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Showing posts with label Heavy-Metal-Detoxification. Show all posts
Showing posts with label Heavy-Metal-Detoxification. Show all posts

Tuesday, August 26, 2008

INFRARED SAUNAS FOR DETOXIFICATION

Toxins such as sodium, alcohol, nicotine, cholesterol and carcinogenic heavy metals (cadmium, lead, zinc, nickel) accumulate in the body during modern daily life. The body eliminates most toxins naturally by sweating. infrared Heat therapy stimulates the sweat glands that cleanse and detoxify the skin. The heat simply speeds up the body's natural process.

BODY POLLUTION
How to maintain your health and vitality through internal cleansing. Continue Reading >>

Saturday, August 16, 2008

Mercury Detoxification Procedures: Amalgam Fillings

By Dr. William G. Drew

Mercury is linked to the most degenerative diseases known to man. In many cases these diseases are iatrogenic - i.e. diseases caused by inappropriate medical / dental treatment.

Mercury is the second most toxic metal known to man; second only to plutonium. But regardless of ranking, mercury has proven to be the most devastating to the health of mankind through its ability to induce diverse, degenerative diseases. In terms of its toll on human suffering, no other metal comes close. Many common medical and mental problems are known to be linked to, if not caused by mercury toxicity.

The majority of mercury that accumulates in our bodies comes from the "silver" amalgam fillings in our teeth. But mercury can be picked up from numerous other sources including artificial flowers, ammunition cartridges, various chemicals including aldehydes, acetic acid, acetone (as in finger nail polish removers), alcohols (as in spirits and rubbing alcohols), chlorine (as in drinking water and chlorine bleaches), disinfectants, cosmetics, Q-tips, dental appliances, dary cell batteries, dyes, electroplated products, felt hats, gold, inks, vapor lamps, mirrors, pharmaceutical products (drugs), pottery, prints, radio tubes, storage batteries, thermometers, wood preservatives, and others. Continue Reading >>



Chemical & Heavy Metal Cleanse Starter Kit

Chemical & Heavy Metal Cleanse Starter Kit

$149.85
[ learn more ]

Add to Cart

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™.

Friday, August 08, 2008

Holistic Oral Care

Increasing evidence surrounding the potential human and environmental hazards of conventional dental techniques has sparked a flurry of alternatives within traditional dental practice.

Holistic dentistry promotes preventative oral care and maintenance, and an environmental commitment to reducing waste and using non-toxic materials.
The holistic dentist eschews the use of mercury and silver-based amalgam fillings and traditional x-rays, which create waste chromium and require other hazardous processing chemicals, in lieu of safe, biocompatible filling materials and digital imaging. Continue Reading >>



Chemical & Heavy Metal Cleanse Starter Kit

Chemical & Heavy Metal Cleanse Starter Kit

$149.85
[ learn more ]

Add to Cart

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™.

Tuesday, April 15, 2008

Heavy Metal Toxicity and dental fillings removal

Heavy Metal Toxicity can be caused by mercury fillings. This video prepares your dental appointment with a holistic dentist or a general dentistry clinic.Fumes of heavy metal while being removed can make you more sick than ever before. Be prepared.





Chemical & Heavy Metal Cleanse Starter Kit

Chemical & Heavy Metal Cleanse Starter Kit

$149.85
[ learn more ]

Add to Cart

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™.

Monday, May 14, 2007

Doctors Frequently Asked Questions About DMPS

Q: Is it legal to prescribe DMPS?

A: It is considered like any other chemical you would order by prescription to be compounded for a patient.

Q: Is DMPS now FDA approved?

A. No. Its current status is as a bulk chemical that may be used in compounding. It is included on the FDA list of Bulk Chemicals That May Be Used In Pharmacy Compounding. Final approval of the list is still pending. The appearance of DMPS or any chemical on this list in no way should be construed as FDA approval. FDA approval generally infers that a drug has been subjected to clinical trials under an IND application to ascertain its safety and efficacy.

This has not been done in the US with DMPS as of this date. (To our knowledge, Heyl is the only DMPS manufacturer with an IND application on file with the FDA.) You may access additional information on the history and the chemicals under consideration through the internet address – http://www.fda.gov/cder/fdama/draft4.pdf

Q: Can DMPS be used orally?

A: Yes. Oral administration is common in other parts of the world. According to Heyl-Berlin, the leading manufacturer of DMPS, oral capsules are the preferred route of administration in chronic metal intoxication with IV administration being reserved for acute poisoning cases or in instances when oral dosing is not possible.

Q: IS DMPS used for conditions other than metal toxicity?

A. The Heyltex Scientific Monograph lists all the known experiments with DMPS in conditions other than metal toxicity on pages 69-71.

Q: Can I use DMPS with DMSA or other chelators?

A: Many physicians alternate use of DMPS with other chelators such as DMSA and EDTA. Heyl does not recommend this. DMPS should not be administered concomitantly with other chelating agents . NOTE: (The manufacturer’s of DMSA do not recommend mixing their chelating agent with any other chelator. DMSA information in the Physcian’s Desk Reference recommends a 4 week "rest" period after the last dose of DMSA before the initiation of any other chelator).
Q: Can you administer DMPS by the IV drip method?

A: DMPS is a dithiol chemical and as such it oxidizes fairly rapidly once in solution when exposed to ambient air. It also oxidizes rapidly at approximately a pH of 7 or greater, therefore IV drip method would probably not be the best route of administration. There is no scientific evidence that oxidized DMPS is of any value in any condition it may used for.

Q: Can I use DMPS as an admixture in a vitamin C IV formula?

A: Oxidation of DMPS is still of concern in this instance. Sodium bicarbonate is generally added to IV-C solutions to adjust the pH. This may cause oxidation, particularly if administered over the usual 2-3 hour time period for this type of IV. (Vitamin C is a reducing agent, it’s possible that it prevents the oxidation of DMPS but this has not been tested or documented. )

Q: What should I mix DMPS with?

A: Generally DMPS should not be mixed with any other chemical or solution. (ie; other chelating agents, normal saline or sodium bicarbonate). This may change the pH which will cause oxidation of the DMPS. A review of the scientific monograph will reveal that it was never mixed with any other solution.

Q: Does DMPS cross over the blood brain barrier?

A: Animal studies indicated that it does not cross over. It also did not carry metal into the brain of animals.

Q: Does DMPS dissolve amalgams in the teeth?

A: DMPS has been used in Germany for a number of years. There have been no reports of dissolved Amalgams.

Q: Is oral DMPS considered a nutritional?

A: Absolutely not. Under no circumstances should DMPS in any form be considered a nutritional product.

Q: Should everyone with suspected metal toxicity receive DMPS?

A: Not necessarily. Data from various researchers around the world indicate that some people spontaneously excrete toxic metals once the individual has been removed from exposure. In the prescribing of any drug or compound, a physician must consider the risk/benefit ratio and make a decision based upon the clinical and laboratory evidence at hand. Not everyone will benefit from the use of DMPS.

Q: Can DMPS be applied topically or as a suppository?

A: According to leading toxicologists and Heyl scientists, there is no benefit to administering DMPS either topically or rectally. There is no data on the absorption of DMPS by these routes of administration. Also of concern is the pH and air exposure of these preparations and the rate of oxidation of the DMPS. The preferred route of administration is oral.

Q: Can DMPS be given to children?

A: Yes. If children are not yet able to swallow capsules, the powder in the capsule can be mixed with cold orange juice (or some other acidic juice) for ingestion.

Q: What is the protocol for administering DMPS?

A: Heyl does not have their own protocol for administering DMPS. Treatment is left to the clinical judgement of the attending physician. Our monograph lists the various dosing protocols for mobilization of heavy metals by several researchers on pages 109-111. The literature describes IV injections of 3mg/kg BW with a maximum dose of 250mg given every four hours for 24-48 hours in severely poisoned individuals, with follow-up oral dosing for several days to several weeks. Acutely poisoned persons are usually hospitalized. Duration of treatment is determined by the continued monitoring of blood and urine samples for excretion of toxic metals. Each physician, who ascertains in their professional and clinical assessment that their patient would benefit from DMPS, must decide the best route to follow for the individual patient.

Q: If I specifically want a prescription I write for DMPS to be filled with the Heyl product, how can I be sure that this will be done?

A: When writing a prescription for any compound, a doctor may specify the manufacturer of the bulk chemical to be used. You may also want to request a copy of the Certificate of Analysis that is provided by the chemicals’ manufacturer.

more discussion: Forum
· Addiction Forum · Ask the Doctors Forum · Ayurveda Forum · Ayurvedic & Thai Herbs Forum · Colon Cleansing Forum · Dental Forum · Diabetes Forum · Diet Forum · General Cleansing Forum · Hepatitis A, B. C Forum · Integrated Medicine Forum · Live Blood Analysis Forum · Ozone-Oxygen-Forum · pH - Alkaline - Acidity Forum · Weight Loss Forum

Chemical & Heavy Metal Cleanse Starter Kit

Chemical & Heavy Metal Cleanse Starter Kit

$149.85
[ learn more ]

Add to Cart

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™.

Wednesday, January 24, 2007

The Teflon Deception

Evidence continues to mount that perfluorochemical (PFC) emissions from synthetic compounds in non-stick cookware and cleaning products produced by DuPont may cause cancer and other health problems.

In particular, perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS), which cannot be broken down by heat, light, or microbes, have been shown to cause tumors in the pancreas, liver, testicles, thyroid, or mammary glands in animal studies.

Workers involved in manufacturing PFOA were also shown to be three times as likely to die of prostate cancer as those who weren't.

PFC concentrations have been found in the blood of fish, dolphins, seals, sea lions, minks, polar bears, gulls, albatrosses, bald eagles, sea turtles, and dozens more species. PFOA is present in the blood of 90 percent to 95 percent of U.S. residents.

DuPont has never conceded that PFCs cause health or environmental problems, although they have attempted to rein in emissions.

Reference: AlterNet January 2, 2007

Here's Why So Many People are Cooking with Saladmaster...

Handle System

Storage has never been easier with our exclusive, detachable handles. Plus, they provide for convenient stove-to-table service, turning a pan into an elegant serving piece with just a click. Cleanup and storage are a breeze, too! Simply remove the handles and place in the dishwasher or cupboard. Versa Loc handles are safer and 200% stronger than industry standard. Best of all no screws means no more loose handles!

Cooking Surface

Regarding the metal, most cookware sold in stores is an 18/10 grade of steel at best. Because of the softness of this grade of metal, when heated, it expands and the food sticks to the pan. You are then forced to cook with oil and the pan becomes difficult to clean. In addition the natural acids and salts contained in our foods can create a chemical reaction with inferior cooking surfaces.

The cooking surface of Saladmaster® cookware is a 316L surgical stainless steel. It is the highest grade of steel used in the cookware industry. It is non-porous, meaning you can cook without oil and its much easier to clean than regular stainless steel. 316L is safe as it does not react with the natural salts and acids of your food.

'The kind of steel used in most stainless steel cookware is not the best metal in which to prepare foods. Most stainless steel cookware sold in stores is of such a nature as to allow chrome and nickel to bleed out into foods as water and food chemicals react with the walls of the vessels as they are heated. The chrome and nickel salts are retained when ingested. They cannot be eliminated. They build up and in time can create troublesome conditions'. - Dr. Shelton's Hygienic Review -

Heat Distribution

Many consumers believe that if a pan is heavy it is good. It's not the weight that's important, it's how quickly the pan heats up, how well it holds the heat and how well it distributes the heat.
Most products on the market have multiple layers of heat conducting alloys on the bottom of the pan only. This means you have to constantly stir your food. Often people become frustrated with traditionally pots 'n pans because they stick and burn at the bottom where the heat source is. Saladmaster's cooking vessel is designed with 7-layers of steel. It is a perfect marriage of metals that distributes the heat 360 degrees. Providing completely even heat allows your food to cook faster at lower temperatures, without the need of stirring.

Temperature Control

All our stoves and fridges have a means of controlling temperature, why doesn't our cookware have one? Since the nutrition of our food can be damaged by high heat, temperature control becomes an extremely important factor to considering the cookware you want to prepare your food in.

Your vitamins and minerals break down when exposed to temperatures above 200ºF. Common cooking methods such as boiling (212ºF), steaming(232ºF) and micro waving (400ºF) can substantially reduce the vitality of your food.

Saladmasters patented Vapo Valve activates below boiling and below steaming. Because it cooks quickly at low heat it preserves the majority of nutrition in your foods.

more information:
http://www.dreddyclinic.com/integrated_med/integrated_med.htm

Chemical & Heavy Metal Cleanse Starter Kit

Chemical & Heavy Metal Cleanse Starter Kit

$149.85
[ learn more ]

Add to Cart

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™.

Saturday, January 13, 2007

A Comprehensive Review of Heavy Metal Detoxification and Clinical Pearls from 30 years of Medical Practice by Dietrich Klinghardt, MD.,Ph.D

A. Introduction:
Heavy Metals appear in the mammalian system because they have become part of our environment.

We are in a constant exchange with our environment which is goverened by the laws of osmosis.

If mercury is in the fish we eat, over time we have mercury in our system. We cannot keep our system pristine and clean, because we are seperated from our toxic environment only by semi-permeable membranes: skin and mucosal surfaces.

Maintaining relative cleanliness requires a number of inherentdetox systems to work overtime against the osmotic pressure of the incoming toxins. As the toxixity of our environment increases so does the osmotic pressure, pushing the often man- made poisons into our body.

Toxins almost never come alone. They come in synergistically acting package-deals. Mercury alone is toxic. Together with zinc it is many times more toxic, add in a little copper and silver, as in dental amalgam fillings and the detrimental effect to the body increases manyfold.

Together with mercaptan and thioether (dental toxins) the toxic amalgam effects grow exponentially.

Add in a little PCB and dioxin, as in fish, and the illness causing effect of the methyl mercury in fish increases manyfold. Toxicology is to a large degree the study of synergistic effects.

In synergy 1 plus 1 = 100. Heavy metals are primarily neurotoxins. There is a synergistic effect between all neurotoxins which is responsible for the illness producing effect.

Making the neurotoxin elimination a major part of my practice has been an amazing experience.

Many illnesses considered intractable respond when the related issues are successfully resolved.

What are Neurotoxins?

Neurotoxins are substances attracted to the mammalian nervous system. They are absorbed by nerve endings and travel inside the neuron to the cell body. On their way they distrupt vital functions of the nerve cell, such as axonal transport of nutrients, mitochondrial respiration and proper DNA transcription. The body is constantly trying to eliminate neurotoxins via the available exit routes: the liver, kidney, skin and exhaled air.

Detox mechanisms include acetylation, sulfation, glucuronidation, oxidation and others. The liver is most important in these processes. Here most elimination products are expelled with the bile into the small intestine and should leave the body via the digestive tract. However, because of the lipophilic/neurotropic nature of the neurotoxins, most are reabsorbed by the abundant nerve endings of the enteric nervous system (ENS) in the intestinal wall. The ENS has more neurons than the spinal chord. From the moment of mucosal uptake the toxins can potentially take 4 different paths:

1. Neuronal uptake and via axonal transport to the spinal chord (sympathetic neurons) or brainstem (parasympathetics) – from here back to the brain.
2. Venous uptake and via the portal vein back to the liver
3. Lymphatic uptake and via the thoracic duct to the subclavian vein
4. Uptake by bowel bacteria and tissues of the intestinal tract

i) Heavy metals:
mercury, lead, cadmium, iron, manganese and aluminum (are the most common).Common Sources: metallic mercury vapor escapes from dental amalgam fillings (they contain about 50% mercury, the rest is zinc, silver copper, tin and trace metals). Cadmium: car fumes, cigarette smoke , pigment in oil paint Lead: outasing from-paint, residues in earth and food chain from time when lead was used in gasoline, contaminated drinking water Aluminum: cookware, drinking water

ii) Biotoxins:
such as tetanus toxin, botulinum toxin (botox), ascaridin (from intestinal parasites), unspecified toxins from streptococci, staphylococci, lyme disease, clamydia, tuberculosis, fungal toxins and toxins produced by viruses. Biotoxins are minute molecules (200-1000 kilodaltons) containing nitrogen and sulfur. They belong to a group of chemical messengers which microorganisms use to control the host´s immune system, host behaviour and the host´s eating habits.

iii) Xenobiotics (man-made environmental toxins):
such as dioxin, formaldehyde, insecticides, wood preservatives, PCBs etc.
iv) Food Preservatives, excitotoxins and cosmetics:
aspartame (diet sweeteners), MSG, many spices, food colourings, fluoride, methyl-andpropyl -paraben, etc.

Heavy Metal Toxicity
Metals can exist in the body with different kinds of chemical bonds and as different molecules. Mercury appears to be the king-pin in the cascade of events in which metals become pathogenic. Mercury can be present as metallic mercury (HgO), as mercury salt (e.g. mercury chloride – HG+), or as methyl mercury (HG++). Methyl mercury is 50 times more toxic than metallic mercury. Methyl-Hg is so firmly bound to the body that it has to be first reduced to HG+ before it can be removed from the cell. This is achieved with reducing agents (“antioxidants”) e.g. intravenous vitamin C and reduced glutathione.

To remove Hg-Salts or metallic Hg from the outside of the cell, other agents are useful Mercury belongs to a group of metals that oxidize in the presence of sulfur and form compounds with sulfur (sulfhydryl affinitive metals). Methyl mercury is already oxidized to its maximum and bound firmly to sulfur in the different proteins of the body. The following metals belong to the sulfhydryl affinitive group and respond to similar detoxification methods: Copper, arsenic, cadmium, lead, mercury. Aluminum and iron for example would not respond a sulfur compound. Some detox agents have multiple mechanisms by which they bind to metals. The algal organism chlorella has over 20 known such mechanisms.

Other metals oxidize with oxygen. Iron turns to rust when oxidized. Rust is nontoxic to the body, whereas iron is. Iron overdose responds to a chemical called desferoximin (desferal). Aluminum responds to the same detoxification agent. A recent Japanese study showed that Chinese parsley, cilantro, is a powerful elimination agent for aluminum stored in bone and the brain.

Other facts:
· Some metals are extremely toxic, even in the most minute dose, whereas others have very low toxicity, even in high doses. However, dependent on the dose, all metals can become toxic to the body. Iron can cause severe oxidative damage, copper may compromise liver function and visual acuity, selenium and arsenic have been known to be used to murder people and so on.
· Most metals serve a functional role in the body. For example, selenium is needed in the enzyme that restores oxidized glutathione back to its functional form as reduced glutathione. Another important function of selenium is its role as a powerful antioxidant in preventing cancer.
· Some metals have a narrow physiological range. That means the difference between a therapeutic dose and toxic overdose is very small. Selenium is an example of this. Magnesium on the other hand has a wide physiological range and thus is more difficult to overdose.
· Some metals have no physiological function. Mercury, lead, aluminum are in this group. Even the smallest amounts have negative physiological-effects.
· biochemical individuality: some people may react more or less than others to the presence of heavy metals in the tissues. Some people may develop a severe chronic illness after exposure of a few molecules of mercury, whereas others may be more resistant to it. Genetic deficiencies in the enzymes responsible for the formation of the metallothioneins and glutathione production and reduction are examples.

Possible side-effects during heavy metal detox:
Every patient can be affected by metals in two ways:
1. Through their non-specific toxic effects
2. Through the system´s allergic reactions to the neurotoxins
Often these two distinctive types of symptoms cannot be easily distinguished. During a detox program, the patient may also temporarily become allergic to the various substances that help to carry out the toxins. This is based on a physiological mechanism called ‘operant conditioning’.

Every time the detoxifying substance is given, mercury emerges from its hiding places into the more superficial tissues of the body, where mercury can now be detected by the immune system. The immune system however is fooled into thinking that the detoxifying substance itself is the enemy. The immune system now starts to react to the detoxifying substance as if it was the mercury itself. This reaction typically resolves spontaneously after six weeks of not using the detox agent in question. This type of conditioned reflex can also be easily treated with simple techniques e.g. NAET, PK (APN), or by giving the detox substance in a homeopathic dilution for a few days. Often the basal membranes in the kidney will swell as a sign of the allergic reaction, causing low back pain, anuria or inability to concentrate urine.

Neuraltherapy or microcurrent stimulation of the kidneys quickly resolves the issue. Muscle aches indicate the redistribution of toxins into the connective tissue and an insufficient program. Depression, headaches, trigeminal neuralgia, seizures, increased pain levels indicate redistribution of metals into the CNS and an inappropriate detox program. Eye problems and tinnitus that occurs during detox indicates redistribution of metals into these organs and requires selective mobilization from these locations before the program is continued. I use a specific type of microcurrent for this purpose

Some recently published findings related to the metal issue:
Iron/mangnese: A recent paper on Parkinsons disease (Neurology June 10, 2003;60:1761-1766)revealedthat just by eating iron and manganese containing foods such as spinach or taking supplements containing Mn or Fe - the risk of developing PD increased almost 2 fold. This demonstrates that even dietary supplements or organically grown foods are amongst the possilbe culprits in metal toxixity.

Methylmercury:
There are two major sources:
1. mercury escaped from dental amalgam fillings is converted by oral and intestinal bacteria to methylmercury, which then is bound firmly to proteins and other molecules. Methyl mercury crosses the blodd brain barrier and the placental barrier leading to massive prenatal exposure. Earlier studies determined that over 90% of the common body burdon of Hg is from dental fillings. Recent studies show that eating fish is starting to compete with amalgam fillings for the leading position as a risk factor.
2.Seafood
A recent study (JAMA, April 2, 2003;289(13):1667-1674) revealed the following It is estimated that nearly 60,000 children each year are born at risk for neurological problems due to methylmercury exposure in the womb. One in 12 U.S. women of childbearing age have potentially hazardous levels of mercury in their blood as a result of consuming fish, according to government scientists. The U.S.FDA recommends that pregnant women and those who may become pregnant avoid eating shark, swordfish, king mackerel, and tile fish known to contain elevated levels of methylmercury, an organic form of mercury. Nearly all fish contain some amount of methylmercury. Mercury accumulates in the system, so larger, longer-lived fish like shark or swordfish contain the highest amounts of mercury and pose the largest threat if eaten regularly.
The National Center for Policy Research for Women & Families published in May 2003, that the following fish are lowest in methyl mercury:
· Catfish (farmed)
· Blue Crab (mid-Atlantic)
· Croaker
· Fish Sticks
· Flounder (summer)
· Haddock
· Trout (farmed)
· Shrimp
The FDA also recommends these fish as safe to eat:
haddock, tilapia, wild alaskan salmon,and sole

Ethylmercury:
A recent quote from Boyd Haley, PhD: “our latest research clearly points to the ethylmercury exposureas being causal in autism. The tremendous enhancement of thimerosal toxicity by testosterone and the reduction of toxicity by estrogen explains the fact that 4 boys to 1 girl getting the disease and the fact thatthe bulk of severe autistics are boys. Most importantly, this autistic situation clearly shows that exposureto levels of mercury that many "experts" considered safe was capable of causing an epidemic of a neurological disease”.

B. Symptoms
Other authors have tried to specify typical symptoms for each metal. Because of the synergistic effects and simultaneous occurence of several toxins at the same time. The best source of literature on the effects of specific metals on the system are the old homeopathic textbooks ‘materia medica’ (Kent, Boericke).

I prefer to look at a client in a systemic way, not focussing on single issues . A manganese typical symptom (ie violent behaviour) may be a lot more worrysome in a given patient then their particular mercury related symptom (ie insomnia). However, the practical focus of detox should be almost always on the mercury first. If mercury is adressed appropriately, the manganese often leaves the body as a side effect of mercury detox. The opposite is not true.
Any illness can be caused by, or contributed to, or exagerated by neurotoxins. Here is a short list:
· Neurological problems: Fatigue, depression, insomnia, memory loss, blunting of the senses, chronic intractable pain (migraine, sciatica, CTS etc.), burning pain, paresthesia, strange intracranial sensations and sounds, numbness. Autism. Seizure disorder. Hyperactivity syndromes. Premature ejaculation and inorgasmia
· Emotional problems: inappropriate fits of anger and rage, timidness, passivity, bipolar disorder, frequent infatuation, addictions, depression, dark mood, obsession, psychotic behaviour, deviant behaviour, psychic attacks, inability to connect with god, etc.
· Mental problems: memory loss, thinking disorder, messy syndrome (cluttering), loss of intelligence, AD, premature aging
· GI problems: candida, food allergy, leaky gut syndrome, parasites, inflammatory bowel disease
· Orthopedic problems: joint arthritis, persisiting musculo-skeletal pain, fibromyalgia, TMD,recurrent osteopathic lesions
· Immunological disorders (autoimmune diseases, hypothyroid disorders, MS, ALS, Sjogen´s Syndrome, CFIDS, MCS etc.)
· Cardiovascular disorders ( vascular disease, arrythmias, angina, increased heartbeat)
· Cancer –mercury, arsenic, copper etc. can be a trigger
· ENT disorders: chronic sinusitis, tinnitus, glandular swelling,
· Eye problems: macular degeneration (dry and wet), optic neuritis, iritis, deteriorating eye sight, etc.)
· Internal medicine problems: kidney disease, hypertension, hypercholesterinemia, syndrome X
· OB/gyn: difficulties of pregnancy, impotence, uterine fibroids, infertility, etc.
C. Diagnosis:
· History of Exposure: (Did you ever have any amalgam fillings? How much fish do you eat and what kind? A tick bite? etc)
· Symptoms: (How is your short term memory? Do you have areas of numbness, strange sensations,etc)- A complete neurotoxin questionaire is available from AANT@425 462 1777
· Laboratory Testing: direct tests for metals: hair, stool, serum, whole blood, urine analysis,breath analysis
· Xenobiotics: fatty tissue biopsy, urine, breath analysis
· Indirect tests: cholesterol (increased while body is dealing with Hg), increased insulin sensitivity, creatinine clearance, serum mineral levels (distorted, while Hg is an unresolved issue), Apolipoprotein E 2/4, urine dip stick test: low specific gravity (reflects inability of kidneys to concentrate urine), persistently low urine ph (metals only go into solution in acidic environments - which supports detoxing), urine porphyrins
· Autonomic Response Testing: (Dr. Dietrich Klinghardt M.D., Ph.D.)
· BioEnergetic Testing (EAV, kinesiology etc.)
· Response to Therapeutic Trial
· Functional Acuity Contrast Test (measure of Retinal Blood Flow)
· Non-specific neurological tests: upper motor neuron signs (clonus, Babinski, hyperreflexia), abnormal nerve conduction studies, EMG etc . non-specific MRI/CT findings: brain atrophy as in AD, demyelination
· Several ‘challenge tests’ are used today. They generally involve measuring the urine metal content,then administering an oral or iv. mobilizing agent and re-mesuring the metal content in the urine after a few hours. Most well known is the DMPS challenge test: However, there is agreement amongst most researchers, that the urine Hg content does not reflect total body burdon – only the currently mobilizable portion of Hg in the endothelium and kidneys. If nothing comes out, there can still be detrimental but non-responsive amounts of Hg in the CNS, connective tissue and elsewhere.
· I have developed a simple approach that works well. I use autonomic response testing (muscle biofeedback) to determine what metal is stored where and what detox agents would be most suitable for this individual. I obtain a hair sample and have it analyzed. It may or may not show any toxic metals. Metals reach the root of the hair via the blood stream. Hair only can show those metals, that have been in the blood in the last 6 weeks. That means, hair only reflects acute toxicity or recently mobilized metals but not the true body burdon. Then we embark on the detox and mobilizing program. In 6 weeks another hair samle is send to the lab and analyzed. If for example manganese is now high, mercury starting to rise (mostly it is methyl Hg, that is reflected in hair), aluminum is at the same value as before, it means, that this program is starting to mobilize Mn ad Hg, but not Al.

Through minor adjustments and following the client closely, we observe as the levels in the hair may rise for months or years before returning to low or absent levels. That is the end point. At that time biochemical challenges with Ca EDTA, DMPS or DMSA can be valuabe to see if there are still hidden pockets of metals somewhere in the system that have been ovrlooked with the other methods. In general, the hair-mineral analysis is often overinterpreted. Hair minerals are a reflection of the toxic-metal induced distortion in mineral metabolism.

D. Treatment:
Why would we want to treat anyone at all? Is it really needed? Can the body not eliminate these toxins naturally on its own?

First we need to consider a multitude of risk factors, which influence later decisions:
Here is a short list of independent risk factors which can either cause accumulation of metals in an otherwise healthy body - or slow down, or inhibit the bodys own elimination processes.
· Genetics – Several genes are involved in coding for the production of inherent detox mechanisms. Example: ApoE being the major repair protein in neuronal damage and responsible for removing mercury from the intracellular environment.

There are 4 different subtypes, one of them making the individual prone to accumulating Hg: (Danik, M. and Poirier, J. Apolipoprotein E and lipid mobilizatin in neuronal membrane remodeling and its relevance to Alzheimer's disease. In: Brain Lipidsand Disorders in Biological Psychiatry, edited by Skinner, E.R.

Amsterdam:
Elsevier Science, 2002,p.53-66). Also well known and studied are the individual genetic differences in glutathione availability. Several companies in the Integrative Medicine Field are offering genetic testing today. So far my clinical results were not impressive when I based my detox program on genetic testing only.

· prior illnesses (i.e. kidney infections, hepatitis, tonsillitis etc.)
· surgical operations (scars often restrict the detoxifying abilities of whole body sections, such as the tonsillectomy scar with it´s effect on the superior cervical ganglion - restricting lymph drainage and blood flow from the entire cranium)
· medication or ´recreational´ drug use (overwhelming the innate detox mechanisms)
· emotional trauma, especially in early childhood. This issue is huge and almost never appropriately adressed
· social status (poor people may still drink contaminated water)
· high carbohydrate intake combined with protein malnutrition (especially in vegetarians)
· use of homeopathic mercury (may redistribute Hg into deeper tissues)
· food allergies (may block the kidneys, colon etc.)
· the patients electromagnetic environment (mobile phone use, home close to power lines etc.Omura showed that heavy metals in the brain act as micro antennae concentrating damaging electro smog in the brain)
· constipation
· compromise of head/neck lymphatic drainage (sinusitis, tonsil ectomy scars, poor dental occusion)
· number of dental amalgam fillings over the patients life-time, number of the patients mothers amalgam fillings

Detox Methods
There are many considerations in choosing detox agents. After choosing the appropriate agent for the individual client and particular metal and exact chemical form of it, we have to consider the body compartment where the metal is stored.

For example, the algae chlorella is ideal for removing virtually all toxic metals from the gut but has too little effect on mercury stored in the brain. Intravenous glutathione may reach the intracellular environment, even in the brain, but is fairly ineffective in removing mercury from the gut.

Each agent has a primary place of action, which determines when, how much and for how long it is used. Agents that have multiple effects on compounds of different metals in the various body compartments are the basis for our detox program. Most specific agents are used for special situations only.

High protein, mineral, fatty acid and fluid intake
Rationale:
· proteins provide the important precursors to the endogenous metal detox and shuttle agents, such as coeruloplasmin, metallothioneine, glutathione and others. The branched-chain amino acids in cow and goat whey have valuable independent detox effects. Amino acid supplements, especially with a concentrate of brached chain amino acids are valuable.

· Metals attach themselves only in places that are programmed for attachment of metal ions.

Mineral deficiency provides the opportunity for toxic metals to attach themselves to vacant binding sites.

A healthy mineral base is a prerequisite for all metal detox attempts (selenium, zinc, manganese, germanium, molybdenum etc.). Substituting minerals can detoxify the body by itself. Just as important are electrolytes (sodium, potassium, calcium, magnesium), which help to transport toxic waste across the extracellular space towards the lymphatic and venous vessels.

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Chemical & Heavy Metal Cleanse Starter Kit

Chemical & Heavy Metal Cleanse Starter Kit

$149.85
[ learn more ]

Add to Cart

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™.

Sunday, January 07, 2007

Doctor, Am I really Toxic?

May I wish you and your family a prosperous, joyous and healthy New Year! As practitioners, no doubt you often talk about toxicity to your patients. The usual question that I am often asked is: "but how do you know that I am toxic doctor?" Well, unless you have run complex tests on blood, urine and faeces using ICP-MS and GC-MS technology, this is really quite a hard one to answer.

WE ARE ALL TOXIC!
One of the most convincing ways that I have found is to simply say, "but we are all toxic – let me prove it to you!" I then summarize scientific studies that have shown that even newborn babies are toxic with a wide variety of toxins.

Please read the interesting .pdf file entitled BodyBurden: The Pollution in Newborns <http://www.detoxmetals.com/mailing/link.php?id=886e884027> written by the Environmental Working Group in July 2005 - I cetainly found it fascinating and very enlightening.

I have a copy in my waiting room which patients can freely read. In summary, it is a detailed analysis of how blood taken from newborn umbilical cords was shown to contain an average of 287 toxins. Of the 287 chemicals detected, 180 cause cancer in humans or animals, 217 are toxic to the brain and nervous system, and 208 cause birth defects or abnormal development in animal tests.

There are other similar studies that have shown that even blood taken from newborns in Greenland from the Inuit Eskimos are showing levels of mercury, lead, cadmium and even DDT - we all think that the North Pole is squeaky clean, but apparently not!

It is not difficult to extrapolate that if newborn babies just entering this world are so toxic, then certainly we as adults MUST be a lot more toxic. It would not be wrong to say for the majority of people that the longer we are on this planet, the more toxic we will be.

SOLUTION?
So what can we do about it doctor?

Well, first we must develop a "detox consciousness" where we simply accept that we cannot escape from these toxins, whereever we may be on this planet.

Therefore, we need to detoxify in much the same way as we take antixodiants and nutritional supplements to protect us against developing chronic disease.

I usually get most of my patients to follow the "Alkaline Detoxification Diet" <http://www.detoxmetals.com/mailing/link.php?id=886e884024> which is a good, all-body cleanse.

This is usually followed by the Gall Bladder Cleanse <http://www.detoxmetals.com/mailing/link.php?id=886e884026> which is a powerful way of cleaning the liver and toxic bile.

there are two choices – one is to use a synthetic chelator such as DMSA, DMPS or EDTA – I think everyone agrees that these synthetic chelators are quite aggressive and can certainly cause side effects, particularly in children and adults with neurological problems, not to mention the elimination of essential minerals too. So what’s the alternative?

NATURAL CHELATORS?
I would like to bring your attention to a natural heavy metal chelator that is very "gentle" in its action with no side effects. This was a synergistic compound of three natural ingredients, namely Chlorella Growth Factor, Coriandrum sativum and a homaccord of Chlorella vulgaris. None of these individual components worked by themselves when tested in double-blind, placebo controlled trials.

However, when combined, there was a "magic" synergy which showed that this compound could chelate aluminium, antimony, arsenic, cadmium, lead, mercury, nickel, thalium and uranium.

I have attached the double blind, placebo controlled study with 350 people that was conducted on this synergistic formula which is now available to all practitioners who are interested in using natural chelators in their practice. The product is called HMD™ and can certainly be combined with synthetic chelators if one wishes.

ADDITIONAL BENEFITS?
Apart from chelating heavy metals, the HMD™ provides many additional benefits due to its individual components such as a hepato-protective effect, immune modulation, can lower blood sugar, detoxifies other xenobiotics, combats damaging free radicals, enhances production of interferon, accelerates and enhances the re-growth of damaged tissue even when ulcerated, burnt and resistant to other healing modalities, it activates cellular functions and increases metabolism, it normalizes the metabolism of fats, activates protein synthesis and promotes rapid healthy growth in children without adverse side effects.

It also helps to resist the effects of premature aging and encourages the rejuvenation of the body’s own DNA/RNA, thus strengthening and improving hair, skin, and nails.

WHO CAN USE IT?
Basically everyone - even young children with ADHD, autism and other neurological problems that may have been caused by heavy metals. HMD™ can also be used in pre-conceptual care by women considering a child – it can be taken 3-4 months before conception to help reduce the toxic load of the mother. It can be used preventatively for all the family, as well as in cases of known heavy metal toxicity. Basically, everyone should be taking a course as part of their detoxification program at least 3-4 months of each year.

more information's at: chelation


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Chemical & Heavy Metal Cleanse Starter Kit

Chemical & Heavy Metal Cleanse Starter Kit

$149.85
[ learn more ]

Add to Cart

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™.

MERCURY DETOXIFICATION

A. ACUTE POISONING
If you suspect you may have ACUTE metal poisoning, you need to obtain medical help immediately. This is considered a medical emergency. Seek the assistance of a qualified medical toxicologist.


B. AMALGAM REPLACEMENT
The most popular detoxification programs involve amalgam replacement. If you are being poisoned by the metal in your mouth, it makes sense to remove the source. I urge caution here, however. Amalgam replacement is surgery. There are risks.

Many dentists will recommend that you replace your amalgams with plastic composites. Blood tests are available which will measure your reaction to the various materials used. You don't want to replace amalgam with a material to which your body will have an allergic reaction.

I replaced my amalgams with composites, and I would not do it again. The placement of plastic composite fillings is very technique-sensitive. There are several steps involved and each one must be followed meticulously. If the dentist doesn't do it properly, the filling will leak, allowing bacteria to reach the dentin resulting in decay, sensitivity, even pain.

Composites are not known for their longevity. While there are improvements and innovations happening, most composites will last only 5 to 7 years, with some lucky patients keeping them for 10 to 12 years. Then they will have to be replaced. That means more trauma to the tooth. In addition, several competent dentists have told me that composites should not be used on occlusal (biting) surfaces, that these materials are not yet strong enough to bear such pressure, and will wear much more quickly on those surfaces.

My dentist replaced six fillings in two hours, and he did a terrible job. My new dentist will use plastic composites only on nonbiting surfaces, and it takes him an hour and a half to do ONE small filling.

If I had it to do over again, I would not use plastic composites. I would use bonded restorations (manufactured inlays) which are superior to plastic composites for durability and longevity. They are more expensive, and it takes two visits instead of one, but I believe that it is best for the health of the tooth (and the body) in the long run. If you're interested in exploring this further, ask your dentist about Cerac, Targis Vectris or Empress manufactured inlays.

Amalgam replacement involves trauma to the tooth, and the chances of fractures, root canals and extractions. If you must have a root canal, I urge you to investigate the use of biocalix as filling material, rather than gutta percha. Recent research indicates that biocalix discourages the growth of anaerobic bacteria in the canals. This provides some measure of assurance for those concerned about the "focal infection" theory. See bioprobe.com and altcorp.com for the latest research by Dr. Boyd Haley and Dr. Curt Pendergrass on biocalix.

C. DETOXING THE BODY
The science of metal detoxification is still in its infancy. Patients who choose this course of treatment should know that they are engaging in experimental medicine with all of its attendant, and sometimes substantial risks.

Detoxification protocols may involve a diet and supplement program, exercise, saunas, and the use of oral or injectable chelators such as DMSA and DMPS. Some doctors will even use injections of procaine. However, the safety of such injections is the subject of significant controversy.

1. Natural detoxification
Remember that mercury detoxification is in evolution. Researchers are learning and adapting their approaches all the time. My belief is that natural methods are the safest approach. I am not a biochemist or nutritionist, so I refer you to others who know much more than I do about natural detox. I most especially recommend Jeff Clark's website (cfsn.com) and Deborah Baker's website (y2khealthanddetox.com).

Basically, you want to make sure your liver, kidneys and gastrointestinal track are functioning as well as possible. Glutathione is the body's natural mechanism for dealing with mercury, so you want those levels to be high normal. Other dietary and nutrient recommendations will be determined by your own individual needs.

Saunas are encouraged in mercury toxic patients, as mercury levels are elevated in the sweat of such patients. Moderate exercise is also recommended, but I am still learning about this, and will post more as I become better informed.

2. Intravenous vitamin C
Some practitioners will recommend intravenous vitamin C at the time of amalgam replacement and during the course of detoxification. I have found no scientific evidence that such administration can reduce mercury toxicity, although it can provide valuable anti-oxidant effects.

I developed painful kidney stones from intravenous vitamin C. I have no known risk factors for stone formation, and there is no history of kidney stones in my family. So for me, intravenous vitamin C is not the answer.

For more on intravenous vitamin C, see the Safety section on the DMPS page.

3. Procaine
One prominent proponent of "neural therapy" claims that procaine will cause the nerve ganglia to release the metal toxins. What is known is that the "caines" (novocaine, lidocaine, procaine, etc.) are broken down in the body into "anilines". Studies have found anilines to be "aggressive carcinogens". So you want to use as little novocaine as you need in the dentist's office, and look with a healthy suspicion at the use of procaine injections.

4. Synthetic chelators
The primary synthetic chelators are DMSA and DMPS. These chelators are life saving drugs in cases of ACUTE metal poisoning.

For chronic metal poisoning, however, their usefulness only infrequently outweighs the risks. In the opinion of several experts, these should be used only as a last resort. Both are effective heavy metal chelators, but both carry risks of harm. Very often, a patient will recover simply from amalgam replacement, and the appropriate diet and supplement program. If you can, give your body a chance before resorting to these powerful drugs.

more information's:
http://www.dmpsbackfire.com/detox/default.shtml

Chemical & Heavy Metal Cleanse Starter Kit

Chemical & Heavy Metal Cleanse Starter Kit

$149.85
[ learn more ]

Add to Cart

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™.

Saturday, December 23, 2006

MERCURY IS A DEADLY POISON!

It is surprising how the controversy regarding mercury still continues even though the research indicating that it is a lethal poison is accumulating rapidly.

This research has shown how detrimental mercury can be to the developing foetus, the newborn, the developing child and the adult.

My intention here is to present a few research studies that will show the various detrimental effects of mercury at all stages of life.


Is there a correlation between the number of amalgams and the amount of mercury excreted in the urine after provocation?

ABSTRACT:

There is a considerable controversy as to whether dental amalgams may cause systemic health effects in humans because they liberate elemental mercury. Most such amalgams contain as much as 50% metallic mercury.

To determine the influence of dental amalgams on the mercury body burden of humans, we have given volunteers, with and without amalgams in their mouth, the sodium salt of 2, 3-dimercaptopropane-1-sulfonic acid (DMPS), a chelating agent safely used in the Soviet Union and West Germany for a number of years. The diameters of dental amalgams of the subjects were determined to obtain the amalgam score.

Administration of 300 mg DMPS by mouth increased the mean urinary mercury excretion of the amalgam group from 0.70 to 17.2 ug and that of the non amalgam group from 0.27 to 5.1 ug over a 9 hour period.

Two-thirds of the mercury excreted in the urine of those with dental amalgams appears to be derived originally from the mercury vapor released from their amalgams.

Linear regression analysis indicated a highly significant positive correlation between the mercury excreted in the urine 2 hours after DMPS administration and the dental amalgam scores. DMPS can be used to increase the urinary excretion of mercury and thus increase the significance and reliability of this measure of mercury exposure or burden, especially in cases of micromercurialism.

Aposhian, H.V., D.C. Bruce, W. Alter, R.C. Dart, K.M. Hurlbut, M.M. Aposhian, "Urinary Mercury after Administration of 2, 3-dimercaptopropane-1-sulfonic acid: Correlation with Dental Amalgam Score" FASEB J. 6: 2472-2476; (1992).

Can dental mercury release from the mother be detected in the foetus?

ABSTRACT:
In humans, the continuous release of Hg vapour from dental amalgam tooth restorations is markedly increased for prolonged periods after chewing. The present study establishes a time-course distribution for amalgam, Hg in body tissues of adult and foetal sheep. Under general anaesthesia, five pregnant ewes had twelve occlusal amalgam fillings containing radioactive 203Hg placed in teeth at 112 days gestation.

Blood, amniotic fluid, faeces, and urine specimens were collected at 1- to 3-day intervals for 16 days. From days 16-140 after amalgam placement (16-41 days for foetal lambs), tissue specimens were analyzed for radioactivity, and total Hg concentrations were calculated. Results demonstrate that Hg from dental amalgam will appear in maternal and foetal blood and amniotic fluid within 2 days after placement of amalgam tooth restorations.

Excretion of some of this Hg will also commence within 2 days. All tissues examined displayed Hg accumulation. Highest concentrations of Hg from amalgam in the adult occurred in kidney and liver, whereas in the foetus the highest amalgam Hg concentrations appeared in the liver and pituitary glands. The placenta progressively concentrated Hg as gestation advanced to term, and milk concentration of amalgam Hg postpartum provides a potential source of Hg exposure to the newborn. It is concluded that accumulation of amalgam Hg progresses in maternal and foetal tissues to a steady state with advancing gestation and is maintained.Vimy, M.J., Y. Takahashi, and F.L. Lorscheider "Maternal-foetal distribution of mercury (203Hg) released from dental amalgam fillings." Am. J. Physiol. 258 (Regulatory Integrative Comp. Physiol. 27): R939-R945 (1990).

Can in utero exposure to mercury cause behavioural disturbances?

ABSTRACT:

Pregnant rats were either 1) administered methyl mercury (MeHg) by gavage, 2 mg/kg/day during days 6-9 of gestation, 2) exposed by inhalation to metallic mercury (Hg) vapour (1.8 mg/m3 air for 1.5 hours per day) during gestation days 14-19, 3) exposed to both MeHg by gavage and Hg vapour by inhalation (MeHg + Hg), or 4) were given combined vehicle administration for each of the two treatments (control).

The inhalation regimen corresponded to an approximate dose of 0.1 mg Hg/kg/day.Clinical observations and developmental markers up to weaning showed no differences between any of the groups. Testing of behavioural functions was performed between 4 and 5 months of age and included spontaneous motor activity, spatial learning in a circular path, and instrumental maze learning for food reward.

Offspring of dams exposed to Hg vapour showed hyperactivity in the motor activity test chambers over all three parameters: locomotion, rearing and total activity; this effect was potentiated in the animals of the MeHg + Hg group. In the swim maze test, the MeHg + Hg and Hg groups evidenced longer latencies to reach a submerged platform, which they had learned to mount the day before, compared to either the control or MeHg group.

In the modified, enclosed radial arm maze, both the MeHg + Hg and Hg groups showed more ambulations and rearings in the activity test prior to the learning test. During the learning trial, the same groups (i.e., MeHg + Hg and Hg) showed longer latencies and made more errors in acquiring all eight pellets.Fredriksson, A., Dencker, L., Archer, T., Danielsson, B.R. "Prenatal Coexposure to Metallic Mercury Vapor and Methyl Mercury Produce Interactive Behavioral Changes in Adult Rats." Neurotoxicol Teratol., 18(2): 129-34, (1996).

ABSTRACT: The total mercury concentrations in the liver (Hg-L), the kidney cortex (Hg-K) and the cerebral cortex (Hg-C) of 108 children aged 1 day- 5 years, and the Hg-K and Hg-L of 46 foetuses were determined. As far as possible, the mothers were interviewed and their dental status was recorded.

The results were compared to mercury concentrations in the tissues of adults for the same geographical area. The Hg-K (n=38) and Hg-L (n=40) of foetuses and Hg-K (n=35) and Hg-C (n=35) of older infants (11-50 weeks of life) correlated significantly with the number of dental amalgam fillings of the mother. The toxicological relevance of the unexpected high Hg-K of older infants from mother with higher numbers of dental amalgam fillings is discussed. Conclusion: Future discussion on the pros and cons of dental amalgam should not be limited to adults or children with their own amalgam fillings, but also include foetal exposure.

The unrestricted application of amalgam for dental restorations in women before and during the child-bearing age should be reconsidered. Abbreviations: Hg-C total mercury concentration in the cerebral cortex (ng/g wet weight). Hg-K total mercury concentration in the renal cortex (ng/g wet weight). Hg-L total mercury concentration in the liver (ng/g wet weight).Drasch et. al. "Mercury Burden of Human Fetal and Infant Tissues" European Journal of Pediatrics (August 1994).

Can mercury amalgam from lactating mothers affect the foetus in utero?

ABSTRACT: Neonatal uptake of Hg from milk was examined in a pregnant sheep model, where radioactive mercury (Hg203)/silver tooth fillings (amalgam) were newly placed. A crossover experimental design was used in which lactating ewes nursed foster lambs. In a parallel study, the relationship between dental history and breast milk concentration of Hg was also examined.Results from the animal studies showed that, during pregnancy, a primary fetal site of amalgam, Hg concentration is in the liver, and after delivery the neonatal lamb kidney receives additional amalgam Hg from mother's milk.

In lactating women with aged amalgam fillings, increased Hg excretion in breast milk and urine correlated with the number of fillings or Hg vapor concentration levels in mouth air.It was concluded that Hg originating from maternal amalgam tooth fillings transfers across the placenta to the fetus, across the mammary gland into milk ingested by the newborn and ultimately into neonatal body tissues.

Comparisons are made to the U.S. minimal risk level recently established for adult Hg exposure. These findings suggest the placement and removal of "silver" tooth filings in pregnant and lactating humans will subject the fetus and neonate to unnecessary risk of Hg exposure.Vimy, M.J., Hooper, D.E., King, W.W., Lorscheider, F.L., "Mercury from Maternal "Silver" Tooth Fillings in Sheep and Human Breast Milk: A Source of Neonatal Exposure" Biological Trace Element Research, 56:143-52, (1997).

Can heavy metals affect human fertility?

ABSTRACT: Heavy metals have been identified as factors affecting human fertility. This study was designed to investigate whether the urinary heavy metal excretion is associated with different factors of infertility.

The urinary heavy metal excretion was determined in 501 infertile women after oral administration of the chelating agent 2,3-dimercaptopropane-1-sulfonic acid (DMPS). Furthermore, the influence of trace element and vitamin administration on metal excretion was investigated. Significant correlations were found between different heavy metals and clinical parameters (age, body mass index, nationality) as well as gynaecological conditions (uterine fibroids, miscarriages, hormonal disorders).

Diagnosis and reduction of an increased heavy metal body load improved the spontaneous conception chances of infertile women. The DMPS test was a useful and complementary diagnostic method. Adequate treatment provides successful alternatives to conventional hormonal therapy.Gerhard, I., Monga, B., Waldbrenner, A., Runnebaum, B., "Heavy Metals and Fertility" Journal of Toxicology and Environmental Health, Part, A, 54:593-611, (1998).

Is mercury associated with cardiac dysfunction?

OBJECTIVES: We sought to investigate the possible pathogenetic role of myocardial trace elements (TE) in patients with various forms of cardiac failure.BACKGROUND: Both myocardial TE accumulation and deficiency have been associated with the development of heart failure indistinguishable from an idiopathic dilated cardiomyopathy.

METHODS: Myocardial and muscular content of 32 TE has been assessed in biopsy samples of 13 patients (pts) with clinical, hemodynamic and histologic diagnosis of idiopathic dilated cardiomyopathy (IDCM), all without past or current exposure to TE.

One muscular and one left ventricular (LV) endomyocardial specimen from each patient, drawn with metal contamination-free technique, were analyzed by neutron activation analysis and compared with

1) similar surgical samples from patients with valvular (12 pts)and ischemic (13 pts) heart disease comparable for age and degree of LV dysfunction;

2) papillary and skeletal muscle surgical biopsies from 10 pts with mitral stenosis and normal LV function, and

3) LV endomyocardial biopsies from four normal subjects.

RESULTS: A large increase (>10,000 times for mercury and antimony) of TE concentration has been observed in myocardial but not in muscular samples in all pts with IDCM.

Patients with secondary cardiac dysfunction had mild increase (< or = 5 times) of myocardial TE and normal muscular TE. In particular, in pts with IDCM mean mercury concentration was 22,000 times (178,400 ng/g vs. 8 ng/g), antimony 12,000 times (19,260 ng/g vs. 1.5 ng/g), gold 11 times (26 ng/g vs. 2.3 ng/g), chromium 13 times (2,300 ng/g vs. 177 ng/g) and cobalt 4 times (86,5 ng/g vs. 20 ng/g) higher than in control subjects.

CONCLUSIONS: A large, significant increase of myocardial TE is present in IDCM but not in secondary cardiac dysfunction. The increased concentration of TE in pts with IDCM may adversely affect mitochondrial activity and myocardial metabolism and worsen cellular function.Frustaci A, Magnavita N, Chimenti C, Caldarulo M, Sabbioni E, Pietra R, Cellini C, Possati GF, Maseri A. Department of Cardiology, Catholic University, Rome, Italy. "Marked elevation of myocardial trace elements in idiopathic dilated cardiomyopathy compared with secondary cardiac dysfunction." From: J Am Coll Cardiol 1999 May;33(6):1578-83

Can dental mercury provoke an increase in antibiotic-resistant bacteria in oral and intestinal flora?

ABSTRACT: In a survey of 640 human subjects, a subgroup of 356 persons without recent exposure to antibiotics demonstrated that those with a high prevalence of Hg resistance in their intestinal floras were significantly more likely to also have resistance to two or more antibiotics. This observation led us to consider the possibility that mercury released from amalgam ("silver") dental restorations might be a selective agent for both mercury- and antibiotic-resistant bacteria in the oral and intestinal floras of primates.

Resistances to mercury and the several antibiotics were examined in the oral and intestinal floras of six adult monkeys prior the installation of amalgam fillings, during the time they were in place, and after replacement of the amalgam fillings with glass ionomer fillings (in four of the monkeys). The monkeys were fed an antibiotic-free diet, and fecal mercury concentrations were monitored.

There was a statistically significant increase in the incidence of mercury-resistant bacteria during the 5 weeks following installation of the amalgam fillings and during the 5 weeks immediately following their replacement with glass ionomer fillings. These peaks in incidence of mercury-resistant bacteria correlated with peaks of Hg elimination (as high as 1mM in the faeces) immediately following amalgam placement and immediately after replacement of the amalgam fillings.

Representative mercury-resistant isolates of three selected bacterial families (oral streptococci, members of the family Enterobacteriaceae, and enterocaocci) were also resistant to one or more antibiotics, including ampicillin, tetracycline, streptomycin, kanamycin, and chloramphenicol. While such mercury- and antibiotic-resistant isolates among the staphylococci, the enterococci, and members of the family Enterobacteriaceae, have been described, this is the first report of mercury resistance in the oral streptococci.

Many of the enterobacterial strains were able to transfer mercury and antibiotic resistances together to laboratory bacterial recipients, suggesting that the loci for these resistances are genetically linked.

Our findings indicate that mercury released from amalgam fillings can cause an enrichment of mercury resistance plasmids in the normal bacterial floras of primates. Many of these plasmids also carry antibiotic resistance, implicating the exposure to mercury from dental amalgams in an increased incidence of multiple antibiotic resistance plasmids in the normal floras of nonmedicated subjects.

Summers, A.O., J.Wireman, M.J. Vimy, F.L. Lorscheider, B. Marshall, S.B. Levy, S. Bennett, and L. Billard, "Mercury Released form Dental "Silver" Fillings Provokes an Increase in Mercury- and Antibiotic-Resistant Bacteria in Oral and Intestinal Floras of Primates", Antimicrobial Agents and Chemotherapy, (April 1993), pages 825 - 834.

Are there increased blood mercury levels in patients with Alzheimer's Disease?

SUMMARY: Alzheimer's disease (AD) is a common neurodegenerative disorder that leads to dementia and death. In addition to several genetic parameters, various environmental factors may influence the risk of getting AD.

In order to test whether blood levels of the heavy metal mercury are increased in AD, we measured blood mercury concentrations in AD patients (n=33), and compared them to age-matched control patients with major depression (MD) (n=45), as well as to an additional control group of patients with various non psychiatric disorders (n=65). Blood mercury levels were more than two fold higher in AD patients as compared to both control groups (p=0.0005, and p=0.0000, respectively). In early onset AD patients (n=13), blood mercury levels were almost three fold higher as compared to controls (p=0.0002, and p=0.0000, respectively).

These increases were unrelated to the patients' dental status. Linear regression analysis of blood mercury concentrations and CSF levels of amyloid B-peptide (AB) revealed a significant correlation of these measures in AD patients (n=15, r=0.7440, p=0.0015, Pearson type of correlation).

These results demonstrate elevated blood levels of mercury in AD, and they suggest that this increase of mercury levels is associated with high CSF levels of AB, whereas tau levels were unrelated. Possible explanations of increased blood mercury levels in AD include yet unidentified environmental sources or release from brain tissue with the advance in neuronal death.C. Hock, G. Drasch, S. Golombowski, F. Muller-Spahn, B. Willershausen-Zonnchen, P. Schwarz, U. Hock, J.H. Growdon, R.M. Nitsch "Increased Blood Mercury Levels in Patients with Alzheimer's Disease" Journal of Neural Transmission, 105: (1998).

Chemical & Heavy Metal Cleanse Starter Kit

Chemical & Heavy Metal Cleanse Starter Kit

$149.85
[ learn more ]

Add to Cart

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™.

Heavy Metals & Health

The word "heavy metal" to most people means a rock band. Heavy metals, however, are one of the most insidious health issues that our society is facing this century, mainly because these nasty toxic metals are just about everywhere on our planet, even in the North and South Poles!

Heavy metal poisoning is so common these days that it is literally impossible to avoid it, as even young newborns have been shown to have heavy metals as soon as they emerge from their mother's womb, as well as receive other metals such as mercury as soon as they are born - from breastfeeding.

A recent report published by Reuters from the Environmental Working Group showed that blood samples of umbilical blood taken by the American Red Cross from ten babies showed an average of 287 contaminants in the blood, including mercury, fire retardants, pesticides and the Teflon chemical PFOA.

Other similar research using neonates born in Greenland, has shown that even in this region of the world which we tend to think as being pristine clean, these babies had mercury, lead, and arsenic in their blood!

If babies are not born with heavy metals they can obtain them immediately when they start to breast feed. For example, research has shown a positive correlation between the level of mercury in mother's breast milk and the number of dental amalgams in their mouth.

The mean levels of mercury in milk of amalgam-free mothers was <>
  • detoxmetals
  • chelation


    • Chemical & Heavy Metal Cleanse Starter Kit

      Chemical & Heavy Metal Cleanse Starter Kit

      $149.85
      [ learn more ]

      Add to Cart

      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™.

      Sunday, November 19, 2006

      Rectal Administration of Chelation Therapy

      The newest, easiest, most convenient, and efficacious technique for detoxifying heavy metals out of the body is by means of rectal chelation therapy.

      The method is to self-apply a patented, trademarked and registered, over-the-counter suppository, Detoxamin.

      People exhibiting toxic metal burdens now are able to chelate themselves while sleeping by use of this non-prescription chelator. Merely insert the firm gelatin pill into the rectum, fall asleep, and awaken in the morning partially detoxified.

      Repeat the procedure until laboratory tests show that there is no more metal poison remaining in the body.

      By this suppository method, the main obstacle to intravenous EDTA chelation therapy has been eliminated. Rather than spending three hours or more per infusion session in a clinic, hooked to an IV, you may take less than a minute to rectally insert the suppository of Detoxamin at home before bedtime.

      Since many people cringe at the thought of getting stuck with a needle for twenty or more such IV treatments, use of a suppository eliminates this psychologically stressful and time-consuming obstacle. Rectal rather than IV administration is less invasive, in no way uncomfortable, and generally preferred.

      In comparison, the treatment price of Detoxamin is half the cost of IV chelation therapy and about the same as oral chelation therapy.
      Detoxamin is readily available to the consumer over-the-counter and by mail order (see the Resource section) and to licensed physicians as a prescription strength chelating agent for dispensing from their offices.

      For adults, each suppository is designed to release 750mg of disodium EDTA, directly into the bloodstream through the colon wall. And the suppository comes in a reduced dosage for children suffering from lead poisoning. It is known to do a highly effective job of heavy metal detoxification.

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      Chemical & Heavy Metal Cleanse Starter Kit

      Chemical & Heavy Metal Cleanse Starter Kit

      $149.85
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      Add to Cart

      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™.

      Tuesday, November 14, 2006

      What is EDTA chelation therapy and what is it used for?

      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 Patients
      Psychiatric 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, Mercury
      Suicidal Behaviors

      Copper, Mercury
      Sleep difficulties / disturbances

      Lead, 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

      Aluminum, Mercury
      Loss 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, Lead
      Poor 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 hearingArsenic, Lead, Mercury
      Abnormal 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 walkingMercury
      Problems with intentional movements or imitation

      Mercury
      Abnormal, 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
      Encephalopathy

      Aluminum, Arsenic, Lead, Thallium
      Cerebrovascular disease

      X metals
      Alterations in nerve conduction velocityLead
      Alterations in the spinal cord

      Thallium
      Accumulates in CNS structures

      Aluminum, Mercury
      Abnormal EEGs

      Arsenic, Lead
      Autonomic disturbances

      Copper, Lead, Mercury, Thallium
      Peripheral Nervous System:
      Peripheral neuropathy

      Arsenic, 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, damage

      Arsenic, Copper, Thallium
      Cirrhosis of the liver; hepatitis

      Copper
      Kidney disease; kidney failure

      Arsenic, Lead, Mercury
      Renal toxicity; tubular proteinosis

      Arsenic, Copper, Lead
      Kidney Damage, histological alterations

      Arsenic, Lead
      Cardiovascular System:
      Blood vessel damage

      Arsenic
      Anemia; decreased red blood cell count

      Arsenic, Copper
      Hypertension; 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, pneumoconiosis

      Arsenic, Aluminum
      Nasal ulcers, perforation of the nasal septum
      X metals
      Immune System:
      Increased incidences of Asthma, autoimmune-like symptoms, & allergies

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

      Lead
      Decreased white blood cell countArsenic, Thallium
      Reproductive System:
      Genital abnormalities

      Aluminum, Thallium
      Disturbances in menstrual cycle; menstrual pains

      Copper, Mercury
      Birth defects; premature births; Spontaneous abortion

      Arsenic, Lead, Mercury
      Reproductive dysfunction

      Arsenic, Aluminum
      Other Physical Disturbances:
      Hypotonia or hypertonia; decreased muscular strength

      X metal
      Rashes, contact dermatitis; eczema, itchy/irritating skin

      Aluminum, Arsenic, Copper, Mercury
      Muscle pain; headache; acrodynia; colic

      Arsenic, Copper, Lead, Thallium
      Alopecia (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

      Chemical & Heavy Metal Cleanse Starter Kit

      Chemical & Heavy Metal Cleanse Starter Kit

      $149.85
      [ learn more ]

      Add to Cart

      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™.

      Dr. Group's Secret to Health Kit

      Dr. Group's Secret to Health Kit

      $39.94
      [ learn more ]

      Add to Cart

      Dr. Group's Secret to Health Kit offers simple at-home solutions for cleansing internally and externally thereby reducing toxins, restoring the body's natural healing process, and helping you achieve true health and happiness.

      Advanced Body Cleansing Kit

      Advanced Body Cleansing Kit

      $147.75
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      Add to Cart

      Advanced Body Cleansing Kit with Livatrex™, Oxy-Powder®, Latero-Flora™ and two bottles of ParaTrex®.