The FDA's Latest Health-Harming Stance on Mercury

Federal health officials have refused to put new restrictions on the use of thimerosal, a mercury-based preservative, in vaccines and other medicines.

The Coalition for Mercury-free Drugs petitioned the FDA for tighter restrictions in 2004, citing evidence that the preservative could be linked to autism. In a reply made public only recently, the FDA rejected the petition.

The Coalition for Mercury-free Drugs currently plans to seek a court order that would force the FDA to remove thimerosal from all vaccines and medicines until it is demonstrated that the preservative is safe.

Thimerosal, which is about 50 percent mercury by weight, is used to kill microbes in vaccines. Since 2001, vaccines given to children 6 and younger have contained at most trace amounts of the preservative. It is still, however, present in some adult vaccines, including most doses of flu vaccine, and in some eye ointments, nasal sprays, and antivenins.

In related news, a government advisory panel has concluded that an FDA safety report suggesting that "silver" mercury amalgam fillings are safe was "unreasonable," and that further study was needed.

The safety report was deemed murky and misleading, and failed to answer concerns regarding why mercury was being used at all. Dental amalgam contains about 50 percent elemental mercury, and studies have shown that with time, mercury vapors leach out of the fillings and may be absorbed into the bloodstream.





Sources:

MSNBC October 24, 2006
http://www.msnbc.msn.com/id/15405274/

Journal of American Medical Association October 25, 2006; 296(16): 1990-1997
http://jama.ama-assn.org/cgi/content/short/296/16/1990


Belleville News Democrat September 29, 2006
http://www.bnd.com/living/15638505.htm

Heavy Metal Detoxification For Your Autistic Child

Autism is a neurological brain disorder. It is often evident when a child does not hit his or her developmental milestones by age of three. The symptoms observered include a delay in speech, unable to interact socially and behavioral disturbances.

Some experts say that autism may be caused by a exposure. Mercury is known to cause neurological disorders as it mainly triggers brain dysfunction. Mercury is likely to be absorbed by the body if it is presented as ethyl mercury that are usually used in thimerosal, preservatives, and additives and even in pediatric vaccines.

Hence to get rid of the mercury, it appears that it is necessary to do a heavy metal detox or a mercury detox. Heavy metal detox is a process where chelating agents aid the body into excreting heavy metals by bonding with the toxic materials and make them less active. Heavy metal detox is in progress when hazardous metals are absorbed by the bloodstream and is excreted safely by the liver or kidney. Continue Reading >>

What Toxic Chemicals & Heavy Metals Affect My Health?

For your benefit and education, we have included the lists below covering the more common toxic heavy metals and chemicals. This page is still under construction and soon we will be uploading detailed descriptions of each of the substances listed below, their related health hazards and sources of exposure.

Common Toxic Metals:

• Arsenic
• Aluminum
• Barium
• Beryllium
• Bismuth
• Cadmium
• Chromium Hexavalent
• Cobalt
• Copper
• Lead
• Mercury
• Nickel
• Tin
• Titanium
• Uranium

Common Toxic Chemicals:

• Antimony
• Asbestos
• Aspartame
• Acesulfame-K
• Acetone Peroxide
• Acrylamide
• Benzene
• Bisphenols
• Chlorine
• DDT
• Dioxins
• Flouride
• Formaldehyde
• HCA's
• Insecticides
• Isopropyl Alcohol
• MSG
• Methyl alcohol
• Pesticides
• Persistant Organic Pollutants
• rBGH
• Nitrates
• Prescription Drugs
• Synthetic Vitamins
• Sodium Chloride
• Refined sugar
• High Fructose Corn Syrup
• Sucralose
• Saccharin
• VOC's
• Carbon Monoxide
• Chlorofluorocarbons
• Perchloroethelyne
• Propane
• Radon
• Toluene
• Phthalates
• Xylene
• n-hexane
• ethyl ketone
• Phenol
• Ammonia
• Sodium Hydroxide
• Carbaryl
• Dichlorophene
• Chlordane

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Chelation Therapy

Here is occlusive coronary atherosclerosis. The coronary at the left is narrowed by 60 to 70%. The coronary at the right is even worse with evidence for previous thrombosis with organization of the thrombus and recanalization such that there are three small lumens remaining.

Atherosclerosis, or "hardening of the arteries", is the cause of two most deadly health problems Unfortunately, it begins quite early in life and continues relentlessly until circulation is so compromised that a heart attack or a stroke is almost certain. The process begins innocently enough, by formation of a small plaque on the wall of an artery. It attracts platelets that form a small blood clot. Later on, additional clotting elements increase the size of the clot. Eventually cholesterol and calcium get deposited into the growing plaque. Calcium completes this process, making the arteries "hard".

This is a normal coronary artery with no atherosclerosis and a wide lumen that can carry as much blood as the myocardium requires. Normally arteries have the ability to expand or contract, depending on the need of the body. But once the calcium is settled on the arterial walls, they become rigid, unable to either expand or contract. That’s where the expression "hardening of the arteries" comes from. The cells of the body require continuous blood supply in order to live. When it stops, most cells die within a few minutes. If this happens in the heart, the result is known as a heart attack. In the brain, it is called a stroke.

MAJOR SYMPTOMS Chest pain (angina) because of decreased circulation within the heart, memory loss, dizziness, poor balance from reduced blood flow to the brain, pain in the legs after walking which is relieved by rest.

TRADITIONAL – TREATMENT Hardening of the arteries is a systemic disease. In other words, it happens throughout the body, not just in one or 2 areas. If you understand this, you will realize that the current approach to treatment is crude, primitive and misguided. Some experts have compared it to putting a band-aid on a major injury.

When a surgeon performs a bypass surgery or an angioplasty, it does nothing to correct the widespread atherosclerosis already present in other parts of the body, such as brain, kidneys, lungs, legs and everywhere else. To complicate matters further, most of the arteries are very small. They are called capillaries, and they comprise the majority of the 40 to 60 thousand miles or arteries feeding the tissues of the body.

The diameter of a capillary is smaller than the size of a red blood cell. This is necessary for the exchange of oxygen and nutrients to take place. Obviously, these arteries can not be bypassed or surgically manipulated. Various medications used for "treatment" of heart disease are designed to deal only with the symptoms, not the real causes of the problem. Clearly, the real treatment for atherosclerosis would be a procedure that removes the plaques from the arteries and restores blood flow all over the body, in large arteries as well as small ones. And this brings us to

CHELATION – THERAPY
Chelation Therapy is probably one of the most effective treatments for hardening of the arteries, yet it is being ignored and even maligned by mainstream medicine. Chelation therapy was used successfully in over 1 million clients over the last 40 plus years. The main ingredient of chelation therapy is a synthetic amino acid known as EDTA (ethylene-diamine-tetra-acetic acid). It has a peculiar ability to strongly attract minerals, especially toxic metals - lead, mercury, cadmium, aluminum and others. Since then, a number of studies published in reputable medical journals have confirmed the effectiveness of IV chelation therapy for treating atherosclerosis and improving blood flow to the heart, the legs and the brain.

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Top 20 Reasons Why You Need A Chemical & Heavy Metals Cleanse:

Top 20 Reasons Why You Need A Chemical & Heavy Metals Cleanse:

1 - One out of every ten women of childbearing age has dangerously high concentrations of mercury "…within one tenth of potentially hazardous levels" in their bloodstream.1
2 - Many people have developed colitis from chronic ingestion of mercury-containing laxatives.
3 - Industrial contaminants (such as dioxins, PCBs, and mercury), microbial contaminants (such as E. coli), and natural contaminants (such as aflatoxin) [can be found in foods]."2
4 - "In 1994, 62% of all food samples tested by the U.S. Department of Agriculture's Pesticide Data Program (PDP) had detectable levels of at least one pesticide."3
5 - "PDP data from 1994-96 … [stated 25] percent of the food samples tested had detectable levels of carcinogenic (cancer causing) pesticides, and 34%" possessed detectable levels of neurotoxic pesticides.4
6 - Some studies estimate 99% of the breastmilk in women residing in the United States contains measurable levels of DDT (Dichloro-Diphenyl-Trichloroethane), the first modern toxic chemical pesticide.
7 - In the United States, eight times more antibiotics are used for the livestock industry than for human inoculation against disease.5
8 - In a study where pigs were fed large amounts of synthetic B vitamins, the pigs produced sterile offspring. Synthetic vitamins provide no nutritional value-they are poisonous!
9 - Chlorine, acetone peroxide, benzoyl peroxide, and nitrogen dioxide are the most common oxidizing agents used during white flour processing in the production of white bread.
10 - The Center for Science in the Public Interest, a nutritional lobbying group, claims that sodium chloride (common table salt) could be "… the single deadliest ingredient in the food supply."6
11 - MSG is a toxic substance and causes adverse reactions, brain lesions, endocrine disorders, and other negative health problems."7
12 - "The chemical, acrylamide, which is used industrially in the manufacturing of some plastics, is also apparently formed by the heating of starches. Foods with especially high levels of the chemical included French fries, potato chips and crackers."8
13 - An alarming study published in the American Journal of Public Health estimates a 95% risk of developing cancer from regular consumption of chlorinated tap water!9
14 - After being inside the body for 20 minutes, Aspartame begins breaking down from its original compound into methanol, formaldehyde (a Class-A carcinogen used to embalm corpses) and formic acid (ant venom).
15 - Over 70% of the world's coffee supply is contaminated with toxic pesticides and chemicals. It's estimated that just one cup of coffee contains more than 2,000 chemicals, many of which are gastrointestinal irritants and cancer-causing agents. Also, the high heat used in roasting coffee beans causes the natural oils to turn rancid, further contributing to its chemical load.
16 - Playing and crawling on a typical floor exposes babies to contaminants such as dust mites, mold and mildew. Just one day of exposure introduces the equivalent of four cigarettes into an infant's lungs.10
17 - "Every year, indoor air pollution is responsible for the death of 1.6 million people - that's one death every 20 seconds…due to pneumonia, chronic respiratory disease and lung cancer…"11
18 - The EPA lists over eighty "regulated" contaminants found in tap water such as chlorine, fluoride, arsenic, and numerous pesticides. This figure doesn't even include unregulated toxins such as perchlorate (a chemical found in rocket fuel!).
19 - The National Resources Defense Council (NRDC) estimates "…as many as 56 million people in the 25 states reviewed by the U. S. Environmental Protection Agency … have been drinking water with unsafe levels of arsenic..."! 12 Arsenic is the number 1 cancer causing agent!
20 - Bottled water, infant formulas, toothpaste, mouthwash and even vitamin supplements, now contain fluoride! Fluorides are more toxic than lead and only slightly less poisonous than arsenic.

Resources:
1 Centers for Disease Control and Prevention. "Blood and Hair Mercury Levels in Young Children and Women of Childbearing Age - United States, 1999." Morbidity and Mortality Weekly Report. Vol. 50, Issue 8. (140-3). Pub. 2 March 2001. Online. Accessed 17 Aug 2007. Available: www.cdc.gov/mmwr/preview/mmwrhtml/mm5008a2.htm

2 United States Environmental Protection Agency. "America's Children and the Environment: A First View of Available Measures." Document # EPA 240-R-00-006. Pub. Dec 2000. Pp. (32-3). Online. Accessed 30 July 2007. Available as PDF: www.yosemite.epa.gov/ochp/ochpweb.nsf/content/ACE-Report.htm/$file/ACE-Report.pdf

3 United States Environmental Protection Agency. "America's Children and the Environment: A First View of Available Measures." Document # EPA 240-R-00-006. Pub. Dec 2000. Pp. (32-3). Online. Accessed 30 July 2007. Available as PDF: www.yosemite.epa.gov/ochp/ochpweb.nsf/content/ACE-Report.htm/$file/ACE-Report.pdf

4 United States Environmental Protection Agency. "America's Children and the Environment: A First View of Available Measures." Document # EPA 240-R-00-006. Pub. Dec 2000. Pp. (32-3). Online. Accessed 30 July 2007. Available as PDF: www.yosemite.epa.gov/ochp/ochpweb.nsf/content/ACE-Report.htm/$file/ACE-Report.pdf

5 Epstien, S. "Potential public health hazards of biosynthetic milk hormones." International journal of health services : planning, administration, evaluation. Vol. 20, Issue 1. (73-84). Online. Accessed 8 Nov 2007. Available: www.ncbi.nlm.nih.gov/sites/entrez?cmd=search&db=pubmed
(PMID=2407676)

6 Michael F. Jacobson, Ph.D. "Press Conference on Salt: the Forgotten Killer." Pub. 24 Feb 2005. Online. Accessed 6 Aug 2007. Available as PDF: www.cspinet.org/new/pdf/final_mj_salt_statement.pdf

7 Truthinlabeling.org "Where is MSG hidden?" Online. Accessed 7 Aug 2007. Available: www.truthinlabeling.org/II.WhereIsMSG.html

8 Kaufman, Marc. "WHO to Talk About Food Carcinogen Finding." The Washington Post. Pub. 27 Apr 2002. Online. Accessed 7 Aug 2007. Available: (Contact Washington Post Archives).

9 Morris, R., Audet, A., Angelillo, I., Chalmers, T. and F. Mosteller. "Chlorination, Chlorination By-products, and Cancer: A Meta-analysis." American Journal of Public Health. Pub. July 1992. Vol. 82, Issue 7. Online. Accessed 14 Aug 2007. Available as PDF: www.ajph.org/cgi/reprint/82/7/955

10 World Health Organization. "Indoor air pollution and health." Online. Accessed 10 Aug 2007. Available: www.who.int/mediacentre/factsheets/fs292/en/index.html

11 World Health Organization. "Indoor air pollution and health." Online. Accessed 10 Aug 2007. Available: www.who.int/mediacentre/factsheets/fs292/en/index.html

12 Natural Resources Defense Council. "Arsenic in Drinking Water." Online. Accessed 14 Aug 2007. Available: www.nrdc.org/water/drinking/qarsenic.asp

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Mercury in Childhood Vaccines Excreted Quickly

(HealthDay News) -- The latest chapter in the debate over whether childhood vaccines can cause autism was written Wednesday with release of a study that showed the controversial mercury-containing preservative thimerosal is rapidly excreted from babies' bodies and can't reach toxic levels.

"Thimerosal has been used for decades, but the surge in vaccinations caused fear that possible accumulations of ethyl mercury, the kind in thimerosal, might exceed safe levels -- at least, when based on the stringent risk guidelines applied to its better-understood chemical cousin, methyl mercury, which is associated with eating fish," lead researcher Dr. Michael Pichichero, a professor of microbiology/immunology, pediatrics and medicine at the University of Rochester, said in a statement.

"One of the unanswered questions when this first popped up as a controversy was, when you got thimerosal as an injection, how long would it stay in your blood," study co-author Dr. John Treanor, a professor of medicine at the University of Rochester Medical Center, said.

The new research, he added, showed that "the levels of thimerosal don't go very high, and they go down right away. By the time it's time for the next dose of vaccine, the levels are right back to where they were at the beginning."

For its study, Pichichero's team tracked 216 infants from R. Gutierrez Children's Hospital in Buenos Aires, Argentina, where thimerosal is still routinely used in vaccines. Use of thimerosal in childhood vaccines was discontinued in the United States after a joint decision in 1999 by U.S. health officials, pediatricians and vaccine manufacturers.

The infants in the study were put into three age groups and their blood-mercury levels were tested both before and after vaccinations were given to newborns, and at their 2- and 6-month checkups.

Pichichero's group found that for all three age groups, the half-life of ethyl mercury in the blood -- the time it takes for the body to get rid of half the mercury, and then another half, and so on -- was 3.7 days. That's significantly less than the half-life of methyl mercury, the kind found in fish, at 44 days.

"Until recently, that longer half-life was assumed to be the rule for both types of mercury. Now it's obvious that ethyl mercury's short half-life prevents toxic build-up from occurring. It's just gone too fast," Pichichero said.

"If you thought thimerosal was responsible for autism, you would be looking at mercury levels that were far below anything anyone's previously thought as being toxic," Treanor added.

"Though it's reassuring to affirm that these immunizations have always been safe, our findings really have greater implications for world health," Pichichero said. "Replacing the thimerosal in vaccines globally would put these vaccines beyond what the world community could afford for its children."

The findings were to be released Monday in the February issue of Pediatrics, but they were released early by the journal's publisher, the American Academy of Pediatrics (AAP), which is requesting that the ABC network cancel the premiere episode of a new show Thursday dealing with the thimerosal-autism controversy.

The findings also follow a recent report from the California Department of Health that rates of autism continue to climb there even after thimerosal has been removed from childhood vaccines.

"A much more fundamental observation has been as mercury has been eliminated from vaccines in many countries the rates at which autism are being diagnosed continue to go up at about the same rate as before the mercury was removed," Treanor noted. "There doesn't seem to be any relationship between the frequency of autism and whether children are getting vaccines with mercury or not."

And they follow a series of studies, including a large-scale U.S. Institute of Medicine review in 2004, that failed to uncover a link between childhood vaccines and autism. The first report of a possible connection appeared in British study in the late 1990s; it has since been discredited.

Current estimates by the U.S. National Institutes of Health say that one American child in 150 has been diagnosed with autism, although experts wonder if that increase is due to better diagnoses and a broader definition of the disorder.

Still, at least one vaccine critic worries that inoculations are making children prone to autism, a developmental disorder characterized by impaired social interaction, communication problems, and unusual, repetitive, or severely limited activities and interests. And if it's not thimerosal, then it must be some other vaccine-related interaction, said Barbara Loe Fisher, co-founder and president of the National Vaccine Information Center.

"There are many biological mechanisms involved in vaccine-induced brain and immune system changes that could quite well lead to autism," she said.

"Mercury doesn't belong in any product," Fisher added. "Mercury doesn't belong in vaccines whether it's proven or not proven that mercury is a problem in vaccines."

In ABC's new TV series Eli Stone, the premiere Thursday focuses on a lawyer arguing that a vaccine caused a child's autism. While the show includes statements that science has refuted a link between autism and vaccines, the program reinforces the connection as the jury awards the mother $5.2 million, according to the AAP.

"If parents watch this program and choose to deny their children immunizations, ABC will share in the responsibility for the suffering and deaths that occur as a result. The consequences of a decline in immunization rates could be devastating to the health of our nation's children," AAP President Dr. Renee R. Jenkins said in a prepared statement.

More information
For more on thimerosal and autism, visit the The Children's Hospital of Philadelphia.

Soy Nuts Lower Blood Pressure in Postmenopausal Women

(HealthDay News) -- Soy nuts may help lower blood pressure in postmenopausal women, a new U.S. study finds.

Researchers at Beth Israel Deaconess Medical Center in Boston studied 60 healthy women -- 12 with high blood pressure (140/90 milligrams of mercury or higher) and 48 with normal blood pressure. All the women ate two kinds of diets for eight weeks each.

One was the Therapeutic Lifestyle Changes (TLC) diet, which consisted of 30 percent of calories from fat (with 7 percent or less from saturated fat), 15 percent from protein, and 55 percent from carbohydrates, 1,200 milligrams of calcium per day, two meals of fatty fish (such as salmon or tuna) per week, and less than 200 milligrams of cholesterol a day.

The other diet had the same calorie, fat and protein content, but the women replaced 25 grams of protein intake with one-half cup of unsalted soy nuts.

"Soy nut supplementation significantly reduced systolic (top number) and diastolic (bottom number) blood pressure in all 12 hypertensive women and in 40 of the 48 normotensive women," the study authors wrote.

"Compared with the TLC diet alone, the TLC diet plus soy nuts lowered systolic and diastolic blood pressure 9.9 percent and 6.8 percent, respectively, in hypertensive women, and 5.2 percent and 2.9 percent, respectively, in normotensive women."

In women with high blood pressure, the soy nuts also decreased levels of low-density lipoprotein ("bad") cholesterol by an average of 11 percent and levels of apoliprotein B (a particle that carries bad cholesterol) by an average of 8 percent.

The study was published in the May 28 issue of the journal Archives of Internal Medicine.

More information
The American Academy of Family Physicians has more about high blood pressure and how to lower it.

Dr. Morton Walker Speaks on Detoxamin

Environmentalists warn us repeatedly that we live on a poisoned planet. Toxins from mercury, lead, aluminum, cadmium, iron, nickel, and about 20 more metallic minerals permeate the Earth's milieu. Heavy and light metals poison us by combining to create deleterious signs and symptoms often referred to collectively as Toxic Metal Syndrome.

This syndrome, an indicator of serious systemic pathology, results in degenerative diseases which affect no less than 92% of the populations of Western industrialized nations, in particular, those people living in apartment high-rises and other polluted city dwellings.

What happens to them?

These poisoned people eventually come down with manifestations of degenerative illnesses such as heart and/or blood vessel deteriorations; pancreatitis; gout, rheumatoid arthritis or osteoarthritis; the syndromes of yeast, chronic fatigue, and/or irritable bowel; Alzheimer's disease, multiple sclerosis, parkinsonism, cancer and many more.

Although a poisoned person's bones remain toxic for life, excellent self-treatment exists to reduce or reverse most symptoms of illness in other body parts. First, get tested for the extent of toxicity, then neutralize metallic poisoning with a chelating agent such as Detoxamin.

By applying the highly efficacious Detoxamin suppository containing Ca-EDTA, you remove toxic metal from cells all over the body. The self-administration is performed rectally before retiring so that as you sleep you remove the toxins. There's no more need for intravenous infusions.

Rectal chelation therapy does the job of detoxifying in a low-cost, convenient manner; it's an effective way to effuse EDTA through the bowel's walls and into your blood stream to clean toxic metals from all body cells.

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Mercury

Mercury is one of the most toxic elements on the planet, probably second only to plutonium, yet (worldwide) people have it in all tissues of their bodies. It continues to be dumped into our waterways and soil, placed into our teeth, and injected into our bodies through vaccinations.

Toxicity caused by excessive mercury exposure is now becoming recognized as a widespread environmental problem and is continuing to attract a great deal of public attention.

A National Academy of Sciences study published in July 2001 estimates that up to 60,000 children born in the USA each year may be affected by mercury toxicity. In March of 2002, an environmental group had charged the FDA of failing to warn the public of the dangers of mercury contamination from eating tuna, which contains high levels of mercury.

Texas researchers have found a possible link between autism and mercury in the air and water. In fact, the incidence of autism has grown in the past 20 years, from one in every 2,000 children to as high as one in every 166! Researchers have been hard-pressed to explain the increase, but many believe mercury to be the culprit.

The World Health Organization (WHO) reports that the amount of mercury absorbed daily by the average human body is 0.3 micrograms (mcg) from water and air, 2.61 mcg from fish, and 17 mcg from dental amalgams (silver fillings). Research points out that 80% of mercury vapor is absorbed into the blood, going directly from the nose to the brain, following nasal nerve pathways. Dentists have four times as much of a body burden of mercury as an average non-dentist.

Dental workers show 50-300% more mercury in hair and fingernails than the average population. Before public awareness campaigns started, it is a notable fact that the preservative thiomerasol (usually added to vaccines) contained mercury. In 1999, the CDC called for the removal of mercury from vaccines. Paradoxically, the CDC still continues to recommend the measles, mumps and rubella vaccine.

If you are one of the millions of Americans who has received silver dental fillings, take notice. Mercury makes up about 50 percent of every amalgam dental filling, also known as “silver” fillings. Amalgam fillings can release mercury for up to 70 years. Someone with eight amalgams, for example, could have 120 mcg released into the saliva per day.

The maximum allowable by the EPA is less than 0.1 mcg per kilogram of body weight per day, to be absorbed into the human body. We now know that the dental mercury/silver amalgam filling is “chemically & electrically active.” Science has proven that every time we eat, drink, or breathe, we may be absorbing disturbing releases of decomposing, toxic particles—mercury included. This chronic, toxic accumulation is being shown to have serious, long-term consequences on our immune system, resulting in a variety of disease and conditions.

Consider that while 78% of Americans have dental fillings, 95% of people with disorders of the central nervous system such as MS, epilepsy, paralysis and migraines also have silver dental fillings. This begs the question: Would you want mercury—one of the most powerful neurotoxins on the planet—embedded in your mouth, only inches from your brain?

The answer is obvious. This is the same reason why you can no longer buy an oral or rectal mercury thermometer.

Toxic Heavy Metals

We have been exposed to heavy metal toxins for an immeasurable amount of time. The industrialization of our planet has drastically increased the environmental burden of heavy metal toxins, to the point that we are dependent upon them for proper functioning.

Industry and commercial processes are actively mining, refining, manufacturing, burning, and manipulating heavy metal compounds for many reasons. Presently, heavy metals are abundant in our drinking water, air and soil due to our increased use of these compounds. They are present in virtually every area of modern consumerism.

Toxic metals are found in construction materials, cosmetics, medicines, processed foods, fuel sources, appliances, personal care products and so much more. It is very difficult, if not impossible, for anyone to avoid exposure to any of the many harmful toxic heavy metals that are so ubiquitous in our environment. It doesn’t look like we will successfully neutralize the threat of heavy metal toxicity in our communities, nor diminish our use of the many commercial goods that they help produce. We can, however, take steps to understand and deal with this threat. Cadmium, aluminum, mercury, antimony, lead and arsenic are some of the heavy metals added to our food chain from upstream industrial discharges, pesticide runoff, incinerator emissions, and smokestacks, as well as aviation.

Heavy metals are found in the air we breathe, from factories, automobiles and in places you wouldn’t imagine. Low-level metal toxicity is recognized by the Environmental Protection Agency (EPA), the Food & Drug Administration (FDA), and the Centers for Disease Control (CDC), as well as by individual state health departments.

The American Heart Association states that blood-levels of lead and cadmium may increase the risk of peripheral artery disease — even at levels currently considered safe. Low-level toxicity from heavy metals and the resulting “oxidative stress” are associated with a depressed immune system, increases in infertility, cancer, cardiovascular disease, and premature mortality.

Emerging evidence shows that blood and bone lead levels, reflecting relatively modest exposures, are also associated with hypertension, renal insufficiency, and cognitive impairment. Studies conducted at the National Academy of Science (NAS) show clear and present danger of heavy metals in our bodies. Tuna, dental fillings and vaccinations containing mercury, can cause problems including birth defects, brain damage, depression, fatigue, hearing loss, vision loss, kidney damage and many more ailments.

The really bad news is that, according to the EPA, 99% of our population contains chemicals that are linked to the development of cancer. Most heavy metals are carcinogenic and can cause free radical damage. They can cause the energy factories in our cells (known as mitochondria) to stop working, which essentially causes cells to die. In the process, the DNA for those affected cells may also be damaged, causing a malfunction in the next generation of cells of this type.

When cells are programmed to die off more quickly or to wildly multiply, we see problems such as weaker tissue, maligned function, or tumors. In short, heavy metals lead to serious illnesses and shorten our lives. There are more than twenty different heavy-metal (environmental) toxins that can impact human health—each toxin producing unique behavioral, physiological, and cognitive changes in an exposed individual.

The degree to which a system, organ, tissue, or cell is affected by a heavy metal toxin depends on the toxin itself and the degree of the individual’s exposure. Here we examine just five of the many hazardous heavy metals that we are commonly exposed to.

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Detoxamin EDTA Chelation Therapy Suppositories are a new patented method of Ca-EDTA chelation therapy medically equivalent to I.V. chelation therapy.

Detoxamin EDTA Chelation Therapy Suppositories are a new patented method of Ca-EDTA chelation therapy medically equivalent to I.V. chelation therapy.

The difference is that Detoxamin introduces a smaller dosage of Calcium Disodium EDTA on a nightly basis.

By applying the highly efficacious Detoxamin suppository containing EDTA, you remove toxic metal from cells all over the body.

The self-administration is performed rectally before retiring so that as you sleep you are taking chelation therapy with EDTA. There's no need for intravenous infusions or quantities of nutritional supplements.

What is EDTA chelation therapy and what is it used for?Chelation (pronounced key-lay-shun) is the process by which a metal or mineral (such as lead, mercury, iron, arsenic, aluminum, etc.) is bonded to another substance-in this case an amino acid called EDTA, Ethylene-Diamine-Tetra-Acetic acid. It is a natural process, basic to life itself. During EDTA chelation therapy, the EDTA infusion bonds with unwanted metals in the body and quickly carries them away in the urine.

Chelation therapy is a safe, effective alternative to drugs and surgeries and is used to treat many illnesses now known to be linked to the presence of toxic heavy metals. Illnesses such as heart disease, strokes, diabetes, circulatory disorders, neuropathies, Alzheimer's disease, atherosclerosis, and adverse reactions to many environmental pollutants. Traditional chelation therapy uses an intravenous drip, and is administered in the outpatient setting.

The number of treatments vary based on each person's individual condition and/or goals of treatment. The average therapy is given one to three times a week for twenty to thirty treatments.How long has EDTA chelation therapy been in use? Why don't more people use it?EDTA chelation therapy for the detoxification for heavy metals has been in continuous use since the 1940s when it was introduced specifically for the treatment of lead poisoning. It was very quickly observed that as the metals were eliminated, not only did the signs and symptoms of lead poisoning abate, but problems related to the circulatory system like heart attacks, angina, strokes, and peripheral vascular disease also improved.

For the past 50 years, well over one million people have received the intravenous form of EDTA chelation. As beneficial and life saving as this therapy has become, it is very expensive and very time-consuming, making it out of reach for most people.Why is Ca-EDTA, Calcium Disodium EDTA, so much better than other types of chelation therapy?According to Dr. Bruce Halstead, "The chemistry of all chelators is such that a change of pH can dramatically effect the process of chemical binding needed to chelate a mineral or metal. When you use a less effective chelator, such as Magnesium EDTA, you lose all chelating ability of the two most essential heavy metals: lead and mercury. Magnesium di-Potassium EDTA has a dramatically lower chelating effectiveness than Calcium EDTA because both magnesium and potassium dramatically decrease the pH in the blood environment to which it is introduced. Any factor decreasing pH renders EDTA less effective.

Once the pH is lowered more than 7.38, it's no longer chemically conducive to any bonding or chelating." (Dr. Halstead is well known as the 'Father of Chelation Therapy'.)

Dr. Morton Walker Speaks on Detoxamin - Toxic Metals Induce Degenerative Diseases; Rectal Chelation Therapy Overcomes Them.

Environmentalists warn us repeatedly that we live on a poisoned planet. Toxins from mercury, lead, aluminum, cadmium, iron, nickel, and about 20 more metallic minerals permeate the Earth's milieu. Heavy and light metals poison us by combining to create deleterious signs and symptoms often referred to collectively as Toxic Metal Syndrome.

This syndrome, an indicator of serious systemic pathology, results in degenerative diseases which affect no less than 92% of the populations of Western industrialized nations, in particular, those people living in apartment high-rises and other polluted city dwellings. What happens to them? These poisoned people eventually come down with manifestations of degenerative illnesses such as heart and/or blood vessel deteriorations; pancreatitis; gout, rheumatoid arthritis or osteoarthritis; the syndromes of yeast, chronic fatigue, and/or irritable bowel; Alzheimer's disease, multiple sclerosis, parkinsonism, and many more which may be deadly-cancer for instance.

Although a poisoned person's bones remain toxic for life, excellent self-treatment exists to reduce or reverse most symptoms of illness in other body parts. First, get tested for the extent of toxicity, then neutralize metallic poisoning with a chelating agent such as Detoxamin. By applying the highly efficacious Detoxamin suppository containing EDTA, you remove toxic metal from cells all over the body. The self-administration is performed rectally before retiring so that as you sleep you are taking chelation therapy with EDTA. There's no need for intravenous infusions or quantities of nutritional supplements.Rectal chelation therapy does the job of detoxifying in a low-cost, convenient manner; it's an effective way to effuse EDTA through the bowel's walls and into your blood stream to clean toxic metals from all body cells.

Do I need Ca-EDTA chelation therapy?
We find ourselves existing in a far more toxic and hostile environment than our bodies were designed to handle. Experts have shown that almost every health problem-from learning disorders to cancer and heart disease-is aggravated by the approximate 1,000% increase in lead levels in our bones. In 1999, it was reliably reported that hearts with some form of disease have 20,000 times more toxic heavy metals than healthy hearts."Human exposure to heavy metals has risen dramatically in the last 50 years as a result of an exponential increase in the use of heavy metals in industrial processes and products." says Maile Pouls, Ph.D (Townsend Letter for Doctors and Patients, July 1999).A recently concluded "Body Burden" study by New York's Mt. Sinai Hospital and the Environmental Working Group was reviewed by University of Oregon Professor Joseph Thornton: "It shows the universality of chemical contamination of people's bodies," Thornton said.

All the studies "confirm the general message that everybody in our society has these chemicals building up. Some people have it worse than others, but everyone has it. No one is clean anymore." (From Being Careful Can't Keep Chemicals Out of Your Body, Miami Herald, February 1, 2003.)Today we know that about one out of every 2.5 Americans will get cancer. Ninety eight percent of cancer is caused by toxic chemicals. When 50% of all men and 33% of all women living now will die of cancer, something is terribly wrong. (Mortality from cancer was reduced by 90% during an 18-year study of 59 patients treated with Calcium-EDTA. This and over 40 other studies prove the efficacy of Ca-EDTA, Calcium Disodium EDTA chelation therapy and Detoxamin. We will all function better and live longer if we lower the overall burden of toxic metals within ourselves. If you eat or breathe, you will probably benefit greatly from chelation therapy.

Is Detoxamin safe for children?
Yes. In fact, Detoxamin case studies were conducted on lead poisoning in children. The study showed no significant increase in BUN or creatinine levels even in very young children. Due to our lower dosage and time release formulation, no renal toxicity was encountered.BEHAVIORAL, STRUCTURAL, FUNCTIONAL ABNORMALITIES ASSOCIATED WITH VARIOUS HEAVY METAL TOXINS.Reference: Published in the August issue of Alternative & Complimentary Therapies (a magazine for doctors) and Published in Townsend Letter for Doctor's and PatientsPsychiatric Disturbances:
Social Deficits, Social withdrawal

Mercury
Repetitive, perseverative, stereotyped behaviors; OCD-typical behaviors
Mercury
Depression, mood swings, flat affect; impaired facial recognition

Arsenic, Copper, Lead, Mercury
Schizoid tendencies; hallucinations; delirium
Mercury
Irritability, aggressive behaviors, temper tantrums
Lead, MercurySuicidal Behaviors
Copper, MercurySleep difficulties / disturbancesLead, Mercury, Thallium
Chronic fatigue (CFS); weakness, malaise
Aluminum, Arsenic, Cadmium, Copper, Lead, Mercury, Thallium
Anorexia; symptoms reflecting eating disorders, loss of appetite/weight
Arsenic, Lead, Mercury
Anxiety; nervous tendencies

Thallium
Attentional problems (ADHD), lacks eye contact, impaired visual fixation
Lead, Mercury

Speech and Language Deficits: Speech disorders
A luminum, MercuryLoss of speech, developmental problems with language Mercury
Speech comprehension deficits

Mercury
Dysarthria; articulation problems; slurred speech, unintelligible speech
Mercury
Cognitive Impairments:Mental retardation, borderline intelligence

Arsenic, Lead, Mercury
Uneven performance on IQ scores, low IQ scores
Copper, LeadPoor concentration, attention deficits (ADHD, response inhibition

Aluminum, Lead
Poor memory (short term, verbal, and auditory)
Aluminum, Lead

Difficulties understanding abstract ideas; difficulty carrying out complex commands

X metals
Dementia; pre-senile and senile dementia
Aluminum
Stupor

Aluminum, Arsenic

Impaired reaction time; lower performance on timed tests

Lead
Sensory Abnormalities:
Abnormal Sensations in the mouth and extremities
Arsenic
Hearing loss, difficulty hearing
Arsenic, Lead, MercuryAbnormal touch sensations; diminished touch sensations, aversion to touch
Arsenic
Blurred vision; sensitivity to light
Arsenic, Mercury
Motor Disorders:
Choreiform movements, myoclonal jerks, unusualpostures

Copper, Mercury
Difficulty walking, swallowing, talking
Copper, Mercury

Flapping, circling, rocking, toe walking
Mercury
Problems with intentional movements or imitation
MercuryAbnormal, gait/posture; incoordination, loss of balance; problems sitting, lying, crawling and walking
Mercury

Decreased locomotor activity
Aluminum, Arsenic
Convulsion; seizure
Aluminum, Arsenic, Copper, Lead, Mercury, Thallium

Physiological Impairment, Brain and Central Nervous System:
Neurofibrillary tangles
Aluminum
Neuritis, retrobulbar neuritis; neuropathy
Aluminum, Arsenic, Lead, Thallium
EncephalopathyAluminum, Arsenic, Lead, Thallium
Cerebrovascular diseaseX metals

Alterations in nerve conduction velocity
Lead
Alterations in the spinal cordThalliumAccumulates in CNS structures
Aluminum, MercuryAbnormal EEGs

Arsenic, Lead
Autonomic disturbancesCopper, Lead, Mercury, Thallium

Peripheral Nervous System:Peripheral neuropathyArsenic, Mercury

Alterations in peripheral nerves
Arsenic
Loss of feeling/ numbness in the extremities; paresthesia

Arsenic, Mercury, Thallium

Gastrointestinal Tract:
Nausea, vomiting, diarrhea; loss of appetite

Arsenic, Mercury

Abdominal pain, stomach cramps; burning of the throat of the mouth

Arsenic, Copper, Lead, Mercury, Thallium

Esophagitis; gastroenteritis; colitis

Arsenic, Mercury, Thallium Cancers (colon, pancreatic, stomach, or rectal) Arsenic

Renal and Hepatic Impairment:Hepatotoxicity; Liver dysfunction, damageArsenic, Copper, Thallium

Cirrhosis of the liver; hepatitis

Copper

Kidney disease; kidney failureArsenic, Lead, MercuryRenal toxicity; tubular proteinosisArsenic, Copper, LeadKidney Damage, histological alterations

Arsenic, Lead
Cardiovascular System:Blood vessel damage

ArsenicAnemia; decreased red blood cell count

Arsenic, CopperHypertension; increased heart rate (tachycardia)

Arsenic, Copper, Lead, Thallium

Electrocardiac disorders, Peripheral vascular disease; cardiovascular disease, vascular collapse

Arsenic, Lead
Respiratory System:Pulmonary Fibrosis

Aluminum, Arsenic
Pulmonary edema

X metals
Pneumonia, laryngitis, pharyngitis, bronchitis

Aluminum, Arsenic, Mercury
Restrictive airway disorders, asthmatic conditions, pneumoconiosisArsenic, Aluminum

Nasal ulcers, perforation of the nasal septumX metalsImmune System:Increased incidences of asthma, autoimmune-like symptoms, & allergies
X metals

Inhibition of lymphocytes, T-cells, monocytes X metals
Immunosuppression

LeadDecreased white blood cell count
Arsenic, ThalliumReproductive System:Genital abnormalitiesAluminum, ThalliumDisturbances in menstrual cycle; menstrual painsCopper, MercuryBirth defects; premature births; Spontaneous abortionArsenic, Lead, MercuryReproductive dysfunctionArsenic, AluminumOther Physical Disturbances:Hypotonia or hypertonia; decreased muscular strengthX metalRashes, contact dermatitis; eczema, itchy/irritating skinAluminum, Arsenic, Copper, MercuryMuscle pain; headache; acrodynia; colicArsenic, Copper, Lead, ThalliumAlopecia (hair loss)Thallium Reference: Published in the August issue of Alternative & Complimentary Therapies (a magazine for doctors) and Published in Townsend Letter for Doctor's and Patients.

Detoxamin Usage Instructions: Detoxamin EDTA Suppositories are solid, bullet-shaped preparations designed for easy insertion into the anus (back passage). Detoxamin is manufactured in a cocoa-butter base, a time-release agent (fatty acid base), and 750 mg of Calcium-Disodium EDTA. Detoxamin will dissolve at body temperature and will gradually spread over the lining of the lower bowel (rectum), where it is absorbed into the bloodstream. Detoxamin is designed to release 750 mg Calcium Disodium EDTA slowly, over an 80-minute period.

A. Detoxamin Protocol for More Severe Cases:
1. Take one suppository at night, prior to bedtime.
2. Take every night for up to 90 days. This will provide the medical equivalence of 30 IV Chelation treatments.
3. Take proper mineral/trace mineral/vitamin replacement every day.
4. Take all other suplementaion every day.B. Detoxamin Protocol for Less Severe Cases/Anti-Aging/Prevention:
1. Take Detoxamin every OTHER night, prior to bedtime.
2. Take Detoxamin every other night for 180 days (90 suppositories). This will provide the medical equivalence of 30 IV chelation treatments.
3. Take proper mineral/trace mineral/vitamin replacement every day.
4. Take all other supplementation every day.

Detoxamin Protocol AFTER A or B is completed:
Your bones are toxic for life. Lead and other heavy metals are stored in the bones and get re-distributed into the bloodstream. Therefore, it is highly recommended to continue maintenance with Detoxamin, this provides the ultimate in Anti-aging benefits.

1. Take 5 Detoxamin suppositories over a 30-day period. This porvides medically equal to about 2 EDTA IV treatments.
2. Take porper mineral/trace mineral/vitamin replacement every day.

Note: Detoxamin is designed to be taken at night, however some patients and physicians prefer taking a suppository in the morning after evacuation. (Optional)

How to Use Detoxamin:
Insert Detoxamin suppositories at night, prior to bedtime.
Eat early in the evening, about 4 hours prior to bedtime. (Reduces any discomfort).
1. Go to the toilet and empty your bowels if necessary.
2. Wash your hands.
3. Remove the plastic wrapping from Detoxamin.
4. Either squat or lie on your side with one leg bent and the other staight.
5. Gently but firmly push the suppository into the rectum, FLAT end first until past the sphincter muscle. By inserting the flat end first opposed to the pointed end, the suppository will travel higher up in the rectum more easily. If necessarey moisten the suppository with a little water. Push it in far enough so it doesn't slip out.
6. Close your legs and sit or lay still for a few minutes.
7. Wash your hands again.
8. Try not to empty your bowels for at least 80 minutes.
9. It is optional to take Detoxamin in the morning, after evacuation.

STORAGE: Store Detoxamin in a cool dark place, but not in the fridge. If Detoxamin suppository gets warm it may melt, put the fridge for a few minutes, this will return the suppository to its original state so it may be inserted.
Shelf Life: 2 Years
More information’s: here Chelation

Help detoxify the body

Lead levels today are 1000 times greater than pre-industrial times.
Toxic metals dangerously compromise our overall health.
Higher IQ and a more efficient immune system are two important reasons to detoxify.

We find ourselves existing in a far more toxic and hostile environment than our bodies were designed to handle. We will function better, and live longer if we lower the overall burden of toxic metals routinely throughout life with some form of detoxification protocol.
Lead levels today are 1000 times greater than pre-industrial time. Mercury is found in our amalgam dental fillings and the fish we eat, cadmium from cigarette smoke and aluminum from cooking. Free metals within our bodies catalyze free radicals and burden our immune system; lead is substituted for zinc within our bodies leading to impaired enzyme function. This imbalance of toxic versus essential trace minerals dangerously compromises our overall health. The idea is to get these toxic metals out of our bodies while supplying our bodies with essential trace minerals. This way, our immune system will be better able to function in the myriad of healing work it performs night and day.

Mercury is one of the most toxic substances commonly encountered

Mercury is one of the most toxic substances commonly encountered, and according to Government agencies causes adverse health effects in large numbers of people in the U.S.[1,2] The extreme toxicity of mercury can be seen from documented effects on wildlife by very low levels of mercury exposure. Because of the extreme toxicity of mercury, only ½ gram is required to contaminate the ecosystem and fish of a 10 acre lake to the extent that a health warning would be issued by the government to not eat the fish [3]. Over half the rivers and lakes in Florida have such health warnings[4] banning or limiting eating of fish, as do approximately 20% of all U.S. lakes, all Great Lakes, 7% of all U.S. river miles, and many bays. Other countries including Canada have similar experience.

More in our Dental Blog

Arizona Judge Amendsd Parenting Plan, Orders Vaccinations

For Immediate Release: November 10, 2004 Arizona Judge Amends Parenting Plan, Orders Vaccinations Can a judge be unbiased when forced to rule whether or not his own order caused permanent injury to children? By Don Harkins (Editor - Idaho Observer) In their efforts to protect two children from family court-ordered vaccinations, Janet and John Burton of Tempe, Arizona, find themselves at center stage in a precedent-setting child custody case. At issue is plaintiff/parent Steven Hutchinson seeking a court order awarding him full custody of two children based on the mother’s insistence that they be lawfully exempted from vaccination. This case is exemplary of a national trend where hundreds, possibly thousands of divorced parents are punished by the state because their ex-spouses choose to use the vaccination issue as a means to gain the custodial upper hand. In many cases, as in the Burton case, one parent may be on record as agreeing with the other parent’s non-vaccination position but changes their mind to enlist the court’s help in undermining the other’s access to the children. Arizona District Judge Larry Grant of Maricopa county has ignored the Burton ’s evidence regarding the dangers of vaccines and upheld Hutchinson’s desire that five-year-old Greyson and seven-year-old Gwyneth be vaccinated. Judge Grant further defied Janet’s well-founded concerns by ordering that Hutchinson may determine what vaccines his children will receive and choose the practitioner who will deliver them. Judge Grant’s order was carried out May 12, 2004. The children were, “…physically restrained and forcefully vaccinated by a reckless, unprofessional ‘health practitioner’ who administered to them 21 vaccines in less than an hour. This ‘kiddie cocktail’ of mercury, aluminum, pathogenic viruses and more may have changed the course of my children’s lives forever,” Janet Burton explained. Neither Hutchinson nor Judge Grant are licensed to prescribe medication in Arizona or any other state. However, armed with Judge Grant’s court order, Hutchinson “prescribed” seven shots (DTaP, IPV, MMR, Hib, Hep B, Varicella and PCV—for a total of 21 vaccines) each for his children. According to the Centers for Disease Control and its “catch-up” schedule, Gwyneth and Greyson should not have received the Hib and PCV shots because they were both past the age of five years. The osteopath Hutchinson used (who is licensed to prescribe medicines) administered the contraindicated vaccines per the judge’s order. Arizona VacLib Chapter Director Kim Medlin has conducted further research into the vaccines administered to Gwyneth and Greyson on May 12. Medlin has found that four of them came from what are called “hot lots”—batches of vaccines known to be causing unusually high numbers of adverse reactions. One of the vaccines is known to be contaminated with bovine spongiform encephalitis—also known as “mad cow” disease. The Burtons have noticed that Gwyneth and Greyson’s personalities have changed since the severe assault of 21 vaccines May 12 and that they are both more sickly. Janet believes the court is getting ready to order that her children be subjected to another round of vaccinations. Several qualified physicians have commented that the first round of vaccinations appear to have caused damage to these two children and concur that additional vaccinations at this time would do more harm than good. Since this case was initiated by Hutchinson last March, Janet has forced the court to review much evidence regarding the dangers of vaccines. They have also enlisted the support of Drs. Muhammad Al-Bayati, Russell Blaylock and William Rae. Judge Grant has demonstrated that he has considered the information provided by Janet when stating for the record that he could not support their position because it would be an admission that, by recommending and ordering vaccines as a policy, the state of Arizona has been engaging in child abuse for decades. The evidence supports Janet’s claims that Hutchinson’s actions are purely vindictive and that he is using his children to punish his former wife for divorcing him last year. “This is the same man that just a few years ago sat me down in front of a computer monitor and proceeded to navigate around various websites in an effort to educate me on the hidden truths about all the risks and cover-ups associated with the ‘experimental’ surgical procedure we all loosely refer to today as childhood immunizations. Of course, as informed, responsible co-parents, we jointly agreed not to vaccinate our children. We made this decision and many other decisions such as birthing our children at home, breastfeeding each baby for a full year and a half and following up with a healthy, organic food plan thereafter. We also agreed that no pharmaceutical medications were to be given and, for certain, we would not mindlessly entrust our children to ignorant, drug-pushing doctors. All of these decisions seemed to serve our two children well as they truly epitomized wellness, vitality and brilliance. Both their father and I were proud of the positions we had taken on issues that pertained to our children’s health and well-being and agreed to continue with what had worked (holistic methods of treatment) for our perfect children when we divorced. Together we outlined our beliefs concerning alternative methods of treatment for our children and made this part of our Parenting Plan—which is on file with the courts to this very day,” Janet explained. Among the documents before Judge Grant are reports of increased risk of adverse reactions in children who receive multiple antigens and letters stating that Gwyneth and Greyson are showing signs of vaccine damage. The Burton’s attorney Wallace Nichols is orchestrating a legal strategy intended to spare Gwyneth and Greyson another round of court-ordered vaccinations. In the process of this child custody case being decided by Judge Grant, the court will be forced to consider the validity of state-recommended vaccination schedules against published science and the expert testimony of qualified neuroscientists, pathologists and medical doctors. And, if the Burtons are able to arrange for her children to undergo a full medical and biochemical analysis by Dr. Rae at the Environmental Health Center in Dallas (EHCD), Judge Grant will be forced to consider the possibility that vaccinations he ordered to appease the wishes of a man seeking retribution on his former spouse have caused two innocent children to suffer permanent injury. The move will also force Hutchinson to legally “trump” the Burton’s medical evidence of vaccine damage by entering into the record an expert second opinion contradicting the findings of Dr. Rae’s EHCD. Burton supporters believe Hutchinson will not be able to discredit the pending EHCD report. “I will take this case as far as it will go,” commented Janet who understands the huge implications this case will have in child custody disputes all over the nation. The EHCD and the work of Dr. Rae in the field of environmental toxicology has come highly recommended by Dr. Sherri Tenpenny and others. The cost for the series of tests to be run on both children is estimated at $3,000. Supporters are willing to supply room and board for the Burtons during the four days they will be in Dallas. The Burtons can use our help in this matter as attorney fees and lost wages are causing them to experience a significant degree of financial hardship. Dr. Rae and the staff at EHCD have excellent credentials and utilize state-of-the-art diagnostic equipment and procedures to arrive at scientifically sound conclusions that stand up in court. To find out more about EHCD, the services it offers and references, go to www.ehcd.com Vaccination Liberation, a national grassroots volunteer association, sees the huge implications of this case and has forwarded a $100 donation to the Burtons to help cover the cost of testing. Vaccination Liberation also requests that medical practitioners nationwide match their donation to this worthy cause. For more information, contact Janet Burton at 480-785-4846. The mailing address for donations and correspondence is Wallace R. Nichols, Esq. 15770 N. Greenway-Hayden Loop, Ste. 104, Scottsdale, AZ 85260 Background of case—from Janet Burton Last March, my former husband Steven Hutchinson, the father of Gwyneth and Greyson, hired legal counsel who announced to the court that his client had a recent change of heart regarding the subject of childhood vaccinations. They asked the judicial ‘system’ to assist Hutchinson in carrying out an act of medically-induced child abuse. And so they did. Though we spent nearly $30,000 on legal fees and were able to generate considerable sympathetic local media coverage, Hutchinson prevailed and was given the opportunity to vaccinate the children with the vaccines of his choice by the health care provider of his choice. This decision was based upon what a judge proclaimed to be a ‘Public Policy’ in the state of Arizona to vaccinate all children. The judge also stated that to rule otherwise would be to admit our government has committed child abuse for decades. With a newly-obtained court order in hand and accompanied by three police cars, Hutchinson and a female accomplice whisked Gwyneth and Greyson away from their school and drove them to a nearby emergency health care clinic. Hutchinson tricked my children by telling them they were only going in for their first check up. Once inside, Hutchinson, along with a woman posing as my children’s mother, authorized a health practitioner (D.O.) to administer cocktails of poisons into Greyson and Gwyneth’s lymphatic systems. This ‘cocktail’ included the DTaP, IPV, MMR, Hib, Hep B, Varicella and PCV vaccines and were given to both children within less than an hour. These vaccines were recklessly combined and, adding insult to injury, two of the vaccines were age inappropriate and one vaccine was from a contaminated lot now known to be infected with BSE or mad cow disease. Virtually no consideration was given to our children’s medical family history, which includes a primary family member (half-sister) who suffered from grand mal seizures for four years after being vaccinated with the MMR vaccine. This family history of seizures puts both of my children at a much greater risk of experiencing seizures than the general population. It is beyond most people’s comprehension how a few unqualified and grossly misguided people can persevere legally to have these toxic vaccines (that are non-emergency medicine) forced upon my children - literally gambling with their lives. And for what medical justification? None was provided. Our five-year-old son and nearly seven-year-old daughter are well past the ages of life-threatening consequences from any of the diseases these CDC-recommended vaccines were supposed to ‘protect’ them from. Greyson and Gwyneth had everything to lose by this insane proposition and nothing to gain. Immunizations (an inaccurate term that leads one to believe that these vaccinations do something to safeguard our little ones from contracting ‘scary’ childhood diseases) are just one grand medical experiment. Time and again, vaccinations have been proven by researchers and non-special interest groups to be ineffective in preventing the spread of infectious diseases and unsafe with consequences ranging from minor irritation at the injection site to death. As a mom, I declared to the children’s father and to the presidingjudge that no one was going to subject my children to such a barbaric, unfounded experiment. The judge exercised his authority to rule otherwise and with the slamming of a gavel, he delivered a ruling for which our children would pay dearly. Approximately 48 hours after the hideous vaccination event May 12, 2004, I was finally able to see my children. I was overwhelmed at the sight of my two children completely dazed and suffering adverse effects such as dehydration, lethargy, dry heaves, headaches, burning eyes, sore throats and, of course, aching thighs with ‘battle scars’ from where needles were drug along my son’s tiny legs as he fought to resist the poison that was being forced hypodermically into his body. Four months later, both Greyson and Gwyneth still show obvious signs of being vaccine damaged. Especially tragic for me is what I witness each day in our son, whose overall health and personality has changed dramatically. It is obvious to me that our son Greyson has been neurologically impaired as a result of being over-vaccinated and is in dire need of diagnostic and remedial care. Instead of a ruling in favor of our motion requesting an “Emergency Stay” be put in place to prevent future vaccinations until I had the opportunity to get both children evaluated and treated for injuries from which they are still suffering, I am instead faced with obstacles placed before us by a judicial system that makes it nearly impossible to get my children medical care and, worse still, appears determined to order our children be re-vaccinated. To date, the court is ignoring the pleadings from several medical experts such as Dr. Russell Blaylock, Dr. Mohammed Al-Bayati, Dr. Doris Rapp, Dr. Stuart Lanson and Dr. Rae – all who have testified that the odds of our two children suffering even more devastating consequences from additional vaccinations would be great and certainly a risk not worth taking. Adding to the absurdity of my family’s case, in July 2004, Hutchinson took me to court in an effort to find me in contempt for not allowing our children to leave with him on a cruise ship to some undisclosed destination off the continental U.S. just 72 hours after receiving 21 vaccinations—while both children were still obviously struggling with the physical and emotional aftermath of this traumatic event. The ruling was handed down three months later that I was indeed ruled to be in ‘contempt’ for my decision to follow my heart, good sense, the advise of medical experts and the recommendations of the CDC suggesting that long distance travel is not a prudent choice for at least three weeks following a child being vaccinated. This recent ruling will cost me upwards of $20,000 once all fines and fees have been paid. We are left with no choice but to appeal this decision to the Court of Appeals or higher. My attorney is confident that we will prevail once a reasonable judge who knows and enforces the laws of our state hears this case. The injustices Greyson, Gwyneth, John and I have suffered are beyond anything I could have dreamed of. Now $30,000 later (my initial attorney fees) and six months down the road, the picture I see of the foreseeable future includes courts, attorneys, doctors and a strangely smirking man who used to be my husband; it also includes two children who have been needlessly damaged at the hands of a judge who empowered their reckless, malice-intending father to carry out the heinous act of forcing an overdose of contaminated and dangerous vaccines on our once perfectly healthy and bright children. It is important to understand that our particular case here in Arizona is one of hundreds all over the country. This same plot is playing all over the nation and those who decide to make the informed choice to abstain from vaccination are subject to having their decision challenged in court by a non-custodial parent, legal guardian or a social worker. And, because the court is the state and the state is recommending the vaccines you wish to avoid, it is not difficult to predict which party will prevail in a child custody dispute where unvaccinated children and family court are involved. We are laying a legal foundation that will allow this case to be heard in the Supreme Court of Arizona. If needed, we are prepared to go all the way to D.C. But, more pressing on my heart today is the children’s need for immediate medical attention. Dr. Rae in Dallas, Texas, has agreed to examine and treat both of my children in an effort to help them recover from the damage that has already been caused and to help ward off the potential for future health-related events and consequences. Dr. Rae is one of only three physicians equipped with the diagnostic equipment necessary to accurately assess the extent to which my children’s brains and bodies have been damaged. These vaccine-related injuries prevent Greyson’s pupils from constricting naturally when exposed to light and Gwyneth is beginning to show signs of a learning disability. Both of my children are continually complaining of aches and pains, and sickliness has replaced their previously robust health. If you are passionate about the rights of parents and children to abstain from state sanctioned medical experimentation and are in a position to contribute financially to our family’s case/cause, make your check or money order payable to Wallace R. Nichols. If you prefer your donation be allocated towards the medical expenses involved in my children’s aftercare, please indicate so in the memo area of your check or money order.

From the bottom of our hearts - Greyson, Gwyneth, John and I ... THANK YOU.
In Unity there is Strength, Janet Burton

Getting Enough Omega-3?

Getting Enough Omega-3?
Provided by: DrWeil.com

Q: Your recent article mentioned one's "omega-3 level." How do I measure mine or find what my level is? I'm trying to increase my intake of omega-3s with flaxseed (ground), fish and lentils. -- Shirley

A: Omega-3 fatty acids are special unsaturated fats our bodies need for optimum health. Unfortunately, most Americans are deficient in omega-3s, and as a result are more likely to develop cardiovascular disease, cancer, inflammatory disorders, and mental and emotional problems. Eating foods rich in omega-3s can reduce these risks and also help treat depression, bipolar disorder, autism, and attention deficit hyperactivity disorder.

I don't think there is any practical way to measure your omega-3 levels. If there were, and if they were low, the solution would be to do what you should do anyway: increase your intake. Instead of worrying about what your levels are, try to calculate how much omega-3s your diet provides.

These fatty acids are found principally in oily fish that live in cold water, primarily wild salmon, mackerel, herring, and sardines. Bluefish is also rich in omega-3s as is - to a lesser extent - albacore tuna, but both of these tasty fish are contaminated by mercury and should be avoided.

Other dietary sources of omega-3s include walnuts, flaxseeds and hemp seeds - and the oils extracted from them - as well as soy and canola oils and specially fortified eggs. If you're eating three ounces of fish two to three times a week, as I recommend, snacking on walnuts and adding flaxseeds to cereals and salads you're probably getting enough omega 3s.

A 3-ounce serving of Alaskan salmon or herring contains about 2 grams of omega-3 fatty acids, while 3 ounces of sardines has about 1.3 grams. You can substitute one ounce of walnuts for a serving of fish, or add a tablespoon or two of freshly ground flaxseed or hemp oil to your diet.

These plant sources provide you with alpha linolenic acid, which the body converts to the omega-3s the body needs. The only problem with plant sources of these nutrients is that some people may not be able to convert alpha-linolenic acid to the longer-chain forms that occur in fish, the forms the body needs.

If you are not getting adequate amounts of omega-3 fatty acids in your diet, I recommend taking a good quality fish oil supplement. This is particularly important if you have high cholesterol, diabetes, symptoms of PMS, coronary artery disease or a family history of heart attack or sudden cardiac death, breast cancer, memory loss, depression, insulin resistance, high cholesterol, or rheumatoid arthritis. Distilled fish oils are free of mercury and other contaminants, and some taste quite good. Start with one to two grams a day.
Andrew Weil, M.D. –

Author of:

• Eight Weeks to Optimum Health
• Spontaneous Healing
• The Natural Mind
• The Marriage of the Sun and Moon
• Health and Healing
• Natural Health, Natural Medicine
• From Chocolate to Morphine (with Winifred Rosen)

Bio-Chelat: Chelation Therapy Clinical Trial - US Study

Clinical Investigation of Bio-Chelat(TM) Chelation Therapy

Results of the Bio-Chelat(TM) Clinical Study with Doctors Data Inc.

The clinical study was conducted over a 14 day-period, starting January 6, 2002 and ending April 18, 2002. Only 11 of the 20 participants fully complied with the experimental protocol and completed the Bio-Chelat(TM) clinical study.

Due to the limited number of observations, David Quig Ph.D. of Doctors Data, was unable to perform the appropriate statistical analysis required for a legitimate evaluation of the trial results. The German Bio-Chelat(TM) study utilized blood, while the U.S. study made use of urine and fecal analysis.

In retrospect, and on close review of all data, Target Your Health, Inc. noticeably sees, that the test design was not fully appropriate because of the specific pharmacokinetics of Bio-Chelat(TM). The decision was therefore made to revise the experimental design study, monitor patient compliance more closely, and conduct another clinical trial utilizing blood in conjunction with Doctors Data.

Nevertheless Dr. David Quig of Doctors Data stated: "Although the U.S. study sample was insufficient, it appears that the preliminary data that was collected show that Bio-Chelat(TM), chelation therapy, brought about elimination of heavy metals of the participants."
To understand how the Bio-Chelat(TM) solution differs and works in comparison to other chelators i.e. (DMPS, DMSA,EDTA, etc), following is a summary description of the pharmacokinetics.

Clinic-Pharmacological Data of Bio-Chelat(TM).
Pharmacokinetics: Bio-Chelat(TM) contains a complex-forming agent (EDTA) and an oxidative catalyst. The oxidative catalyst has the following function:1. To oxidize the SH-groups into SO3 2- groups or SH-ions into sulfate. SH-groups or SH-ions are ubiquitous in the GI tract and form very strong bonds with heavy metals.

The bonds of the newly formed SO32-groups or sulfate groups are reduced, thus allowing this very low concentrated (homeopathic) dosage of EDTA to easily bind with the heavy metal ions. In an acidic environment (i.e. stomach, intestines etc), EDTA forms a high complex bond with mercury, cadmium and lead. Because of this, heavy metals coming from the food, teeth roots, bile etc. are chelated and excreted with the feces.

By decreasing the uptake of mercury ions into the blood stream and creating a high electric-magnetic gradient in the GI-tract, new heavy metal ions are pulled from the body into the blood stream and stomach/intestine and excreted (Law of Isotonicity).

One example: When taking Bio-Chelat(TM), (DL) the urine clearly showed an increased amount of Cadmium and Nickel. On the other hand, fecal excretion of Cadmium, Mercury, Lead decreased.Analysis: When Bio-Chelat(TM) is absorbed into the GI tract, heavy metals are chelated and excreted with the feces.

This "clean-up" of the GI tract can last between 24 hours to 1 week and depends on the patient. During this period higher values of excreted heavy metals can be seen. Once the "clean-up" is completed, a lower concentration of heavy metals is then found in the feces. Lesser heavy metals are now absorbed into the blood, creating an imbalance between the blood and the deposits, which then will pull new heavy metals into the blood stream from the deposits, which are then excreted via the urine and feces.

As formulated by Dr. Leman in the German study:
Bio-Chelat((TM), chelation therapy, will indirectly intensify the body's physiologic elimination mechanism of heavy metals. When comparing values prior to Bio-Chelat(TM) intake, due to the minimization of heavy metals into the blood (blood doesn't receive anymore metals from the GI-tract), the balance between heavy metal depots and blood is disturbed, and heavy metals spill over (are pulled) into the blood, and are then discarded via the kidneys and intestines.

An increase in the heavy metal concentration of the urine and feces should not be measurable, because even the blood level of heavy metals should now be inferior compared to the pre-therapeutic level. For long-term therapy, this physiological mechanism can be utilized to eliminate heavy metals.

Final Conclusion
The therapeutic value of Bio-Chelat(TM) in the context of chelators currently on the market is seen as follows:

a) Chelators work relatively fast, but they are also very strong with a relative high washout of important trace elements and a high degree of specific side effects.

b) Bio-Chelat(TM), chelation therapy, works much gentler and is easier as most common chelators.

c) Bio-Chelat(TM) is not suitable for acute care of heavy metal toxicity or a very high toxic ion loads.

d) Bio-Chelat(TM) has its greatest value as a middle and long-term therapy for chronic heavy metal toxicity and especially in preventing heavy metal toxicity through the today's overall heavy metal exposition. For this it is the optimal product.

e) The side effects of Bio-Chelat(TM) are minimal when compared to the overall effect. Those side effects can be totally eliminated through a modification of intake and dose. No associated risks are connected with the use of Bio-Chelat(TM).
Because of this, Bio-Chelat(TM), chelation therapy, is excellent in view of the numerous patients carrying a chronic heavy metal ion load.
It is a necessary solution.

more info at:
http://www.dreddyclinic.com/integrated_med/chelation.htm

Bio-Chelat: Chelation Clinical Trial - German Study

Clinical Investigation of Bio-Chelat(TM)
This investigation was done according to the recommendation of 83/571 EWG, Part IV, dated 11/28/1983 (EG#L332).

Planning, methodology, completion, evaluation and documentation went according to the appropriate principles for clinical drug testing, dated 12/09/1987 (Banz. Page 16-617).
Clinic-Pharmacological Data

1. Pharmacological Dynamics
For this clinical evaluation, a standard dose of 3x20 drops was used and well tolerated by most patients. We recommend taking the chelation solution before meals. With associated dryness of the mouth, follow the solution with water. We also recommended decreasing the dosage to 3x15 or a minimum of 3x10 or 2x15 drops per day when a decrease of saliva was noted. Dryness of the mouth was rarely experienced with the reduced dose and whenever it was an issue, most symptoms disappeared 3-4 weeks after taking the Bio-Chelat(TM).

There was an obvious connection between the release of mercury ions from amalgam fillings using Bio-Chelat(TM) Chelation therapy, and the subsequent depressive effect of this release on the salivary glands. It turns out that the amount of liquid taken by the participant is of particular importance. Participants were instructed to drink a minimum of 2 liters of water per day to ensure adequate mercury excretion by the kidneys. However, not all participants followed the recommendation. Those participants, who drank less increasingly complained of mouth dryness.

The time-relationship-effect concludes that Bio-Chelat(TM) is fast absorbed and its' maximum effect occurs during the first 1-3 hours when the most excretion takes place. Because of this, it is necessary and indicated to take the solution 3 times per day. The increased digestibility after a few weeks concludes that either a tolerance occurs or that the mercury elimination is sufficiently advanced.

To see the chelation effect on the body, blood panels must be assessed (especially calcium, magnesium, zinc as well as heavy metals), to check for toxic consequences within the kidneys and to determine mercury excretion. Also, liver panels to determine metabolic performance and evaluate possible hepatotoxic action of Bio-Chelat(TM). According to the published data, there were no negative responses when observing blood count; life essential mineral concentration also did not change. Only zinc was significantly decreased, and therefore, zinc supplementation should be considered whenever necessary. Thrombocyte count also decreased slightly, while leucocytes increased minimally. On the other hand, mercury levels decreased, as well as other heavy metal ions (lead, cadmium), which is seen as a positive finding.

Specific kidney parameters showed no negative consequences to the kidneys. In regards to the liver panel, we recognized a small insignificant increase of gamma-GT-values. The observed changes in LDH and GOT are not significant. This is most likely because of the increased demand placed on this organ with the excretion of toxic metal ions.

2. Pharmacokinetics and Bio-availability

A pharmacological determination of absorption, distribution, change, and excretion of Bio-Chelat(TM) or its by-products did not occur. This is unusual with homeopathic diluted agents. The optimum dose is a compromise between desired effect on one hand and side effects on the other. Here it was a minimal dose of 3x10 drops and an optimal dose of 3x20 drops. The maximal dose should not be strived for.

3. Effect with continued use
The therapeutic goal of mercury elimination can39;t be achieved in a short time because mercury is either deposited or bound to various organs. A fast mobilization using chelation therapy can bring considerable side effects.

Because of this it is normal and appropriate to take Bio-Chelat(TM) over at least a 3-month time span. Longer time periods are only indicated when, for example, there are mercury extractions, removal of amalgam fillings or new fillings are being placed.

We know that Bio-Chelat(TM) is an excellent solution as long as the mercury concentration in the serum, urine or sputum continues to be high, and there are occasionally new chemical exposures that would make it useful to continue taking the solution daily.

4. Side effects
None are known. In this study, no patient gave such an indication, although it should be mentioned that all participants had a naturopathic medical orientation and do not take pharmaceuticals.

Clinical Therapeutic Data
The results of this study was based on 74 participants and was documented statistically, including side effects. Each patient was questioned about side effects of the chelation therapy during the exit interview. Questions centered on how the solution was taken, as well as how they felt during the trial and how they tolerated the solution. This information is given whenever known.

· All users were clients from the HG Homeopathic Clinic, which is the practices of Drs. Pieper/Bender, Hautzel, Rebien and Schneider, as well as from the dental practices of Drs. Obermayer and Obreschko.

· Testing Method: More than 60 participants were examined, all having mercury-amalgam-fillings; their mercury and heavy metal load was checked and the effects of the Bio-Chelat(TM) on this heavy metal burden.

· Hypothesis: Will Bio-Chelat(TM) reduce this load significantly after taking it for 3 months? For verification and documentation, blood, urine, and sputum examination was used, as demonstrated on the enclosed table. Absorption spectrometry, done at the Diagnostic Center for Mineral Analysis and Spectroscopy (Lowensteinst. 9, Michelrieth), was the specific method used to measure these metals within the serum.

· The company Hormonology produced Bio-Chelat(TM) (a liquid solution enriched with minerals in addition to 100 ml of oxygen). The standard dose recommended by the manufacturing company was 3 x 20 drops/day. It was recommended to take a teaspoon of Bio-Chelat(TM) before meals, followed with water. The dose was modified when necessary for the participant.
· The test was done over a 3-month period. Because it took 3 months to find appropriate test participants, the complete study lasted from January 1, 1995 until July 31, 1995.

· No additional therapies were done or recommended.
· The desired effect was a decrease of the serum mercury, lead, cadmium, and palladium concentrations upon completion of the program.
· Undesirable effects were any associated dryness of the mouth, stomach problems and occasional nausea. These were present in a few cases and Bio-Chelat(TM) was discontinued. Those problems generally decreased after 3-4 weeks. Nevertheless, in a few cases an adjustment of the dosage was necessary. Side effects were generally only noted for 1-2 hours and did not cause any further problems.
· The therapeutic value of the Bio-Chelat(TM) in the context of other chelators that are currently on the market is seen as follows:
Chelators work relatively fast, but they are also very strong with a relative high washout of important trace elements and a high degree of specific side effects.

Bio-Chelat(TM) works much gentler than with most common chelation therapies.

Although during the treatment a significant decrease of the body's heavy metal ion load was seen, this is accomplished without greatly disturbing the mineral and trace element relationships. The reduction of zinc should be looked at with caution and may easily be corrected throughout the treatment.

A small increase in the liver panel is, as mentioned earlier, partly due to the increased load on the liver while eliminating heavy metal ions. In a few isolated cases, it was observed that those values completely approached normal levels within a few days or weeks, particularly when liver supportive and excreting therapies were simultaneously administered. All liver panel values were normal upon completion of the Bio-Chelat(TM) study.

Should a patient have liver damage, and have for example an increased transaminase value, Bio-Chelat(TM) should be given very carefully while evaluating the risks.

Bio-Chelat(TM) is not suitable for acute mercury poisoning or very high new toxic ion loads.Bio-Chelat(TM) has its greatest value as a middle and long-term therapy for sub-acute or chronic mercury toxicity. For this it is the optimal product.

The side effects of Bio-Chelat(TM) are minimal when compared to the overall effect. Those side effects can be totally eliminated through a modification of intake and dose. No associated risks are connected with the use of Bio-Chelat(TM). After discontinuance of the Bio-Chelat(TM) any effects disappear within hours.

Because of this, Bio-Chelat(TM) is an excellent chelation therapy that will fill today's market niche, in view of the numerous patients carrying a chronic toxic mercury and heavy metal ion load. It is a necessary solution for that particular market.

more information at: Chelation

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