CHILDHOOD ILLNESS PREVENTED BUT AT WHAT COST?

How do we define good health? Is it being vaccinated against every imaginable disease? Or is it having a healthy immune system that is able to function appropriately when required?

Do we really need to protect our children from every known childhood illness at the possible cost of damaging the immune response to such an extent that the child suffers a lifelong battle with diabetes, asthma, psoriasis, systemic lupus etc? Is this a real possibility?

For those of us who can recall the days when children regularly caught measles, mumps, chicken pox, rubella etc. there is something that simply doesn’t add up nowadays. Today’s children might be protected from childhood illnesses but the amount of allergies, food intolerances and auto-immune issues were unknown in previous generations. I recovered from all the above just as my schoolmates did. In contrast I cannot recall sickly schoolmates on special diets or medication. Why is this?

Research into auto-immune disease accidentally revealed that auto-immune responses appeared after several vaccinations.

The Most Damning Vaccination Study not Publically Disclosed to Date

By Paul Fassa – Natural News –

There have been reports from epidemiological studies confirming  suspicions that those who are vaccinated often don’t do as well with long-term  health as those who are vaccination free. Those epidemiological studies  (statistical surveys) have shown that bad health is more common among the  vaccinated who survive without serious injury than children not  vaccinated. But how and why has not come under controlled animal lab  studies until Japan’s Kobe University animal lab study of  2009. This study was reported and peer reviewed in the PLOS One Open  Journalat the end of 2009, but has not received much if any public  attention. It was brought to public’s attention very recently by homoeopathist  and health writer Heidi Stevenson’s article on her Gaia Health blog. (Source  below)

Japanese study summary

Here’s the conclusion quoted from the Kobe  University study’s journal report: “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.) The initial  purpose of this independently funded study was to understand how autoimmune  diseases develop from autoimmunity. It was not an effort to prove vaccination  safety or danger. The researchers used mice that were bred to avoid  autoimmune diseases and injected them with solutions that contain antigens.  Antigens generate antibodies to protect against invading disease pathogens.  Antibodies can turn against the host if they become self generated, causing  autoimmune diseases. A vaccination  injects cultured vaccine antigens of weakened or dead viruses to create an  immune response of antibodies to that antigen, supposedly for creating immunity  to that particular disease. It’s not very unusual for cytokine storms (immune system  overreactions) to overwhelm one who has been vaccinated. Vaccine adverse  reactions have caused injuries of permanent disability, autism spectrum  disorders, or death more often than publicly disclosed. The Kobe  researchers injected the mice that were bred to not develop autoimmune diseases  repeatedly with antigens, much like vaccinations are administered to infants and  children, to study how an  immune system could turn on itself to create autoimmune diseases. They  were pushing the mice’s immune systems to see if and when they would no longer  bend, but break. They used Staphylococcus entertoxin B (SEB) as their  injected antigens. The study report did not mention including any  toxic adjuvants or preservatives such as mercury, aluminum, or formaldehyde  used in vaccines. Antigens were used without the toxic additives normally used  in vaccinations. 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. 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. (Source below)

Conclusion

This study should put to rest the notion that “greening”  vaccines, that is removing or withholding vaccines’ normal toxic additives,  would make the childhood vaccination schedule of close to 40 vaccinations by 18  months of age more agreeable. The Kobe animal trials demonstrated how  autoimmune reactions were created as a consequence of repeated antigen only inoculations with long enough breaks between each injection to allow  complete recoveries. Autoimmune diseases have increased in quantity and  variety as childhood vaccination schedules increased and more vaccines were made  available for naive recipients. Even infectious diseases that vaccines are  supposed to immunize against have appeared among the vaccinated more often than  publicly admitted. The very basis of creating immunity with even  “greened” vaccinations is worse than false, it is actually  unhealthy. Sources for this article include: Heidi’s  article: http://gaia-health.com The Japanese study’s journal  report: http://www.plosone.org Antigens explained: http://en.wikipedia.org/wiki/Antigen Recommended  vaccination schedule for children to age six: http://aapredbook.aappublications.org About the  author: Paul Fassa is dedicated to warning others about the current  corruption of food and medicine and guiding others toward a direction for better  health with no restrictions on health freedom. You can visit his blog at http://healthmaven.blogspot.com

http://www.naturalnews.com/036806_vaccination_studies_side_effects_immune_system.html#ixzz23eMUyJlA

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