Editor’s Note: I told People this was the case more than 30 yrs ago when I was a med student. Of course, everyone in mainstream medicine and education thought I was NUTS. Finally, I’m vindicated. Praise God Almighty.
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PLOS ONE: Self-Organized Criticality Theory of Autoimmunity.
If Publicized, this Study Would be a Vaccination Schedule Bombshell
Paul Fassa | Natural Society | November 8, 2013
Several epidemiological surveys show vaccinated children suffer from poorer chronic health more then unvaccinated kids, but it means little to vaccine pushers and advocates.
Well, here is another study which shows how over-stimulating the immune system (through vaccines) inevitably leads to autoimmune diseases.
The Japanese Study Summarized
Here’s the Kobe University study’s conclusion:
“Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host’s immune ‘system’ by repeated immunization with antigen, to the levels that surpass system’s self-organize criticality.” (Emphasis added.)
Ironically, the initial purpose of this independently funded study was to understand how autoimmune diseases develop. It was not originally intended as an effort to prove vaccination safety or danger.
The researchers even used mice that were bred to avoid autoimmune diseases. They were injected with solutions that contained antigens without toxic additives.
Antigens generate antibodies to protect against invading disease pathogens. Antibodies can turn against the host if they become overly and unnecessarily self generated, causing long term autoimmune diseases, such as asthma, food allergies, arthritis, MS, and a host of neurological disorders that plague us much more than infectious diseases.
A vaccination injects cultured vaccine antigens of weakened (attenuated) or dead viruses to create an immune response of antibodies to that antigen, supposedly for creating immunity to that particular disease.
Read: Study Detracting Vaccine-Autism Link Backfires
The researchers injected the mice repeatedly with the antigen Staphylococcus entertoxin B (SEB) with just enough time between each injection to recover from immediate antigen reactions. They wanted to ascertain the specific mechanics of how an immune system could turn on itself to create autoimmune diseases if it was over-stimulated.
Toxic adjuvants or preservatives normally used in vaccines were not part of the study. After seven injections, the mice recovered each time with their immune systems intact. But after the eighth injection, problems with key immunity cells began arising. Looks like “greening” vaccines is useless.
Damaged cells were observed microscopically and showed signs of early autoimmunity. Their immune systems had started to self generate antibodies for autoimmune reactions after repeated antigen inoculations.
As expected, this lab study summarized here has not received much if any public attention. The findings were echoed by others, including retired neurosurgeon and author Dr. Russell Blaylock. He expressed concern over the over-stimulation of young people’s immune systems with repeated antigen vaccinations, even without toxic additives. Here is the video interview.
Conclusion
This study should put to rest the notion that “greening” vaccines by removing or withholding vaccines’ normal toxic additives would make the childhood vaccination schedule of close to 40 vaccinations by 18 months of age more acceptable. It is also a direct challenge to the theory and practice of vaccinations.
With the CDC’s vaccination schedule, human infants and children are usually not given enough “recovery time”, which was allowed for the study mice.
The very basis of creating immunity with even “greened” vaccinations is worse than false, it is actually very unhealthy.