Heavy Metals and Toxicity in the Body

What are the signs or symptoms of heavy metal toxicity? Symptoms of heavy metal toxicity include mental confusion, pain in muscles and joints, headaches, short-term memory loss, gastrointestinal upsets, food intolerances/allergies, vision problems, chronic fatigue, and others. The symptoms are so vague that it is difficult to diagnose based on symptoms alone. Read more

Everyone today is exposed to heavy metals and toxic chemicals

Everyone today is exposed to heavy metals and toxic chemicals. Particularly for slow metabolizers, a very good method to detoxify the body is the far-infrared sauna. Its dry, warming energy is highly compatible with the human body. It heats the tissues several inches deep, enhancing metabolic processes. Read more

Heavy Metals Can Taint Wine

(HealthDay News) -- The cardiac benefits of wine have been touted for years, but heavy metal contamination found in some European red and white wines could turn a health benefit into a hazard, British researchers report.

Heavy metals have been linked to neurological problems such as Parkinson's disease and may also increase oxidative stress, which can lead to chronic inflammatory disease and cancer, the researchers noted.

"We used literature reports of concentrations of metals in wines originating from 16 countries to determine the Target Hazard Quotients (THQ) for these wines," said lead researcher Declan Naughton, a professor of biomolecular sciences at Kingston University in South West London. "Many of the wines gave very high THQ values, which is concerning."

Among wines from Portugal, Austria, France, Spain, Czech Republic, Hungary, Germany, Serbia, Argentina, Brazil, Italy, Jordan, Macedonia, Slovakia and Greece, only three countries had wines that posed no hazard from heavy metals.

Based on the wines analyzed, only those from Argentina, Brazil and Italy had THQ values that were below 1.0.

The report was published in the Oct. 30 online edition of Chemistry Central Journal.

For the study, Naughton and his colleague Andrea Petroczi used the THQ, a formula developed by the U.S. Environmental Protection Agency to look for seven heavy metals in wines. These included vanadium, copper, manganese, nickel, zinc, chromium and lead.

Naughton and Petroczi found that most wines had THQ values much higher than 1.0. In fact, THQ values typically ranged from 50 to 200. Red and white wines from Hungary and Slovakia reached THQ levels of 300.

"For consumption of 250 mL (8.5 oz.) daily, these wines give very high THQ values and may present detrimental health concerns through a lifetime," Naughton said.

Because heavy metals can pose a health threat, Naughton and Petroczi recommend that levels of metal ions should appear on wine labels. "This would help inform customer choice," Naughton said. "In addition, where necessary, further steps should be introduced to remove key hazardous metal ions during wine production."

No wines from the United States were included in the study, so it is not possible to tell the heavy metal content of wines produced in this country. One critic of the study does not think U.S. wines contain dangerous levels of heavy metals.

"The U.S. [Alcohol and Tobacco] Tax and Trade Bureau routinely performs market basket surveys in the U.S. to test wine and alcohol for a number of components, including heavy metals," explained Gladys Horiuchi, communications manager at the Wine Institute of California.

Joan R. Davenport, a professor of soil science in the Department of Crop and Soil Sciences at Washington State University, thinks a lot more study needs to be done to figure out how these heavy metals are ending up in wine.

"Knowing what I know about not only growing wine grapes but the whole process of turning them into wine and looking at some of the countries where these wines came from, it makes me wonder what may happen in the processing," Davenport said.

A lot of the heavy metals found in the wines in the study, exist in only very small quantities in soil, Davenport said. "The likelihood of that being in the grapes isn't very likely," she said. The contamination could be coming from the metal barrels used in processing the wine, she added.

Davenport isn't worried that these metals are a health problem. "I'm not going to drink any less wine," she said. "Enjoy what you enjoy in moderation. But if you like only Hungarian wine, you might be in more trouble than if you like Argentinean wine."

More information

For more about wine and heart disease, visit the American Heart Association.

THE DANGERS OF TOXIC METALS

by Dr. Lawrence Wilson

Toxic metals comprise a group of minerals that have no known function in the body and in fact are harmful. Today mankind is exposed to the highest levels of these metals in recorded history, thanks to their industrial use and burning of coal, petroleum and incineration of waste material. They affect everyone and are a major cause of illness, aging and even genetic defects.

The study of toxic metals is part of nutrition and toxicology, areas not emphasized in medical schools. For this reason, these important causes of disease are accorded little attention in conventional mainstream medicine. This article focuses on the extent of toxic metal problems ≠ sources of toxic metals, symptoms and how to remove them. Continue Reading >>

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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

Chemical & Heavy Metal Cleanse Starter Kit $149.85 [ learn more ] The Chemical & Heavy Metal Starter Kit was designed by Dr. Group for individuals that are new to the cleansing process, or are simply looking for an easy-to-perform, cost effective cleanse program. The Heavy Metal Starter Kit is comprised of LIFE Detox Foot Patches™, NDF Plus™, and Quantum Zeolite™.

The Secret To Health - Part 1 of 8

The Secret to Health reveals information that has been suppressed by the medical establishment for over 100 years! Learn how you can restore your health, increase your energy and vitality, and take control of your body again!

90% of Disease is Caused by Toxins Entering the Body!

Every single day, your body absorbs millions of toxins from Ngenetically modified foods, pesticides, meat, dairy, soy, white flour, table salt, MSG (monosodium glutamate), microwaved foods, refined sugar, and artificial sweeteners. You also receive toxins from caffeine, alcohol, electromagnetic radiation, heavy metals, parasites, industrial chemicals, and prescription drugs. These impurities contaminate nearly everything we eat, drink, touch, or breathe and they are the root cause of disease!

Did You Know? * You should have three bowel movements every day, not two or three per week! * Constipation and other digestive disorders afflict 1 out of every 5 people in America, with the average person carrying up to 15lbs of impacted waste in their colon ! * Experts estimate 9 out of 10 people have parasites in their bodies and don't know it! * Playing on a typical floor exposes babies' lungs to the equivalent of four cigarettes in the form of contaminants from mold, mildew, and dust mites! * Most pharmaceutical drugs list constipation as a major side effect! * Unnecessary medical procedures and prescription drug use in the U.S. accounts for over 700,000 deaths annually!




More informations here:

• Live_blood Analysis
• Live_Blood_Analysis Darkfield Microscopy Courses
• dark field microscopy
• pleomorphism
• Günther Enderlein

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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.

more information: Chelation

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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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Aluminum

Aluminum toxicity is a serious condition that occurs when a person absorbs excessive amounts of aluminum—a metal that often deposits itself in the brain. Aluminum is the most abundant metallic element in the earth’s crust and is introduced into the body through the digestive system, lungs and skin, before it is absorbed into the tissues.

The highest exposure to aluminum is most frequently due to chronic consumption of aluminum-containing antacid products. Research shows that aluminum builds up in the body over time, creating an increased health hazard as people get older.

Aluminum toxicity can lead to symptoms similar to Alzheimer’s disease and osteoporosis and can impair kidney function. Aluminum toxicity can also lead to colic, rickets, gastrointestinal problems, poor calcium metabolism, anemia, headaches and decreased liver function. A disturbing pattern of aluminum accumulation and interference with normal neurological function appears to be supported in many scientific arenas.

Recent studies suggest that aluminum contributes to neurological disorders such as Alzheimer’s disease, Parkinson’s disease, senile and pre-senile dementia, clumsiness of movements, staggering when walking, and the inability to pronounce words properly. Autopsies, performed on people who have died of Alzheimer’s disease, showed accumulations of up to four times the normal amount of aluminum in the nerve cells of the brain. Levels were especially high in the hippocampus, which plays a central role in memory.

There are also geographical links between Alzheimer’s disease and high aluminum in drinking water. Elevated hair aluminum has been observed in Alzheimer’s patients. Amyotrophic lateral sclerosis, another neurodegenerative disease, may also be linked to aluminum content of water supplies. Behavioral difficulties among schoolchildren have also been associated with elevated levels of aluminum and other neurotoxic heavy metals. Studies show that dyslexic children have higher levels of aluminum in their hair, when compared with controls.

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Cadmium

Cadmium is a widespread heavy metal in the environment and in our bodies. It is very poisonous, and we only excrete cadmium in very small amounts.

Cadmium can cause damage to all types of body cells. By damaging the cell membrane, cadmium increases the permeability of the cells, one of the consequences being that the transfer of other heavy metals into the cells is facilitated. In the acute stage, cadmium intoxication causes enteritis. A slow accumulation of cadmium takes place, mainly in the kidneys; the liver and bones are other important sites for cadmium storage.

Food products account for more than 90 percent of human exposure to cadmium, except in the vicinity of cadmium-emitting industries, according to the Agency for Toxic Substances and Disease Registry. Cadmium has fast uptake through the roots to edible leaves, fruits and seeds. Cadmium builds up in animal milk and fatty tissues. A 1990 study showed that acute cadmium toxicity from food is rare, but chronic exposure at lower levels increases cadmium in certain body organs.

One source of cadmium in our environment, and main reason for cadmium accumulating in the body, is tobacco smoke. One cigarette contains 16-24 mcg. of cadmium of which the body absorbs approximately half. In addition to this, 5 - 10% of the cadmium from our food and other sources is absorbed; therefore, a substantial amount of cadmium is stored in our body system over a number of years.

Prolonged accumulation of cadmium in the body stains the teeth. It can cause damage to the nervous system, decrease the detoxification power of the organism, it can cause high blood pressure and atherosclerosis, damage the immune system; most importantly the antibody production, decrease fertility, cause anemia, emphysema, and cancer.

Increased concentrations of cadmium had been found in the placenta of women who have given birth to children with low birth weight, neural damage, and Down’s syndrome. Children who are exposed to large concentrations of cadmium in their environment often have learning disabilities.

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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.

Chemical & Heavy Metal Cleanse Starter Kit $149.85 [ learn more ] The Chemical & Heavy Metal Starter Kit was designed by Dr. Group for individuals that are new to the cleansing process, or are simply looking for an easy-to-perform, cost effective cleanse program. The Heavy Metal Starter Kit is comprised of LIFE Detox Foot Patches™, NDF Plus™, and Quantum Zeolite™.

Detoxamin CaEDTA Suppositories to Treat Elevated Blood Lead Levels in Children

Detoxamin CaEDTA Suppositories to Treat Elevated Blood Lead Levels in Children
Ted Rozema, MD

Summary: The test results clearly demonstrate the high level of effectiveness of removing lead from the human body with Calcium disodium EDTA rectal suppositories. The effect of lead poisoning on high percentages of the pediatric population is cause for concern.

Lead poisoning is one of the most common and preventable pediatric health problems today. Currently, the primary form of medical intervention consists of expensive and painful CaEDTA intramuscular injection.

The availability of an easily administered effective medical treatment is an important component in controlling the worldwide lead poisoning epidemic.

Introduction: Childhood lead poisoning is one of the most common pediatric health problems in the world today, and it is entirely preventable and reversible.

Enough is now known about the sources and pathways of lead exposure, about ways of preventing this exposure, and about ways of reducing the lead content of the body to begin the efforts to eradicate this disease permanently.

The persistence of lead poisoning, in light of all that is known, presents a singular and direct challenge to public health authorities, clinicians, regulatory agencies, and society. Lead is ubiquitous in the human environment as a result of industrialization. It has no known physiologic value.

Children are particularly susceptible to lead's toxic effects. Lead poisoning, for the most part, is silent: most poisoned children have no symptoms.

The vast majority of cases, therefore, go undiagnosed and untreated. Lead poisoning is widespread. It is not solely a problem of inner city or minority children. No socioeconomic group, geographic area, or racial or ethnic population is spared.

Previous lead statements issued by the Center for Disease Control (CDC) have acknowledged the adverse effects of lead at lower and lower levels. In the most recent previous CDC lead statement, published in 1985, the threshold for action was set at a blood lead level of 25 mcg/dL, although it was acknowledged that adverse effects occur below that level.

In the past several years, however, the scientific evidence showing that some adverse effects occur below levels at least as low as 10 mcg/dL in children has become so overwhelming and compelling that it must be a major force in determining how we approach childhood lead exposure.

It is not possible to select a single number to define lead poisoning. Epidemiological studies have identified harmful effects of lead in children at blood lead levels at least as low as 10 mcg/dL. Some studies have suggested harmful effects at even lower levels, but the body of information accumulated so far is not adequate for effects below about 10 mcg/dL to be evaluated definitively. As yet, no threshold has been identified for the harmful effects of lead.

Because 10 mcg/dL is the lower level of range at which effects are now identified, primary prevention activities are typically directed at reducing children's blood lead levels below 10 mcg/dL or 14 mcg/dL. While the overall goal should be to reduce children's blood lead levels below 10 mcg/dL, there are entrenched reasons for not attempting to do interventions directed at individual children to lower blood lead levels of 10-14 mcg/dL. First, practical medical interventions for children with blood lead levels in this range have previously been unavailable.

Second, the sheer numbers of children in this range would preclude effective case management in established intravenous therapy. Clearly, a simply and effective therapy such as suppository is needed. The single, all-purpose definition of childhood lead poisoning has been replaced with a multi-tiered approach, described in the following table:
CLASS
Blood leadconcentration (mcg/dL)

COMMENT
I 10 A child in Class I is not considered to be lead poisoned. IIA 10-14 Many children (or a large proportion of children) with bloodlead levels in this range should trigger community wide childhood lead poisoning prevention activities.

Children in this range may need to be rescreened more frequently. A decrease in blood lead level would be beneficial. IIB 15-19 Child should receive nutritional and educational interventionsand more frequent screening. If the blood lead level persists inthis range, environmental investigation and intervention should be done.

Non-invasive medical intervention should be done. III 20-44 Environmental evaluation, remediation and a medical examination should take place. Such a child needs pharmacological treatment of lead poisoning. IV 45-69 A child in Class IV will need both medical and environmentalinterventions, including even I.M. chelation therapy. V 69>

A child with Class V lead poisoning is a medical emergency. Medical and environmental managment must begin immediately.

Background: Lead is a poison that affects virtually every system in the body. The risks of lead exposure are not based on theoretical calculations.

They are well known from studies of children themselves and are not extrapolated from data on laboratory animals or high-dose occupational exposure.Since 1970, our understanding of childhood lead poisoning has changed substantially. As investigators have used more sensitive measures and better study designs, the generally recognized level for lead toxicity has progressively shifted downward.

Before the mid-1960's, a level above 60 mcg/dL was considered toxic (Chisholm and Harrison, 1956). By 1978, the defined level of toxicity had declined 50% to 30 mcg/dL.Lower blood lead levels cause adverse effects on the central nervous system, kidney and hematopoietic system. Blood lead levels as low as 10 mcg/dL, which do not cause distinctive symptoms, are associated with decreased intelligence and impaired neurobehavioral development (Davis and Svendsgaard, 1987; Mushak et al, 1989).

The concern about adverse effects on central nervous system functioning at blood lead levels as low as 10 mcg/dL is based on a large number of rigorous epidemiological and experimental studies. Several well-designed and carefully conducted cross-sectional and retrospective cohort studies in many different countries have been conducted (Lansdown et al., 1986; Fulton et al., 1987; Fergusson et al., 1988; Silva et al., 1988; Bergomi et al., 1989; Hansen et al., 1989; Hatzakis et al., 1989; Winneke et al., 1990; Lyngbye et al., 1990; Needleman et al., 1990; Yule et al., 1981; Hawk et al., 1986; Schroeder et al., 1985) Some inconsistencies can be found in the results of these studies, but the weight of the evidence clearly supports the hypothesis that decrements in children's cognition are evident at blood lead levels well below 25 mcg/dL.

No threshold for the lead-IQ relationship is discernable from these data. Recent evaluation of 24 major cross-sectional studies provides strong support for the hypothesis that children's IQ scores are inversely related to lead burden (Needleman and Gatsonis, 1990).According to the Natural Resources Defense Council, blood lead levels as low as 10 mcg/dL, which do not cause distinctive symptoms, are associated with reading and learning disabilities, reduced attention span and behavioral problems.

The ramifications of the proliferation of lead pollution from industrialization combined with the devastating effects of health are sobering. A simple and effective therapy, such as EDTA chelation via suppository, is urgently needed.Methods: A cluster of previously untreated children with high blood lead levels was desired for the purpose of testing the efficacy of Calcium disodium EDTA rectal suppositories to remove toxic metals from the human body. 1.) Determinization of study area: Friends of Lead Free Children, a non-profit organization connected to Columbia University and Fordham University, assisted in the search. A residential neighborhood in Haina, Dominican Republic as selected.

The residential neighborhood was located adjacent to a battery recycling plant. All preliminary testing indicated 100% of residents as markedly toxic with lead.2.) The selection of subjects into the study: Children who had been identified with blood lead levels over 10 mcg/dL were determined in a twenty four (24) hour urine collection by Ion Coupled Plasma Emission Spectroscopy.

Hg. Analysis was determined by cold vapour mercury analysis. 3.) Individual treatment of lead overload: Cautious removal of lead from body depots was achieved through the use of Calcium disodium EDTA rectal suppositories . The use of suppositories provided for the prevention of local corrosive action of toxic metals on mucous membranes.4.) Compensation: Compensation was not paid to subjects; however, no charges were incurred by participants for the drug and laboratory testing.5.) Safety: By determining the concentration of heavy metals in the urine following provocative stimulation, the therapy with EDTA was scientifically determined, providing a safe treatment program.

The study simultaneously provided diagnostic information regarding heavy metal burden as well as a defined treatment protocol for lead toxicity in a pediatric population. EDTA is a substance with low systemic and local toxicity and is generally well tolerated. The drug, per se, has been classified GRAS by the FDA, no cases of anaphylaxis have been reported through the oral administration of EDTA or through its use as a food additive.6.)

Alternative therapies: Alternative therapies were available for the treatment of metal intoxications, including (R,S)-2,3-dimercapto propane-1-sulfonic acid (DMPS) as well as its close standing analog DMSA. A significant advantage of using EDTA suppositories in a pediatric population include:—a) Cooperative binding constant for lead.—b) The suppository route of administration at bedtime was (is) an— easy and acceptable delivery system.—c)

The antioxidant/free radical quenching role of EDTA made it— superior over the other agents available due to the fact that— neurological dysfunction was (is) recognized as a result of free— radical mediated damage.—d) EDTA was already approved for oral administration by the FDA — and is on the GRAS list.—e) EDTA is an ANTIDOTE to counteract the TOXIC action of — lead from the environment.7.) Medical care: Medical care was provided by Universidad de Autonomia de Santa Domingo. In the event of a medical emergency connected with the study, subjects were to contact the appropriate center, but this was never necessary. In addition, all participants could receive product and clinical information by calling: Ted Rozema, M.D., and principal investigator.8.) Data coordination: Data was coordinated and maintained by the principal investigator, all data was statistically analyzed. Information was made available to all appropriate authorities, including IRB of the GLCCM and the FDA.

9.) Clinical laboratory: Clinical laboratory facilities and medical support was provided by AmScot Medical Laboratories, Inc. To ensure the safety and integrity of the study, the following analyses were assessed: — a) Baseline: — Smac 18 with CBC - manual differential Blood lead determination — Urine (24-hour collection) —heavy metals to include: Pb, Cd, Hg, As, Ni, Al — B2 - micro globulin (serum) Anti - TPO Total Ca/Ca2+ Mg/Mg2+ Pt/APTT PTH — b) Provocative EDTA challenge: — Blood lead determination — Urine (9-hour) - heavy metals - Pb, Cd, Hg, As, Ni, Al — B2 - micro globulin (serum) Total Ca/Ca2+ Mg/Mg2+ Pt/APTT PTH —c) Mid-study laboratory evaluation: — Blood lead determination — CBC - manual differential Urine (9-hour) - heavy metals - Pb, Cd, Hg, As, Ni, Al — B2 - micro globulin (serum) — Total Ca/Ca2+ Mg/Mg2+ — Pt/APTT PTH —d) Post study (6 weeks): — Blood lead determination — SMAC 18 with CBC - manual differential — Urine (9-hour) - heavy metals - Pb, Cd, Hg, As, Ni, Al — B2 - micro globulin (serum) — Total Ca/Ca2+ Mg/Mg2+ — Anti-TPO — PTH

Research Protocol: A study to determine the efficacy of Calcium disodium EDTA used as a rectal suppository in removing toxic metals from the human body. Subjects: children with proven lead toxicity (blood lead levels >10mcg/dL). Study design: 1.) Enrollment. 2.) Blood lead levels drawn to enter into study with simultaneous determination of urine lead excretion (total urine minerals - if possible with parental assistance). 3.) Treatment phase. 4.) Placement of a rectal suppository containing 2 grams of Calcium Disodium EDTA nightly for 10 days, then 10 days without EDTA, then placement of the EDTA suppository for 10 days, continue this program for two courses of treatment. 5.) Laboratory determinations:

PRE
AFTER 10 DAYS
AFTER 10 DAYS
AFTER 10 DAYS
BLOOD
XX — Supp
XX — No supp
XX — Supp
XX
URINE
XX — Supp
XX — No supp
XX — Supp
XX

Purpose is to demonstrate gradual reduction of both blood and urine lead levels over time with a simple and cost-effective method. It was anticipated that methods to reduce lead intake would be in place during and after this study. Unfortunately, no environmental mitigation was ever enacted.Specimen Collection Regimen: Pre-study: 1.) Collection of 3 to 5 ml of whole blood in heparinized, lead-free curettes. 2.) Collection of 9 hours of urine.

This was measured from the time the child went to bed until 9 hours later. It was anticipated that the children were not getting up at night to urinate and mother would need to watch to catch the first morning specimen then determine when is the 9 hour point and collect the additional urine to make the complete collectionThis provided a base line for both blood levels and excretion on a daily basis.

Just before the first suppository: 1.) Collection of 1 to 5 ml of whole blood in heparinized, lead-free curettes. 2.) Insertion of the first suppository in the child's rectum, high as possible, just before the child goes to sleep, preferable with the child already in the bed.

The morning after the first suppository: 1.) Collection of 9 hours of urine. This was measured from the time the child went to bed until 9 hours later. It was anticipated that the children were not getting up at night to urinate and mother would need to watch to catch the first morning specimen then determine when is the 9 hour point and collect the additional urine to make the complete collection. The morning before the 10th suppository: 1.) Collection of 3 to 5 ml of whole blood in heparinized, lead-free curettes. The morning after the 10th suppository: 1.) Collection of 9 hours of urine. This was measured from the time the child went to bed until 9 hours later. It was anticipated that the children were not getting up at night to urinate and mother would need to watch to catch the first morning specimen then determine when is the 9 hour point and collect the additional urine to make the complete collection.

The morning of the 19th day: This is the last day without a suppository before the next ten days of suppository administration. 1.) Collection of 3 to 5 ml of whole blood in heparinized, lead-free curettes. 2.) Collection of 9 hours of urine. This was measured from the time the child went to bed until 9 hours later. It was anticipated that the children were not getting up at night to urinate and mother would need to watch to catch the first morning specimen then determine when is the 9 hour point and collect the additional urine to make the complete collection.This gave us a determination of equilibration after no treatment for 10 days.The morning of the 30th day: 1.) Collection of 3 to 5 ml of whole blood in heparinized, lead-free curettes.

The morning after the 30th suppository: 1.) Collection of 9 hours of urine. This was measured from the time the child went to bed until 9 hours later. It was anticipated that the children were not getting up at night to urinate and mother would need to watch to catch the first morning specimen then determine when is the 9 hour point and collect the additional urine to make the complete collection. All specimens were taken to the laboratory of Dr. Conrado Depratt at the Instituto De Quimica of the Universidad Autonoma de Santo Domingo.Results: Average 20 children test data:
BLOOD LEAD LEVELS


Pre-study
66.64
mcd/gL
After 10 days of suppositories
39.09
mcd/gL
After 10 days without suppositories
61.45
mcd/gL
After 10 more days on suppositories
83.67
mcd/gL

URINE LEAD EXCRETION LEVELS


Pre-study
004.23
mcd/gL
After 1st suppository
325.55
mcd/gL
After 10 days of suppositories
061.445
mcd/gL
After 10 days without suppositories
009.04
mcd/gL
After 10 more days on suppositories
022.71
mcd/gL

The data clearly demonstrates that Detoxamin , (EDTA delivered in rectal suppository form), effectively removes lead from children with lead poisoning. The continued high excretion level, after 10 days without Detoxamin is of special interest. Also of special interest is the rebound effect in the blood lead levels. It's degree reflecting the high amount of stored lead in the tissue and bones and the attendant mobilization effect.

Each time the blood lead level was diminished, additional lead was mobilized from the tissues and bones. It was anticipated that methods to reduced lead intake would be in place during and after this study. Unfortunately, no environmental mitigation was ever enacted. Ideally, environmental intervention would have been enforced and the Detoxamin Calcium disodium EDTA rectal suppository therapy would have continued for a 6-month duration. This circumstance was not possible.

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Chemical & Heavy Metal Cleanse Starter Kit $149.85 [ learn more ] The Chemical & Heavy Metal Starter Kit was designed by Dr. Group for individuals that are new to the cleansing process, or are simply looking for an easy-to-perform, cost effective cleanse program. The Heavy Metal Starter Kit is comprised of LIFE Detox Foot Patches™, NDF Plus™, and Quantum Zeolite™.

An End to Prostate Problems?

Breakthrough Detoxification Research Now Being Conducted

California, August 30, 2006. Prostate conditions such as prostatitis, enlarged prostate and prostate cancer are affecting men worldwide. In fact, more than 50% of all men 50 and over suffer from an enlarged prostate (Benign Prostate Hyperplasia or BPH).

The problem gets worse as men age. That’s just one possible prostate condition. Another widespread affliction is prostatitis. It affects younger as well as older men. This week, World Health Products received full Investigational Review Board (IRB) approval to conduct clinical trial on an innovative detoxifying product, Detoxamin®, in conjunction with the antibiotic, tetracycline. Pre-study trials indicate that this combination therapy will reduce or eliminate prostate problems.

The study is slated to begin September 9, 2006 at the Tustin Longevity Center in Tustin, California under the direction of Rita Ellithorpe, MD, a specialist in integrative medicine.

A recent discovery has revealed a minute life form, much smaller than the smallest bacteria. It’s called nanobacteria. Many medical scientists believe these culprits cause hardening of the arteries, kidney stones and other degenerative conditions. These ultra microbes are thought to encase themselves in a shell of calcium.

Researchers involved in this current study have uncovered convincing evidence pointing to nanobacteria forming calcifications or stones on the prostate. These continually growing stones are thought to cause pressure on the prostate giving rise to prostatitis and BPH. Studies suggest that calcium biofilm surrounding the nanobacteria can removed by an amino acid, EDTA, contained in a product called Detoxamin.

The nanobacteria are exposed and then destroyed by tetracycline. This one-two approach of killing the nanobacteria with tetracycline and dissolving the calcium deposits with Detoxamin is the foundation for conducting this study. There is evidence that EDTA also has beneficial results in diminishing hardening of the arteries, atherosclosis. Detoxamin also chelates or binds poisonous heavy metals within deep tissues and enables the body to easily eliminate the toxins through urine and feces. “Our clinical trial will determine if prostate calcifications will either reduce in size or be eliminated altogether.

Furthermore, we will also find out if symptoms decrease or disappear,” says Larry Clapp, PhD, co-investigator and author of Prostate Health in 90 Days.
Toxic heavy metals have been implicated in many diseases of aging from Alzheimer’s, to cardiovascular disease. “I have over 500 patients with a variety of conditions in my practice that I placed on Detoxamin; the reason, because mostly everyone I have tested has a variety of heavy metal build up in their bodies.

Detoxamin is a safe, effective and convenient way to remove these menacing toxins. Therefore, we eliminate the causative agents so that other therapies can work in combination and repair the damage heavy metals cause to cells, tissues and organs,” as stated by Dr. Ellithorpe, the Principle Investigator of the study. This new clinical study supports the use of combination therapy to curtail or eliminate the growing prostate problems.

more information at: Chelation

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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