Effects of Magnesium Di-Potassium EDTA suppositories on blood chemistry values Spencer Feldman September 2002.
ABSTRACT: Two studies were completed using 21 and 16 patients
respectively measuring the effects of Magnesium Di-Potassium EDTA suppositories on standard blood chemistry values. Liver enzymes remain unchanged.d BUN/creatinine ratios, bilirubin levels and prothrombin times all showed normalization towards optimal values whether initially high or low. 92% of the subjects had an increase in CO2 levels indicating increases in metabolism. We conclude that magnesium di-potassium EDTA suppositories are absorbed, safe and effective. Methods and Materials - EDTA Chelation Therapy21 subjects had their blood drawn, and then they inserted one 333 mg Magnesium Di-Potassium EDTA suppository rectally. 30 minutes later their blood was drawn again. Subjects were told not to change their lifestyle or eating habits. The subjects were then given ten more suppositories and were told to take one per night for ten nights. 11 days later, the subjects had their blood drawn again. Some clients had their blood drawn on the12th day and they were given 2 extra suppositories. Of the 21 subjects initially begun with, 5 did not take a second blood draw. Results Figures one and two show the normalizing effect of the suppository form of Magnesium Di-Potassium EDTA on kidney function. Figures 3 and 4 show that there is no stress to the liver as measured liver enzymes remaining stable. Figure 5 shows a normalizing effect on prothrombin time. Figure 6 shows a global increase in the blood CO2 levels indicating an increase of oxygenation and increase in metabolic efficiency. Figure 7 shows a normalizing effect on bilirubin. Figure 1 shows the change in BUN/creatinine ratios after 10 days. The X-axis represents the original BUN/creatinine ratio; the Y-axis represents the change in that ratio after the Magnesium Di-Potassium EDTA. Figure 2 is the same data with the non-conforming data-point removed. This client’s BUN went from 30 to 18 and her creatinine went from 1.2 to 0.7. While this does not yield a change in the BUN/creatinine ratio it obviously implies an incredible regeneration of kidney function in a short period of time. |
Figure 3 SGOT levels (10 days) Figure 4 SGPT levels (10 days)
Discussion Of Chelation TherapyIn redesigning both the method of administration and the type of ingredient used in chelation, there are two questions to answer, is it safe, and is it effective. Figures one and two show that not only is there no apparent damage to the kidney function, there is actually an improvement as measured by the normalization of the BUN/creatinine ratios. Low values went higher and the high values went lower. In addition, the farther from the norm the values initially were, the greater the change seen towards the norm. I.V. chelation also shows this normalizating effect1 but typically only after an initial and reversible glomerulonephritis. We believe that the smaller and more frequent application of suppository EDTA is safer on the kidneys than the less frequent but more intense therapies given intravenously as evidenced here. Figures three and four show no effect on liver enzymes, further indication of the safety of this protocol. Chelation by suppository with Magnesium Di-Potassium EDTA in
suppository form is both safe and effective and represents a valid alternative
to intravenous chelation with Di-sodium EDTA. In addition, Magnesium
Di-Potassium EDTA also has shown to have certain beneficial effects not
associated with the traditional Di-sodium form of EDTA. References 1 The effect of EDTA chelation therapy and supportive multivitamin/trace mineral supplementation upon renal function. A study in Serum Creatine. E.W. McDonagh, DO, C.J. Rudolph, PhD, DO, and E. Cheraskin, MD, DMD . 2 Balancing body chemistry with nutrition seminars. Third
Revision – January 2000 page 39. The following is a letter
from Dr. Halstead, considered by many to be the father of modern chelation An Open Letter To Whom It May Concern 31 May 2000
I have been involved in the development of the EDTA suppositories since the idea
was first conceived seven years ago. The suppository delivery system was developed because it meets a special need. The primary purpose was to
produce a drug delivery system that was painless and effective for children and for adults that found it difficult to take chelation therapy because of time
constraints. Research studies showed that the uptake of EDTA was effective by the colonic route. The low molecular weight of EDTA of 292.1 facilitates efficient absorption through the colon wall. Moreover, there is an additional safety factor because it is in a special time release formulation. There is clinical evidence available that the suppository is not only safe, but it is effective. It is my professional opinion that approximately 90% or more of the EDTA is absorbed through the colon. For
additional information on this subject it will be helpful to review my book, The Scientific Basis of EDTA Chelation Therapy, by Halstead and Rozema 1977. Keep up the good work. Best Regards, Bruce W. Halstead, M.D. Director |
One reason we don't have a shopping cart page to sell ten thousand of these marvel per day is credibility.
Let's face it - when people make money doing something, only the fewest do so with mutual or universal benefit in mind.
Whether it's Medicardium or DeToxamin, another high-quality natural chelative agent,
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We all take in toxic metals; it's important to remove it safely, non-invasively, and effectively.
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cure or prevent any disease.
They are intended to help strengthen and support
the human body's natural ability to heal
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