The U.S. Food and Drug Administration (FDA) is declaring war on our children and it’s on each of us to be unrelenting as we defend the next generation from Big Pharma and its allies. We must stop the FDA’s attack, beginning with a campaign to end unethical and unsubstantiated Emergency Use Authorizations (EUA) that will subject our younger and most vulnerable children to the unnecessary risks of COVID shots.
The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) is scheduled to meet on four separate occasions in June to discuss additional EUAs that would provide cradle-to-grave COVID shots and consider a “Future Framework” that will permanently lower the bar for safety and efficacy going forward.
Their itinerary is as follows:
June 7 — Emergency Use Authorization for Novavax’s COVID shot for adults.
June 14 — Amendment to Moderna EUA to include primary series to children and adolescents 6 through 17 years of age.
June 15 — Amendment to Moderna’s EUA to include primary series for children 6 months to 5 years and amendment to Pfizer’s EUA to include the primary series to children 6 months through 4 years of age.
June 28 — Proposed “Future Framework” for COVID shots.
Dr. Toby Rogers aptly calls the June meetings a “blitzkrieg” because it is an overwhelming all-out attack (on informed consent) designed to create psychological shock and demoralizing chaos. But we can change the outcome by arming up with real data and creating a blitzkrieg of our own.
We need Defenders like YOU to hold the line and stop the approval of EUA amendments that profoundly impact the health and safety of our kids. Tell VRBPAC members that:
There is no COVID emergency for children.
Children under 18 with no comorbidities have virtually no risk of death from COVID. They have a 99.995% recovery rate and the vast majority of children have minimal symptoms. A study published in Nature described how children between 3 and 11 years of age mount effective, robust and sustained immune responses to COVID. The CDC’s own data show that at least 75.2% of children ages 0 to 11 years and 74.2% of adolescents ages 12 to 17 years already have superior natural immunity.
mRNA shots offer little in the way of protection.
There is no clinically significant health benefit from the mRNA vaccines. Moderna’s own press release acknowledges that “the absence of any severe disease, hospitalization or death in the study precludes the assessment of vaccine efficacy against these endpoints.” Preliminary data showed the shots were only about 44% effective at preventing symptomatic infection in children 6 months to 2 years old, and 37% effective in children ages 2 to 5 years old — both below the 50% level that regulators had generally called the minimum level for EUA approval in 2020. In New York, officials observed that Pfizer’s efficacy against Omicron plummeted from 68% to 12% after 7 weeks in children ages 5 to 11.
Injuries from COVID shots in children are catastrophic.
Vaccinated children face a substantial risk of myocarditis. Moderna’s EUA application, originally filed in June 2021, has already been held up because of a clear safety signal for myocarditis, which has prompted a number of European countries to prohibit its use in young people. Additionally, the Vaccine Adverse Events Reporting System (VAERS) has over 48,500 reports of adverse events in children, including 112 deaths (as of May 20, 2022) and a growing number of reports of encephalopathies, clotting issues, diabetes and neurological issues in children following COVID shots.
The FDA is poised to make decisions regarding our children and the future of this country that may have a devastating impact on children’s health.
Please send a message to FDA and CDC officials, VRBPAC members and elected representatives demanding that they reject the Pfizer and Moderna EUA applications for children and ensure our government agencies are following the science.
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