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Chelation of Heavy Metals.
BENEFITS of H2O2 and Chelation
- Reduction of liver-produced cholesterol
- Lowered insulin requirements in diabetics
- Lowered blood cholesterol levels
- Reduced high blood pressure
- Normalization of cardiac arrhythmias
- Relief from leg muscle cramps
- Reduction in allergic symptoms
- Normalized weight
- Improved psychological and emotional status
- Enhanced sensory input: better sight, hearing, taste
- Fewer excessive heart contractions
- Lessened varicose vein pigmentation
- Lightened age spots
- Fewer aches and pains, arthritic and otherwise
- Less reliance on pain medication
- Hair loss stopped and reversed
- Reversal of impotence
- Alzheimer's Disease symptoms reversed
- Reduced need for duiretics
- Cold extremities warmed
- Chronic Fatigue Syndrome overcome
- Memory, and mental concentration improved
- Post-cataract surgery vision loss restored
- Cosmetic changes, including more lustrous hair, added eye sparkle, stronger unsplit nails, better skin color, fewer visible wrinkles and a more youthful appearance.
Chelation Therapy
Binding of toxic metals and excretion of them from the body.
EDTA is the main component.
Eat before and after treatment to maintain blood sugar levels.
There are both Long Drip and Short Drip treatments.
Mercury is best eliminated by a Short 10 minute chelation.
EDTA, removes toxic metals, improves circulaton, enhances the immune system and inhibits the creation of "free radicals". Free Radicals are now believed by many scientists to be an important contributing cause of atherosclerosis (hardening of the arteries), cancer, diabetes, alzheimer's and other diseases of aging.
DMPS
Treatment of Mercury Intoxication with Dimercaptopropanesulfonate
International Journal of Pharmaceutical Compounding
Mar/Apr 2005 by Smith, Barry, Golden, Patrick, Pingree, Carrie
http://www.findarticles.com/p/articles/mi_qa4101/is_200503/ai_n13510963
Currently there are several proposed methods of chelation and subsequent removal of mercury from the body, including dimercaptopropanesulfonate, dimercaptosuccinic acid, intravenous vitamin C and edetate.
Mercury also binds to the sulfur in thiol groups in the body, which interferes with protein formation and a variety of enzyme reactions. The most common source of mercury toxicity is amalgam dental fillings, which millions of people possess. The mercury in the fillings interacts with saliva to produce a toxic vapor, which is slowly inhaled over the years. In addition, constant wear breaks off minute pieces of amalgam, which are ingested. Normal bacterial flora converts the inorganic mercury in amalgam to methyl mercury, an organic form of mercury. Mercury toxicity may manifest as vague symptoms, ranging from fatigue, weakness, headache and anxiety to skin irritations and digestive disorders.
The main objective of mercury chelation therapy is to achieve mercury levels of less than 3 pg/g creatinine. Mercury attaches itself to the sulfur in dimercaptopropanesulfonate (DMPS), which forms a mercury-DMPS complex that is removed by renal excretion. It is believed that excretion occurs through the organic anion transporter in the basolateral membrane of the proximal tubule. An estimated 3.8 to 21 pg of mercury leaks from amalgam fillings per day, and DMPS therapy may remove up to 1 mg of mercury per day. Listed below are some of the common side effects reported for dimercaprol, the parent drug of DMPS:5
- Agitation
- Burning sensation of mouth, throat and eyes
- Chest constriction
- Headache
- Nausea
- Tachycardia
- Tingling of extremities
- Vomiting
DMPS is an extracellular chelating agent that was first developed in China. It has a high affinity for mercury, copper and zinc. Once mercury-containing amalgam has been removed, DMPS is used as a challenge test to determine whether or not the patient carries a greater than desirable mercury load.
Interpretation of post-treatment urine tests is difficult because the level of mercury reflected in the urine represents the amount excreted after a single dose of DMPS. Since DMPS remains intracellular, a patient might have a significantly lower total body mercury burden after a series of DMPS treatments, but that same patient may have an elevated value in the follow-up urine test. This reflects that there was likely more intracellular mercury available to be chelated and excreted into the urine after the single follow-up dose of DMPS.
The patients involved in the study exhibited few side effects from DMPS. A few patients complained of nausea or an upset stomach, side effects that appeared to diminish by giving the dose with food. One patient experienced numbness, tingling and burning in the legs, and swelling of the hands, face and ankles; the reaction was considered serious enough to discontinue treatment. Another patient reported swollen lips and a rash but elected to continue treatment. A third patient complained of increased tiredness.
Therapy Costs:
$300 to $110. Regular appointment for small/large peroxide or chelation or EDTA
$150 to $ 75. Introductory interview, consulting.
COMMENT:
If you have either systemic mutated Candida or a FUIRERIA, you may find it necessary to take more hydrogen peroxide treatments than chelation treatments in that you may need the H2O2 more often than once per week.
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