Dear Mr. HHS Secretary,
Please make these bold moves
LIMIT COVERED PERSONS
Under their government contracts, both Pfizer and Moderna are “protected from liability under a declaration issued under the PREP Act, or a successor COVID-19 PREP Act Declaration of equal or greater scope.”
One solution to avoid a breach of contract between Moderna and Pfizer and the DOD/HHS would be to take away immunity for all other covered persons —Distributors, Pharmacies, Schools, Localities. Then, the products will just sit there (or be administered at their own risk).
(A)Flexibility of period
The [HHS] Secretary may, in describing periods under paragraph (2)(B), have different periods for different covered persons to address different logistical, practical or other differences in responsibilities.
The Secretary has unfettered power to make this call.
No court of the United States, or of any State, shall have subject matter jurisdiction to review, whether by mandamus or otherwise, any action by the Secretary under this subsection.
The Covid-19 Emergency ends December 31, 2029. This emergency protection cannot end (yet) but it can certainly be modified.
STOP HHS FROM DECLARING THAT ALL EUA VACCINES ARE SAFE AND EFFECTIVE
All Covid-19 vaccines are not safe and effective. Children’s COVID-19 vaccines are only EUA which means they ‘may be effective,’ as they have not undergone the safety testing required to permit licensing.
There are still no licensed COVID-19 vaccines available for children under 12, so all COVID-19 vaccines given to young kids are EUA products.
The FDA’s website on EUA for medical products states that EUA vaccines only have to meet the standard of “may be effective” as long as if, “based on the totality of the scientific evidence, it is reasonable to believe that the product may be effective for the specified use.”
“The ‘may be effective’ standard for EUAs provides for a lower level of evidence than the ‘effectiveness’ standard that FDA uses for product approvals,” the website states.
Before a vaccine can be fully licensed, the vaccine maker typically is required to conduct numerous clinical trials to demonstrate that the product is safe. However, the safety requirements for EUA are more flexible.
CANCEL MODERNA’S $590M AWARD to speed the development of mRNA vaccines against potential pandemic flu viruses and other emerging infectious diseases (to design up to four other novel pandemic flu vaccines and do the phase 1 clinical studies).
On January 17, 2025, HHS stated that the award was made to speed the development of an H5N1 avian flu mRNA vaccine that matches the strains circulating in cows and birds and expand its clinical data that would support the use of mRNA vaccines, if needed, against other flu strains that have pandemic potential.
Please pause all mRNA technology.
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Radically transparent safety monitoring will make the point of how many people die. But, it is within your power to stop most of it before it happens, sir.
Ray L. Flores II
This amount, or any amount, is rediculous. No gov funds should be spent on a product that maims and kills. I am almost 89 and have not had vaccines in decades, even though I was warned I should 0pdue to my age. One of the reaslons that I HAVE LIVED TO THIS AGE IS BECAUSE I avoid assaults on my immune system with vaccines and phatmaceuticals.
That all sounds good Ray. I have a question, maybe you can answer it: Since the Pfizer “vaccine” that went through clinical trials and received FDA approval were manufactured by a different process than the Comirnaty product that was actually injected into the arms of the public is there possibly grounds for claim of fraud? The two products are not the same.