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Here is a detail of the open letter to RFK Jr and his colleagues sent by policy experts disappointed by today's HHS policy direction, and consider the mRNA rulings a betrayal of campaign commitments:
"MAHA is not the possession of Secretary Kennedy, Commissioner Marty Makary, advisor Calley Means, or Surgeon General nominee Dr. Casey Means. MAHA is the voice of millions of desperate parents, many with injured or deceased children. Those furious parents were active before any of you were in office, and their activism will outlast any administration. The MAHA vote, especially of independent moms, is an historic game-changer. Neither MAGA nor the Democrats could have won without this critical swing vote.
We ask you to deliver our actual policy goals in the near term....
1. Ban mRNA/gene therapy-derived technologies for all vaccines, due to definitively demonstrated abject failure regarding safety, efficacy and disease prevention in the real-world setting of over 4 years of deployment and billions of administered doses.
2. Terminate the PREP Act declaration for COVID injections, as there is no emergency.
Extension of this declaration, with its ironclad liability shield for manufacturers and administrators, serves no public health interest whatsoever.
3. Recommend that Congress repeal the PREP Act entirely, due to numerous Constitutional conflicts.
4. Ban pharmaceutical direct-to-consumer advertising, as is the case in every other country except New Zealand.
5. Review and revise current HHS level policies that create perverse incentives for healthcare providers for medical coercion, including but not limited to vaccinations.
6. End conflicts of interest at CDC, FDA, NIH and NIAID.
The FDA has rejected its strongest safety warning for Covid mRNA vaccines despite acknowledging that children were killed by the products.
This news surfaced during a televised Bloomberg interview with FDA Commissioner Marty Makary, who said the agency has “no plans” to apply its strongest safety warning to Covid mRNA vaccines.
In that interview, Makary confirmed that the FDA’s own safety and epidemiology centre had formally recommended a boxed warning — a step reserved, under FDA rules, for drugs with “special problems, particularly ones that may lead to death or serious injury.”
