Reply #10: You are the one spreading misinformation- and you don't have a case [View All]

[philb]

The expereince of the clinics in all states treating autism is the same. I've posted the statements of the MDs in several of those clinics, what they find is that the kids are virtually all mercury toxic and also with other toxic metals like lead, etc.
And they clearly got the mercury thimerosal from vaccines.
And the experience of the clinics is all the same, regarding outcome. They all improve signif. after metals detoxification and nutritional measures to deal with the metabolic blockages that mercury causes. I've posted documentation from the medical literature that mercury is documented to block virtually all body metabolic processes at very low levels of exposure.
The've done hundreds of thousands of tests by medical labs, and the results were clear. Mercury toxicity. And they've treated thousands and the results are similar.

The test discussed here is widely studied and documented in the medical literature as a test for mercury toxicity. There is scientific consensus on this like most of the other things you keep bringing up. Find me a credible expert who disagrees about this test and what it means.
They find that not only those with autism, but also most with CFS, MS, Lupus, etc. are mercury toxic when they do these tests, though the source is amalgam rather than vaccines and the clinics testing them are often different from these.


J.S. Woods et al, “Urinary porphyrin profiles as biomarker of mercury exposure: studies on dentists”, J Toxicol Environ Health, 40(2-3):1993, p235-; & “Altered porphyrin metabolites as a biomarker of mercury exposure and toxicity”, Physiol Pharmocol, 1996,74(2):210-15, & Canadian J Physiology and Pharmacology, Feb 1996; & M.D.Martin et al, “Validity of urine samples for low-level mercury exposure assessment and relationship to porphyrin and creatinine excretion rates”, J Pharmacol Exp Ther, Apr 1996 & J.S. Woods et al, “Effects of Porphyrinogenic Metals on Coproporphrinogen Oxidase in Liver and Kidney” Toxicology and Applied Pharmacology, Vol 97, 183-190, 1989; & (b) Strubelt O, Kremer J, et al, Comparative studies on the toxicity of mercury, cadmium, and copper toward the isolated perfused rat liver. J Toxicol Environ Health. 1996 Feb 23;47(3):267-83; & (c)Kaliman PA, Nikitchenko IV, Sokol OA, Strel'chenko EV. Regulation of heme oxygenase activity in rat liver during oxidative stress induced by cobalt chloride and mercury chloride. Biochemistry (Mosc). 2001 Jan;66(1):77-82; &(d) Kumar SV, Maitra S, Bhattacharya S. In vitro binding of inorganic mercury to the plasma membrane of rat platelet affects Na+-K+-Atpase activity and platelet aggregation. Biometals. 2002 Mar;15(1):51-7: & (e) A cascade analysis of the interaction of mercury and coproporphyrinogen oxidase (CPOX) polymorphism on the heme biosynthetic pathway and porphyrin production. Heyer NJ, Bittner AC, Echeverria D, Woods JS. Toxicol Lett. 2006 Feb 20;161(2):159-66. Epub 2005 Oct 7.

I don't understand why you keep saying such things since the science and results of the hundreds of thousands of tests by MDs on these thousands of patients is clear and consistent, and I've never seen any evidence that there is credible evidence to the contrary, and you surely haven't presented any. I know that you can't, since the evidence has long been clear and consistent.