Fluoride is a multi-system poison. The Natural Solutions Foundation strongly opposes compulsory drugging through its addtion to the water systems of communities. We believe that this is both medically reckless and unconstitutional.
The Natural Solutions Foundation’s strongly anti-fluoride position for infants and children is now echoed by the American Dental Association (ADA) which says that children under 1 year should not be exposed to fluoride.
Although the US supported fluoride in infant formula during the 2006 Codex Committee on Nutritiona and Foods for Special Dietary Uses meeting in Chiang Mai, Thailand which dealt with infant formula and other special purpose foods, using data provided by the Natural Solutions Foundation, South Africa pushed the restriction on fluoride in healthy infants’ formula through, despite strong US objection.
Long a proponent of fluoridation of children’s teeth, the ADA joins the Natural Solutions Foundation in pointing out the dangers of the now-debunked toxin in infant’s bodies.
Rather than deal with the expense of safe disposal, the mining industry created the false belief that fluoride should be added to water, toothpaste, supplements, etc. That way, mining companies make a profit instead of taking a loss on fluoride which is expensive to dispose of according to EPA regulations. Despite propaganda to the contrary, fluoride has no known place in human metabolism and increases disease in those exposed to it. It is toxic to the brain, kidneys, bones, teeth, causes bone and other cancers at levels far lower than those permitted in water and has no known positive impact on human health despite oft-repeated but deeply flawed research claims to the contrary. Recent re-evaluation of the original research and other data make it clear that fluoride in any amount is a cumulative biological poison.
Although the United States has sought to add Fluoride to infant formula in the US and internationally, the World Health Organization recommends that infant formula be prepared in water which has no fluoride. Fluoridating water supplies means that infants will necessarily be exposed to amounts of fluoride which are toxic to them. “Little is known of the particular susceptibility of infants to fluoride but what we do know makes it clear that infant formula should be mixed with fluoride free water because fluoride is so toxic to them. Since infants are generally more sensitive to toxins than adults, banning it from formula is the only sensitive alternative,” according to Rima E. Laibow, MD, Medical Director of the Natural Solutions Foundation (http://www.HealthFreedomUSA.org).
Despite its wide acceptance as a water and food additive, and even as a “nutritional supplement,” fluoride is actually a dangerous metabolic poison with permanent effects at levels much lower than 1 part per million (ppm). Exposure is cumulative since fluoride is a bio-accumulator which remains in the body and can cause cancer, kidney failure, bone disease, including bone cancers, structural damage to bone and teeth, thyroid poisoning, pineal gland calcification, reproductive failure, synergistic increases in lead poisoning when both are present, endocrine disruption leading to diabetes, other cancers and decreases in the availability of essential nutrients like magnesium.
In addition to water, the FDA allows sodium aluminum fluoride (cryolite) to be sprayed on more than 30 fruits and vegetables at up to 7 ppm. The USDA set a 1.2 ppm limit for arsenic and fluoride pesticides in 1933 since they are equally toxic. While arsenic sprays have been phased out, fluoride ones are increasingly popular and now can be used not only on food but on food storage areas as well. Current FDA water fluoridation standards allow up to 4 ppm and assure on-going fluoride contamination for most Americans.
Industry pressure is strong to increase the amount of fluoride we ingest: DOW Chemical uses extremely high fluoride tolerances on a wide number of common foods including 98 ppm for wheat germ, 40 ppm for wheat bran, 31 ppm for rice bran, 30 ppm for some nuts, 28 ppm for corn meal, 26 ppm for corn flour, 25 ppm for millet, wild rice, sorghum and wheat grains and 17 ppm for oat grain.
Leading scientists have called for a ban on all fluoride usage in light of its devastating impact on health and a recent evaluation of the data upon which fluoridation was initially approved by the FDA for municipal water supplies was deeply and fraudulently distorted when presented to the FDA and the public since toxic results were not revealed in the group receiving fluoridated water.
Vaccines often contain fluoride as an adjuvant or immune system irritant to provoke the immune system into producing more antibodies with fewer antigens since antigens are the expensive part of vaccines. Since vaccines also frequently contain aluminum hydroxide, the synergistic toxicity of the two toxins is significantly more than the toxicity of either toxic metal alone at the same dosage. This problem is repeated in municipal water supplies since fluoride is added for its alleged dental health benefits while aluminum salts are added to “polish” the water and give it an appealing gleaming appearance.
Fluoride as an additive has a dark past: it was first added to water in the Soviet Gulag (prison system) since it is a neurological poison and made political and other difficult prisoners complacent and therefore easier to manage. It was added to the water supplies of the Nazi death and slave labor camps for the same reason. Fluoride is widely used as an additive although the scientific evidence upon which its use rests is either fraudulent or flawed. Long a staple of water treatment, sodium fluoride has been replaced by other, even more toxic fluoride compounds like sulfuryl fluoride which has never been tested in water supplies nor approved for use in them.
The New York State Attorney General has expressed support for banning this dangerous but widely used pesticide. Fluoride contamination from either natural sources or its addition to liquids and products used by children results in dental fluorosis, a permanent mottling of teeth which is both cosmetic and structural, and similar structural damage to bone associated with increased fractures, osteoporosis (bone loss) and demineralization of bone. IQ loss and other neurological damage is due both to the fluoride itself and the dangerous interaction of fluoride with lead since fluoride renders lead even more toxic to the brain. Fluoride without lead leads to loss of higher cognitive functions including decision-making and IQ.
Yours in health and freedom,
Dr. Rima
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
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Think about it for a moment: unlabeled GMOs with medical consequences, including, as in this case, sterility, constitutes the force feeding of industrial toxins to a global population. You might call it forced drugging, and you would be right.
One would tend to assume that food sold to consumers would not have intended or unintended medical consequences like birth defects, cancer, auto immune diseases, infertility or sterility. One would be wrong. Since FDA and USDA do not conduct, or examine, safety studies except once very early on in the approval process when they review preliminary safety testing provided by the corporation developing the product (!), these “foods” (Frankenfoods, really) are launched into the market place with neither safety testing nor review of safety testing by our supposed “watchdog” agencies.
Natural Solutions Foundation believes in your health freedom. Apparently, the FDA and USDA do not. If they did, they would not permit dangerous, untested and unlabeled (that is, forbidden to be labeled!) GMO “food” to be sold in the US as “food” (for people) and “feed” (for animals who are, ultimately, eaten by people). You see, we believe that your right to safe, unadulterated foods and it also includes your right to have children if you want to, and grandchildren, too.
Seven months ago we noted that a little-known genetic bioengineering firm in California, Epicyte, announced the development of genetically engineered corn which contained a spermicide which made the semen of men who ate it sterile in 2001. At the time Epicyte had a joint venture agreement to spread its technology with DuPont and Syngenta, two of the sponsors of the Svalbard Doomsday Seed Vault. Epicyte was since acquired by a North Carolina biotech company. It was astonishing to learn that Epicyte had developed its spermicidal GMO corn with research funds from the US Department of Agriculture, the same USDA which, despite worldwide opposition, continued to finance the development of Terminator technology, now held by Monsanto.
Every independent scientific review of safety of which I am aware documents the serious, potentially lethal, and now, sterility-inducing impact of these “foods”. One has to wonder whether the Epicyte human sterility gene is part of the NK 603xMon810 genome now since its impact is sterility.
Whether it is or not, what is clear is that the consumption of the unlabeled “foods” or their by products and derivatives poses as great a threat to humanity as the ever-promised Avian Flu Pandemic. Eat them at your own risk. And get involved to pressure your Congressional members to become co-sponsors of, and strongly support, the 2 excellent bills before Congress now which would require safety testing and labeling of all GMO foods. Click here (http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=25920) to send you strong message to Congress for your food rights.
Genetically Modified “foods” do not have names. They have numbers
Real food has names, usually less than 3 syllables. GMO “foods” and “feeds” hide behind initials and numbers like the biochemicals they are: e.g., NK 603 and Mon810. Those are genetically engineered corn types permitted for human and animal food in the US and the EU and elsewhere in the world. Neither corn (or “maize” as it is also called) has EVER been properly tested for safety by an independent governmental agency. No safety review of independent, non-industry studies has ever been done by a government agency anywhere in the world. Independent studies have never been commissioned by any government agency before these foods were approved, strictly on the basis of corporate assurances that these “foods” were safe in the US, Europe and elsewhere.
The reality is that when independent studies are conducted on these “foods”, they are neither safe nor benign.
The FDA thinks it is perfectly fine to take those rights, and your posterity, away from you without your knowledge or consent. By allowing genetically modified (GMO) “foods” which are known to reduce fertility in animals (we are, reproductively speaking, biologically similar to the animals being tested) and forbidding labeling of GMO foods or ingredients, the FDA says that foods like NK603 and Mon810 are acceptable to them. Is the truth that this is part of a long-stanidng, wide-ranging depopulation program using multiple ways to eliminate your ability to reproduce?
Who cares? You do, and so do we.
Thanks for your continuing support. Without it, the Natural Solutions Foundation could not continue its important work.
Yours in health and freedom,
Dr. Rima
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsMedia.tv
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Natural Solutions Foundation
Genetically-engineered food: potential threat to fertility
Study shows that genetically engineered maize affects reproductive health in mice
Vienna, Austria, 11 November 2008 – A study published today by the Austrian government identified serious health threats of genetically engineered (GE) crops. In one of the very few long-term feeding studies ever conducted with GE crops, the fertility of mice fed with GE maize was found to be severely impaired, with fewer offspring being produced than by mice fed on natural crops. Considering the severity of the potential threat to human health and reproduction, Greenpeace is demanding a recall of all GE food and crops from the market, worldwide. Of course, that would mean changing the happy approval of Codex of all “foods” genetically modified and all GMO “feeds” as well. We’ll need your strong support to build the coalition to mass the muscle to reopen those issues. It can be done, of course, but we need your help.
Your only protection on your table and in your cupboards right now, of course, is to eat, grow and source organic food. Only organic food. Too expensive? What is your health worth and, if you are of child bearing age, the ability to have children or have your children have children? A few dollars more in food per week? Probably. If you can’t afford the expense, start doing intensive gardening in a corner of your apartment, on your patio or in a small corner of your garden. Foot Square Gardening references abound on the internet, at your library and in your book store. Take a look. Even in the winter it’s pretty simple to do indoors. Don’t delay, though. The damage from these Frankenfoods is cumulative.
The study, sponsored by the Austrian Ministries for Agriculture and Health, was presented today at a scientific seminar in Vienna, Austria. Prof. Dr. Jürgen Zentek, Professor for Veterinary Medicine at the University of Vienna and lead author of the study, summarised the findings: Mice fed with GE maize had less offspring in the third and fourth generations, and these difference were statistically significant. Mice fed with non-GE maize reproduced more efficiently. This effect can be attributed to the differences in the food source.
“GE food appears to be acting as a birth control agent, potentially leading to infertility – if this is not reason enough to close down the whole biotech industry once and for all, I am not sure what kind of disaster we are waiting for,†said Dr. Jan van Aken, GE expert at Greenpeace International. “Playing genetic roulette with our food crops is like playing Russian roulette with consumers and public healthâ€.
The Austrian scientists performed several long-term feeding trials with laboratory mice over a course of 20 weeks. One of the studies was a so-called reproductive assessment by continuous breeding (RACB) trial, in which the same parent generation gave birth to several litters of baby mice. The parents were fed either with a diet containing 33% of a GE maize variety (NK 603 x MON 810), or a closely related non-GE variety. A decrease in litter size and weight was found to be statistically significant in the third and fourth litters in the GE-fed mice compared to the control group.
Owned by Monsanto, the GE maize variety tested in this study is tolerant to a herbicide and resistant to certain insect pests. It has been approved for planting and food use in a variety of countries, including the US, Argentina, Japan, Philippines and South Africa. In Mexico and the European Union(1), it is approved for food and feed use.
“This study is yet another example that the food and feed safety of GE crops and food cannot be guaranteed. The reproductive toxicity of this GE maize was a totally unexpected result, but regulators around the world had considered this GE maize variety as safe as non-GE varieties – a potentially devastating error,†said Dr. van Aken.
Contacts:
Dr. Jan van Aken, Greenpeace International agriculture expert, +49 151 1805 3415
Dr. Janet Cotter, Greenpeace International Science Unit, +44 7812 174783
Notes to Editors:
(1) In 2005, the European Food Safety Agency EFSA gave a green light for this variety. Without conducting any independent studies and just relying on Monsanto’s data, EFSA wrote it “considers it unlikely that NK603 x MON810 maize will have any adverse effect on human and animal healthâ€. This exemplifies how flawed and ill-designed the European risk assessment for GE crops is.
There are two articles which follow this introduction which have great bearing on your health and, eventually, your ability survive.
Agricultural chemicals have been known since their inception to pose significant threats to human, animal and environmental health. They are, in fact, only approved for use on the food supply of people and animals because, in my opinion, of the enormous wealth which chemical companies, which are, in essence, a branch of the pharmaceutical industry, have have available to throw at compliant regulators and legislators, plus deceptive and misleading advertising bulwarked by corporate junk science.
Agricultural chemicals are not, however, limited to herbicides, fungicides, pesticides and fertilizers. Other chemicals quality for that designation, too. For many years, the US has permitted the spraying of fluoride and mercury on crops after harvest to prevent mold growth during storage despite the well characterized dangers of those substances.
Now, another toxin, also well known for its adverse effect on the brain, the nervous system, the endocrine system, perception, mood and vascular integrety has been approved by the supposed guardians of our health, the FDA, EPA and USDA for direct application, without any upper limit, on our foods.
Read this article and ask yourself whether you ever want to eat non organic food again. Then ask yourself why regulators are permitting known toxins in our food.
And then click on this link (https://staging.drrimatruthreports.com/index.php?page_id=189) to make a donation to the Natural Solutions Foundation, a totally donation-supported Non governmental organization (NGO) devoted to your right to make your own choices in your health. Among the freedoms that we believe belong to you and that we are fighting for on your behalf, and ours, is the right to know what your food has been sprayed with, genetically modified with, contaminated with or irradiated with. In short, if food is contaminated you have a right to know it.
And you have another right, too, as I see it.
You have a right to be protected by the regulators from the self-interested companies that do not care at all about the damage their chemicals and processes bring to you and yours. That is, after all, what we believe regulatory agencies are supposed to do. But the sad truth is that we need to be protected FROM the regulatory agencies.
That’s one of the things that Natural Solutions Foundation does, in fact. And, of course, we need your help. Click here (https://staging.drrimatruthreports.com/index.php?page_id=189) to become a supporting sponsor with a tax deductible recurring donation. And visit the Natural Solutions Foundation home page, www.HealthFreedomUSA.org, to sign up for our free, secure Health Freedom eAlerts.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
MSG is being sprayed right on fruits, nuts, seeds, grains, and vegetables as they grow —
even those used in baby food
In the 1970s, reluctant food processors “voluntarily” took processed free glutamic acid (MSG) out of baby food. Today it’s back, in fertilizers called “Omega Protein Refined/Hydrolyzed Fish Emulsion” and “Steam Hydrolyzed Feather Meal,” both of which contain hydrolyzed proteins; and in a product called AuxiGro WP Plant Metabolic Primer (AuxiGro) produced by Emerald BioAgriculture (formerly Auxein Corporation), which contains both hydrolyzed protein(s) and “monosodium glutamate.” AuxiGro is being sprayed on some of the vegetables we and our children will eat, into the air we and our children must breath, and onto the ground from which it can move into drinking water. Head lettuce, leaf lettuce, tomatoes, potatoes, and peanuts were among the first crops targeted. On September 12, 2000, the Auxein Corporation Web site gave the following information:
Crops registered include: Celery; Fresh Market Cucumbers; Edible Navy and Pinto Beans; Grapes; Bulb Onions; Bell, Green and Jalapeno Peppers; Iceberg Head Lettuce; Romaine and Butter Leaf Lettuce; Peanuts; Potatoes; Snap Beans; Strawberries; Processing Tomatoes; Fresh Tomatoes; and Watermelons.
Today, there is no crop that we know of that has not been approved for treatment with MSG by the U.S. Environmental Protection Agency (EPA).
Even in California — the only state where there are any restrictions on the use of AuxiGro — AuxiGro has been approved for use on a number of crops, and Emerald BioAgriculture continues to push for more. Field tests in California have been — and may continue to be — conducted on a variety of crops, and those AuxiGro treated crops may be sold in the open market without revealing that they have been treated. We can’t tell you which crops those are because the CDPR has refused to send records of test trials (which are public information) to the Truth in Labeling Campaign.
As of June 13, 2002, AuxiGro was registered for use in California on tomatoes, almonds, apricots, cherries, plums, nectarines, peaches, prunes, grapes (including grapes to be used in wine), and onions. At that time, the California Department of Pesticide Regulation said they were not aware of any testing of AuxiGro for use on other crops. They also said that they did not have any proposals presently in house to register additional crops for AuxiGro. It would appear, however, that what the CDPR said was not true, for the CDPR subsequently announced that Emerald BioAgriculture had applied for permission to use AuxiGro on tomatoes (new use), and on melons (new crop) — and, to the best of our knowledge, approval is always preceded by field testing.
On July 7, 2004, Emerald BioAgriculture requested approval of use of AuxiGro as a desiccant, disinfectant, fertilizer, fungicide, growth regulator – for increased yield and prevention of powdery mildew in various crops such as almonds, grapes, and melons. They also asked to add cole crops (including broccoli, brussels sprouts, cabbage, cauliflower, kale, collards, turnips, rutabaga, mustard, watercress, and kohlrabi) to the list of crops approved for AuxiGro use.
Approval for use on organic crops–in all states–has been requested.
What’s wrong with using glutamic acid, an amino acid found in protein, as a spray on crops?
– In protein, amino acids are found in balanced combinations. Use of free glutamic acid as a spray on crops throws the amino acid balance out of kilter.
– It’s not the glutamic acid found in protein that is being sprayed on crops, it’s a synthetic product. The spray being used most widely is called AuxiGro. The “free glutamic acid” or so called “L-glutamic acid” component being used by its manufacturer, Emerald BioAgriculture, contains L-glutamic acid, an amino acid found in protein; but it also contains D-glutamic acid, pyroglutamic acid, and other chemicals referred to in the industry as “contaminants.” The free glutamic acid used in AuxiGro is processed free glutamic acid. It is manufactured — in chemical plants — where certain selected genetically engineered bacteria — feeding on a liquid nutrient medium — excrete the free glutamic acid they synthesize outside of their cell membrane into the liquid medium in which they are grown. In contrast, the free glutamic acid found in protein, and the free glutamic acid involved in normal human body function, are unprocessed. free glutamic acid, and contain no contaminants.
– No one knows what the long term effects of spraying processed free glutamic acid on crops will be.
– That the processed free glutamic acid (MSG) will be absorbed into the body of the plant and into the fruit, nuts, seeds, or vegetable it produces seems undeniable. If it were not, the plant would not be stimulated to grow. Neither Emerald BioAgriculture or the EPA will address this issue.
– That there will be residue left on crops has not been disputed by Emerald BioAgriculture. But no study of either the amount of that residue, or the least amount of processed free glutamic acid needed to cause a reaction in an MSG-sensitive person, has ever been done. “It should wash off” doesn’t mean it will wash off. “It seems unlikely that such a small amount would cause a reactions” doesn’t mean that a small amount will not cause a reaction or have long term health effects.
– Free glutamic acid is known to be toxic to the nervous system. But the neurotoxic effects that processed free glutamic acid will have on animals that consume the plants on which it is sprayed – effects over and above any effects caused by external glutamic acid residue – have never been evaluated. Neither are there data on the effects that spraying processed free glutamic acid will have on drinking water.
– Consider, also, that children are most at risk from the effects of processed free glutamic acid. Their undeveloped blood-brain barriers leave them most at risk from exposure to processed free glutamic acid. It has been repeatedly demonstrated that infant animals fed processed free glutamic acid when young develop neuroendocrine problems such as gross obesity, stunted growth, and reproductive disorders later in life, and that they also develop learning disabilities. Emerald BioAgriculture did not address that particular safety issue in its application to the EPA.
– No one knows how little glutamic acid is needed to kill a single brain cell or to trigger an adverse reaction.
– Free glutamic acid is a neurotransmitter. It causes nerves to fire, carrying nerve impulses throughout the nervous system.
– Free glutamic acid is a neurotoxin. Under certain circumstances, free glutamic acid will cause nerves to fire repeatedly, until they die.
– Processed free glutamic acid kills brain cells. The free glutamic acid ingested by laboratory animals that caused brain lesions and neuroendocrine disorders was very often given in the form of the food ingredient “monosodium glutamate.” “Monosodium glutamate” is the name of a particular food additive. Processed free glutamic acid is the reactive component in “monosodium glutamate,” just as processed free glutamic acid is a reactive component in AuxiGro.
The glutamate industry research done in the 1970s that was submitted to the EPA by the Auxein Corporation, that pretended to find that processed free glutamic acid is “safe,” has been long refuted by independent scientists. Indeed, at the present time, neuroscientists attempting to develop drugs to block the toxic effects of free glutamic acid are using processed free glutamic acid to selectively kill certain kinds of brain cells.
– Processed free glutamic acid causes neuroendocrine disorders in maturing animals that ingest processed free glutamic acid early in life.
– Processed free glutamic acid causes learning disorders in maturing animals that ingest processed free glutamic acid early in life.
– Processed free glutamic acid crosses the placental barrier and causes learning disabilities in animal offspring of dams that ingest it.
– Processed free glutamic acid has access to the brain through the blood-brain barrier, which is not impervious to the unregulated flow of processed free glutamic acid. The blood-brain barrier is immature at birth and may continue to develop up to puberty. In certain areas called the circumventricular organs, the blood barrier is never impervious to the unregulated flow of free glutamic acid. In addition, the blood-brain barrier is easily damaged by such events as high fever, a blow to the head, drug use, stroke, ingestion of processed free glutamic acid, and the normal process of aging.
– The National Institutes of Health recognize glutamic acid as being associated with addiction, stroke, epilepsy, degenerative disorders such as Alzheimer’s disease, Parkinson’s disease, and ALS, brain trauma, neuropathic pain, schizophrenia, anxiety, and depression.
– For years, free glutamic acid has been produced and used in food additives with names such as monosodium glutamate, sodium caseinate, and hydrolyzed soy protein. In some people, the processed free glutamic acid in food additives causes adverse reactions that include migraine headache, asthma, arrhythmia, tachycardia, nausea and vomiting, depression, and disorientation. The processed free glutamic acid in prescription and non-prescription drugs, food supplements, and cosmetics can also cause adverse reactions.
There are badly flawed industry-sponsored studies that have pretended to find that processed free glutamic acid does not cause adverse reactions. Inappropriate procedures used by the glutamate industry have included limiting subjects to people virtually guaranteed not to be sensitive to processed free glutamic acid, and/or using processed free glutamic acid or other similarly reactive substances in placebos as well as in test material. The Food and Drug Administration (FDA) has based its claim that processed free glutamic acid causes only mild and transitory reactions on those badly flawed industry-sponsored studies.
– Even the EPA admits that the food additive called “monosodium glutamate” causes adverse reactions.
– Even the FDA admits that the food additive “monosodium glutamate” contains processed free glutamic acid.
<>– Even the FDA admits that many consumers refer to all free glutamic acid as “MSG.”
The EPA’s approvals of use of MSG in agriculture are simple, straightforward, and in violation of the Federal Food, Drug, and Cosmetic Act
In reviewing the application of Auxein Corporation (now Emerald BioAgriculture) for use of processed free glutamic acid in a spray to be applied to crops as they grow, the EPA failed to conform to the requirements of the Federal Food, Drug and Cosmetic Act, which require, in part, that the EPA review any proposed action for validity, completeness, reliability, and relationship to human risk. The EPA also ignored Executive Order 13045 which requires government agencies to consider available information concerning the variability of the sensitivities of major identifiable subgroups of consumers, including infants and children. For example, Auxein Corporation sent the EPA 14 industry-sponsored toxicological studies from the literature, all done in the 1970’s, but failed to mention hundreds of studies in the literature that refuted those 14 studies. Auxein Corporation even failed to send the EPA independent studies that appeared in the same book(s) as the industry-sponsored studies sent to the EPA. For example, although processed free glutamic acid causes brain lesions and neuroendocrine disorders in infant animals, this special hazard faced by infants was ignored by Auxein Corporation. It would appear that Auxein Corporation restricted its consideration of “available information” to information made available by the glutamate industry; and the EPA, even after having been sent abstracts from other “available information,” has not challenged the Auxein Corporation applications. A more complete discussion of the shortcomings of the EPA approvals granted to Auxein Corporation has been submitted to the EPA.
Questions about the safety of spraying processed free glutamic acid on plants and into the environment have been raised by the Truth in Labeling Campaign and by individual consumers. The EPA has refused to address those concerns. The EPA, and, in particular, EPA spokesperson Dr. Janet Andersen, has failed to respond to allegations that in approving the spraying of processed free glutamic acid, the EPA failed to consider the reliability, validity, and completeness of the Auxein Corporation application or comply with Executive Order 13045 entitled Protection of Children from Environmental Health Risks and Safety Risks, except to say that the EPA had complied with executive order 13045. Moreover, while responding to letters that asked direct questions of the EPA, Andersen failed to respond to most, if not all, of the direct questions contained in those letters.
AuxiGro, the first MSG-laced plant “growth enhancer” to hit the market, has been approved for spraying on every crop we know of, with no restrictions on the amount of processed free glutamic acid (MSG) that may remain in and/or on crops when brought to market. Even before consumers had an inkling that crops were being sprayed, the Truth in Labeling Campaign received reports that MSG-sensitive consumers had gotten sick from head lettuce and potatoes.
Federal Register notices chronicling the application and approval of processed free glutamic acid are available on the Web via GPO Access, the Federal Register, through: http://www.gpoaccess.gov/fr/index.html. Application for approval of use of AuxiGro was made to the EPA in 1997. Testing of the product was also approved in that year, and many of the test crops sprayed with AuxiGro were brought to market without notifying consumers. Glutamic acid was granted an exemption from establishment of a tolerance limit in January, 1998. AuxiGro was also approved for use on a number of crops in January, 1998, and approved for use on other crops later. No announcement of these approvals was made in the Federal Register.
Due to a technical glitch in the system, the glutes came to need one more approval to make their California registrations work. The glutes were asking for AuxiGro to be approved for use as a fungicide in California, but the EPA had only approved AuxiGro for use as a pesticide produce or plant growth enhancer. And when application was made for this addition to their approvals, the application was brought to our attention; and the Truth in Labeling Campaign filed a formal protest to this approval of AuxiGro. The Formal Objection of the Truth in Labeling Campaign was filed on August 16, 2001 with the EPA.
By law, formal objections filed in a timely manner must be responded to within six months. Also, by law (we were told) even though the Final Rule had not been promulgated, this additional use of AuxiGro would be considered approved unless and until the EPA determined that it should be otherwise. In July, 2004, we received a conference call from Dr. Andersen and a number of other EPA players, including an EPA lawyer — a “courtesy call” telling us that our objections had been discounted and that the Final Rule allowing use of AuxiGro as a fungicide would be published shortly in the Federal Register.
What’s wrong at the EPA?
Neither the EPA nor Janet Andersen, Ph.D., director of the Biopesticides and Pollution Prevention Division (BPPD), are stupid. Rather, all evidence would appear to suggest that the EPA, which is charged with protecting the health of Americans, says it is protecting the health of Americans, when in fact the EPA acts to protect the bottom line of big business. Don’t think for a moment that MSG is the only toxin unleashed on the American public by the EPA. Let the words “methyl parathion” and “DDT” jog your memory.
The EPA, in granting the chemical referred to as “L-glutamic acid” an exemption from the requirement of a tolerance for residues of “L-glutamic acid” on all food commodities when applied/used in accordance with good agricultural practices (thereby allowing unrestricted amounts of processed free glutamic acid (MSG) residue to remain in and on any and all food crops that come under the EPA’s jurisdiction) violated Section 408(c)(2)(A)(i), Section 408(c)(2)(ii), Section 408(c)(2)(B), and Section 408(b)(2)(D) of the Federal Food, Drug, and Cosmetic Act.
Neither “L-Glutamic Acid and Gamma Aminobutyric Acid; Exemptions from the Requirement of a Tolerance; Final Rule” (Federal Register June 21, 2001) nor “Glutamic Acid; Pesticide Tolerance Exemption; Final Rule” (Federal Register January 7, 1998), which preceded it, met the criteria established by law for granting exemptions from the restriction of a tolerance.
How did spokesperson Andersen excuse the fact that the EPA approved processed free glutamic acid for use in an EPA approved spray? First, said Andersen, the free glutamic acid used in the spray is naturally occurring, and it’s 99.3 per cent pure pharmaceutical grade L-glutamic acid. Yet, in admitting that the free glutamic acid in AuxiGro is not 100 per cent pure L-glutamic acid, and that it is pharmaceutical grade, Andersen contradicted herself, and actually made the point that 1) if the free glutamic acid used in AuxiGro were truly natural, it wouldn’t be “pharmaceutical grade;” and 2) if the free glutamic acid used in AuxiGro were truly natural it would be 100 per cent, not 99.3 per cent pure L-glutamic acid.
Andersen said something else very interesting. She said that the EPA is well aware of the fact that MSG causes adverse reactions. However, when Andersen used the term “MSG” she was referring to the one food ingredient called “monosodium glutamate,” and not to the free glutamic acid in “monosodium glutamate” that causes adverse reactions. Failure to define terms, as Anderson did (and does) so handily, is both deceptive and misleading.
What Andersen did is very clever. What she said makes no sense at all. No one has ever claimed that the processed free glutamic acid in AuxiGro comes out of a box labeled “monosodium glutamate.” So for her to say it doesn’t, is meaningless. On the other hand, the claim has been made that the free glutamic acid in AuxiGro will cause the same brain lesions, neuroendocrine disorders, adverse reactions and other diverse disease conditions that are caused by the free glutamic acid in “monosodium glutamate” and the other food additives that contain processed free glutamic acid. That claim is true, but Andersen does not address it. How do you refute someone who ignores legitimate questions and spews out irrelevant statements as though they pertained to your legitimate questions? You don’t. The EPA defense of its approval of use of processed free glutamic acid in plant “growth enhancers” and its registration of AuxiGro has two parts to it: 1) ignoring those who question EPA actions, and 2) making the irrelevant statement that AuxiGro does not contain MSG (monosodium glutamate).
Neither Andersen nor anyone else at the EPA ever addressed the criticism that approvals given by the EPA to allow the use of free glutamic acid and the product AuxiGro were inappropriate.
The EPA, which approved the used of processed free glutamic acid in plant “growth enhancers,” made a grievous error. But instead of recognizing and remedying that error once it was pointed out to them, the EPA began a cover-up. That cover-up included use of ambiguous words and phrases, half-truths, and downright lies told to consumers. The cover-up continued (and continues still) with a variation of those ambiguous words and phrases, half-truths, and downright lies told to legislators who inquire about spraying MSG into the environment.
You might find the Emerald BioAgriculture sales literature interesting
Sales literature promoting AuxiGro was once found on their Web site, but is now long gone. While Federal Register notices included the fact that there is processed free glutamic acid (MSG) in AuxiGro, the sales literature from Auxein Corporation did not mention the fact that their product contains free glutamic acid until the Truth in Labeling Campaign began to broadcast that information. In November, 1999, Auxein added deceptive, misleading, and untrue statements in an elaboration of its Product Page, wherein they essentially make the untrue assertion that the glutamic acid used in AuxiGro is chemically and biologically identical to that found in plants and animals.
Sales literature did (on September 12, 2000), however, contain the following:
“PRECAUTIONARY STATEMENTS
HAZARDS TO HUMAN AND DOMESTIC ANIMALS – CAUTION”
If you think you might be reacting to AuxiGro sprayed on crops, you might want to try to (contact Emerald BioAgriculture (formerly Auxein Corporation) at the addresses that follow. (A friend recently told us that he tried to contact them by e-mail, but his e-mail was returned unopened.) By law, the company is required to forward reports of adverse reactions to the EPA. You might want to ask the EPA if Emerald BioAgriculture did so.
John L. Mclntyre, Ph.D.
President & CEO
Emerald BioAgriculture (formerly Auxein Corporation)
3125 Sovereign Drive, Ste. B
Lansing, MI 48911-4240
Phone: (888) 828-9346
Fax: (517) 882-7521
E-Mail: mailto:%20sales@auxein.com
(From time to time, their web page, http://www.auxein.com , can be accessed by password only.)
www.Truthout.org
Evidence of poison
Fiona Macleod
08 March 2007 11:59
A Limpopo medical doctor has documented a string of physical abnormalities — including
breasts on a five-year-old girl — that he believes are directly linked to the unregulated
use of agricultural chemicals.
Dr Johan Minnaar (44) has produced evidence of serious illnesses and disorders among his
patients in Groblersdal, where commercial farmers are spraying large amounts of
pesticides on crops.
Horrific cases include teenage boys temporarily “growing breasts” during spraying
seasons, miscarriages, partial facial paralysis, cancers and ear malfunctions. Many of his
patients suffer from milder poisoning symptoms, such as asthma, sinusitis, headaches,
dizziness and depression.
Minnaar, who has been practising as a doctor in Groblersdal since 1997, took the unusual
step of coming forward with his evidence after unsuccessful attempts to get government
and regulatory authorities to intervene.
He said: “Groblersdal is surrounded by farms growing mostly citrus and grapes, but also
cotton, vegetables and maize. Throughout the year there is constant crop spraying with
pesticides containing organophosphates and carbamates. No one has informed the
community what pesticides are being used, even though the law states people must be
notified before spraying.”
Minnaar started investigating after realising that symptoms he had experienced over six
years followed a pattern.
“I experienced chronic fatigue, nausea, muscle aches and pains, skin rashes and arthritis,
particularly from August till November, when there is a noticeable increase in the spraying.
On investigation, it became clear that other people had these symptoms at the same time.”
Last August, he became so ill that he had to stay at home for two weeks. His wife and
three children also showed symptoms. He began regularly testing his and his spouse’s
blood and the tests showed they were exposed to organophosphates and carbamate
pesticides.
Minnaar laid complaints with the registrar of the national agriculture department, the
water affairs department and the labour and health departments of the Limpopo
government. He also tackled the farmers, chemical companies and crop sprayers.
The spraying continued and, on two days in February this year, large amounts of
carbamate were released during the aerial spraying of citrus orchards. Residents were not
warned beforehand. Among those who later showed signs of poisoning were pupils of two
schools located in the orchards.
Minnaar said pupils regularly played on the sports fields during spraying. The teenage
boys who had consulted him about “growing breasts” in the spraying seasons attended the
schools.
In late January, a woman brought a five-year-old girl who had developed breasts to his
consulting rooms. Minnaar suspected it could be linked to poisoning and referred her case
to Limpopo government officials, who he met two days later.
“As with many patients, she had no access to medical facilities or funds. The authorities
undertook to get her medical testing and treatment, but we’ve heard nothing,” he said.
According to Professor Leslie London of the University of Cape Town’s health sciences
faculty, premature puberty and other hormonal abnormalities are symptoms of
contamination by pesticides containing “endocrine disruptors”.
A 2005 study of girls in Mexican farming areas, titled Altered Breast Development in Girls,
indicated that pesticides could affect breast development and lead to early puberty.
Said London: “It has been shown that endocrine disruptors can also affect sexual
maturation and differentiation. A study in Sri Lanka of a pesticide called endosulfan found
that boys living in villages below cashew nut plantations sprayed with endosulfan had
impaired sexual maturity and other reproductive impairments.”
London researched aerial crop spraying around Groblersdal in 2005, with a focus on risks
to small farmers rather than health impacts. Last year, he published research on possible
links between aerial organophosphate spraying in the Northern Cape and Guillain-Barré
Syndrome, a neurological disorder.
“The problem of rural towns affected by agricultural application of pesticides is
ubiquitous,” he said. “Present regulatory and safety management methods really don’t
address this problem sufficiently.
“I think there is a view that if you choose to live in the country, you should accept this as a
way of life. That is a societal value decision, not a matter of science.”
The health department’s directorate of environmental health has announced plans to
launch a chemical safety programme in Groblersdal at the end of March. According to its
draft concept document, “the aim is to launch the programme to inform provinces that
national [government] is willing to assist them in the management of chemicals”.
The draft programme identifies schoolchildren, women, farmers and farmworkers, shack
dwellers, informal traders and manufacturers as the “most vulnerable communities in
municipalities that lack capacity to properly and satisfactorily deal with chemical safety
issues”.
South Africa is a signatory to international conventions aimed at promoting chemical
safety, and the labour ministry said in October that chemical safety was “high on the
minister’s agenda”. But crop spraying is a highly technical industry, and pinpointing
contamination is difficult.
London said it was almost impossible for applicators in planes to control the drift of
chemical sprays. “Aerial application has been shown in some studies to drift more than
2km, even in the absence of strong winds.”
European countries strictly regulate the industry through buffer zones around residential
areas and warning systems, he added.
Gerrit van Vuuren, an aerial application consultant at Croplife South Africa, blamed mist-
spraying of crops on the ground. “It is absolutely wrong to conclude that because there is
a yellow aircraft spraying agrichemicals in an area, it must the reason for ill health effects,”
he said.
Van Vuuren said mist-blowers apply more than 1 000 litres of spray mixture a hectare,
compared to 30 to 40 litres in the case of aerial spraying. They also blow a significant
volume of the spray higher than 6m into the air.
“A couple of mist-blowers spraying thousands of litres of spray mixtures at night are less
visible than an aircraft spraying a couple of hundred litres in the morning.”
He said it was up to farmers to notify inhabitants and issue warnings. They were also
supposed to ensure no one entered their fields during spraying.
The environmental health unit at the Elias Motsoaledi municipality, under which
Groblersdal falls, said it was “busy investigating the usage of pesticides being sprayed
from aeroplanes, as nuisances do occur from these activities”.
But Minnaar is frustrated by government promises to investigate. “For all practical
purposes, the supposed controls are not working. While they keep promising to sort it out,
we are getting poisoned,” he said.
The Natural Solutions Foundation keeps a close eye on the continuing disinformation of Big Pharma to try to convince you that there is no reason to, or good reason not to, take dietary supplements. It is like Honda telling you that there is no reason to buy, or good reason not to buy, a Toyota.
You see, dietary supplements are the direct economic competitor of drugs. Dietary supplements, like clean, unadulterated food, keep you healthy and get you back to health if you have become ill.
Compared to drugs, they are cheap, safe, easy to use and controllable by you or a helpful nutritionally knowledgeable person. And, at least in the US, they are classified as foods so they cannot be regulated the way drugs would be.
Of course, the FDA is always on the look out to undermine that freedom, recognized by the 1994 Dietary Supplements Health and Education Act (DSHEA) — unanimously adopted by Congress — which this Agency publicly calls “the worst act ever passed by the US Congress”. Why? Because the FDA is run by and for industry and the drug industry is a leading source of FDA funds through User Fees. The big players in the food industry, who pay no user fees to the FDA are, none the less, very important buddies of the organization, so food is regulated for the interests of big industry and drugs are regulated to promote the drug industry, at the expense of anything that might get in the way, like, for example, dietary supplements, or the public good.
Recently pro-industry legislators created an Adverse Event Reporting system for dietary supplements that tries to ignore the role of the many drugs many people use in distorting their metabolism and leading to . Naturally, this created a great PR opportunity to bash and diminish the importance and safety of dietary supplements which do not kill people. Drugs kill people. Foods which are not contaminated do not and dietary supplements are foods!
Dr. Ron Paul, Congressman from Texas, last year called one FDA maneuver an “abuse of power…” and Congress passed dangerous bill under the guidance and force of Senator Ed. Kennedy that further enhanced the power of the FDA. In this case, though, the Health Freedom movement had a partial victory in that we insisted that Congress add a clause to the bill, protecting Dietary Supplements… and Congress, responding to the hundreds of thousands of messages that advocates of health freedom, generated, through our Action Items and otherwise, adopted the protective language.
Yet we recall that genetically modified yeast which produced contaminated Tyrptophane did kill people, giving the FDA the excuse it was seeing to remove this safe and effective sleep and calming amino acid from the market. It was, after all, cutting into the drug market heavily. The FDA did not take genetically modified products off the market. And the company which produced the contaminated shipment in Japan had a sudden and very mysterious fire which destroyed the factory – and any evidence of contamination – almost immediately after the incident was revealed.
Such is the corruption of an agency which regulates both food and drugs. Clearly, those functions must be separated and a new agency which is consumer controlled must be created. Click here () to make sure that happens!
In the meantime, read the important analysis of the latest “Dietary Supplements are Poisonous” disinformation and make a recurring 100% tax deductible donation (https://staging.drrimatruthreports.com/index.php?page_id=189) to the Natural Solutions Foundation so that we can continue to provide information and strategic input to keep your health freedom free.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsMedia.tv
1:12 PM
FOR IMMEDIATE RELEASE
Orthomolecular Medicine News Service, October 9, 2008
(OMNS, October 9, 2008) “Dietary supplements cause 600 ‘adverse events'”, reported USA Today on 22 Sept, 2008. In an article that looks much like an official US Food and Drug Administration press release, it said that “Serious side effects from the use of food supplements resulted in 604 “adverse-event” reports – a list that includes at least five deaths – through the first six months that such accounts have been required by law.” (1)
Good grief! Looks like all those supplement-popping health nuts really are nuts after all. Food supplements simply must be dangerous!
Or are they?
Later on in the article, far from the headline, USA Today conceded that “An adverse event can be anything from a concern that a supplement isn’t working to a serious illness that follows consumption.” And, FDA spokesman Michael Herndon admitted that of the five deaths and 85 hospitalizations reported, “Some of these deaths were likely due to underlying medical conditions.”
FDA’s method of gaining data is suspect at best and biased at worst. Their “Dietary Supplement Adverse Event Reporting” webpage,
http://www.cfsan.fda.gov/~DMS/ds-rept.html, states: “FDA would like to know when a product causes a problem even if you are unsure the product caused the problem or even if you do not visit a doctor or clinic.” The measure of uncertainty involved in publicly soliciting adverse reports “even if you are unsure that the product caused the problem” is noteworthy.
But most significant of all is that FDA refused to disclose exactly which supplements allegedly were causing problems. Doesn’t the public have a right to know? In the absence of FDA disclosure to the contrary, it is likely that the five or fewer deaths attributed to “food supplements” were in fact due to medicinal substances marketed as dietary supplements. FDA acknowledges this in a round-about way at their website
(http://vm.cfsan.fda.gov/~dms/mwgblghb.html).
There you will find an “Important Message” which asks health professionals to “Report Serious Adverse Events Associated with Dietary Supplements Containing GBL, GHB, or BD . . . a group of products sold as dietary supplements for bodybuilding, weight loss and sleep inducement which have been determined to pose a significant public health hazard. These products are chemically related ! to gamma butyrolactone (GBL), gamma hydroxybutyric acid (GHB), and 1,4 butanediol (BD), and can cause dangerously low respiratory rates (intubation may be required), unconciousness/coma, vomiting, seizures, bradycardia and death. GBL, GHB and BD have been linked to at least 122 serious illnesses reported to FDA, including three deaths.”
But these substances are not foods. They are not vitamins, and they are not minerals, and they are not amino acids. They should not be considered with or as food supplements. Over half of all Americans safely take nutritional supplements every day. If each of those persons took only one tablet per day, that would be some 145,000,000 individual doses daily, for a total of over 53 billion doses annually. Many healthy people take more. And yet, according to national statistics compiled by the authoritative American Association of Poison Control Centers, there is not even one death per year from vitamins. (2) Look at the reports, which detail each individual vitamin, mineral, amino acid and herb, and see for yourself at
http://www.aapcc.org/dnn/NPDS/AnnualReports/tabid/125/Default.aspx
By comparison, FDA acknowledges that prescription drugs resulted in 482,154 adverse-event reports in the year 2007. That is nearly 400 times as many adverse events from prescription drugs per six-month period. And this much higher number does not include over-the-counter drugs, a striking omission. Many non-prescription drugs, such as Tylenol (acetaminophen), are a long way from safe. Liver toxicity from acetaminophen poisoning is by far the most common cause of acute liver failure in the United States. Acetaminophen accounted for 51% of all acute liver failure cases in 2003. (3) Indeed, the Associated Press previously reported that common drug dangers are so bad that “Harmful reactions to some of the most widely used medicines – from insulin to a common antibiotic – sent more than 700,000 Americans to emergency rooms each year.” (4)
Vitamin supplements compete with FDA-sponsored drugs. FDA has been trying to eliminate availability of vitamin supplements for over 45 years. As early as 1962, writes constitutional attorney Jonathan W. Emord, “FDA perceived a competitive threat emerging to drug regulation from the sale of dietary ingredients at above RDA doses.” In 1966, “FDA published a rule that any dietary supplement exceeding 150% of the RDA for a vitamin or mineral would automatically be regulated as a drug.” In 1976, after a “public outcry,” the Proxmire Amendment prohibited FDA from deeming a vitamin or mineral a drug solely because of potency. “Undaunted,” continues Emord, “FDA tried yet again to rid the market of vitamins in the 1970s by claiming on a case by case basis that they were adulterated based on their potency.” FDA also tried to have supplements declared to be unapproved food additives. “FDA’s position was a logical absurdity: Single ingredient dietary supplements were food additives b! ecause the ingredients were added to a gelatin capsule which was, FDA said with a wink and a smirk, a food. . . The United States Court of Appeals for the Seventh Circuit described FDA’s position as an “Alice in Wonderland” approach.” In 1980, FDA tried to get vitamins classified as over-the-counter drugs. . . FDA has repeatedly exceeded the limits of its statutory authority to bring about changes designed to protect drug companies from competition.” (5)
Additional evidence comes directly from FDA, whose own Dietary Task Force Report, released June 15, 1993, said: “The task force considered many issues in its deliberations including to ensure that the existence of dietary supplements on the market does not act as a disincentive for drug development.” There is also this statement was made by FDA Deputy Commissioner for Policy David Adams, at the Drug Information Association Annual Meeting, July 12, 1993: “Pay careful attention to what is happening with dietary supplements in the legislative arena . . . If these efforts are successful, there could be created a class of products to compete with approved drugs. The establishment of a separate regulatory category for supplements could undercut exclusivity rights enjoyed by the holders of approved drug applications.”
FDA wants control of vitamins. Their latest ploy is to frighten the public into thinking vitamin supplements are dangerous, without proof, and without even naming the supplements they accuse. Don’t fall for what Abram Hoffer, M.D., calls “the FDA’s grand lie that, if told over and over again, is accepted as somehow true.”
Vitamin supplements are not the problem. Poor eating habits, and too many medicines, are the problem. Food supplements are a solution. They are effective, and vastly safer than drugs. The US Food and Drug Administration knows this full well.
References:
(1) Perez AJ. Dietary supplements cause 600 ‘adverse events’. USA Today, Sept 22, 2008:
http://www.usatoday.com/news/health/2008-09-22-supplements-adverse-events_N.htm
or http://www.usatoday.com/news/health/2008-09-22-supplements-adverse-events_N.htm?POE=click-refer
(2) Annual Reports of the American Association of Poison Control Centers’ National Poisoning and Exposure Database, 3201 New Mexico Avenue, Ste. 330, Washington, DC 20016. Download any report from 1983-2006 at
http://www.aapcc.org/dnn/NPDS/AnnualReports/tabid/125/Default.aspx
free of charge. The “Vitamin” category is usually near the end of the report. Summary and commentary at:
http://www.doctoryourself.com/vitsafety.html
(3) Larson AM et al Acetaminophen-induced acute liver failure: results from a United States multicenter, prospective study. Hepatology 2005;42:1364-1372. See also:
http://www.medpagetoday.com/Psychiatry/Depression/tb/2233
(4) Associated Press, Oct 17, 2006.
http://www.msnbc.msn.com/id/15305033/
(5) Emord JW. FDA violation of the rule of law. Speech from the Health Freedom Exposition in Richmond, Virginia September 23, 2006.
http://www.emord.com/events/speeches/fda_violation.htm
Nutritional Medicine is Orthomolecular Medicine
Orthomolecular medicine uses safe, effective nutritional therapy to fight illness. For more information:
http://www.orthomolecular.org
The peer-reviewed Orthomolecular Medicine News Service is a non-profit and non-commercial informational resource.
Editorial Review Board:
Damien Downing, M.D.
Harold D. Foster, Ph.D.
Steve Hickey, Ph.D.
Abram Hoffer, M.D., Ph.D.
James A. Jackson, PhD
Bo H. Jonsson, MD, Ph.D
Thomas Levy, M.D., J.D.
Erik Paterson, M.D.
Gert E. Shuitemaker, Ph.D.
Andrew W. Saul, Ph.D., Editor and contact person.
Email: omns@orthomolecular.org
http://alobar.livejournal.com/3062139.html
Compulsory drugging is wrong, as far as I am concerned. Mandatory vaccination is compulsory drugging and is not only wrong, it is unnecessary and dangerous. Disinformation is easily found claiming that vaccination is both safe and effective. These falsehoods are so far from the truth that the Natural Solutions Foundation has filed a Citizens Petition with the Federal Trade Commission urging it to hold public hearings and ban all advertising and information to patients and doctors which claims that vaccination is either safe, effective or both. (That Citizens Petition has been “lost” and illegally denied a total of at least 4 times so far!)
The reality is that vaccination is dangerous and ineffective, despite hundreds of year of propaganda to the contrary.
When the act to establish the Vaccine Police, BARDA, was under consideration, I published an article called “The Syringe of Death: Coming Soon to a Police Station Near You” in which I argued that establishment of BARDA, the Biomedical Advanced Research and Development Agency by the Richard Burr’s Biodefense and Pandemic Vaccine and Drug Development Act of 2005 was a very bad, and very dangerous secret agency and should not be created. BARDA was created, none the less, and now serves as the mandatory vaccination police of the Patriot Act “Public Health” fascism.
“The Syringe of Death” is published in full below. Although BARDA was then under consideration and is now a reality, the discussion of this frightening agency is relevant to today’s discussion as is a look at the 4 myths upon which the barbaric, unnecessary and dangerous treatments called “vaccination” or “inoculation” rest.
Frighteningly, the creation of BARDA was announced on April 26, 2007 by the Department of Health and Human Services. Its Secretary at that time, Mike Leavitt, said in his Press Release, “The creation of BARDA enhances the opportunity for innovation in our efforts to develop effective medical countermeasures against a host of public health threats, either natural or man made,†Secretary Leavitt said. “I am pleased that Congress recognized the importance of advanced development in the establishment of BARDA, and the President’s FY 2008 budget request of $189 million for this purpose will help further the department’s efforts to bridge the gap between the National Institutes of Health’s research and development programs and Project BioShield.â€
BARDA, however, is, in essence, a secret Vaccination Police which can, once a “Pandemic” is declared, with or without reason or evidence, require mandatory vaccination for the real or imagined “Pandemic”. If vaccinations were safe or effective, assuming a real Pandemic, of course, perhaps there would be some faint justification for such totalitarian police state tactics in the approach to public health. In fact, vaccination is such a risky activity that it is classified as an un-insurable risk since no insurance company or underwriter in the world will guarantee the financial compensation of those harmed by it – and they are, as we now know, legion.
Documentation of extensive, shameful cover-ups by industry (now absolved from all liability for dangerous vaccines and drugs by a compliant FDA) and government abound and are sadly, old news. Documentation of vaccination dangers abound as well, ranging from the well known tragic and nearly totally preventable autism epidemic to life long neurological dysfunction of many sorts to asthma and immune suppression, leukemias and other cancers, infertility (secondary to UN/US/WHO sponsored vaccination programs in Africa, South and Central America allegedly for diseases like small pox and tetanus but which secretly induce permanent sterility) and a host of other conditions and diseases. But still the beat goes on: one state after another decides that yet another vaccine must be added to the vaccination schedule. New Jersey, for example, has decided that ineffective, but financially productive, mandatory seasonal flu vaccine, which often contains mercury, but always contains other horrific contaminants and toxic substances, MUST be administered to every child from the age of 6 months to 18 year EVERY YEAR (twice in the first year, by the way). Never mind that in the winter of 2007-8, the CDC announced that this same vaccine was ineffective at least 60% of the time. Never mind the dangers. Just focus on the profits!
And just focus on the social control, as well. It is well known by now that the Patriot Acts, the BIOSHIELD Acts and other US laws make mandatory vaccination a reality once the world “Pandemic” is invoked. And those who resist will, says the law, be interred or quarantined for an indeterminate period.
The propaganda war continues: Those who opt out of this questionable procedure are endangering us all, they say. But is that true? No, not at all.
Vaccination is, in fact, based on 4 major myths or, if you want to be more precise, lies.
Vaccination is based on junk science, and has been since the first “experiments” by that mountebank enshrined by history, Edward Jenner, the founder of virology and vaccination. In 1796, when Jenner transferred “cowpox”, actually syphilis, from the hand of milk maid Sarah Nelmes to 8 year old James Phipps, allegedly protecting James from smallpox. In fact, James and Jenner’s own son died from the repeated immune challenges induced by Jenner’s repeated inoculation.
Within 60 years, it was clear that Jenner’s procedures were neither safe nor effective. Since the British Parliament decided that although Jenner’s now-mandatory vaccination against small pox was causing deadly epidemics of syphilis and leprosy in otherwise healthy babies, it would be embarrassing to admit its error to the British public. Rather than reverse its support of both vaccination and Jenner, it chose to protect its own face at the expense of its citizens’ well-being, therefore laying the groundwork for today’s government position on vaccinations.
Much has been written about the dangers of vaccination and those who are interested in learning what vaccination is really about and how to avoid it for themselves and their children are invited to join the Natural Solutions Foundation vigorous and informative No-Forced-Vaccination Forum at http://groups.yahoo.com/group/no-forced-vaccination/join
The article, “The Syringe of Death” is more timely than ever since BARDA was established last year and the United States Government is determined to add both voluntary and mandatory vaccinations to our lives at ever-accelerating rates, despite common sense and good science.
To stop compulsory vaccination and drugging, click on each of the following action steps and ask your friends and neighbors to do the same:
Stop Compulsory Vaccination and Drugging
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=21833
Protect Philosophical Exemptions to Vaccinations
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=23087
Sign the Tiburon Declaration on Compulsory Vaccination
https://staging.drrimatruthreports.com/index.php?p=460
Remember, your voice is the one that can make the difference.
Yours in health and freedom,
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.Organics4U.org
www.NaturalSolutionsFoundation.org
The Syringe of Death, Coming Soon To A Police Station Near You
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
Senator Richard Burr (R-NC) thinks he owns your body. If he’s right, you will have no
say over what gets injected into it and no recourse under the law if it harms or kills you.
That is, if Burr gets what he’s after and S. 1873 passes the US Senate. Burr’s bill,
“Biodefense and Pandemic Vaccine and Drug Development Act of 2005”, establishes the
Biomedical Advanced Research and Development Agency (BARDA), a secretive and
secret agency exempt from public scrutiny, the Freedom of Information Act and the
Federal Advisory Committee Act. BARDA will be the only agency which can declare a
pandemic condition and may do so for any (or no) reason. Operating in secret, BARDA
will be responsible for the advanced research and development of drugs and vaccines (in
partnership with pharmaceutical companies), and, because the contents of those vaccines
will remain shrouded in BARDA darkness, any injuries and deaths caused by drugs and
vaccines which BARDA labels “countermeasures†to any BARDA-declared threat may
never be known.
Even if those contents do become known, S. 1873 cancels any manufacturer liability for
the companies that made the vaccines or drugs. Injured parties will have no legal means
of securing compensation from either the government or the companies themselves.
And BARDA can declare a pandemic (at any time) and require mandatory universal
forced vaccination.
Can we assume that these vaccines will provide us any protection at all? Perhaps, but
it’s not likely. First, clearly understand that under BARDA you may be (legally)
subjected to experimental drugs – drugs which have no track record at all – and, second,
with or without the advent of BARDA, it is now more important than ever that the real
truth about vaccines be widely and quickly disseminated. There are reported to be more
than 200 new vaccines “in the pipelineâ€. If they, along with the ones in use now, are not
safe, we, and our children, are not safe.
All of us have been carefully conditioned to believe that vaccines are safe. But the truth
is ugly and, with BARDA staring us in the face, more than a little frightening. Here are
the cold, hard facts:
Cold, Hard Fact # 1: Vaccines are not safe: vaccines are dangerous. The evidence is
abundant that the tragic cost of loading babies and children up with toxic brews of
mercury, aluminum, formaldehyde, injected foreign protein, stealth viruses and, in the
second generation vaccines, the deadly immune enhancer squalene, is unacceptably high.
Lives are ruined and lost in these children when toxins overwhelm their immune systems
and brains and cause tragic, totally preventable suffering and death. Autism (occurring in
4 children per 10,000 when I graduated from medical school in 1970) now afflicts a
minimum of 1 child in 168 in the US. Children have not changed: the poisons we give
them have. Gulf War Syndrome, a pervasive, progressive, deadly auto-immune disease
afflicting over half a million US veterans, appears to be a deadly vaccine reaction to an
experimental vaccine (Anthrax) which the US used on soldiers without their consent in
clear violation of the Helsinki Declaration and the Nuremberg Protocols, international
conventions and agreements which prohibit human experimentation without full
informed consent.
The concept of informed consent, is, of course, is meaningless in the face of compulsory
vaccination with secret ingredients and no manufacturer accountability.
Contaminants make vaccines tremendously dangerous. Swine flu (for a pandemic which
never materialized) was contaminated with polio virus in 1976. Over 45 million
Americans were vaccinated in just 77 days and although there were only 6 cases of Swine
flu in the entire country the vaccine reportedly caused at least 565 cases of polio paralysis
(renamed “Guillain-Barre Syndrome†for the occasion), 60 deaths and other serious
problems, including blindness and impotence. (There is no reason to feel reassured
because this particular disaster occurred in the past: every flu vaccine is capable of
passing along Guillain-Barre (polio) and other unsuspected viral diseases.)
Cold, Hard Fact # 2: Vaccines have not eradicated diseases: vaccines spread diseases.
Attenuated viruses (infective, weakened versions of the dangerous ones) are commonly
used in vaccines so that your body will develop an immune ‘memory’ for that virus. The
next time your immune system meets that specific virus, it rapidly combats it by
producing large numbers of antibodies. This practice and theory derive from the dawn of
vaccination: Edward Jenner’s pioneering use of cowpox pus inoculations to eliminate
smallpox. This innovative and surprising medical treatment is touted as one of the
triumphs of modern medicine. It makes a wonderful story but, in fact, inoculation not
only spread smallpox, it caused well-documented epidemics of syphilis and leprosy in
inoculated people, especially babies (who have immature immune systems). In spite of
the documented associated dangers of leprosy, syphilis, smallpox, death and blindness,
England provided free vaccination in 1840, made it compulsory in 1853, and punished
lack of vaccination with seizure of property and imprisonment in 1857 (which should
sound familiar). It took a British Royal Commission some 41 years more to put a stop to
the deaths and disease that Jenner’s unproven technique caused. Finally, in 1898,
England’s compulsory smallpox vaccination laws were overturned.
In 1854, the first year of British compulsory vaccination, deaths from syphilis in infants
under 1 year increased by 50% and continued to rise steadily after that. In 1802 Jenner
was paid 10,000 pounds by the House of Commons. Shortly afterwards, it became clear
that vaccines did not work. Rather than lose face, the House of Commons granted Jenner
another 20,000 pounds in 1807 and 3,000 pounds a year thereafter.
Jenner knew that milk maids who milked with active pus-filled sores on their hands
transmitted pox to their cows. Local superstition held that the cow’s pus was a
preventive against small pox. Jennings learned from a local farmer, Benjamin Jestey, that
he had inoculated his wife and 3 children with cowpox pus by jabbing them with a
darning needle and they did not contract small pox. Jenner assumed that this meant they
were protected against smallpox. To the modern ear this is absurd. In Jenner’s day,
neither methodology nor the scientific method were part of the culture.
Jenner, a village apothecary who purchased a University of Edinburgh MD for 15
pounds, was a showman who made much of his “discovery†and hastened to induce
Sarah Nelmes, a young milk maid with a fresh lesion on her finger, to allow him to
collect pus from her sore. He inoculated an 8 year old named James Phipps who
developed a fever and a pustule on his skin. Seventeen days later he inoculated the boy
again, this time with small pox. Since the boy did not develop smallpox, Jenner
concluded that “protection was completeâ€.
Jenner hawked his inoculation but people started to complain because they were
developing smallpox (and syphilis) after vaccination with Jenner’s cowpox. Jenner
switched to infected material from horses’ heels instead (“Horse-greaseâ€). John Baker,
the child he inoculated with horse-grease, however, died before he could expose him to
small pox. Undeterred, he inoculated 6 more children with horse-grease and was so
convinced that the results would be positive that he rushed to London to publish them
before there were any results. The [untested] “success†of James Phipps’ inoculation and
his London paper established Jenner’s method and his success. Revolted by the idea of
horse-grease inoculations, people demanded cowpox inoculations again. Jenner
complied.
But just what is cow pox? In tropical countries it is cutaneous smallpox plus leprosy (a
non-lethal disease often present along with leprosy) while in more moderate climates the
milk maids were transferring syphilis to the cattle along with their cutaneous smallpox.
Jenner was making his brew from the cowpox pus and the results were
nothing short of disastrous for untold numbers of people.
Modern small pox vaccines are produced in much the same way: lesions are induced on
the skin of calves and, after they are “sacrificed†[and sold for veal?], the harvested
material from their lesions is cultured in eggs and prepared as vaccines.
However, although immunity fails to develop more than 80% of the time, serious side
effects are distressingly common from the modern small pox vaccines: At least 52 people
out of every million will have life threatening events and 1-2 will die. Permanent damage
to heart, brain, skin and GI effects are also well known side effects. The Center for
Disease Control (CDC) notes that serious side effects and dangers probably occur much
more often since many people can be harmed by live virus vaccines: immune
compromised people (on steroids, with eczema or psoriasis, nursing babies, pregnant
women and their fetuses, people with HIV/AIDs, transplant patients, chemotherapy and
radiation patients, people with auto-immune diseases, young children, asthmatics, etc.)
are at serious risk for contracting the same disease that the inoculation is designed to
prevent or worse.
In the US, the CDC classifies more than 60 million people as immune compromised.
People who are re-inoculated after many years are particularly susceptible to severe and
life threatening reactions. Those who are ill are likely to develop sever effects as well.
In fact, Tommy Thompson, former Health and Human Services boss, said that he would
not take the vaccine although the US is stock piling “a dose of smallpox vaccine with
every American’s name on itâ€. Perhaps the one with his name has been changed so it
reads, “To Whom It May Concernâ€.
S. 1873 and BARDA would, according to its proponents, allow absolutely no exemptions
for medical conditions or personal conviction. None.
Dr. Mike Lane, former director of the CDC’s so-called “smallpox eradication programâ€
in the 1970’s, is a proponent of mass vaccination with no exemptions saying, “Medical
contraindications would not apply… there would be NO exceptions. [In India] I’m sure
that we killed a few people, but we did the best that we could….If the person is exposed
there will be no exemptions, medical or otherwise.â€
When a live virus is used in the vaccine, infective virus is shed for anywhere from 4 to 21
days (or more) and, during that time, inoculated persons can give the disease, or the side
effects of the inoculation, to any vulnerable person they come into contact with.
So, while it may be true that vaccines have spread disease, isn’t it true that vaccines have
eliminated the epidemic diseases of the past? No, actually they have not. Neither
Jenner’s cowpox inoculation nor modern smallpox inoculation did anything to eliminate
smallpox (quite the contrary). The fact is, Dr. Charles A. R. Campbell discovered that
smallpox is transmitted by the flying bedbug, Cimex lectularius, and that eliminating this
parasitic insect from human habitation eliminates smallpox, too. Personal hygiene and
better housekeeping eliminated the deadly scourge. (Dr. Campbell also discovered that
the disfiguring pocks of the disease could be prevented by a diet high in Vitamin C.)
When the World Health Organization (WHO) declared the planet “smallpox free†in
1980, they did so administratively, not medically: small pox incidence was reduced, but
not gone, despite nearly universal vaccination. What to do? WHO solved the problem
cleverly: they renamed the disease “cowpox†and “monkey poxâ€. Shazam: a smallpox
free planet, quicker than you can say, “Junk Science!â€
Other epidemic diseases were in sharp decline at the end of the 19th and early 20th
centuries as a direct consequence of improved hygiene and other life-style changes.
Measles, Diphtheria, Whooping Cough, Polio and Hepatitis B were all in sharp decline
long before vaccines were introduced. The contribution to the decline made by vaccines,
however, was negligible or non-existent. Scarlet Fever, typhoid fever and cholera, for
which inoculation either did not exist or was never wide-spread, declined on the same
sharp curve for the same reasons. So do we need inoculations because of the public
health hazard? Despite the considerable hype, in fact, there is no unbiased evidence
which connects disease prevention with inoculation.
Cold, Hard Fact # 3: Flu vaccines do not protect people from flu-related deaths.
The CDC claims that an astonishing 36,000 people die from flu in an average year. But
according to the former Secretary of Health and Human Services, Tommy Thompson, 68
people under 65 die from flu each year in the US. The truth is that in 4 years, a total
4,440 people, mostly elderly, died from flu, no where near the CDC’s touted 144,000
deaths. While that figure is great for flu vaccine sales, it derivers not from reality but
from the CDC’s industry-friendly statistical trick of classifying all pneumonia-related
deaths, despite any lack of evidence, as flu deaths. Discussing this nonsense, Lone
Simonsen of the National Institute of Allergy and Infectious Disease/NIH, writes in The
Archives of Internal Medicine “We could not correlate increasing vaccination coverage
after 1980 with declining mortality rates in any age group. Because fewer than 10% of all
winter deaths were attributable to influenza in any season, we conclude that observational
studies substantially overestimate vaccination benefit.”1
Cold, Hard Fact # 4: Potential pandemic viral diseases like the Bird Flu do not have safe
and effective vaccines to prevent them and there are no drugs to treat them effectively.
Despite that fact, on September 15, 2005 the US purchased $100 Million of a French
experimental flu vaccine designed to protect against bird flu. It’s so experimental, in fact,
that although we have purchased megabucks worth of the stuff, the French manufacturer,
Sanofi-Pasteur, is planning to experiment with adjutants (immune response enhancers) to
rev up human response to it. Perhaps the adjuvant is the same one that the Army used in
the deadly Vaccine A against anthrax: squalene. The purchase is real, but there is
currently no such thing as a vaccine for pandemic bird flu.
Unfortunately, even if vaccines did work (they don’t) and were safe (they’re not), a virus
has to actually exist before you can make a vaccine that can control the disease. The
pandemic version of the latest bird flu does not yet exist. Vaccines are very specific: they
train the immune system to make antibodies to a particular protein sequence. Because
those antibodies are highly specific, guessing wrong on which flu strain is coming soon
to a droplet near you has led to an embarrassing history, year after year, of ineffective flu
shots against the wrong strain of virus. People developed side effects, but the shots did
not ward off the flu since the vaccine misfired with regard to the virus it was supposed to
be protecting people against. And, oh by the way, experimental vaccines are not even
alleged to be safe. No one knows what effects they will have. And, under BARDA, no
one (least of all the manufacturer) will need to worry about that.
Allegedly, the bird flu pandemic version has not yet mutated and therefore does not exist
so there is no way whatsoever to make a vaccine against it. Not even the US Government
can make a vaccine against an imaginary virus. But that is just what the government
wants us to believe they can do. Clearly, the French experimental flu vaccine purchase is
a political, not a public health one. IF the bird flu mutates and becomes pandemic, it
would take between 4 and 18 months to gear up to make commercial quantities of the
1
(http://archinte.ama-assn.org/cgi/content/abstract/165/3/265)
vaccine. In the meantime, anyone getting the bird flu and surviving it would have natural
antibodies to the disease. But right now, unless the already-mutated pandemic H5N1
virus is being stock-piled in a laboratory for convenient release at an opportune moment
(which is certainly possible), the virus needed to make a real bird flu vaccine exists only
in fearful imagination. So what would BARDA inoculate you with? Who knows? A
nanochip to track you, perhaps? The technology exists. An experimental drug, maybe?
Something that someone wants to test on huge numbers of people whether they like it or
not? Squalene? Perhaps. Perhaps not. Only BARDA would know. You won’t.
BARDA would be above the law and beyond investigation. Consider: the anthrax vaccine
currently being tested on US 2nd and 3rd graders contains squalene. The experiment is
therefore not about anthrax (the vaccine is only approved for cutaneous anthrax, a non-
life threatening disease highly unlikely to be used, therefore, as a bio-weapon) but rather
about what happens to children given a deadly substance which stimulates their immune
systems to destroy their bodies over time. After World War II, the managers of IG
Farben, the vast German industrial combine, were imprisoned for Crimes Against
Humanity for precisely this kind of activity. Who will be convicted this time? The head
of super-secret BARDA? On what secret evidence? This is what the
government/pharmaceutical cabal is doing now in full view of the public and of
Congress. Can you imagine what would happen if there were no public scrutiny at all
and no legal liability for any ill deeds whatsoever? Only if you can imagine BARDA.
BARDA is a medical Gestapo. It would have the power to initiate a medical marshal law
from which the only escapes would be prison, death, fleeing the country or rebellion.
Bill S. 1873 has five powerful Republican co-sponsors: Republican Senate Majority
Leader Bill Frist (R-TN), Senate Health, Education, Labor and Pensions Committee
Chairman Mike Enzi (R-WY), Senate Budget Committee Chairman Judd Gregg (R-NH),
Elizabeth Dole (R-NC) and Alexander Lamar (R-TN).
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