchestrated by the industry. What these seniors don’t know is that the only way they would lose their Medicare HMO is if the insurance company dumps them because they don’t think they’re profitable enough anymore. That happened back in the nineties, Cigna did it, Aetna did it—all the insurance companies that participated in the Medicare HMO program did it. That’s when Congress reduced the reimbursements a little bit, these big insurance companies dumped seniors by the millions...
Guernica: You’ve said that Cigna purges small businesses whose employees have serious health problems by raising premiums on these businesses until they can’t pay them. Senator Rockefeller recently asked Cigna about this practice, but I believe they denied it.
Wendell Potter: Cigna denied it, but there is evidence in a transcript that Rockefeller has in which the president of Cigna Healthcare uses the exact word: purging. So within the last couple of days, Rockefeller sent them a letter asking them to prove that they don’t purge. Because Cigna is saying they don’t [purge], but there’s evidence that they do. So essentially Rockefeller has caught them in a lie.
Guernica: How do we get other health insurance industry executives to see this from the point of the view of the uninsured?
Wendell Potter: It’s hard. My own process of doing this—it was the hardest thing I’ve ever done in my life. To say: “Okay, I’ve got a good job here, I’ve got a family to support, I’ve got a mortgage, I’ve got kids in college; but I’m going to quit my job and do what’s right”—that just doesn’t happen every day. And when you’re in a company, you also are thinking, “I am making a positive difference?” The people who work at these companies by and large are not evil people. But they only see their small part of it; they don’t see the broader picture of what the industry is doing to our healthcare system.
Guernica: If you had a few minutes in a room with some of these executives—maybe some of your former colleagues and friends like Hanway and Petren—who look only at profits. What would you say to them to get them to change their minds?
Wendell Potter: I’d say: “Look at what has happened to our healthcare system and look honestly at the role the insurance industry has played in that. Be honest as you look at this. You know what I’m saying is true. If you were like me, you probably don’t want to think about it. But look at what I’ve been saying, and you’ll recognize what I’m saying as true. You know it’s true. Do the right thing—which in my view is stepping away from the industry and speaking out.” I would also like to say to the critics of healthcare reform: “Open your minds a little bit and take a realistic look at our healthcare system and what has happened to it and the reasons for it. I think you’ll come to the same conclusions that I did.”
Guernica: Knowing people like Hanway, Petren—do you think they will ever come around to seeing things your way?
Wendell Potter: I’m doubtful. I’ve read that people are basically hard-wired to feel the way they do and see the world the way they do. Many people are just born Republican and Conservative. They’re just inclined to believe that the free market is the best thing regardless of in what sense of the economy it is. They have that element; those are the people who control these companies. They might just be hard-wired to see the world like that.
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Compensation fund - James Hardie non-executive directors barred from being directors - accountability (think ACC's Board)
Why the Hardie finding will be good for corporate governance Date: August 21 2009
By Elisabeth Sexton
Since the former board of James Hardie was found guilty of corporate misconduct in April, a torrent of business commentary has suggested that the law expects too much, particularly of non-executive directors.
These are the part-time stewards of a company charged with setting strategy and supervising its management.
The gist has been that the NSW Supreme Court decision was just about a single media release.
OK, it was about the politically sensitive subject of compensation for asbestos diseases. And, yes, it turned out the rosy assertion in 2001 that a new $293 million trust would be ''fully funded'' was, by 2004, about $1.5 billion out.
Even so, the argument goes, the non-executive directors had paid too heavy a price in the damage to their reputations and careers for a one-off lapse about PR. And more broadly, Justice Ian Gzell's ruling had set an unrealistic standard by expecting boards to check every media release and micro-manage executives.
This sentiment was summed up in a June headline in The Australian Financial Review: Is this the death of the non-executive director?
If it wasn't clear enough from Justice Gzell's decision in April, his reasons yesterday for banning the directors from boardrooms for five years spell out that their breach of duty was more than an inadvertent slip. The board's approval of the media release in 2001, ''while isolated, was highly significant,'' the judge said yesterday.
The non-executive directors knew from their board papers that James Hardie had to convince the public there were sufficient funds in the new trust to meet all legitimate asbestos claims, he said. They were aware of the significance of what the release would say about the level of funding. The advice they had received did not support its emphatic wording.
Their approval of the release was a deliberate attempt to gain acceptance of the plan to remove asbestos claims from the James Hardie group into the new trust.
''This was a serious breach of duty and a flagrant one,'' the judge said.
These views might be overturned on appeal in a higher court. But that possibility does not alter the gravity of what was at stake in this case.
It was about convincing the federal and state governments that, in undertaking a major corporate restructure, James Hardie could be trusted to look after people suffering from vicious diseases.
Thousands of Australians are expected to contract mesothelioma and asbestosis from exposure to James Hardie products for decades to come.
One testimonial filed in the case was from the investment banker Peter Hunt, who advised the then chairman Meredith Hellicar during the three-year negotiations for the new compensation scheme which replaced the underfunded trust in 2007.
Hunt, the executive chairman of Caliburn, described a task made difficult by uncertainties - in projecting future claims, economic growth rates, investment returns and James Hardie's performance and funding capacity for at least 40 years - and by the complexity of the legal issues involved and the public and media spotlight on the negotiations.
Hunt praised Hellicar for her hard work yet his account of how much was involved in achieving the new scheme underlined the directors' shabby job of addressing these same uncertainties and complexities in 2001.
Directors and advisers hyperventilating about the wider impact of the penalties handed down yesterday should consult a note sent by law firm Arnold Bloch Leibler to its clients about Justice Gzell's main decision in April. ABL was involved in the case, representing the former non-executive director Dan O'Brien.
It began by noting the judgment had caused ''widespread alarm within the business community'' and that ''some in the media have gone so far as to label the decision 'a blow against good corporate governance' which will distract directors from their primary function of guiding a company's strategy''.
The law firm said rather than being such an attack on good governance, ''the case simply reaffirms that directors must actively participate and scrutinise matters discussed at board meetings'' and should satisfy themselves about the accuracy of ''announcements of importance to the company and the public''.
You don't need to be an expert in corporate law to work that out.
Despite the success of the Veterans Health Administration, the Bush administration has restricted access to the V.A. system.
Let me tell you about two government-financed health care programs. One, the Veterans Health Administration, is a stunning success � but the administration and Republicans in Congress refuse to build on that success, because it doesn�t fit their conservative agenda. The other, Medicare Advantage, is a clear failure, but it�s expanding rapidly thanks to large subsidies the administration rammed through Congress in 2003. ... The key to the V.A.�s success is its long-term relationship with its clients: veterans, once in the V.A. system, normally stay in it for life. This means that the V.A. can ... make much better use of information technology than other health care providers. ... which reduces both costs and medical errors. The long-term relationship ... also lets the V.A. save money by investing heavily in preventive medicine, an area in which the private sector � which makes money by treating the sick, not by keeping people healthy � has shown little interest.
The result is a system that achieves higher customer satisfaction than the private sector, higher quality of care by a number of measures and lower mortality rates � at much lower cost per patient. Not surprisingly, hundreds of thousands of veterans have switched from private physicians to the V.A. The commander of the American Legion has proposed letting elderly vets spend their Medicare benefits at V.A. facilities, which would lead to better medical care and large government savings.
Instead, the Bush administration has restricted access to the V.A. system, limiting it to poor vets or those with service-related injuries. And as for allowing elderly vets to get better, cheaper health care: �Conservatives,??? writes Time, �fear such an arrangement would be a Trojan horse, setting up an even larger national health-care program and taking more business from the private sector.???
Think about that: they won�t let vets on Medicare buy into the V.A. system, not because they believe this policy initiative would fail, but because they�re afraid it would succeed.
Meanwhile, the Bush administration is pursuing a failed idea from the 1990�s: channeling Medicare recipients into private H.M.O.�s. The theory was that H.M.O.�s, by bringing private-sector efficiency and the magic of the marketplace to health care, would be able to do what the V.A. has achieved in practice: provide better care at lower cost. But ... [y]ears of experience show that H.M.O.�s actually have substantially higher costs per patient than conventional Medicare...
In 2003, however, the Bush administration pushed through the Medicare Advantage program, which offers heavy subsidies to H.M.O.�s. According to the independent Medicare Payment Advisory Commission, Medicare Advantage plans cost the government 11 percent more per person than traditional Medicare. Oh, and mortality rates in these plans are 40 percent higher than those of elderly veterans covered by the V.A. But thanks to the subsidy, membership in Medicare Advantage plans is surging.
On one side, then, the administration and its allies in Congress oppose expanding the best health care system in America, even though that expansion would save taxpayer dollars, because they�re afraid that allowing a successful government program to expand would undermine their antigovernment crusade and displease powerful business lobbies.
On the other side, ideology and fealty to interest groups make them willing to waste billions subsidizing private H.M.O.�s.
Remember that contrast the next time you hear some conservative going on about excessive spending on entitlements, and declaring that we need to cut back on Medicare and Medicaid benefits.
A handful of Brazil nuts a day can reduce the risk of eight types of cancer by up to 76 per cent, scientists said yesterday. They are packed with the mineral selenium, which can help prevent cancer of the liver, lung, stomach, prostate, pancreas, brain, kidney and oesophagus by blocking the formation of tumours.
Selenium also fights tumours once they appear, improving the chances of survival.
Dr Margaret Rayman of the University of Surrey, told the British Association Festival of Science in Exeter that people should aim for a daily intake of around 200 micrograms (mcg) of the mineral.
That cuts risk by between 46 per cent in the case of lung cancer and 76 per cent for prostate cancer, studies have found.
A handful of Brazil nuts a day is enough. Other sources are liver, kidney and shellfish.
People also get some selenium from the soil, through crops such as wheat. However Britons get on average only 30 mcg in their diet today, half the level of the early 1970s.
Doctor Rayman says this is partly because when we joined the forerunner of the European Union, we changed from importing wheat from selenium-rich Canada to European sources, where the soil contains a lot less of the mineral.
She warned that taking more than 450 mcg of selenium a day can cause some toxic effects.
A medical conference in London heard how the spice turmeric, which helps give curries their distinctive flavour and colour, can help protect against leukaemia in children.
Scientists suspect some children are born with a predisposition to the blood cancer and that it is triggered by environmental factors. Infections, viruses, radiation and pesticides are suspected culprits
Professor Moolky Nagabhushan, of the Loyola Medical Centre in Chicago, told the conference, organised by the charity Children with Leukaemia, that studies suggest turmeric and its colouring curcumin, protect against these "triggers". Daily Mail, September 2004
By edema excessive fluid gather in body parts or greater areas of the body, making the areas swollen. Edema is most often a problem in the legs, but can occur anywhere in the body.
There are several types of edema, and many cases are also a mixture of more than one type. By lymphedema the drainage from the tissues through the lymph vessels are impaired or excessive fluid goes through the blood capillary walls into the spaces between the cells in a tissue. Edema can also occur because of poor drainage of blood through the veins towards the heart. Edema can further be caused by general accumulation of excessive fluid in the body.
The causes of edema are many. Edema is a symptom by most inflammations. Insufficient heart action by congestive heart failure can cause edema. A too high intake of salt can cause general water retention in the body. Sitting and standing long in the same position can cause edema in the lower limbs. A still sitting life without exercise can cause or aggravate edema.
Insufficiencies of the liver or kidneys can cause fluid retention and thereby edema. Edema can be a side effect of antihypertensive drugs, steroids surgery and radiation therapy. Further causes of different types of edema are varicose veins, cancer, hypothyroidism, blood clots, constipation and physical injuries.
To treat edema, it is important to treat the underlying disease or injury. However, medical treatment does not always cure the underlying condition or the cause is wholly or partially lifestyle aspects. Therefore various measures targeted directly against the edema are useful. These are presented here:
Pharmacological treatments: The physician will sometimes prescribe diuretics to reduce fluid retention in the body and thereby reduce edema. This treatment should however be used for serious edema or edema persistent when other measures do not work.
Salt intake restriction: Restriction of salt intake is an important measure by edema. People suffering from edema should avoid adding great amount of salt into their food or consume preprocessed food with a salty taste.
Diet: A good general diet that alleviates chronic inflammation is useful. The diet should especially contain enough sources of omega-3-fatty acids and monounsaturated fatty acids, like: Fat fish, seafood, flax oil, olive oil, almonds, rape oil and canola oil. Also vegetables and fruit in a natural shape are useful.
Avoiding constipation: Constipation should be treated, since a stomach engorged by excessive content can cause impairment of fluid circulation.
Variation of corporeal position: You should avoid sitting or standing still a long time during the day. When sitting during work or rest, you should change position with regular intervals.
Exercise: Every day you should have some exercise adjusted to your health condition. This could be walking, cycling, swimming, running or any other sport activity where you use greater parts of your body. Doing regular stretching exercises or yoga is useful. By severe edema special therapeutic exercises should be prescribed by a professional.
High position of limb: When you are sleeping or resting the swollen body parts can be placed in an elevated position by means of pillows, pads or by resting in an adjustable bed or chair.
Massage: By minor edema yourself, your spouse or a friend can massage the affected body part to alleviate the edema. The massage should be done in the direction of natural flow of blood and lymph that is towards the heart. You should however avoid massaging distinctly injured or distinctly inflamed body parts. By severe edema a professional massager should be engaged to perform the massage type called "manual lymphatic drainage".
Elastic bandaging: You can use elastic gloves, stockings, tapes or bandages around the swollen body parts during the day or during physical activities after instruction from a professional person.
Inflatable garments: There are inflatable garments to be found that can be used around the engorged body parts some times of the day. Also these should be used after professional instruction.
Sequential gradient pump therapy: One can get special electric pumps connected to inflatable garments. The pump inflates and deflates the garments repeatedly. Each garment has several rooms that are inflated sequentially in the direction of the natural fluid stream towards the heart. In this way the fluid is dynamically pumped the right way out of the engorged body part. This type of therapy is used in professional settings or at home after instruction from a professional.
Skin care: The skin on a body part affected by severe edema should attain special care to avoid and treat sores. Proper cleaning, daily use of moisturing creams, proper rinsing of skin injuries, antiseptic creams by injuries.
Complete decongestive therapy: This is a complete set of edema treatment techniques done by a professional person combined with self-care instructed by the professional. The techniques used are: Manual lymphatic drainage, compression bandaging, therapeutic exercise and skin care.
Herbal and natural products: Many herbs and products composed of a blending of these herbs are used against edema. Such herbs are: Dandelion, Gingko biloba, horse chestnut, buchu, goldenrod, corn silk, horsetail, juniper, butchers broom, cleaver and ginger. Some people have experienced a good effect from using apple cider vinegar.
The flavonide rich product pycnognenol extracted from the bark of the French maritime pine has shown promising effects against edema according to scientific studies. The flavonides hydroxyethylrutosides also seem to have good effect against edema. Other natural substances that may help to treat edema are the flavonids diosmin and hesperidin and vitamin C.
Oil pulling: The procedure called "oil pulling" may help for edema. It consists of rinsing the mouth with one tablespoon of natural oil for 15-20 minutes and then spitting the oil out. It is done in the morning before eating. Sesame or sunflower oils are usually recommended for this use.
Contrary to popular belief, recent studies have found that there are probably ways to regenerate brain matter.
Animal studies conducted at the National Institute on Aging Gerontology Research Center and the Johns Hopkins University School of Medicine, for example, have shown that both calorie restriction and intermittent fasting along with vitamin and mineral intake, increase resistance to disease, extend lifespan, and stimulate production of neurons from stem cells.
In addition, fasting has been shown to enhance synaptic elasticity, possibly increasing the ability for successful re-wiring following brain injury. These benefits appear to result from a cellular stress response, similar in concept to the greater muscular regeneration that results from the stress of regular exercise.
Additional research suggests that increasing time intervals between meals might be a better choice than chronic calorie restriction, because the resultant decline in sex hormones may adversely affect both sexual and brain performance. Sex steroid hormones testosterone and estrogen are positively impacted by an abundant food supply. In other words, you might get smarter that way, but it might adversely affect your fun in the bedroom, among other drawbacks.
But if your not keen on starving yourself, there are other options. Another recent finding, stemming from the Burnham Institute for Medical Research and Iwate University in Japan, reports that the herb rosemary contains an ingredient that fights off free radical damage in the brain. The active ingredient, known as carnosic acid (CA), can protect the brain from stroke and neurodegeneration such as Alzheimer’s and from the effects of normal aging.
Although researchers are patenting more potent forms of isolated compounds in this herb, unlike most new drugs, simply using the rosemary in its natural state may be the most safe and clinically tolerated because it is known to get into the brain and has been consumed by people for over a thousand years. The herb was used in European folk medicine to help the nervous system.
Another brain booster that Bruce N. Ames, Ph.D., a professor of biochemistry and molecular biology at the University of California, Berkeley, swears by his daily 800 mg of alpha-lipoic acid and 2,000 mg of acetyl-L-carnitine, chemicals which boost the energy output of mitochondria that power our cells. Mitochondrial decay is a major factor in aging and diseases such as Alzheimer's and diabetes. Elderly rats on these supplements had more energy and ran mazes better.
Omega-3s fatty acids DHA and EPA found in walnuts and fatty fish (such as salmon, sardines, and lake trout) are thought to help ward off Alzheimer's disease. (In addition, they likely help prevent depression and have been shown to help prevent sudden death from heart attack).
Turmeric, typically found in curry, contains curcumin, a chemical with potent antioxidant and anti-inflammatory properties. In India, it is even used as a salve to help heal wounds. East Asians also eat it, which might explain their lower rates (compared to the United States) of Parkinson's disease and Alzheimer's disease, in addition to various cancers. If curry isn’t part of your favorite cuisines, you might try a daily curcumin supplement of 500 to 1,000 mg.
Physical exercise may also have beneficial effects on neuron regeneration by stimulating regeneration of brain and muscle cells via activation of stress proteins and the production of growth factors. But again, additional research suggests that not all exercise is equal. Interestingly, some researchers found that exercise considered drudgery was not beneficial in neuronal regeneration, but physical activity that was engaged in purely for fun, even if equal time was spent and equal calories were burned, resulted in neuronal regeneration.
Exercise can also help reduce stress, but any stress-reducing activity, such as meditation and lifestyle changes, can help the brain. There is some evidence that chronic stress shrinks the parts of the brain involved in learning, memory, and mood. (It also delays wound healing, promotes atherosclerosis, and increases blood pressure.)
It should go without saying that short-term cognitive and physical performance is not boosted by fasting, due to metabolic changes including decrease in body temperature, decreased heart rate and blood pressure and decreased glucose and insulin levels, so you’re better off not planning a marathon or a demanding work session during a fasting period.
As part of a healthy lifestyle the prescription of moderating food intake, exercising, and eating anti-oxidant rich foods is what we’ve long known will boost longevity, but it’s good to know that we can bring our brains along with us as we make it into those golden years without being the 1 in 7 who suffers from dementia. Keep your fingers crossed and eat some rosemary chicken.
Little or No Evidence Supports Conventional Medical Treatments
by Barbara L. Minton
(NaturalNews) Do you ever get the feeling that your doctor doesn't know what he's doing? Well, you are probably right. There is little or no evidence that today's $2 trillion-dollar medical system works any better than various other alternatives. Whether you have diabetes, heart trouble, back pain or cancer, this judgment applies. If you are contemplating surgery, you should know that the orthodox disease establishment doctors have little clue about the success rates for the procedures they endorse.
Dr. David Eddy, a consultant for healthcare giant Kaiser Permanente and leader in the development of clinical evidenced based guidelines admits that the medical profession does not know what its doing, according to an article published by Alan Stang. Even today, with a high-tech health-care system that costs the nation so much money, there is little or no evidence that many widely used treatments and procedures actually work.
Eighty-five percent of what doctors do is not backed by hard evidence, which presumably means that only fifteen percent is. "Doctors dangerously over treat patients, because they get paid to treat; they don't get paid not to treat," claims Stang.
A hundred and fifty years ago, Ignaz Semmelweis claimed that his fellow physicians were killing women delivering babies in Vienna's hospitals. Women were so terrified of hospitals that they considered a hospital stay the same as a death sentence. Their families had to bring them there by force because the women would try to escape. Semmelweis suspected that the reason for the deaths was that doctors were going from surgery to surgery without washing their hands. When he demanded that they scrub and sterilize their hands, the death rate dropped dramatically.
Although you would suspect that modern practitioners certainly wash their hands between patients, especially between surgeries, you would be wrong. Eighty percent of hospital infections happen today because doctors don't wash their hands, resulting in deaths of thousands of people and costs of over a billion dollars a year. For instance, more than one-quarter of the University of Pittsburgh Medical Center's doctors don't wash, because proper washing takes time and costs them money they would otherwise be making, according to an article in Business Week that interviewed some of the nation's leading doctors.
According to these doctors, some of their colleagues are killing and robbing thousands of Americans a year. And these unindicted felons are the same critics calling for the power of the government to raid health food stores and throw so-called "alternative" practitioners into jail. These are also the same moral miscreants who use government propaganda to warn disease victims to reject any other treatment and therapy except theirs. They are the ones in collusion with the pharmaceutical companies who are trying to ban nutritional supplements with Codex Alimentarius. They point with their unwashed hands at anyone who dares to contradict them.
Stang recalls the story of Abraham Cherrix who had Hodgkin's disease. The doctors told him to take chemotherapy so he did. It failed and the cancer returned. The chemo had left Abraham so weak that he couldn't walk. He didn't want to do it again, wanting instead to try "alternative" treatments to restore his immune system. Doctors used the courts to force him to again take the same chemotherapy that had failed him and left him so weak.
Abraham's dad asked the social worker, "What will you do with my little boy? Will you take him somewhere and strap him down and put duct tape on his mouth and pump him full of this stuff if he doesn't want it?" The social worker replied, "No, I will come to your house with a uniformed officer, and I will take your son by force if he resists. And I will take him to somebody else who will do that." As the result of the huge public outrage over this case, Abraham finally won and was returned to his parent's custody.
How could this have happened? The disease establishment is willing to do anything to protect and maintain its multi-billion dollar control of the people. Establishment medicine as practiced in the U.S. is monopoly medicine. Any threat to that monopoly is taken seriously. The four big players in monopoly medicine are the government, the AMA (American Medical Association), the drug companies, and the medical schools.
No matter how beneficial prevention modalities and alternative treatment modalities are to the people, they must be concealed, controlled, and done away with. There is a kind of psychic disconnect practiced by the establishment mentalities that want to do away with the means to prevent and treat conditions that may eventually threaten their own lives.
As the drug companies and politicians try to line us up for forced vaccinations and treatments, it's good to remember that forced medical treatment was one of the main principles of Nazism. The Holocaust did not begin with the extermination of Jewish people. It ended with them.
The Holocaust began with the doctors when Hitler was still in jail during the Weimar Republic established after World War I. The Allies had promised Germany there would not be a punitive peace. Of course they lied and ended up imposing a ruinous war debt at the Versailles Conference. When Germany could not pay, the doctors decided to do their patriotic duty by eliminating "useless eaters". They began with handicapped children and worked their way to criminals and beyond. Since doctors were running the program, the public swallowed it as just being "humane". Only years later was this program known as the Holocaust, which many people today wrongly believe only exterminated the Jewish.
The fact that Business Week was able to publish much of this information in their cover story suggests that the disease establishment may be losing some of its control. But like many large beasts, monopoly medicine is probably more dangerous in its death throws.
Sources:
Author not noted, "Medical Guesswork", Business Week, May 29, 2006.
Stang, Alan, "Today's American Medicine: The Cure," (www.AlanStang.com) .
About the author
Barbara is a school psychologist, a published author in the area of personal finance, a breast cancer survivor using "alternative" treatments, a born existentialist, and a student of nature and all things natural.
Mercury Fillings Shattered! FDA, ADA Conspiracy to Poison Children with Toxic Mercury Fillings Exposed in Groundbreaking Lawsuit
by Mike Adams
(NaturalNews) The FDA has, for decades, ridiculously insisted that mercury fillings pose no health threat whatsoever to children. While dismissing hundreds of studies showing a clear link between mercury amalgam fillings ("silver fillings") and disastrous neurological effects in the human body, the FDA denied the truth about mercury and effectively protected the mercury filling racket that has brought so much harm to so many people. For over a hundred years, a cabal of "mercury mongers" made up of the American Dental Association, mercury filling manufacturers and indignant dentists have reaped windfall profits by implanting toxic fillings into the mouths of children, all while insisting that mercury -- one of the most toxic heavy metals known to modern science -- posed no health threat whatsoever.
Today, that reign of toxicity is about to end. Thanks to the tireless, multi-year efforts of people like Charles Brown, National Counsel for Consumers for Dental Choice (www.ToxicTeeth.org), the FDA has now been forced to acknowledge a fact so fundamental that, by any measure of honest science, it should have adopted the position decades ago. What position is that? Simply that mercury is toxic to humans.
Why the FDA has to be sued to do its job of protecting consumers
The FDA's stonewalling on this issue has been nothing less than a circus of politically-motivated denials, much like the Big Tobacco executives swearing under oath that "Nicotine is not addictive." In similar style, the FDA insisted for decades that "Mercury is not toxic." Both statements, as any sane person can readily conclude, are the outbursts of lunatics. Sadly, those lunatics somehow remain in charge of our nation's food, drugs and cosmetics (and dental care), meaning that any real progress to protect the People must come from outside the FDA.
And that's exactly what just happened. Consumers for Dental Choice teamed up with Moms Against Mercury (www.MomsAgainstMercury.org) to sue the FDA and its commissioner whose name sounds like an evil-minded villian right out of a Marvel comic book: Von Eschenbach. The lawsuit, entitled, Moms Against Mercury et al. v. Von Eschenbach, Commissioner, et al was concluded earlier this week with a reluctant agreement by the FDA to both change its website on the issue of mercury and to reclassify mercury within one year, following a period of public comment (which the agency will no doubt try to drag out as long as possible in order to avoid actually sticking to the terms of the lawsuit agreement).
Remarkably, the FDA's website no longer claims mercury is harmless. The language has now been changed in dramatic fashion, reading: "Dental amalgams contain mercury, which may have neurotoxic effects on the nervous systems of developing children and fetus."
There's still a lot of fudging there. Note the careful use of the word "may," which means the FDA still isn't sure whether mercury is neurotoxic, but it might be. This is the FDA's way of continuing to stonewall this issue, even as it lost its lawsuit. For any FDA officials who don't yet think mercury is toxic to the human nervous system, I invite them to chug a few milliliters of the substance themselves and find out what the effects might be. It certainly couldn't make them any more mad than they are already!
Why the FDA is as mad as a hatter
Speaking of people going mad with mercury, that's the history of the term "as mad as a hatter." As explained by Wikipedia:
There is scientific evidence behind the meaning of insanity. Mercury was used in the process of curing felt used in some hats. It was impossible for hatters to avoid inhaling the mercury fumes given off during the hat making process. Hatters and other men in working mills died early due to the residual mercury caused neurological damage, as well as confused speech and distorted vision. As the mercury poisoning progressed to dangerously high levels, sufferers could also experience psychotic symptoms, such as hallucinations. See http://en.wikipedia.org/wiki/Mad_hatter... to read more.
Interestingly, the symptoms of mercury toxicity quite accurately describe the mental state of the top decision makers at both the FDA and the American Dental Association, both of which have hallucinated for decades that mercury was safe for children to swallow! These people also exhibit symptoms of serious neurological damage such as malfunctioning frontal lobes -- the part of the brain responsible for reasoning. They also seem to lack proper functioning in the part of brain responsible for empathy and compassion towards fellow human beings.
Perhaps top FDA and ADA officials have been chemically lobotomized in some way, and there's no question that the leaders in conventional dentistry suffer from advanced stages of psychosis, too. This could very well be due to the fact that their ongoing use of mercury fillings has exposed them to decades of mercury vapors and airborne particles which have entered their nervous systems and damaged their brains, making them appear quite mad.
Thus, the modern version of "mad as a hatter" might be, "mad as a dentist."
Not all dentists are mad, mind you, but the ones that still work with mercury no doubt suffer very real neurological damage as a result.
What's next for the FDA
Despite this lawsuit victory, please keep in mind that the FDA has not agreed to immediately ban toxic mercury fillings. They have merely agreed to consider reclassifying mercury at some future date -- a commitment they will probably break, given their history of lying about mercury and refusing to do what they've agreed to do on this subject (see the interview, below, for more details on that).
At every opportunity throughout recent history, the FDA has gone out of its way to censor the truth about the toxicity of mercury fillings, thereby directly supporting the continued exposure of literally hundreds of millions of children, adults and senior citizens to a substance that every reasonable scientist in the modern world knows to be highly toxic to the human nervous system. And in this way, the FDA is guilty of crimes against the People. To know that a substance is highly toxic, and yet to continue allowing it to be implanted into the mouths of children, teens and adults (even when you have the power to ban it) is not merely irresponsible, it is downright criminal.
I can only hope that a nationwide class action lawsuit against the ADA, the FDA, local dentists and mercury manufacturers will emerge from this action. Countless Americans have been poisoned by mercury fillings, and the whole scam has been orchestrated by the usual suspects: Powerful corporations and industry groups that sought to exploit the People for profits, regardless of the harm it might cause them. The fact that a substance as toxic as mercury has been allowed to be implanted into the mouths of children for so long reveals precisely how corrupt, outdated and downright dangerous our system of modern dentistry has really become. Much of what comes out of the mouths of dentists, it turns out, is pure poison... and not coincidentally, that's exactly what those same dentists put into the mouths of their own patients!
But I don't want to give the impression that all dentists are evil. In fact, more and more dentists are now practicing mercury-free dentistry, and I strongly recommend that if you need to see a dentist in the future, insist on seeing one that has given up using mercury. This is more than a personal health issue, it's also an environmental issue. Where do you think all the mercury goes after you chew on those silver fillings and swallow little mercury bits? The mercury molecules that aren't absorbed by your body and lodged in your brain cells are eliminated from the body and flow right into the environment. Ever wonder why all the seafood bring harvested from the ocean these days is contaminated with mercury? Well now you know: It's due to all the toxic consumers peeing away the mercury they've swallowed from their silver fillings!
The FDA remains steadfastly clueless about mercury
So now, thanks to this lawsuit, the FDA has changed its website to read: "Pregnant women and persons who may have a health condition that makes them more sensitive to mercury exposure, including individuals with existing high levels of mercury bioburden, should not avoid seeking dental care, but should discuss options with their health practitioner."
This sentence says nothing conclusive of course, and it doesn't urge consumers to avoid mercury in any way, but it does at least imply that perhaps there is a link between dental care and mercury poisoning. If you're interested in being amused, you can read all this distorted language yourself at: http://www.fda.gov/cdrh/consumer/amalgams.html
This document, by the way, reveals the outright stupidity of FDA "experts" as they stumble from one topic to the next. For example, one question asked on the page is:
Should pregnant women and young children use or avoid amalgam fillings?
The FDA's answer to that is: The recent advisory panel believed that there was not enough information to answer this question.
In other words, the FDA advisory panel selectively chose to avoid all the evidence showing mercury to be extremely harmful to the nervous system of a fetus or a child, and they have decided to pretend to be uninformed on the subject rather than take any real stance on protecting human beings from the toxicity of mercury. Wow, and to think, these are the people running our national food supply and drug approval processes, too! Is it any wonder so many drugs are deadly? If the FDA thinks mercury is safe, no wonder they think deadly pharmaceuticals don't harm people either!
Exclusive interview with Charles Brown, Consumers for Dental Choice
In the days leading up to this lawsuit with the FDA, I spoke to Charles Brown over the phone and explored the timeline of events involving the FDA and mercury. This interview, published below, is nothing short of astonishing! In it, you'll learn about the FDA's stonewalling tactics, the lies and deceptions of the American Dental Association, and why it took an outside consumer group suing the FDA to get the agency to do its job of protecting consumers from toxic mercury.
Mike: The story here is that you and the organization – Consumers for Dental Choice are now suing the Food & Drug Administration to seek removal of mercury fillings from the U.S. marketplace. Can you give us some details about this lawsuit? Why you think suing the FDA is the best way to go here.
Charlie: Well sure Mike, the FDA is the spoke of the wheel here. I mean they are the ones that make decisions on whether products should be on the market or should not be on the market. They approve, they classify. In the case of devices – a device is something that is used in healthcare and it is separately regulated under a set of rules. One category of devices is implants. Implants are what goes in the body but does not dissolve. It stays in the body at least six months and does not dissolve.
Dental fillings are an implant. The FDA is deciding instead of classifying, instead of regulating it, it will do nothing and it has done nothing on mercury amalgam – encapsulated mercury fillings - decade after decade. They continue to promise to act and actually, last year they made me a written promise and I foolishly believed them. I actually thought when they promised, in writing, that they would begin the classifying process and put together the first step.
They promised me specifically what the step would be, I naively thought, "Well, gee maybe these people are honorable and telling the truth." Actually, once again, they have just pretended. Under pressure, they will say they are going to do something – pressure from Congress, pressure from the Courts, pressure from petitioners, pressure from the press.
They will say, "Sure, we are going to do something." They do nothing. They have left this mercury amalgam out there unclassified, unregulated with no warnings and just a few news releases, which have nothing to do with what they are supposed to be doing.
Mike: So mercury fillings – let me just get this straight from the beginning here, have never been classified by the FDA, which means they have never been really approved by the FDA, correct?
Charlie: Correct, this is a primitive filling in the first place but the pre-primitive – the pre-historic system in the 19th and early 20th Century was where was the dentist mixed the mercury with a powder. That lasted until the 20th Century with the old-fashioned offices. It is now prohibited in several states but that was the way where the dentists would mix a bottle of mercury and powder. That has been classified – not together, but the powder has been classified and the bottle of mercury.
No dentist does that anymore. They are not allowed to do it that way where the ADA tells them not to do it. The state government tells them not to do it. Everybody tells them they cannot do it that way and they do not do it that way. They take the capsule that they receive in the mail. The capsule has never been classified. The FDA knows to classify. Any step that the FDA takes, that the Food & Drug Administration takes toward addressing mercury fillings they know it is the beginning of the end.
Mike: That is my next question. Do you think there will be a cascading effect here? I mean if the FDA honestly begins to apply the law; it would then have to mean the end of mercury.
Charlie: It is the end of the mercury fillings if they apply law so they have intentionally done nothing. If they classify amalgam, they know they are going to have to classify it similar to other mercury devices so they do not do it.
Mike: They just try to delay this and hope no one notices.
Charlie: They will delay until they retire – not delay until next week. They will delay until they retire. Then they will get the golden retirement egg from the American Dental Association. They also know that if they did an Environmental Impact Statement it is the end of mercury fillings.
Mike: Well, that is my next question.
The environmental impact of mercury fillings in dentistry
Charlie: Environmental... yes, sure – the Environmental Impact Statement says it does not require you to go a certain step but if you say if we use mercury fillings, it is the largest source of mercury in the wastewater. Its cremation is the largest source of mercury in the air except in communities that have many power plants is something.
In communities with no other industrial mercury uses it is the largest source of mercury in the air and is the largest source of mercury in the water in every community in America -- the huge contributor in coming out of cemeteries and so on. So you say if we continue mercury fillings, it is an environmental disaster. If we ban them, it is environmentally the right thing to do. Once they have done that the logical step since you could go either way is to take the environmentally friendly move.
They will not do an Environmental Impact Statement. It is a conscious decision inside FDA of protectors of mercury fillings – people like Susan Runner, people like Norris Alderson who have decided that they will protect the use of these fillings on behalf of organized dentistry and they will defy the laws of the land to do so.
Mike: I have so many questions to ask you about this. Let us start with one that I think any intelligent reader would be asking himself or herself and that is if this mercury is so toxic to human biochemistry and if it has such a detrimental impact on the environment, how could so many dentists and the American Dental Association be in such strong support of it.
Charlie: Yes, it is amazing. It is amazing. It really goes to the foundation stone. Clearly if we had it to do over again we would not build the combustion engine. The invention of the combustion engine may have been the decision that destroys our planet unless we can reverse that. I mean clearly that is the main reason we are turning our planet into a heat box.
However, the foundation stone is the combustion engine in which Henry Ford put us. The foundation stone of dentistry is mercury fillings. If there had been no mercury fillings, there would have been no dental profession. That is a certainty. We now have physicians of the ear, nose, and throat. In the 19th Century, there were physicians of the mouth. They said to use mercury is malpractice.
The barbers put the mercury in. It worked better than gold, which was very hot then. It hurt you to go in. Whereas, the mercury was nice and smooth and people were drinking mercury for syphilis so they were able to put it in there because medicine had not yet pushed it out of their profession. They pushed it out again not counting vaccines but they pushed it out of medicine around 1900, but dentistry was something different.
By then dentistry had gotten their market niche. Their market niche was we are going to take care of the mouth. They created an entirely different profession – one that basically is not related to healthcare. They take the position the mouth is so different from the rest of the body we will just worry about the mouth and nothing else and you doctors will not worry about the mouth at all. We have the most grotesque healthcare system where physicians even refuse to look at the mouth. People in the hospital – you can be in the hospital, you can be so sick and nobody is going to look at your mouth except the dentist.
It is like a division of labor where they both make their money and the person harmed is the public, so organized dentistry took the position since mercury is safe by definition because we use it and we are doctors, anything we put in the mouth is safe. They just put in... they put beryllium in there.
They put anything in there with the idea of we are immune because we are doctors. We know what we are doing and it is just a tragedy. It is just unbelievable that we ended up with a profession so wedded to the most neuro-toxic element on the planet.
Why dentists are walking away from mercury fillings
Mike: Well, you hinted at the arrogance of the professionals who continue to support this mercury and you mentioned the history quite a bit there. I have to wonder that given that nearly a hundred years have passed since this was being widely introduced into dentistry and with all the information about mercury's toxicity over the years, how could dentists still say that this substance is not harmful? What is their argument now?
Charlie: Well, half of them do not use it now. See half of them have walked away from it. Here is what happened – enter the institutional powerhouse, the American Dental Association, to impose a top down system. The ADA realizing that they had a secret. The ADA became the whole player on the field. The ADA is opposite the AMA in many ways and I am not – believe me I am not a supporter of the American Medical Association. I do not mean to say that but in this one area the AMA has a set of ethics that make sense, which is we do not endorse products for money. The AMA ventured into that I think in about the '30s and decided they had better stop and then they ventured into it again in the '90s and they realized they could not.
They promised their membership. They had to fire their executive director, break this contract with Sunbeam, and promise they will never endorse products for money. That is the AMA's ethical position and it is an ethical position. The ADA – the American Dental Association has no such ethics, Mike. They endorse products for money.
The ADA, starting in the '50s really, the 1950's, they really took off at that point. A product endorsement system, business studies show that Crest was a minor toothpaste product compared to Colgate. Crest surpassed Colgate because the they poured money into the ADA coffers and the ADA, in turn, gave their name to Crest to say we endorse this Crest toothpaste. It became such an advantage for Crest that the other toothpaste makers decided they would slop money to the ADA too, which they did.
The ADA was not only unethically telling the public a product is safe when they did not know if it was safe. They were not testing it. The ADA was even taking money from their members for joining and then turning around and saying to their members you should use this product because we endorse it, because it is safe and effective when they had no idea if it was safe and effective.
They were serving two masters but the corporate master to ADA was paramount and so they took these sums of money from every dental products manufacturer, became a dental products endorsement machine more than a professional group – much more than a professional group. You had that basic powerhouse – the ADA saying go buy these products.
Then the ADA saw the criticism of mercury amalgam coming in the 1980's and they knew they had to do something because they were getting money from the manufacturers and they had dentists that did not want the public to know. The ADA adopted a gag rule in their code of ethics in 1987 and it said that dentists should not tell anybody about the toxicity of mercury.
Mike: Really?
Charlie: Yes, absolutely.
Mike: They adopted a gag rule about mercury fillings?
Charlie: They adopted a gag rule. In the Goldwater Center, the Phoenix based Goldwater Center wrote an essay condemning the gag rule in 1998 – a decade later. They were the first ones to do it.
They are a think tank, kind of a libertarian think tank I guess you would call it – the Goldwater Center. Modeled after the thinking of their namesake of the group, of course, Senator Goldwater... he did not found it but it was founded on his principles and Congressman Flake was the executive director. He is now a Congressman.
When he was executive director, Mark Gingrich – a former reporter at the Arizona Republic, who joined that group, wrote a whole report on the gag rule and how bad it was. That was the libertarian from the right if you will. The libertarian on the left – the American Civil Liberties Union, took the same position. They sued the Connecticut Dental Board here on the other coast, said you cannot have this gag rule, and won.
Then the attorney general of Oregon, the attorney general of Iowa said you have to stop the gag rule so bit by bit, piece by piece, the gag rule has been dismantled but the value of it was the ADA protecting its product.
I will tell you something else when they adopted the gag rule, I left this out: the ADA had patents on mercury amalgam. Not only did they get money for promoting the product. They even got patents on amalgam to protect its use, then told dentists do not talk about this product.
Mike: This sounds like just a financial racket here.
Charlie: The ADA is a financial racket. There is no question about it. To break the control over mercury fillings you not only have the history, they have to protect their profession, which was founded on mercury. I mean it is not that now but it was founded on mercury – the foundation stone. They have to protect their own history and their own pocketbooks.
Now with the gag rule crumbling they have many problems. The ADA has huge problems with this. They are in retreat. Mike, the one thing is they are definitely this year they began retreating. We gave them an exit strategy. December of 2006 I sat down in the ADA headquarters and said you guys know you have to get out of this and I have a cost-free exit strategy that will not destroy your reputation. We presented – Consumers for Dental Choice presented the ADA – the American Dental Association with an exit strategy on mercury fillings based on the environment where the ADA could say they would not have to concede any health issues. They would say we recognize that mercury amalgam is an environmental problem. Alternatives exist, therefore, we are announcing a phase out over the following number of years.
I asked for one year and they said it would have to be longer and I said okay, but I said we have to have an end. People have said to me well let us take them on like cigarettes and I will tell that is about the worst prototype I can think of where the lawyers became billionaires and kids are still smoking.
I am not going to tolerate that kind of end where a bunch of people get rich and the kids are still harmed... because poor kids are still getting mercury fillings and poor Latino pregnant women and Native American children and so on are getting this. We are not going to accept that. There has to be an end date.
They were willing to do it. The lawyers were willing to do it at this discussion – December 14, 2006 at the ADA offices in Chicago but they just could not pull the trigger with the ADA. They just could not have a second meeting. They have decided instead through 2007 they are doing a gradual retreat. There is no question they are. It is coming, but the gradual retreat continues to harm millions of people in America and around the world. Their gradual retreat is not acceptable. We are not going to have a Vietnam ending where we have eight years to withdraw.
Mike: Right, now, I mean obviously the ADA does not want to admit that mercury fillings were ever a hazard because then they could open themselves up to huge class-action lawsuits, right.
Charlie: Absolutely and I told them I hope they do get huge class-action lawsuits and some day they will because they would not walk away from it. They had their chance and they continued to give this nonsensical stuff about how mercury exposure is okay as long as they do it. It is just outrageous. It is morally outrageous and they know it.
The scientific reports that they produce are cooked. They are unethical. They have no scientific aspect. They are simply PR machines where they find some dentist – not a real scientist but just their fellow dentists to write reports. It is an effort to say we are going to protect ourselves, we are going to have our government do it, the government is going to do it for us, and the FDA is about as compliant a government agency as ever existed.
Mike: Now, what happens if your lawsuit succeeds with the FDA? I mean essentially, what has to happen next for the FDA to ban mercury fillings?
Charlie: Well, they could take many routes. They could just ban it. They could start doing their job. If they start the classifying process then amalgam is gone. The ADA has admitted that. The ADA warned its members the FDA is probably going to put restrictions on amalgam. That process has started. They promised us they were starting then the FDA just stopped. They just stopped because within the organization they reversed the course and decided effectively that dentists are more important to them than consumers. It is just so tragic that dental economics out-trumps children's health but that is the way the FDA operates.
Mike: Well but that cannot be a surprise to anyone who follows the FDA...
Charlie: Well it is a surprise to those of us that had an assumption that we actually believed what we were told. I know if you follow FDA, it is not a surprise. The FDA needs to be totally reorganized. They need to stop having a system where those with a self-interest in the product are the ones that get to make the decisions.
The idea that Susan Runner, a practicing dentist, is at the FDA doing the work for the ADA and has actually had a sort of agenda to cover up mercury decade after decade and it is still being covered up in the Dental Devices Branch. The fact that Dan Schultz – the physician who's head of Devices will not remove her or allow anybody but a dentist to be in charge, this shows the professional courtesy that physicians give to dentists. Schultz simply closes his eyes.
He knows it is a problem but he is a physician. He wants dentists in charge because that is the deal they made a hundred years ago that dentists are in charge of the mouth and the public is shut out and physicians are to blame as well on this for shutting their eyes. Dan Schultz is as morally culpable and legally culpable at the FDA as Susan Runner is. That is why we sued him and sued her both and several other people.
Arresting top FDA officials and charging them with crimes against the People
Mike: Now, I am on the record saying that I believe the FBI should march into the FDA offices and arrest these individuals and we should prosecute them for criminal behavior against the American people. Do you think that is going way too far or do you think that's quite reasonable?
Charlie: That is probably not going too far. We filed a series of complaints with the Inspector General. We filed complaints with the in-house FDA Inspector and then filed a complaint with the U.S. Inspector General last Fall. They have decided they will not comply with the law. They know they have to classify mercury amalgam. They will not do it.
They know environmental impact statements are required or environmental assessments are required – the first step. They will not do it. They know that they warn about all of the mercury exposures such as fish or they warn against as a matter of precaution mercury exposure to children from all other sources. They banned mercurochrome years ago. They took it out of childhood vaccines – actually not of them but they said they would take it out of all of them.
They gave warnings on fish for children and pregnant women. They have decided that they will stand silent on mercury and it is truly a conspiracy of silence. That is why our lawsuit did not just sue the FDA. We sued five deep into the bureaucracy. We know whom the players are who are ignoring their duty and we have named them because we are tired of the FDA having a system where they all can hide behind each other. I hope that system ends and our lawsuit plays a role in exposing it.
Mike: Now, you just mentioned mercury in fish and that is a great point. Do you happen to know how many times more mercury there is in a typical filling than would be found in a serving of fish?
Charlie: Well, it is a more severe exposure because in the fish it is locked in. The mercury from the fish is mainly going through the body. It is a lesser exposure. The mercury in the amalgam is implanted. The mercury in the fillings is thousands of times more because it is half a gram. That is 500,000 micrograms per filling.
Mike: Where we are talking micrograms in the fish, right?
Charlie: Yes, yes we are. We are so I mean it is so much more but it is a way for medicine and dentistry to change the subject and to blame the fish. It is the fish's fault.
Mike: So the FDA says well, mercury in fish is dangerous to you but mercury in your mouth, in your teeth is harmless.
Charlie: Well, the FDA has said that. You know the FDA does not speak through its news releases. The FDA speaks through its regulations and its warnings. It has never officially said anything about mercury amalgam. They know it cannot stand the light of day. Yes, they make off-the-cuff comments.
They come out with a white paper, which has nothing to do with a regulation – and they refuse to say who wrote it. If FDA staff has furtively sneaked out interviews, white papers, other ways to say mercury fillings are safe but officially, FDA is not saying that at all. Officially, FDA is taking the position that they have never taken a position that it is safe.
When forced by the Court to say is mercury safe or not in the first lawsuit we filed, the first bombs against mercury versus FDA, the FDA admitted five times that it does not know if mercury fillings are safe. I can give you all five quotations from their brief or I can give people the website to look it up.
Meet Consumers for Dental Choice
Mike: Can you tell us a little bit, about where your passion comes from on this topic and people would like to know a bit about your background and your organization – Consumers for Dental Choice.
Charlie: Well, sure. Consumers for Dental Choice were founded a decade ago. Came up with the idea in 1996 – it was an idea of Bob Jones who is an inventor from Colorado and now in Texas. He is a former airline pilot, former U2 pilot earlier than that. He is just an outstanding man and inventor and an engineer. He has many patents.
He got very sick from mercury fillings and realized the impact of them was severe. He got to know many of the pioneering dentists like Hal Huggins and Scott McAdoo. He was out west and in the east Sue Ann Taylor, a journalist in Atlanta came up with the idea that we really need a consumer movement to fight this. Bob Jones had a conference, which he paid for and sponsored in Denver in 1996.
I was in a law firm that represented a lot of alternative health practitioners and interests and consumer groups in the kind of cutting edge alternative health issues many of which no longer were cutting edge because of the work of the senior partner, Jim Turner.
Anyway so Jim Turner and I went to that and we decided we would start up the group but Jim came up with the idea we called it the Consumers for Dental Choice and it became a project of another non-profit and then became its own organization in 1999.
Then it became a spin off, I left the law firm with it in 2002 to become a full-time consumer group with an office and so on. It has been around for 12 years. It has been a stand-alone organization for six. I got into it representing alternative health groups. I represented many alternative health ideas. I have been a state attorney general of West Virginia in the 1980's. I have been a political activist in the past and had interesting kinds of legal challenges I think.
This has just appealed to me and I guess the more I get into it the more I realize how many children are being hurt and how many animals are being poisoned and we have to do something. The way to do it is to have a very aggressive activist organization. It needs to get right in the face of federal or state regulators or the private sector interests like manufacturers or the ADA.
Mike: What about your funding? Where does your funding come from?
Charlie: We get some money from foundations – the Garfield Foundation is a wonderful funder, has funded us for seven years. For a long time we were funded by the Wallis Research Foundation, a family foundation. The patriarch was H. B. Wallis, an inventor from Iowa. He then lived in Scottsdale near you Mike.
He died a couple of years ago and that funding ended at that point from the Wallis Research Foundation but Garfield funds us and then individual dentists and that number grows each year... dentists who have decided to give money off their credit card every month or give an annual contribution and it is very exciting. These people are mercury-free. They are the people who know the ADA is wrong and know we need to fight and they are so much a part of our team that quite a few of them give money. It is terrific.
Mike: How quickly is that movement accelerating towards mercury-free dental care?
Charlie: Well, fast. The number of mercury-free dentists, if that is any measurement, was 9% in 1995. This is according to the Clinical Research Associates run by the preeminent dentist scholar, very neutral. He has no dog in our fight – Gordon Christensen out of Orem, Utah.
One of the things he surveys in dentists is who is mercury-free and it was 9% in 1995. Then 27% of dentists were mercury-free by 2001; by 2005, it was 32%. In 2007, a different survey – this was by a dental magazine said that 52% of the dentists are now mercury-free. It may have reached that number. It may have reached half. It may have reached the tipping point. The progress on dentists is huge. The progress of consumers, the number of mercury fillings was far over 50% when we started, like 60% or something like that I believe or more.
The ADA says it is fewer than 30%. I am sure it is but that is the good news. The bad news is it could well get frozen at that number where we have two-tier dentistry where middle-class adults get no mercury but the poor, the children, the working class people, minorities, children, they keep getting mercury and that is absolutely both immoral and unacceptable.
Mike: How much mercury is actually released into the environment or put into people's mouths each year through dentistry?
Charlie: Well, I do not have that but the expert is the Mercury Policy Project and Michael Bender. They are really the experts. Their website is www.MercuryPolicy.org. Michael has written just some seminal reports on this. About every two years, he writes another one. If the folks want to go to www.MercuryPolicy.org they will definitely see what they need to do.
Mike: While we are mentioning websites, I want to mention yours again. It is www.ToxicTeeth.org
Charlie: Yes it is.
Mike: Can consumers also financially support your organization with a donation?
Charlie: Sure, our address is 316 F Street Northeast, Suite 316, Washington, D.C. 20002 and again our website is www.ToxicTeeth.org
Why conventional dentists are so arrogant about mercury and fluoride
Mike: Okay and I will check out www.MercuryPolicy.org too. I will take a close look at that. Getting back to the dentists themselves it is encouraging to see that perhaps as many as half of practicing dentists are now shunning the use of mercury. You have to wonder what the other half are thinking though.
I have had numerous conversations, debates, arguments with dentists. I find that those who are still using mercury also still support mass fluoridation of the water supply. They are some of the most arrogant people I have ever met. It is infuriating because his or her position is that no one has any right to question mercury or fluoridation. It makes you wonder. Where are these people coming from that they think they already know so much about mercury that they have declared it to be harmless and no one can challenge that?
Charlie: Albert Einstein once said it is always unusual to find someone for whom curiosity survives a formal education. There are so many dentists and they are not alone in this among professionals who get that degree and now they can turn off their brain and make money. These people have decided just to read the ADA propaganda and that is it.
You hear that these pro-mercury dentists defend their use of mercury fillings and they will not use the word "mercury" they will give false information as if it is inert. It is not. They know it is not. If they read anything, they know it is not inert.
They may just decide to believe it themselves and their big rationale and every pro-mercury dentist that you talk to will give this rationale within the first two minutes. We know it is safe because we have used it for 150 years. Now, I guess the first response to that is what other part of pre-civil war medicine do you endorse?
The second point is that it is the most absurd scientific reasoning to say something has been used a long time and therefore is safe. I mean cigarettes must be safe. I have this article, a copy of it, from the British Lancet. Lancet is the British equivalent of the American Medical Association Journal but it is much better. It is much less sleazy in its connection to special interest groups, which the AMA Journal certainly is.
The Lancet had an article in 1860, an editorial in 1860 that said cigarettes are the universal product around. If it were dangerous as if its critics said people would be dropping dead in the streets, and clearly its universal use proves that it is safe and it is time to quit criticizing it. That is what things are with amalgam. They make jokes. Well, nobody dropped dead in my office, they say.
Well, if somebody gets sick later he or she does not go back to the dentist. The dentist says I am just in charge of the mouth and just the metals I put in the mouth. I do not have any other role. If I cut you while I am putting it in, well I know I have to deal with that because then I have done something that is in the mouth.
Any total body effect of what I do leaves with the patient. They get that patient out of the office. They are done with them and then they have this wall of silence and nobody can get back in and beat them in court, although we are going to beat them in court soon. Dentists literally say it is safe because we have done it for 150 years. Does that make it good? – is this good if we do it for 150 years?
It was the same argument for slavery. It was the same argument for cigarettes. It is the same argument for everything. If we do it long enough it must be good. That is just the most absurd thing for a man of science or a woman of science to say but by goodness, they do.
Mike: Yes, they do. I know you are not focusing on fluoridation but of course, this issue extends to fluoridation where I personally find many of the same similarities – a complete lack of scientific evidence supporting it, a denial of the dangers of fluoridation and the extreme arrogance and unwillingness to consider any possibility that they might be wrong.
Charlie: Yes, absolutely, absolutely and I think that is why you would say well how could this continue for so long. I mean how segregation could continue for a hundred years. I mean how could it take 70 years to ban lead in gasoline?
In the early 1920's as they started to mass produce gasoline with lead in it the people started dying. Workers died. Workers died in large numbers and everyone knew lead was the culprit... I mean everyone knew. Just as everyone knows mercury is toxic. Everyone knew lead in the 1920's knew lead was toxic.
The gasoline industry and the oil industry came up with two solutions. One is they thought of the funny word that said we have added ethyl to the gas. It means lead but they thought just as the dentists say silver fillings or amalgam. To protect the workers they raised the steam stacks in the plants where the gasoline was made.
In other words, rather than the workers getting sick and dying immediately from the lead exposure, the chimneys were raised so high that the lead went into the higher atmosphere and started just polluting the whole country. The workers were semi-saved in the sense they were not dying on the spot and the whole country was getting to the point of huge toxicity.
The study showed that as we took the lead out of gasoline in the '70s the level of violence committed by teenagers started going down immediately because each year they were less lead-toxic and the ones growing up were not starting out with lead toxicity. Lead toxicity like mercury toxicity causes people to be violent because they are poisoned. They just strike out.
It took from the '20s to the late '70s and everybody knew it was toxic and again with mercury fillings because the oil industry had such well-placed lobbyists and they were able to revert the question, saying we do not have to prove it is safe, you have to prove it is unsafe. That is what the dentists keep doing. We have done it for 150 years so prove it. Well, okay we can prove it. But they say, now you are not going to prove it with us having the government in our pocket.
The government people are in their pocket. Randall Luter, who had a lot of promise, he was Deputy Commissioner. He has just decided to sleep on it. Let the dentists and the bureaucrats' be back in charge of this issue at FDA; those people have decided we do not care. We are going to protect special interest groups or we are going to let others at FDA protect special interest groups so we have a similar resolve.
How to stop the FDA with a lawsuit
Mike: To conclude this – getting back to the lawsuit itself, if you win the lawsuit can it force the FDA to rule on this? Why cannot the FDA just say we will deal with it later? I mean can they not just continue to delay even if you win the lawsuit?
Charlie: Well, that is a challenge. You pointed to that. I mean if a court just looks at the FDA and says hurry up and do it, the FDA will nod, oh your honor we certainly will. We will hurry as fast as we can. In that sense, it may not do anything. We are trying to build accountability of public officials and that is why we have asked for the remedy that the court should simply take it off the market until FDA does its job.
Then I will bet they start moving fast. That is a challenge – a challenge to get that kind of remedy. Nonetheless, we have to begin. We sued them in the U.S. Court of Appeals. The Court of Appeals gave us a roadmap to go to district court. We were all set to file in May of 2007 and the FDA said no they would like a meeting. Please do not file. They would like a meeting. We had a meeting. We said we need an answer in 30 days.
In 30 days, the FDA answered and said yes, we will do an advanced notice and a proposed rule. I got a letter from the lawyer for the FDA, Wendy Vincente saying speaking for the FDA we will do this... we assumed that the FDA was telling us the truth. We were wrong so we waited and waited and waited because we would have filed this suit in June.
The FDA just bought six, seven months of time simply by telling another bald faced lie, which was that they were going to start moving forward to classify amalgam when... I think some people at the FDA probably have that intention. I think there was good faith from some people but the bureaucrats – the ones that want to keep mercury fillings unclassified, protected for dentistry like Susan Runner - have won out.
The FDA is so badly organized, its lead scientist – the Associate Commissioner for Science, the top science person of the agency, degree is in veterinarian medicine.
Mike: Their degree is in veterinarian medicine?
Charlie: Veterinarian medicine – not a toxicologist, not a chemist, the top person has a degree in veterinarian medicine.
Mike: Well, let me just say right here let me offer that when it comes time to apply grassroots pressure give me a call because we can put out an action alert to our reader base, which is now over one million people.
Charlie: That is fantastic.
Mike: If we coordinate it with what you are doing then we can create this real surge of grassroots pressure because I think what you are finding out is that if you take the FDA's word on anything, then nothing is done. If we can pressure them from another angle that can really assist your lawsuit effort or other efforts in applying pressure. What we need is a re-launch of a campaign as you had "Mothers Against Mercury." We need, what I call, a Web sticker – like a bumper sticker on the Web. We need a little graphic, name like that "Mothers Against Mercury", launch this campaign, and let it go viral all across the Web tied to action items such as grass roots complaints or protests – those kinds of things.
Charlie: Well, I will tell you where we are going to work grass roots and I am happy because I have already told the company we are, Dentsply, is the second largest manufacturer of mercury fillings. They make others. They make resin. They make composite.
They also make the alternatives – porcelain and so on I think. I know they make a resin composite. They make many other dental products and Wall Street report said Dentsply would be better off if amalgam was banned, they would be more profitable. Dentsply nonetheless has dug in its heels and said we are going to keep making mercury fillings. Basically, Dentsply has turned its back on its own shareholders.
The Wall Street has said stop and they said we are not going to stop. Now whether this is just some kind of backroom deal with the ADA or pressure from the ADA that they cannot stand or some other reason that they will not explain to me. I have written them and their counsel wrote me back a "back of the hand" letter... about a two-paragraph letter or three paragraphs saying [nothing substantial]. Dentsply is not only harming consumers and dentists – dental employees, dental workers, the environment all of which they could be sued for.
They have an easy exit route. They could make the non-mercury fillings. That is an area we are going to work on – they are based in York, Pennsylvania. I think their day is going to come.
Mike: Well, what if we can organize all kinds of protests around that company even maybe not in person but phone calls, faxes, emails...
Charlie: Well, why not in person? Anybody who is listening to this and wants to contact me or anybody around the York, PA area or anybody in Pennsylvania that wants to help us ought to contact me that want to go in person. My email is
This e-mail address is being protected from spambots. You need JavaScript enabled to view it
We would like to get people to write but we want folks that are somewhere in the Maryland, eastern half of Pennsylvania...
Mike: We have readers all over the country and I know we could get people there. I do not know how many. I do not know if it is ten, 100, or what but I know we have people emailing us all the time asking what we can do. What can we do to fight these evil corporations? If we get some people out there protesting with signs – "Mercury poisoned my child" on their sign. If we get that up on YouTube this could have just a huge domino effect not only make more people aware of your organization but also the mercury toxicity issue.
Charlie: Okay, I will. Thank you sir.
Prologue
Following this interview, Charles Brown won a significant court victory over the FDA, and now the FDA has promised it will reclassify mercury by June, 2009. Between now and then, NaturalNews will be working closely with ToxicTeeth.org to rally grassroots support for an outright ban on mercury amalgam fillings.
Stand by for action alerts on internet protests, petitions, and perhaps even in-person protests. We must work together to demand that toxic mercury fillings be banned. Then we will end the hundred-year reign of neurotoxic terror that has been orchestrated by the ADA, the FDA and the conventional dentistry industry. We will also support a national class-action lawsuit against not just the ADA and FDA, but even against the individual dentists who have installed these toxic mercury fillings into the mouths of children over the last ten years, despite the incredible amount of scientific evidence proving that mercury fillings cause irreparable harm to human health.
It is time to stop poisoning our children and our planet with mercury. The era of mercury poisoning must come to an end. NOW. And those responsible for this chemical attack against our people must be made to compensate for the harm they have unleashed and serve time for their crimes against the People.
The revolution will be announced via e-mail.
If you're not already subscribed to NaturalNews, get on our e-mail list right now by signing up here: www.NaturalNews.com/readerregistration.html
In the months ahead, we'll announce key action items via e-mail. Join us in protesting against the ADA and FDA about the toxicity of mercury fillings, and be prepared to hammer your Senators and other lawmakers in Washington to urge them to support an outright ban on mercury in dental care.
This poison must be stopped! And it is up to you to help us achieve this important goal for the future of the human race. Literally, it is that important. We are talking about the future of human life on this planet. If we hope to live, if we hope to have seafood, or ocean ecosystems, or fully-functioning brains and healthy babies, we must stop mercury now.
Join the revolution. Stay tuned to NaturalNews. Watch your e-mail for important announcements from us.
And be sure to visit www.ToxicTeeth.org and join their e-mail list, too. Stay informed. Empower yourself. Demand real change. And when the day comes, I ask for your support in urging the arrest and prosecution of the criminals at the ADA the FDA who have orchestrated this mass poisoning of the American people. It is time to arrest, prosecute and imprison these criminals who are, in every sense, an imminent threat to the health and safety of the American people.
I do not believe in using violence to resolve problems, and I do not believe that these people should be dragged out of their offices and hanged in a public forum, as some other writers have suggested, but I do believe that we must strip them of their power and influence, and we must hold a public court session so that all the world can see the degree of evil that has been operating inside the ADA and FDA for so many years. We must bring this issue into the light, and let the truth be told about this hundred-year lie so that future generations can learn what happens when you allow corporate profits to dictate health regulatory decisions in any society.
I'm writing to alert readers to a crucial email from a I'm I'm I'm writing to alert readers to a crucial email from a physician who has evidence vitamin D is protective against H1N1 and to ask you, the reader, to contact your representatives in Washington to help protect Americans, especially children, from H1N1 before winter comes.
Dear Dr. Cannell:
Your recent newsletters and video about Swine flu (H1N1) prompted me to convey our recent experience with an H1N1 outbreak at Central Wisconsin Center (CWC). Unfortunately, the state epidemiologist was not interested in studying it further so I pass it on to you since I think it is noteworthy.
CWC is a long-term care facility for people with developmental disabilities, home for approx. 275 people with approx. 800 staff. Serum 25-OHD has been monitored in virtually all residents for several years and patients supplemented with vitamin D.
In June, 2009, at the time of the well-publicized Wisconsin spike in H1N1 cases, two residents developed influenza-like illness (ILI) and had positive tests for H1N1:
one was a long-term resident; the other, a child, was transferred to us with what was later proven to be H1N1.
On the other hand, 60 staff members developed ILI or were documented to have H1N1:
of 17 tested for ILI, eight were positive. An additional 43 staff members called in sick with ILI. (Approx. 11-12 staff developed ILI after working on the unit where the child was given care, several of whom had positive H1N1 tests.)
So, it is rather remarkable that only two residents of 275 developed ILI, one of which did not develop it here, while 103 of 800 staff members had ILI. It appears that the spread of H1N1 was not from staff-to-resident but from resident-to-staff (most obvious in the imported case) and between staff, implying that staff were susceptible and our residents protected.
Sincerely,
Norris Glick, MD
Central Wisconsin Center
Madison, WI
Dear Dr. Glick:
This is the first hard data that I am aware of concerning H1N1 and vitamin D. It appears vitamin D is incredibly protective against H1N1.
Dr. Carlos Carmago at Mass General ran the numbers in an email to me. Even if one excludes 43 staff members who called in sick with influenza, 0.73% of residents were affected, as compared to 7.5% of staff. This 10-fold difference was statistically significant (P<0.001). That is, the chance that this was a chance occurrence is one less than one in a thousand.
Second, if you read my last newsletter, you will see that children with neurological impairments, like the patients at your hospital, have accounted for 2/3 of the childhood deaths for H1N1 so far in the USA. That is, the CDC knows, because they reported it, that patients with neurological impairments are more likely to die from H1N1.
The problem is that I cannot get anyone in authority at the CDC or the NIH to listen. I need readers to email or call their senators and congresspersons in Washington.
Ask your senator or congressperson to contact the CDC and NIH to complain about CDC and NIH inaction on Vitamin D and H1N1. Also, ask your senators and representative to demand congressional hearings on Vitamin D and H1N1, before it is too late. Here is the link below, just click it and follow instructions to contact your own represenatives.
Even though the virus is not becoming more deadly the vaccine army comes marching on. However, they have not been able to scare nurses, doctors or in England pregnant women.
When will they give up?
No one knows what treatment will be effective against the H1N1 Flu. However, the data from Dr. Norris is very compelling, that Vitamin D will be protective for H1N1.
To lower your families incidence of colds and flu this winter and to lower your probability of Swine Flu, start by measuring their vitamin D levels, keep it above 50ng/ml and by giving the whole family daily probiotics and vitamin D.
Twenty-two years ago, Drs. Cedric Garland and his brother, Frank, proposed that many cases of cancer were caused by lack of vitamin D. The medical community treated these respected epidemiologists as if they were nuts. Vitamin D was discovered in 1922 as the vitamin that prevents and treats rickets, a disease that causes children and adults to have such weak bones that they bend.
The Garland brothers showed that people who live in the northern parts of the United States have more than three times as many colon cancer deaths as those who live in the South. They explained that very few Americans meet their needs for vitamin D from the food, so we have to meet our needs for vitamin D from sunlight. Sunlight is less intense in the northern latitudes, and people in the colder climates often do not go out in the winter; therefore, they often suffer from lack of vitamin D.
The July, 2002 issue of the American Journal of Clinical Nutrition shows that 42 percent of African American women have low blood levels of vitamin D, compared to only 4.2 percent in Caucasians. That means that African Americans are ten times more likely to suffer from vitamin D deficiency than Caucasians. Lack of vitamin D interferes with immunity and a person's ability to kill germs and cancer cells. Every day, the human body makes millions of cancer cells. Your immunity then filters out these cells and prevents them from growing. When immunity is impaired, the cancer cells can grow to form solid cancers, such as cancer of the breast, prostate or colon.
All men will develop prostate cancer if they live long enough, but the average Caucasian develops prostate cancer after age 85, while the average African American develops it many years earlier. People of color require far more ultraviolet light to make vitamin D than those who have lighter skins. Lack of vitamin D damages immunity to cause cancers, diabetes and infections.
My advice is for you to think about your vitamin D status. A person with light skin can get enough vitamin D from a few minutes spent in sunlight each day, but the darker your skin, the more sun exposure you need to meet your daily requirements. You can get vitamin D from vitamin supplements, fish oils, fish, breakfast cereals, and a tiny bit from milk fortified with vitamin D. If you do not eat fish at least four times a week, take vitamin D supplements or vitamin D fortified breakfast cereals. If you are not sure if you are getting enough vitamin D from food or sunlight, go to your doctor and request a blood test for vitamin D. If your blood level of vitamin D is below 15 micrograms /liter, you should take 400 international units or 5 micrograms of vitamin D each day. I am convinced that you will be protecting yourself from cancer and infections. Women will also be protecting their future babies from infections and possibly birth defects. Don't wait for the medical community to agree on this.
5 Myths About Health Care Around the World by T.R. Reid
As Americans search for the cure to what ails our health-care system, we've overlooked an invaluable source of ideas and solutions: the rest of the world. All the other industrialized democracies have faced problems like ours, yet they've found ways to cover everybody -- and still spend far less than we do.
I've traveled the world from Oslo to Osaka to see how other developed democracies provide health care. Instead of dismissing these models as "socialist," we could adapt their solutions to fix our problems. To do that, we first have to dispel a few myths about health care abroad:
1. It's all socialized medicine out there.
Not so. Some countries, such as Britain, New Zealand and Cuba, do provide health care in government hospitals, with the government paying the bills. Others -- for instance, Canada and Taiwan -- rely on private-sector providers, paid for by government-run insurance. But many wealthy countries -- including Germany, the Netherlands, Japan and Switzerland -- provide universal coverage using private doctors, private hospitals and private insurance plans.
In some ways, health care is less "socialized" overseas than in the United States. Almost all Americans sign up for government insurance (Medicare) at age 65. In Germany, Switzerland and the Netherlands, seniors stick with private insurance plans for life. Meanwhile, the U.S. Department of Veterans Affairs is one of the planet's purest examples of government-run health care.
2. Overseas, care is rationed through limited choices or long lines.
Generally, no. Germans can sign up for any of the nation's 200 private health insurance plans -- a broader choice than any American has. If a German doesn't like her insurance company, she can switch to another, with no increase in premium. The Swiss, too, can choose any insurance plan in the country.
In France and Japan, you don't get a choice of insurance provider; you have to use the one designated for your company or your industry. But patients can go to any doctor, any hospital, any traditional healer. There are no U.S.-style limits such as "in-network" lists of doctors or "pre-authorization" for surgery. You pick any doctor, you get treatment -- and insurance has to pay.
Canadians have their choice of providers. In Austria and Germany, if a doctor diagnoses a person as "stressed," medical insurance pays for weekends at a health spa.
As for those notorious waiting lists, some countries are indeed plagued by them. Canada makes patients wait weeks or months for nonemergency care, as a way to keep costs down. But studies by the Commonwealth Fund and others report that many nations -- Germany, Britain, Austria -- outperform the United States on measures such as waiting times for appointments and for elective surgeries.
In Japan, waiting times are so short that most patients don't bother to make an appointment. One Thursday morning in Tokyo, I called the prestigious orthopedic clinic at Keio University Hospital to schedule a consultation about my aching shoulder. "Why don't you just drop by?" the receptionist said. That same afternoon, I was in the surgeon's office. Dr. Nakamichi recommended an operation. "When could we do it?" I asked. The doctor checked his computer and said, "Tomorrow would be pretty difficult. Perhaps some day next week?"
3. Foreign health-care systems are inefficient, bloated bureaucracies.
Much less so than here. It may seem to Americans that U.S.-style free enterprise -- private-sector, for-profit health insurance -- is naturally the most cost-effective way to pay for health care. But in fact, all the other payment systems are more efficient than ours. U.S. health insurance companies have the highest administrative costs in the world; they spend roughly 20 cents of every dollar for nonmedical costs, such as paperwork, reviewing claims and marketing. France's health insurance industry, in contrast, covers everybody and spends about 4 percent on administration. Canada's universal insurance system, run by government bureaucrats, spends 6 percent on administration. In Taiwan, a leaner version of the Canadian model has administrative costs of 1.5 percent; one year, this figure ballooned to 2 percent, and the opposition parties savaged the government for wasting money.
The world champion at controlling medical costs is Japan, even though its aging population is a profligate consumer of medical care. On average, the Japanese go to the doctor 15 times a year, three times the U.S. rate. They have twice as many MRI scans and X-rays. Quality is high; life expectancy and recovery rates for major diseases are better than in the United States. And yet Japan spends about $3,400 per person annually on health care; the United States spends more than $7,000.
4. Cost controls stifle innovation.
False. The United States is home to groundbreaking medical research, but so are other countries with much lower cost structures. Any American who's had a hip or knee replacement is standing on French innovation. Deep-brain stimulation to treat depression is a Canadian breakthrough. Many of the wonder drugs promoted endlessly on American television, including Viagra, come from British, Swiss or Japanese labs.
Overseas, strict cost controls actually drive innovation. In the United States, an MRI scan of the neck region costs about $1,500. In Japan, the identical scan costs $98. Under the pressure of cost controls, Japanese researchers found ways to perform the same diagnostic technique for one-fifteenth the American price. (And Japanese labs still make a profit.)
5. Health insurance has to be cruel.
Not really. American health insurance companies routinely reject applicants with a "preexisting condition" -- precisely the people most likely to need the insurers' service. They employ armies of adjusters to deny claims. If a customer is hit by a truck and faces big medical bills, the insurer's "rescission department" digs through the records looking for grounds to cancel the policy, often while the victim is still in the hospital. The companies say they have to do this stuff to survive in a tough business.
Foreign health insurance companies, in contrast, must accept all applicants, and they can't cancel as long as you pay your premiums. The plans are required to pay any claim submitted by a doctor or hospital (or health spa), usually within tight time limits. The big Swiss insurer Groupe Mutuel promises to pay all claims within five days. "Our customers love it," the group's chief executive told me. The corollary is that everyone is mandated to buy insurance, to give the plans an adequate pool of rate-payers.
The key difference is that foreign health insurance plans exist only to pay people's medical bills, not to make a profit. The United States is the only developed country that lets insurance companies profit from basic health coverage.
In many ways, foreign health-care models are not really "foreign" to America, because our crazy-quilt health-care system uses elements of all of them. For Native Americans or veterans, we're Britain: The government provides health care, funding it through general taxes, and patients get no bills. For people who get insurance through their jobs, we're Germany: Premiums are split between workers and employers, and private insurance plans pay private doctors and hospitals. For people over 65, we're Canada: Everyone pays premiums for an insurance plan run by the government, and the public plan pays private doctors and hospitals according to a set fee schedule. And for the tens of millions without insurance coverage, we're Burundi or Burma: In the world's poor nations, sick people pay out of pocket for medical care; those who can't pay stay sick or die.
This fragmentation is another reason that we spend more than anybody else and still leave millions without coverage. All the other developed countries have settled on one model for health-care delivery and finance; we've blended them all into a costly, confusing bureaucratic mess.
Which, in turn, punctures the most persistent myth of all: that America has "the finest health care" in the world. We don't. In terms of results, almost all advanced countries have better national health statistics than the United States does. In terms of finance, we force 700,000 Americans into bankruptcy each year because of medical bills. In France, the number of medical bankruptcies is zero. Britain: zero. Japan: zero. Germany: zero. Given our remarkable medical assets -- the best-educated doctors and nurses, the most advanced hospitals, world-class research -- the United States could be, and should be, the best in the world. To get there, though, we have to be willing to learn some lessons about health-care administration from the other industrialized democracies.
The mainstream media are now reporting the onset of a swine flu “emergency.” Yet controversy is raging over the safety and efficacy of the government-approved vaccine.
The strain known as H1N1 supposedly hits children and young people the hardest. The elderly are said to be similarly at risk. Deaths are being reported, as are shortages of vaccine at some locations.
Government officials are making the TV rounds, including Secretary of Health and Human Services Kathleen Sebelius, who says the vaccine is “safe and secure” and “right on target with an immune response.”
Yet Americans are deeply skeptical. According to a poll by AOL news, 61 percent say they do not plan to get the vaccine. Only 21 percent are “very worried” about the flu outbreak.
In fact the alliance between the federal government and the big pharmaceutical companies to push the H1N1 vaccine has ignited a populist revolt. The debate that is raging on Capitol Hill over national health care insurance had already exposed the health care industry as being far more concerned with profits than they are with people. H1N1 came along just in time to carry the revolt a step further.
An example of how the pharmaceutical industry is obsessed with the bottom line is shown by the difference in prices between proprietary medicines and their generic equivalents. A report by Life Extension magazine found that such well-known drugs as Celebrex, Lipitor, and Prozac had enormous mark-ups, topped by Xanaz, marked-up from 2.4 cents to $136.79 per 100 tablets!
No wonder many people are turning to alternative remedies, including improved nutrition or use of supplements such as vitamin C. To combat this, the government has gone on the attack, with the Food and Drug Administration and the Federal Trade Commission sending warning letters to over 140 product vendors. On the list is famed alternative healer Dr. Andrew Weil for statements on his website about his Immune Support Formula containing astragalus, an herbal mainstay of traditional Chinese medicine that is said to increase the body’s immune response.
Another natural preventive for flu and many other illnesses is simply to drink plenty of clean, filtered water, preferably fresh spring or well water, or water that has been ionized through an alkanization process. Recently the Natural News website published an interview done several years ago with a Dr. Batmanghelidj, who published extensive research that demonstrates how many illnesses for which doctors prescribe expensive and dangerous drugs are really caused by dehydration, including many diseases affecting the elderly. Click Here
One result of dehydration, for instance, is deterioration of the walls of blood vessels. In order to repair the damage, the body produces more cholesterol, which Dr. Barmanghelidj calls “a waterproof bandage” for the cardio-vascular system. Then, when this extra cholesterol shows up in blood tests, doctors prescribe powerful drugs like Lipitor which can have devastating side-effects. It would most likely be better simply to tell people to drink more water.
Finally, the enormous pressure being brought to bear on the population to take the H1N1 vaccine has added to a huge and growing controversy over whether vaccines are safe at all. An increasing number of commentators are linking the growing use of vaccines to what some call an epidemic of childhood autism and other neurological disorders. Recall that the swine flu scare of 1976 led to discontinuation of the vaccine back then when it caused a number of deaths and a surge in paralysis from Guillan-Barre syndrome.
See for instance, the work of Dr. Andrew Moulden of Canada, whose work has linked vaccines to a “sludging” effect in the tiniest blood vessels in the brain which may be related to onset of such diseases as dementia, multiple sclerosis, autism, and even schizophrenia, along with many childhood learning disabilities. Dr. Moulen has even suggested a possible link between the frequent administration of flu vaccines to the elderly and the onset of alzheimer’s. Click Here
But there is an even deeper problem with modern medicine, which is that it is almost completely materialistic in its assumptions and approach.
Modern medicine views disease as a mechanistic process, caused either by “germs,” chemical imbalances, or genetics. This leads to the assumption that for every illness, there is a physical cure, either by killing the offending micro-organism, restoring chemical balance through a pill, or cutting out the failed or offending body part by surgery.
The materialistic outlook has even taken over the practice of psychiatric medicine. If a person is depressed, disturbed, anxious, or unhappy, don’t look at the possible causes in that person’s outlook, environment, diet, habits, addictions, or value system. Just give them an anti-depressent or even an anti-psychotic. Never mind that these drugs may just suppress symptoms or even reduce the person to almost a vegetative state. On the surface, at least, they seem to be “getting better” or at least causing less trouble!
But in some circles, an entirely different world-view is emerging. We know, for instance, about the holistic approach to medicine that sees a person as not just a bundle of chemical reflexes but a complete human being with a mind, heart, body, and spirit, all of which need to work more or less in harmony for optimum health to result.
But how often is this knowledge really practiced by people day-in and day-out?
A whole new industry of holistic health practitioners has come into existence, including those who practice acupuntrure, acupressure, reiki, hypnosis, massage, and body-work, including yoga, tai-chi, qi-gong, etc.There is also a growing awareness that a regular practice of prayer and spiritual devotion also benefits the whole person, including the physical body.
The deepest of these holistic practices may in fact be meditation. Meditative or contemplative prayer is a central component of religious practice within both the Catholic and Orthodox faiths, and meditation is the central discipline of all lines of Buddhism. Yoga also includes meditation, and in some types of yogic practice is the core discipline.
Are people who meditate more healthy? I am not aware of any scientific studies, but based on my own experience with many different types of meditation which includes association with various groups, schools, and teachers of meditation, I would have to say they appear to be. Or at least they worry less about their physical health, take illness more in stride, and are able to recover faster when it occurs.
One thing is sure: long-term practice of meditation on a daily basis seems to raise the energy level of the body. This makes a difference because the body is like an energy-filled vessel. If this energy leaks through negative emotions, unnecessary physical tension, and the constant churning of the mind, the body will suffer a general state of depletion, which is bound to make it more susceptible to disease. It also makes a difference if one avoids much of the jarring imagery churned out by the mass media through violent and disturbing films, TV programming, video games, etc.
These health-related factors which have been understood by traditional societies for millennia are also starting to be realized by millions of ordinary people in every walk of life. Combined with a nutritious diet, physical exercise, positive relationships, and productive work, a rich inner life of prayer and meditation produces a multitude of benefits, not the least of which seems to be improved physical health and greater resistance to infections such as swine flu.
People with high cholesterol live the longest. This statement seems so incredible that it takes a long time to clear one´s brainwashed mind to fully understand its importance. Yet the fact that people with high cholesterol live the longest emerges clearly from many scientific papers. Consider the finding of Dr. Harlan Krumholz of the Department of Cardiovascular Medicine at Yale University, who reported in 1994 that old people with low cholesterol died twice as often from a heart attack as did old people with a high cholesterol.1 Supporters of the cholesterol campaign consistently ignore his observation, or consider it as a rare exception, produced by chance among a huge number of studies finding the opposite.
But it is not an exception; there are now a large number of findings that contradict the lipid hypothesis. To be more specific, most studies of old people have shown that high cholesterol is not a risk factor for coronary heart disease. This was the result of my search in the Medline database for studies addressing that question.2 Eleven studies of old people came up with that result, and a further seven studies found that high cholesterol did not predict all-cause mortality either.
Now consider that more than 90 % of all cardiovascular disease is seen in people above age 60 also and that almost all studies have found that high cholesterol is not a risk factor for women.2 This means that high cholesterol is only a risk factor for less than 5 % of those who die from a heart attack.
But there is more comfort for those who have high cholesterol; six of the studies found that total mortality was inversely associated with either total or LDL-cholesterol, or both. This means that it is actually much better to have high than to have low cholesterol if you want to live to be very old.
High Cholesterol Protects Against Infection
Many studies have found that low cholesterol is in certain respects worse than high cholesterol. For instance, in 19 large studies of more than 68,000 deaths, reviewed by Professor David R. Jacobs and his co-workers from the Division of Epidemiology at the University of Minnesota, low cholesterol predicted an increased risk of dying from gastrointestinal and respiratory diseases.3
Most gastrointestinal and respiratory diseases have an infectious origin. Therefore, a relevant question is whether it is the infection that lowers cholesterol or the low cholesterol that predisposes to infection? To answer this question Professor Jacobs and his group, together with Dr. Carlos Iribarren, followed more than 100,000 healthy individuals in the San Francisco area for fifteen years. At the end of the study those who had low cholesterol at the start of the study had more often been admitted to the hospital because of an infectious disease.4,5 This finding cannot be explained away with the argument that the infection had caused cholesterol to go down, because how could low cholesterol, recorded when these people were without any evidence of infection, be caused by a disease they had not yet encountered? Isn´t it more likely that low cholesterol in some way made them more vulnerable to infection, or that high cholesterol protected those who did not become infected? Much evidence exists to support that interpretation.
Low Cholesterol and HIV/AIDS
Young, unmarried men with a previous sexually transmitted disease or liver disease run a much greater risk of becoming infected with HIV virus than other people. The Minnesota researchers, now led by Dr. Ami Claxton, followed such individuals for 7-8 years. After having excluded those who became HIV-positive during the first four years, they ended up with a group of 2446 men. At the end of the study, 140 of these people tested positive for HIV; those who had low cholesterol at the beginning of the study were twice as likely to test postitive for HIV compared with those with the highest cholesterol.6
Similar results come from a study of the MRFIT screenees, including more than 300,000 young and middle-aged men, which found that 16 years after the first cholesterol analysis the number of men whose cholesterol was lower than 160 and who had died from AIDS was four times higher than the number of men who had died from AIDS with a cholesterol above 240.7
Cholesterol and Chronic Heart Failure
Heart disease may lead to a weakening of the heart muscle. A weak heart means that less blood and therefore less oxygen is delivered to the arteries. To compensate for the decreased power, the heart beat goes up, but in severe heart failure this is not sufficient. Patients with severe heart failure become short of breath because too little oxygen is delivered to the tissues, the pressure in their veins increases because the heart cannot deliver the blood away from the heart with sufficient power, and they become edematous, meaning that fluid accumulates in the legs and in serious cases also in the lungs and other parts of the body. This condition is called congestive or chronic heart failure.
There are many indications that bacteria or other microorganisms play an important role in chronic heart failure. For instance, patients with severe chronic heart failure have high levels of endotoxin and various types of cytokines in their blood. Endotoxin, also named lipopolysaccharide, is the most toxic substance produced by Gram-negative bacteria such as Escherichia coli, Klebsiella, Salmonella, Serratia and Pseudomonas. Cytokines are hormones secreted by white blood cells in their battle with microorganisms; high levels of cytokines in the blood indicate that inflammatory processes are going on somewhere in the body.
The role of infections in chronic heart failure has been studied by Dr. Mathias Rauchhaus and his team at the Medical Department, Martin-Luther-University in Halle, Germany (Universitätsklinik und Poliklinik für Innere Medizin III, Martin-Luther-Universität, Halle). They found that the strongest predictor of death for patients with chronic heart failure was the concentration of cytokines in the blood, in particular in patients with heart failure due to coronary heart disease.8 To explain their finding they suggested that bacteria from the gut may more easily penetrate into the tissues when the pressure in the abdominal veins is increased because of heart failure. In accordance with this theory, they found more endotoxin in the blood of patients with congestive heart failure and edema than in patients with non-congestive heart failure without edema, and endotoxin concentrations decreased significantly when the heart’s function was improved by medical treatment.9
A simple way to test the functional state of the immune system is to inject antigens from microorganisms that most people have been exposed to, under the skin. If the immune system is normal, an induration (hard spot) will appear about 48 hours later at the place of the injection. If the induration is very small, with a diameter of less than a few millimeters, this indicates the presence of "anergy," a reduction in or failure of response to recognize antigens. In accordance, anergy has been found associated with an increased risk of infection and mortality in healthy elderly individuals, in surgical patients and in heart transplant patients.10
Dr. Donna Vredevoe and her group from the School of Nursery and the School of Medicine, University of California at Los Angeles tested more than 200 patients with severe heart failure with five different antigens and followed them for twelve months. The cause of heart failure was coronary heart disease in half of them and other types of heart disease (such as congenital or infectious valvular heart disease, various cardiomyopathies and endocarditis) in the rest. Almost half of all the patients were anergic, and those who were anergic and had coronary heart disease had a much higher mortality than the rest.10
Now to the salient point: to their surprise the researchers found that mortality was higher, not only in the patients with anergy, but also in the patients with the lowest lipid values, including total cholesterol, LDL-cholesterol and HDL-cholesterol as well as triglycerides.
The latter finding was confirmed by Dr. Rauchhaus, this time in co-operation with researchers at several German and British university hospitals. They found that the risk of dying for patients with chronic heart failure was strongly and inversely associated with total cholesterol, LDL-cholesterol and also triglycerides; those with high lipid values lived much longer than those with low values.11,12
Other researchers have made similar observations. The largest study has been performed by Professor Gregg C. Fonorow and his team at the UCLA Department of Medicine and Cardiomyopathy Center in Los Angeles.13 The study, led by Dr. Tamara Horwich, included more than a thousand patients with severe heart failure. After five years 62 percent of the patients with cholesterol below 129 mg/l had died, but only half as many of the patients with cholesterol above 223 mg/l.
When proponents of the cholesterol hypothesis are confronted with findings showing a bad outcome associated with low cholesterol--and there are many such observations--they usually argue that severely ill patients are often malnourished, and malnourishment is therefore said to cause low cholesterol. However, the mortality of the patients in this study was independent of their degree of nourishment; low cholesterol predicted early mortality whether the patients were malnourished or not.
Smith-Lemli-Opitz Syndrome
As discussed in The Cholesterol Myths (see sidebar), much evidence supports the theory that people born with very high cholesterol, so-called familial hypercholesterolemia, are protected against infection. But if inborn high cholesterol protects against infections, inborn low cholesterol should have the opposite effect. Indeed, this seems to be true.
Children with the Smith-Lemli-Opitz syndrome have very low cholesterol because the enzyme that is necessary for the last step in the body’s synthesis of cholesterol does not function properly. Most children with this syndrome are either stillborn or they die early because of serious malformations of the central nervous system. Those who survive are imbecile, they have extremely low cholesterol and suffer from frequent and severe infections. However, if their diet is supplemented with pure cholesterol or extra eggs, their cholesterol goes up and their bouts of infection become less serious and less frequent.14
Laboratory Evidence
Laboratory studies are crucial for learning more about the mechanisms by which the lipids exert their protective function. One of the first to study this phenomenon was Dr Sucharit Bhakdi from the Institute of Medical Microbiology, University of Giessen (Institut für Medizinsche Mikrobiologie, Justus-Liebig-Universität Gießen), Germany along with his team of researchers from various institutions in Germany and Denmark.15
Staphylococcus aureus α-toxin is the most toxic substance produced by strains of the disease-promoting bacteria called staphylococci. It is able to destroy a wide variety of human cells, including red blood cells. For instance, if minute amounts of the toxin are added to a test tube with red blood cells dissolved in 0.9 percent saline, the blood is hemolyzed, that is the membranes of the red blood cells burst and hemoglobin from the interior of the red blood cells leaks out into the solvent. Dr. Bhakdi and his team mixed purified α-toxin with human serum (the fluid in which the blood cells reside) and saw that 90 percent of its hemolyzing effect disappeared. By various complicated methods they identified the protective substance as LDL, the carrier of the so-called bad cholesterol. In accordance, no hemolysis occurred when they mixed α-toxin with purified human LDL, whereas HDL or other plasma constituents were ineffective in this respect.
Dr. Willy Flegel and his co-workers at the Department of Transfusion Medicine, University of Ulm, and the Institute of Immunology and Genetics at the German Cancer Research Center in Heidelberg, Germany (DRK-Blutspendezentrale und Abteilung für Transfusionsmedizin, Universität Ulm, und Deutsches Krebsforschungszentrum, Heidelberg) studied endotoxin in another way.16 As mentioned, one of the effects of endotoxin is that white blood cells are stimulated to produce cytokines. The German researchers found that the cytokine-stimulating effect of endotoxin on the white blood cells disappeared almost completely if the endotoxin was mixed with human serum for 24 hours before they added the white blood cells to the test tubes. In a subsequent study17 they found that purified LDL from patients with familial hypercholesterolemia had the same inhibitory effect as the serum.
LDL may not only bind and inactivate dangerous bacterial toxins; it seems to have a direct beneficial influence on the immune system also, possibly explaining the observed relationship between low cholesterol and various chronic diseases. This was the starting point for a study by Professor Matthew Muldoon and his team at the University of Pittsburgh, Pennsylvania. They studied healthy young and middle-aged men and found that the total number of white blood cells and the number of various types of white blood cells were significantly lower in the men with LDL-cholesterol below 160 mg/dl (mean 88.3 mg/l),than in men with LDL-cholesterol above 160 mg/l (mean 185.5 mg/l).18 The researchers cautiously concluded that there were immune system differences between men with low and high cholesterol, but that it was too early to state whether these differences had any importance for human health. Now, seven years later with many of the results discussed here, we are allowed to state that the immune-supporting properties of LDL-cholesterol do indeed play an important role in human health.
Animal Experiments
The immune systems in various mammals including human beings have many similarities. Therefore, it is interesting to see what experiments with rats and mice can tell us. Professor Kenneth Feingold at the Department of Medicine, University of California, San Francisco, and his group have published several interesting results from such research. In one of them they lowered LDL-cholesterol in rats by giving them either a drug that prevents the liver from secreting lipoproteins, or a drug that increases their disappearance. In both models, injection of endotoxin was followed by a much higher mortality in the low-cholesterol rats compared with normal rats. The high mortality was not due to the drugs because, if the drug-treated animals were injected with lipoproteins just before the injection of endotoxin, their mortality was reduced to normal.19
Dr. Mihai Netea and his team from the Departments of Internal and Nuclear Medicine at the University Hospital in Nijmegen, The Netherlands, injected purified endotoxin into normal mice, and into mice with familial hypercholesterolemia that had LDL-cholesterol four times higher than normal. Whereas all normal mice died, they had to inject eight times as much endotoxin to kill the mice with familial hypercholesterolemia. In another experiment they injected live bacteria and found that twice as many mice with familial hypercholesterolemia survived compared with normal mice.20
Other Protecting Lipids
As seen from the above, many of the roles played by LDL-cholesterol are shared by HDL. This should not be too surprising considering that high HDL-cholesterol is associated with cardiovascular health and longevity. But there is more.
Triglycerides, molecules consisting of three fatty acids linked to glycerol, are insoluble in water and are therefore carried through the blood inside lipoproteins, just as cholesterol. All lipoproteins carry triglycerides, but most of them are carried by a lipoprotein named VLDL (very low-density lipoprotein) and by chylomicrons, a mixture of emulsified triglycerides appearing in large amounts after a fat-rich meal, particularly in the blood that flows from the gut to the liver.
For many years it has been known that sepsis, a life-threatening condition caused by bacterial growth in the blood, is associated with a high level of triglycerides. The serious symptoms of sepsis are due to endotoxin, most often produced by gut bacteria. In a number of studies, Professor Hobart W. Harris at the Surgical Research Laboratory at San Francisco General Hospital and his team found that solutions rich in triglycerides but with practically no cholesterol were able to protect experimental animals from the toxic effects of endotoxin and they concluded that the high level of triglycerides seen in sepsis is a normal immune response to infection.21 Usually the bacteria responsible for sepsis come from the gut. It is therefore fortunate that the blood draining the gut is especially rich in triglycerides.
Exceptions
So far, animal experiments have confirmed the hypothesis that high cholesterol protects against infection, at least against infections caused by bacteria. In a similar experiment using injections of Candida albicans, a common fungus, Dr. Netea and his team found that mice with familial hypercholesterolemia died more easily than normal mice.22 Serious infections caused by Candida albicans are rare in normal human beings; however, they are mainly seen in patients treated with immunosuppressive drugs, but the finding shows that we need more knowledge in this area. However, the many findings mentioned above indicate that the protective effects of the blood lipids against infections in human beings seem to be greater than any possible adverse effects.
Cholesterol as a Risk Factor
Most studies of young and middle-aged men have found high cholesterol to be a risk factor for coronary heart disease, seemingly a contradiction to the idea that high cholesterol is protective. Why is high cholesterol a risk factor in young and middle-aged men? A likely explanation is that men of that age are often in the midst of their professional career. High cholesterol may therefore reflect mental stress, a well-known cause of high cholesterol and also a risk factor for heart disease. Again, high cholesterol is not necessarily the direct cause but may only be a marker. High cholesterol in young and middle-aged men could, for instance, reflect the body’s need for more cholesterol because cholesterol is the building material of many stress hormones. Any possible protective effect of high cholesterol may therefore be counteracted by the negative influence of a stressful life on the vascular system.
Response to Injury
In 1976 one of the most promising theories about the cause of atherosclerosis was the Response-to-Injury Hypothesis, presented by Russell Ross, a professor of pathology, and John Glomset, a professor of biochemistry and medicine at the Medical School, University of Washington in Seattle.23,24 They suggested that atherosclerosis is the consequence of an inflammatory process, where the first step is a localized injury to the thin layer of cells lining the inside of the arteries, the intima. The injury causes inflammation and the raised plaques that form are simply healing lesions.
Their idea is not new. In 1911, two American pathologists from the Pathological Laboratories, University of Pittsburgh, Pennsylvania, Oskar Klotz and M.F. Manning, published a summary of their studies of the human arteries and concluded that "there is every indication that the production of tissue in the intima is the result of a direct irritation of that tissue by the presence of infection or toxins or the stimulation by the products of a primary degeneration in that layer."25 Other researchers have presented similar theories.26
Researchers have proposed many potential causes of vascular injury, including mechanical stress, exposure to tobacco fumes, high LDL-cholesterol, oxidized cholesterol, homocysteine, the metabolic consequences of diabetes, iron overload, copper deficiency, deficiencies of vitamins A and D, consumption of trans fatty acids, microorganisms and many more. With one exception, there is evidence to support roles for all of these factors, but the degree to which each of them participates remains uncertain. The exception is of course LDL-cholesterol. Much research allows us to exclude high LDL-cholesterol from the list. Whether we look directly with the naked eye at the inside of the arteries at autopsy, or we do it indirectly in living people using x-rays, ultrasound or electron beams, no association worth mentioning has ever been found between the amount of lipid in the blood and the degree of atherosclerosis in the arteries. Also, whether cholesterol goes up or down, by itself or due to medical intervention, the changes of cholesterol have never been followed by parallel changes in the atherosclerotic plaques; there is no dose-response. Proponents of the cholesterol campaign often claim that the trials indeed have found dose-response, but here they refer to calculations between the mean changes of the different trials with the outcome of the whole treatment group. However, true dose-response demands that the individual changes of the putative causal factor are followed by parallel, individual changes of the disease outcome, and this has never occurred in the trials where researchers have calculated true dose-response.
A detailed discussion of the many factors accused of harming the arterial endothelium is beyond the scope of this article. However, the protective role of the blood lipids against infections obviously demands a closer look at the alleged role of one of the alleged causes, the microorganisms.
Is Atherosclerosis an Infectious Disease?
For many years scientists have suspected that viruses and bacteria, in particular cytomegalovirus and Chlamydia pneumonia (also named TWAR bacteria) participate in the development of atherosclerosis. Research within this area has exploded during the last decade and by January 2004, at least 200 reviews of the issue have been published in medical journals. Due to the widespread preoccupation with cholesterol and other lipids, there has been little general interest in the subject, however, and few doctors know much about it. Here I shall mention some of the most interesting findings.26
Electron microscopy, immunofluorescence microscopy and other advanced techniques have allowed us to detect microorganisms and their DNA in the atherosclerotic lesions in a large proportion of patients. Bacterial toxins and cytokines, hormones secreted by the white blood cells during infections, are seen more often in the blood from patients with recent heart disease and stroke, in particular during and after an acute cardiovascular event, and some of them are strong predictors of cardiovascular disease. The same is valid for bacterial and viral antibodies, and a protein secreted by the liver during infections, named C-reactive protein (CRP), is a much stronger risk factor for coronary heart disease than cholesterol.
Clinical evidence also supports this theory. During the weeks preceding an acute cardiovascular attack many patients have had a bacterial or viral infection. For instance, Dr. Armin J. Grau from the Department of Neurology at the University of Heidelberg and his team asked 166 patients with acute stroke, 166 patients hospitalized for other neurological diseases and 166 healthy individuals matched individually for age and sex about recent infectious disease. Within the first week before the stroke, 37 of the stroke patients, but only 14 of the control individuals had had an infectious disease. In half of the patients the infection was of bacterial origin, in the other half of viral origin.27
Similar observations have been made by many others, for patients with acute myocardial infarction (heart attack). For instance, Dr. Kimmo J. Mattila at the Department of Medicine, Helsinki University Hospital, Finland, found that 11 of 40 male patients with an acute heart attack before age 50 had an influenza-like infection with fever within 36 hours prior to admittance to hospital, but only 4 out of 41 patients with chronic coronary disease (such as recurrent angina or pervious myocardial infarction) and 4 out of 40 control individuals without chronic disease randomly selected from the general population.28
Attempts have been made to prevent cardiovascular disease by treatment with antibiotics. In five trials treatment of patients with coronary heart disease using azithromyzin or roxithromyzin, antibiotics that are effective against Chlamydia pneumonia,yielded successful results; a total of 104 cardiovascular events occurred among the 412 non-treated patients, but only 61 events among the 410 patients in the treatment groups.28a-e In one further trial a significant decreased progression of atherosclerosis in the carotid arteries occurred with antibiotic treatment.28f However, in four other trials,30a-d one of which included more than 7000 patients,28d antibiotic treatment had no significant effect.
The reason for these inconsistent results may be that the treatment was too short (in one of the trials treatment lasted only five days). Also, Chlamydia pneumonia, the TWAR bacteria, can only propagate inside human cells and when located in white blood cells they are resistant to antibiotics.31 Treatment may also have been ineffective because the antibiotics used have no effect on viruses. In this connection it is interesting to mention a controlled trial performed by Dr. Enrique Gurfinkel and his team from Fundación Favaloro in Buenos Aires, Argentina.32 They vaccinated half of 301 patients with coronary heart disease against influenza, a viral disease. After six months 8 percent of the control patients had died, but only 2 percent of the vaccinated patients. It is worth mentioning that this effect was much better than that achieved by any statin trial, and in a much shorter time.
Does High Cholesterol Protect Against Cardiovascular Disease?
Apparently, microorganisms play a role in cardiovascular disease. They may be one of the factors that start the process by injuring the arterial endothelium. A secondary role may be inferred from the association between acute cardiovascular disease and infection. The infectious agent may preferably become located in parts of the arterial walls that have been previously damaged by other agents, initiating local coagulation and the creation of a thrombus (clot) and in this way cause obstruction of the blood flow. But if so, high cholesterol may protect against cardiovascular disease instead of being the cause!
In any case, the diet-heart idea, with its demonizing of high cholesterol, is obviously in conflict with the idea that high cholesterol protects against infections. Both ideas cannot be true. Let me summarize the many facts that conflict with the idea that high cholesterol is bad.
If high cholesterol were the most important cause of atherosclerosis, people with high cholesterol should be more atherosclerotic than people with low cholesterol. But as you know by now this is very far from the truth.
If high cholesterol were the most important cause of atherosclerosis, lowering of cholesterol should influence the atherosclerotic process in proportion to the degree of its lowering.
But as you know by now, this does not happen.
If high cholesterol were the most important cause of cardiovascular disease, it should be a risk factor in all populations, in both sexes, at all ages, in all disease categories, and for both heart disease and stroke. But as you know by now, this is not the case
I have only two arguments for the idea that high cholesterol is good for the blood vessels, but in contrast to the arguments claiming the opposite they are very strong. The first one stems from the statin trials. If high cholesterol were the most important cause of cardiovascular disease, the greatest effect of statin treatment should have been seen in patients with the highest cholesterol, and in patients whose cholesterol was lowered the most. Lack of dose-response cannot be attributed to the knowledge that the statins have other effects on plaque stabilization, as this would not have masked the effect of cholesterol-lowering considering the pronounced lowering that was achieved. On the contrary, if a drug that effectively lowers the concentration of a molecule assumed to be harmful to the cardiovascular system and at the same time exerts several beneficial effects on the same system, a pronounced dose-response should be seen.
On the other hand, if high cholesterol has a protective function, as suggested, its lowering would counterbalance the beneficial effects of the statins and thus work against a dose-response, which would be more in accord with the results from the various trials.
I have already mentioned my second argument, but it can’t be said too often: High cholesterol is associated with longevity in old people. It is difficult to explain away the fact that during the period of life in which most cardiovascular disease occurs and from which most people die (and most of us die from cardiovascular disease), high cholesterol occurs most often in people with the lowest mortality. How is it possible that high cholesterol is harmful to the artery walls and causes fatal coronary heart disease, the commonest cause of death, if those whose cholesterol is the highest, live longer than those whose cholesterol is low?
To the public and the scientific community I say, "Wake up!"
References
1. Krumholz HM and others. Lack of association between cholesterol and coronary heart disease mortality and morbidity and all-cause mortality in persons older than 70 years. Journal of the American Medical Association 272, 1335-1340, 1990.
2. Ravnskov U. High cholesterol may protect against infections and atherosclerosis. Quarterly Journal of Medicine 96, 927-934, 2003.
3. Jacobs D and others. Report of the conference on low blood cholesterol: Mortality associations. Circulation 86, 1046–1060, 1992.
4. Iribarren C and others. Serum total cholesterol and risk of hospitalization, and death from respiratory disease. International Journal of Epidemiology 26, 1191–1202, 1997.
5. Iribarren C and others. Cohort study of serum total cholesterol and in-hospital incidence of infectious diseases. Epidemiology and Infection 121, 335–347, 1998.
6. Claxton AJ and others. Association between serum total cholesterol and HIV infection in a high-risk cohort of young men. Journal of acquired immune deficiency syndromes and human retrovirology 17, 51–57, 1998.
7. Neaton JD, Wentworth DN. Low serum cholesterol and risk of death from AIDS. AIDS 11, 929–930, 1997.
8. Rauchhaus M and others. Plasma cytokine parameters and mortality in patients with chronic heart failure. Circulation 102, 3060-3067, 2000.
9. Niebauer J and others. Endotoxin and immune activation in chronic heart failure. Lancet 353, 1838-1842, 1999.
10. Vredevoe DL and others. Skin test anergy in advanced heart failure secondary to either ischemic or idiopathic dilated cardiomyopathy. American Journal of Cardiology 82, 323-328, 1998.
11. Rauchhaus M, Coats AJ, Anker SD. The endotoxin-lipoprotein hypothesis. Lancet 356, 930–933, 2000.
12. Rauchhaus M and others. The relationship between cholesterol and survival in patients with chronic heart failure. Journal of the American College of Cardiology 42, 1933-1940, 2003.
13. Horwich TB and others. Low serum total cholesterol is associated with marked increase in mortality in advanced heart failure. Journal of Cardiac Failure 8, 216-224, 2002.
14. Elias ER and others. Clinical effects of cholesterol supplementation in six patients with the Smith-Lemli-Opitz syndrome (SLOS). American Journal of Medical Genetics 68, 305–310, 1997.
15. Bhakdi S and others. Binding and partial inactivation of Staphylococcus aureus a-toxin by human plasma low density lipoprotein. Journal of Biological Chemistry 258, 5899-5904, 1983.
16. Flegel WA and others. Inhibition of endotoxin-induced activation of human monocytes by human lipoproteins. Infection and Immunity 57, 2237-2245, 1989.
17. Weinstock CW and others. Low density lipoproteins inhibit endotoxin activation of monocytes. Arteriosclerosis and Thrombosis 12, 341-347, 1992.
18. Muldoon MF and others. Immune system differences in men with hypo- or hypercholesterolemia. Clinical Immunology and Immunopathology 84, 145-149, 1997.
19. Feingold KR and others. Role for circulating lipoproteins in protection from endotoxin toxicity. Infection and Immunity 63, 2041-2046, 1995.
20. Netea MG and others. Low-density lipoprotein receptor-deficient mice are protected against lethal endotoxemia and severe gram-negative infections. Journal of Clinical Investigation 97, 1366-1372, 1996.
21. Harris HW, Gosnell JE, Kumwenda ZL. The lipemia of sepsis: triglyceride-rich lipoproteins as agents of innate immunity. Journal of Endotoxin Research 6, 421-430, 2001.
22. Netea MG and others. Hyperlipoproteinemia enhances susceptibility to acute disseminated Candida albicans infection in low-density-lipoprotein-receptor-deficient mice. Infection and Immunity 65, 2663-2667, 1997.
23. Ross R, Glomset JA. The pathogenesis of atherosclerosis. New England Journal of Medicine 295, 369-377, 1976.
24. Ross R. The pathogenesis of atherosclerosis and update. New England Journal of Medicine 314, 488-500, 1986.
25. Klotz O, Manning MF. Fatty streaks in the intima of arteries. Journal of Pathology and Bacteriology. 16, 211-220, 1911.
26. At least 200 reviews about the role of infections in atherosclerosis and cardiovascular disease have been published; here are a few of them: a) Grayston JT, Kuo CC, Campbell LA, Benditt EP. Chlamydia pneumoniae strain TWAR and atherosclerosis. European Heart Journal Suppl K, 66-71, 1993. b) Melnick JL, Adam E, Debakey ME. Cytomegalovirus and atherosclerosis. European Heart Journal Suppl K, 30-38, 1993. c) Nicholson AC, Hajjar DP. Herpesviruses in atherosclerosis and thrombosis. Etiologic agents or ubiquitous bystanders? Arteriosclerosis Thrombosis and Vascular Biology 18, 339-348, 1998. d) Ismail A, Khosravi H, Olson H. The role of infection in atherosclerosis and coronary artery disease. A new therapeutic target. Heart Disease 1, 233-240, 1999. e) Kuvin JT, Kimmelstiel MD. Infectious causes of atherosclerosis. f.) Kalayoglu MV, Libby P, Byrne GI. Chlamydia pneumonia as an emerging risk factor in cardiovascular disease. Journal of the American Medical Association 288, 2724-2731, 2002.
27. Grau AJ and others. Recent bacterial and viral infection is a risk factor for cerebrovascular ischemia. Neurology 50, 196-203, 1998.
28. Mattila KJ. Viral and bacterial infections in patients with acute myocardial infarction. Journal of Internal Medicine 225, 293-296, 1989.
29. The successful trials: a) Gurfinkel E. Lancet 350, 404-407, 1997. b) Gupta S and others. Circulation 96, 404-407, 1997. c) Muhlestein JB and others. Circulation 102, 1755-1760, 2000. d) Stone AFM and others. Circulation 106, 1219-1223, 2002. e) Wiesli P and others. Circulation 105, 2646-2652, 2002. f) Sander D and others. Circulation 106, 2428-2433, 2002.
30. The unsuccessful trials: a) Anderson JL and others. Circulation 99, 1540-1547, 1999. b) Leowattana W and others. Journal of the Medical Association of Thailand 84 (Suppl 3), S669-S675, 2001. c) Cercek B and others. Lancet 361, 809-813, 2003. d) O’Connor CM and others. Journal of the American Medical Association. 290, 1459-1466, 2003.
31. Gieffers J and others. Chlamydia pneumoniae infection in circulating human monocytes is refractory to antibiotic treatment. Circulation 104, 351-356, 2001
32. Gurfinkel EP and others. Circulation 105, 2143-2147, 2002.
About the Author
Dr. Ravnskov is the author of The Cholesterol Myths and chairman of The International Network of Cholesterol Skeptics (thincs.org).
There is one risk factor that is known to be certain to cause death. It is such a strong risk factor that it has a 100 percent mortality rate. Thus I can guarantee that if we stop this risk factor, which would take no great research and cost nothing in monetary terms, within a century human deaths would be completely eliminated. This risk factor is called "Life."
Many doctors believe that most patients with familial hypercholesterolemia (FH) die from CHD at a young age. Obviously, they do not know the surprising finding of the Scientific Steering Committee at the Department of Public Health and Primary Care at Radcliffe Infirmary in Oxford, England. For several years, these researchers followed more than 500 FH patients between the ages of 20 and 74 and compared patient mortality during this period with that of the general population.
During a three- to four-year period, six of 214 FH patients below age 40 died from CHD. This may not seem particularly frightening but as it is rare to die from CHD before the age of 40, the risk for these FH patients was almost 100 times that of the general population.
During a four- to five-year period, eight of 237 FH patients between ages 40 and 59 died, which was five times more than the general population. But during a similar period of time, only one of 75 FH patients between the ages of 60 and 74 died from CHD, when the expected number was two.
If these results are typical for FH, you could say that between ages 20 and 59, about 3 percent of the patients die from CHD, and between ages 60 and 74, less than 2 percent die, in both cases during a period of 3-4 years. The authors stressed that the patients had been referred because of a personal or family history of premature vascular disease and therefore were at a particularly high risk for CHD. Most patients with FH in the general population are unrecognized and untreated. Had the patients studied been representative for all FH patients, their prognosis would probably have been even better.
This view was recently confirmed by Dr. Eric Sijbrands and his coworkers from various medical departments in Amsterdam and Leiden, Netherlands. Out of a large group they found three individuals with very high cholesterol. A genetic analysis confirmed the diagnosis of FH and by tracing their family members backward in time, they came up with a total of 412 individuals. The coronary and total mortality of these members were compared with the mortality of the general Dutch population.
The striking finding was that those who lived during the 19th and early 20th century had normal mortality and lived a normal life span. In fact, those living in the 19th century had a lower mortality than the general population. After 1915 the mortality rose to a maximum between 1935 and 1964, but even at the peak, mortality was less than twice as high as in the general population.
Again, very high cholesterol levels alone do not lead to a heart attack. In fact, high cholesterol may even be protective against other diseases. This was the conclusion of Dr. Sijbrands and his colleagues. As support they cited the fact that genetically modified mice with high cholesterol are protected against severe bacterial infections.
"Doctor, don’t be afraid because of my high cholesterol." These were the words of a 36-year-old lawyer who visited me for the first time for a health examination. And indeed, his cholesterol was high, over 400 mg/dl.
"My father’s cholesterol was even higher," he added. "But he lived happily until he died at age 79 from cancer. And his brother, who also had FH, died at age 83. None of them ever complained of any heart problems." My "patient" is now 53, his brother is 56 and his cousin 61. All of them have extremely high cholesterol values, but none of them has any heart troubles, and none of them has ever taken cholesterol-lowering drugs.
So, if you happen to have FH, don’t be too anxious. Your chances of surviving are pretty good, even surviving to old age.
Scientific Steering Committee on behalf of the Simon Broome Register Group. Risk of fatal coronary heart disease in familial hypercholesterolaemia. British Medical Journal 303, 893-896, 1991; Sijbrands EJG and others. Mortality over two centuries in large pedigree with familial hypercholesterolaemia: family tree mortality study. British Medical Journal 322, 1019-1023, 2001.
From The Cholesterol Myths by Uffe Ravnvskov, MD, PhD, NewTrends Publishing, pp 64-65.
This article appeared in Wise Traditions in Food, Farming and the Healing Arts,
the quarterly magazine of the Weston A. Price Foundation, Spring 2004.
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There is a daunting amount of research studies showing that the widely acclaimed benefits on fluoride dental health are more imagined than real. My main concern however, is the effect of sustained fluoride intake on general health. Again, there is a huge body of research literature on this subject, freely available and in the public domain.
But this body of work was not considered by the York Review when their remit was changed from “Studies of the effects of fluoride on health” to “Studies on the effects of fluoridated water on health." It is clearly evident that it was not considered by the BMA (Britsh Medical Association), British Dental Association (BDA), BFS (British Fluoridation Society) and FPHM, (Faculty for Public Health and Medicine) since they all insist, as in the briefing paper to Members of Parliament - that fluoridation is safe and non-injurious to health.
This is a public disgrace, I will now show by reviewing the damaging effects of fluoridation, with special reference to thyroid illness.
It has been known since the latter part of the 19th century that certain communities, notably in Argentina, India and Turkey were chronically ill, with premature ageing, arthritis, mental retardation, and infertility; and high levels of natural fluorides in the water were responsible. Not only was it clear that the fluoride was having a general effect on the health of the community, but in the early 1920s Goldemberg, working in Argentina showed that fluoride was displacing iodine; thus compounding the damage and rendering the community also hypothyroid from iodine deficiency.
Highly damaging to the thyroid gland
This was the basis of the research in the 1930s of May, Litzka, Gorlitzer von Mundy, who used fluoride preparations to treat over-active thyroid illness. Their patients either drank fluoridated water, swallowed fluoride pills or were bathed in fluoridated bath water; and their thyroid function was as a result, greatly depressed. The use in 1937 of fluorotyrosine for this purpose showed how effective this treatment was; but the effectiveness was difficult to predict and many patients suffered total thyroid loss. So it was given a new role and received a new name, Pardinon. It was marketed not for over-active thyroid disease but as a pesticide. (Note the manufacturer of fluorotyrosine was IG Farben who also made sarin, a gas used in World War II).
This bit of history illustrates the fact that fluorides are dangerous in general and in particular highly damaging to the thyroid gland, a matter to which I shall return shortly. While it is unlikely that it will be disputed that fluorides are toxic - let us be reminded that they are Schedule 2 Poisons under the Poisons Act 1972, the matter in dispute is the level of toxicity attributable to given amounts; in today’s context the degree of damage caused by given concentrations in the water supply. While admitting its toxicity, proponents rely on the fact that it is diluted and therefore, it is claimed, unlikely to have deleterious effects.
They could not be more mistaken
It seems to me that we must be aware of how fluoride does its damage. It is an enzyme poison. Enzymes are complex protein compounds that vastly speed up biological chemical reactions while themselves remaining unchanged. As we speak, there occurs in all of us a vast multitude of these reactions to maintain life and produce the energy to sustain it. The chains of amino acids that make up these complex proteins are linked by simple compounds called amides; and it is with these that fluorine molecules react, splitting and distorting them, thus damaging the enzymes and their activity. Let it be said at once, this effect can occur at extraordinary low concentrations; even lower than the one part per million which is the dilution proposed for fluoridation in our water supply.
The body can only eliminate half
Moreover, fluorides are cumulative and build up steadily with ingestion of fluoride from all sources, which include not just water but the air we breathe and the food we eat. The use of fluoride toothpaste in dental hygiene and the coating of teeth are further sources of substantial levels of fluoride intake. The body can only eliminate half of the total intake, which means that the older you are the more fluoride will have accumulated in your body. Inevitably this means the ageing population is particularly targeted. And even worse for the very young there is a major element of risk in baby formula made with fluoridated water. The extreme sensitivity of the very young to fluoride toxicity makes this unacceptable. Since there are so many sources of fluoride in our everyday living, it will prove impossible to maintain an average level of 1ppm as is suggested.
What is the result of these toxic effects?
First the immune system. The distortion of protein structure causes the immune proteins to fail to recognise body proteins, and so instigate an attack on them, which is Autoimmune Disease. Autoimmune diseases constitute a body of disease processes troubling many thousands of people: Rheumatoid Arthritis, Systemic Lupus Erythematosis, Asthma and Systemic Sclerosis are examples; but in my particular context today, thyroid antibodies will be produced which will cause Thyroiditis resulting in the common hypothyroid disease, Hashimoto’s Disease and the hyperthyroidism of Graves’ Disease.
Musculo Skeletal damage results further from the enzyme toxic effect; the collagen tissue of which muscles, tendons, ligaments and bones are made, is damaged. Rheumatoid illness, osteoporosis and deformation of bones inevitably follow. This toxic effect extends to the ameloblasts making tooth enamel, which is consequently weakened and then made brittle; and its visible appearance is, of course, dental fluorosis.
The enzyme poison effect extends to our genes; DNA cannot repair itself, and chromosomes are damaged. Work at the University of Missouri showed genital damage, targeting ovaries and testes. Also affected is inter uterine growth and development of the foetus, especially the nervous system. Increased incidence of Down’s Syndrome has been documented. Fluorides are mutagenic. That is, they can cause the uncontrolled proliferation of cells we call cancer. This applies to cancer anywhere in the body; but bones are particularly picked out. The incidence of osteosarcoma in a study reporting in 1991 showed an unbelievable 50% increase. A report in 1955 in the New England Journal of Medicine showed a 400% increase in cancer of the thyroid in San Francisco during the period their water was fluoridated.
My particular concern is the effect of fluorides on the thyroid gland
Perhaps I may remind you about thyroid disease. The thyroid gland produces hormones which control our metabolism - the rate at which we burn our fuel. Deficiency is relatively common, much more than is generally accepted by many medical authorities: a figure of 1:4 or 1:3 by mid life is more likely. The illness is insidious in its onset and progression. People become tired, cold, overweight, depressed, constipated; they suffer arthritis, hair loss, infertility, atherosclerosis and chronic illness. Sadly, it is poorly diagnosed and poorly managed by very many doctors in this country. What concerns me so deeply is that in concentrations as low as 1ppm, fluorides damage the thyroid system on 4 levels.
1. The enzyme manufacture of thyroid hormones within the thyroid gland itself. The process by which iodine is attached to the amino acid tyrosine and converted to the two significant thyroid hormones, thyroxine (T4) and liothyronine (T3), is slowed.
2. The stimulation of certain G proteins from the toxic effect of fluoride (whose function is to govern uptake of substances into each of the cells of the body), has the effect of switching off the uptake into the cell of the active thyroid hormone.
3. The thyroid control mechanism is compromised. The thyroid stimulating hormone output from the pituitary gland is inhibited by fluoride, thus reducing thyroid output of thyroid hormones.
4. Fluoride competes for the receptor sites on the thyroid gland which respond to the thyroid stimulating hormone; so that less of this hormone reaches the thyroid gland and so less thyroid hormone is manufactured. These damaging effects, all of which occur with small concentrations of fluoride, have obvious and easily identifiable effects on thyroid status. The running down of thyroid hormone means a slow slide into hypothyroidism. Already the incidence of hypothyroidism is increasing as a result of other environmental toxins and pollutions together with wide spread nutritional deficiencies.
141 million Europeans are at risk
One further factor should give us deep anxiety. Professor Hume of Dundee, in his paper given earlier this year to the Novartis Foundation, pointed out that iodine deficiency is growing worldwide. There are 141 million Europeans are at risk; only 5 European countries are iodine sufficient. UK now falls into the marginal and focal category. Professor Hume recently produced figures to show that 40% of pregnant women in the Tayside region of Scotland were deficient by at least half of the iodine required for a normal pregnancy. A relatively high level of missing, decayed, filled teeth was noted in this non-fluoridated area, suggesting that the iodine deficiency was causing early hypothyroidism which interferes with the health of teeth. Dare one speculate on the result of now fluoridating the water?...