Guest guest Posted September 8, 2006 Report Share Posted September 8, 2006 n Wendrow, RE: LABELS (and paradigms) Since neither autism nor Asperger's nor PDD-NOS nor OCD nor ... are " diseases " that one has but rather " conditions " (disorders/syndromes) that are defined by the symptoms displayed, technically no one can " have " them -- they exhibit only exhibit the symptoms of these " conditions, " one appropriate answer may be: " My 'child' has been diagnosed with 'autism' (or 'Asperger's' or 'PDD-NOS' or 'OCD') or, for that matter, 'ADHD,' for example. Current reality seems to indicate that the major " disease " conditions that lead to a diagnosis within the " ASD spectrum " are, in order of approximate percentage [ " ~n% " ], for children who have been given a " complete " differential diagnosis: 1. Mercury (or Mercury plus other heavy metal) poisoning [~80-85%], 2. Viral encephalitis (in the US and the UK, mainly from the measles virus but some instances have also implicated that the varicella virus can be a factor when varicella occurs with measles) [~10%], 3. A named genetic defect (e.g., Fragile X and Rhett) or an unnamed one [~1-2%], 4. Some combination of the preceding [~10% in total], or 5. Unidentifiable [<1%]. Thus, the parents of these damaged children should be proactively changing the paradigm and, AFTER appropriate differential diagnosis, should be initially telling those who ask, using 'autism' as our example: 1. " My 'child' has been mercury poisoned to the point that he has a diagnosis of 'autism,' " or 2. " My 'child' has had a viral encephalitis that has left him with a diagnosis of 'autism' " or 3. " My 'child' has been diagnosed with a 'Fragile X' gene problem that has contributed to a diagnosis of 'autism'. " For children who are in a program and recovering, a parent could say: 1. " My 'child' is recovering from being mercury mercury poisoned but still has a diagnosis of 'autism' (or, when the child improves, 'Asperger's' or 'OCD' or 'PDD-NOS') " , or 2. " My 'child' is recovering from viral encephalitis but still has a diagnosis of _________, " or 3. " My 'child' has been diagnosed with 'Fragile X' but has improved to the point that his (her) current neurodevelopmental diagnosis is ___________. " Based on the approximate frequency of the results of differential diagnostic work-ups that the engaged medical community seems to be finding, most parents should recognize that their children who have been diagnosed (labeled) with " autism " are most probably mercury poisoned (seemingly in ~85% of the cases). For those who are students of history, the current mercury poisoning by drugs (mostly Thimerosal poisoning by Thimerosal-preserved vaccines and serum drugs with contributons by: a. Topical drug products that were finally outlawed in 1998 [OTC topicals containing Thimerosal and Mercurochrome] and b. Thimerosal-preserved ear, eye and throat preparations that are still approved by the FDA) shares many parallels with the previous mercury poisoning by drugs (mostly Calomel poisoning by teething powders and some worming and other preparations): 1. In both cases, these mercury-containing drugs were claimed to be safe WITHOUT any proof of safety, 2. In both cases, the healthcare establishment chose to diaggnosis " causeless " conditions ( " Pink Disease " and " Acrodynia " for the symptoms caused by Calomel-containing drugs; Autism, PDD-NOS, OCD, ADHD, etc. for the symptoms caused by Thimerosal-containing drugs) instead of mercury poisoning. 3. In both cases, the toxicologists raised concerns about mercury poisoning that the healthcare establishment dismissed 4. In both cases, the main target was our developing children. 5 .. In both cases, not all who received the mercury-compound-containing drugs developed the severe adverse health conditions observed and the onset of clinical symptoms occurred after some period of exposure. 6. The symptoms for both types of mercury poisoning are very similar or the same. Apparently, based on the chronological history, Thimerosal was chosen as a " replacement " for Calomel based on a false generalization that " organic mercury compounds " are, as a class, LESS toxic than " inorganic mercury compounds, " principally Calomel, which the American public was increasingly demanding be removed from their medicines or proven safe in the 1930s. Moreover, based on the studies published in the 1930s and 1940s, the marginal perforamnce of a 0.01% Thimerosal level as a preservative and the toxicity of Thimerosal at levels below 20 parts-per-BILLION (0.02 parts-per-MILLION [0.000002% by weight per volume]) to human cells and tissues were clearly established. In both instances, the healthcare establishment continued to claim that the mercury-containing products were safe while refusing to conduct the in-depth toxicological studies to prove what was the safe level. In the Calomel-based mercury-poisoning history, the healthcare establishment steadfastly refused to admit that Pink Disease and Acrodynia were mercury poisoning and simply quietly withdrew the Calomel-laced drugs from products from the market starting in the 1930s and complete in the US by the 1940s (but not until the 1950s in Australia) while quietly introducing the Thimerosal-preserved vaccines and sera and Thimerosal-based antiseptics beginning in the 1930s in the US with, again, UNSUPPORTED claims that these were " safe " and, in the case of antiseptics, that " they 'promoted " healing " even though the scientifically sound independent toxicological data clearly indicated that Thimerosal was not safe at the nominal " 0.01% " level in Thimerosal-preserved drugs much less at the nominal " 0.1% " level in OTC antiseptics and vaginal spermicides. In spite of the lack of proof of safety and FDA study reports in the early 1980s that CLEARLY established that organic-mercury-based antiseptics and vaginal contraceptives were toxic to those exposed to them and that these organic-mercury- based antiseptcs did NOT promote healing but rather caused cell death, it took the FDA until 1998 to ban the use of Thimerosal and other mercury compounds in OTC topical skin products and vaginal contraceptives. However, in spite of the lack of proof of safety, the FDA REFUSED and, to date, continues to REFUSE to: a. Require PROOF of SAFETY or b. Ban all uses of Thimerosal or any other mercury- containing compound in the manufacture of drugs. The US history of the mercury poisoning of children by medicine (using Calomel-laced teething powders and worming preparations) spans the period from the late 1800s to about 1940 (a period of at least 6 decades). The on-going US history of the mercury poisoning of fetuses, babies and children (using Thimerosal- preserved vaccines and sera and other drug products) began in about 1930 and is still continuing (a period that will, if NOT stopped immediately, certainly exceed 8 decades). As was the case with the mercury poisoning of our children and ourselves by inorganic mercury compounds (principally Calomel), our children and ourselves are being mercury poisoned by organic mercury compounds (principally Thimerosal) that continue to be allowed to be used in vaccines and other drugs without PROOF of safety and with PROOF of human neural toxicity CURRENTLY at levels below 0.001 parts-per-million (less than 1 part-per billion; < 0.0000001% Thimerosal [more than 100,000 times lower than the 0.01% level found inm for example, the Thimerosal-preserved human influenza vaccines). Hopefully, after considering this email, the reader will redouble his or her demand that the healthcare establishment either: 1. PROVE safety in the appropriate TOXICITY studies (acute, sub-acute, mult-generational reproductive, and short-, intermediate- and long- term) with a requirement that the minimum safety factor allowed must be 100, or 2. STOP using all mercury compounds in any medical procedure or the manufacture of any medicine. Futhermore, UNTIL the REQUIRED PROOFS of SAFETY and be generated, the reader will DEMAND that the FDA: 1. Suspend the US license and/or approval of all drugs in which any mercury species is used in that drug's manufacture, including use in the manufacture of any component of a drug) and 2. " Request " that all in-date product be voluntarily recalled and held off the US market pending the outcome of the REQUIRED safety testing. Should the TOXICITY studies find that the current products have mercury levels that are toxic to some, then, for products on the market or in the drug-development pipeline, where the drug producers failed to prove safety before submitting an application to the FDA for FDA review and licensing or approval, the American people should demand that the FDA revoke the licenses or approvals and reject with prejudice any such drug product formulations that are under review. In addition, the government should assess each producer of any such mercury-containing drug product a fine of not less than $ 1,000,000.00 for each month a product was on the market (from the day it was licensed or approved), or, if in review by the FDA, not less than $ 100,000.00 for each day a drug submission where mercury-based compounds were used in the production of the drug was in review by the FDA -- with the funds collected earmarked to pay for the care and therapy for the hundreds of thousands of children who have been significantly damaged. In addition, the firms fined should be prohibited from passing these fines on to the American consumers in any manner and barred from advertising any drug they produce until after the fines levied and any interest that might acrue if the fines are paid off under an installment plan have been paid in full. [NOTE: These fines should be applied to all firms for the period of time that they marketed any Thimerosal-containing drug product WITHOUT rigorous proof of safety even when that firm no longer makes any such drugs.] Respectfully, Dr. King http://www.dr-king.com PS: I am still opposed to the CAA bill because it princiaplly funds activities of agencies (NIH and CDC) who have been proven to be involved in the knowing mercury poisoning of Americans starting in the womb. ++++++++++++++++++++++++++++++++++++++++++ At 06:55 9/7/06 -0700, n Wendrow wrote: > > I have noticed that many people refer to >their kids or others as being " Autistic " >as opposed to saying " he/she has Autism " > Labels are very demeaning, and they >seriously affect how others treat a person. >They often imply negative connotations >which in turn lead to negative stereotypical >assumptions being made about the abilities >of the person to whom the label is ascribed. > Just thought for consideration > take care > n > Quote Link to comment Share on other sites More sharing options...
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