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Reference:
Stephanie Seneff at CDC on October 19, 2016
And there are complementary links to further studies at the bottom of the page.
I have added extra line breaks to highlight important points.
I am a senior research scientist at MIT and I am deeply concerned about the autism epidemic we face in America today.
Whatever the CDC puts on the information sheet for the MMR vaccine is of less concern to me than the issue of the CDC shirking responsibility to guarantee that the vaccine is not contaminated with unintended ingredients that may be causing a great deal of harm to children. In particular, I am most concerned about the recent evidence that multiple vaccines, but the MMR vaccine in particular, are contaminated with glyphosate. This is entirely plausible, and, in fact, I predicted it would be true based on the fact that MMR live measles virus is grown on gelatin derived from the ligaments and bones of pigs and cows fed large doses of glyphosate in their GMO Roundup Ready corn and soy feed.
Both Zen Honeycutt and Anthony Samsel have now tested multiple vaccines for glyphosate contamination. Those few vaccines that were free of contamination were not manufactured from live virus grown on gelatin. MMR had at least nine times as much glyphosate as any of the other vaccines. It should be the responsibility of the CDC, not random citizens, to perform such tests.
I have compared the adverse reactions for the MMR vaccine in the recent data in the FDA's Vaccine Adverse Event Reporting System (VAERS) against the earlier data. Specifically, I separated the data into two equal halves, one spanning the years from 1990 to 2002 and the other spanning the data after 2002. Alarmingly, the reactions during the past decade or so are far more acute, statistically, than those in the earlier data. Hospitalization, autism, asthma, eczema, hives, seizures, shortness of breath, anaphylactic shock, hyperventilation, infection, and irregular heart rate were all statistically significantly more common in the latter half of the data. Furthermore, there were 50% more adverse events reported in the latter half.
As far as I am aware, the vaccine formulation has not changed, so I believe that these alarming differences may be explained by glyphosate contamination in the later vaccines.
I want to add that recent research by Anthony Samsel and myself strongly supports the idea that glyphosate's insidious cumulative toxicity to humans is mainly due to its ability to get into proteins by mistake in place of glycine.
This concept of a non-coding amino acid substituting by mistake for a coding amino acid is not novel. In fact, there are at least four known naturally produced toxins that work exactly through such a mechanism: Aze, BMAA, L-canavinine, and glufosinate. Glufosinate, which substitutes by mistake for glutamate, is also a popular herbicide, like glyphosate.
The paper where Anthony Samsel and I present our evidence for glyphosate substitution for glycine is titled, "Glyphosate pathways to modern diseases V: Amino acid analogue of glycine in diverse proteins," and is published in the Journal of Biological Physics and Chemistry 16 (2016) 9-46. I hope members of the CDC will take the time to read this paper and many of the associated 353 references provided therein.
Glyphosate contamination in MMR can be predicted to result in the synthesis of a version of haemagglutinin by the measles virus that is resistant to proteolysis by human immune cells due to glyphosate contamination within the protein.
A series of papers by Prof. Singh et al. at Utah State University have shown convincingly that antibodies to measles haemagglutinin from the MMR vaccine can lead to autoantibodies to myelin basic protein in the brain through molecular mimicry. Such autoantibodies have actually been identified in a large percentage of autistic children who had very high antibody titers to haemagglutinin. I think this may be a major factor in the autism epidemic. Please check out the paper by Vijendra Singh et al, "Abnormal Measles-Mumps-Rubella Antibodies and CNS Autoimmunity in Children with Autism," published in J Biomed Sci 2002;9:359-364.
I attach copies of the two papers referred to above.
Please contact me directly if you would like to learn more about my work.
These are the two downloads referenced by this commentary entry: (no links here)
"Glyphosate pathways to modern diseases V:
Amino acid analogue of glycine in diverse proteins"
and
"Abnormal Measles-Mumps-Rubella Antibodies
and CNS Autoimmunity in Children with Autism"
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