10/19/2022
The United States has been in a National Public Heath Emergency since Trump was president. His administration issued this proclamation on 1/31/2020. Current President Biden extended that public health emergency yet again. It has been extended several times for 90 days at a clip. We saw current President Biden say in Detroit that the “pandemic is over”. I guess it is not over as the emergency was extended yet again. This is the first small story, the routine extension of the emergency.
Matters To Be Considered: The agenda will include discussions on influenza vaccines, pneumococcal vaccine, meningococcal vaccines, respiratory syncytial virus vaccine, rotavirus vaccine, dengue vaccines, adult immunization schedule, child/adolescent immunization schedule, COVID-19 vaccines and Chikungunya vaccine. Recommendation votes on pneumococcal, adult immunization schedule, child/adolescent immunization schedule and COVID-19 vaccines are scheduled. A Vaccines for Children (VFC) vote on COVID-19 vaccine is scheduled. Agenda items are subject to change as priorities dictate. For more information on the meeting agenda visit https://www.cdc.gov/vaccines/acip/meetings/meetings-info.html .
Why do these two seemingly small stories matter to the average person and why are they related. Under the 2005 Public Readiness and Preparedness Act, vaccine manufacturers are exempt from liability. Nobody to date has won a lawsuit because the burden of proof is willful misconduct. More can be seen about this from RFJ Jr.’s article here. What it basically means is that these products that has been mandated and taken by millions of Americans that have given us no (or very little) protection from Covid and massive amounts of side effects including death, have no liability for these manufacturers (JnJ, Pfizer, Moderna).
If the drug was fully approved and there was no emergency, there would be liability for these manufacturers. Currently there is a health emergency and there is an FDA approved version of these vaccines. The FDA approved versions have not been given in the USA. In the case of Pfizer it is called Comirnaty. You cannot get this FDA approved version in the USA, we are told that it is the same formulation as the EUA’d version, but who really knows.
I am getting to why these stories are related. In 1986 the National Childhood Vaccine Injury Act (NCVIA) of 1986 (42 U.S.C. §§ 300aa-1 to 300aa-34) was signed into law by President Reagan.
According to Wikipedia, “NCVIA's purpose was to eliminate the potential financial liability of vaccine manufacturers due to vaccine injury claims[1] to ensure a stable market supply of vaccines, and to provide cost-effective arbitration for vaccine injury claims.[2] Under the NCVIA, the National Vaccine Injury Compensation Program (NVICP) was created to provide a federal no-fault system for compensating vaccine-related injuries or death by establishing a claim procedure involving the United States Court of Federal Claims and special masters.”
This means if a vaccine gets onto the ACIP recommended childhood vaccine schedule, the liability protection is there for vaccine manufacturers. This may be why they changed the definition of vaccine. So if Biden did not extend the emergency, that he said was over himself, the vaccine manufacturers would have two choices.
The first choice would be to allow the “Comirnaty” in the case of Pfizer to be administered without liability protection because the Public Health Emergency would have been over. The second choice would be to pull the EUA’d vaccine and not allowed any Americans to get the jabs until the ACIP could reinstate their liability protection by adding it to the recommended childhood vaccine schedule. If they chose the second choice, even the Americans that thought nothing is wrong with the shots would start to question why they can’t get the booster or bivalent booster after months of promotion of these products by our governments, the news media, and manufacturers.
Neither of these choices would have been good for Pfizer or Moderna (no one takes the JnJ one anymore). Biden came in and saved the day by extending the emergency to get these shots on the recommended childhood vaccine schedule, thus allowing Pfizer and Moderna to not have to choose between a rock and a hard place.
What does this mean when the ACIP inevitably does quietly add these mRNA shots to the recommended childhood schedule? Thanks to the 10th amendment, all 50 states have to decide to listen to this recommendation by the ACIP or not. Being that less that 10% of kids got these jabs, there will be parents fighting these implementations in all 50 states. The manufacturers won’t really care, they still get their liability protection from the 1986 law. We will start to see the fight as the ACIP will definitely recommend adding these to the schedule. They don’t really care about our kids, they care about Pharma’s bottom line.