OK, just to put a fork in it and call it done, this means that the fact that the vaccines were not effective at preventing infection, replication, and transmission of the virus were known to the Response Coordinator of the White House Coronavirus Task Force during the Trump administration, and furthermore, Dr. Birx explicitly acknowledged that the clinical trials were not designed to assess whether the genetic vaccines could enable herd immunity (to achieve which requires a product that can block or seriously reduce transmissibility of the pathogen). Therefore, these facts were known by Dr. Birx well before the time when the Washington Post was accusing me of being a liar for stating precisely this truth on the steps of the Lincoln Memorial. Of course Youtube has deleted videos of that speech, but it can still be found on Rumble, and the prepared text is still available here.
Suffice to say, Hope concerning effectiveness of a vaccine using previously untested genetic modification technology is not sufficient justification for federal action to block early treatment options, mandate administration of unlicensed Emergency Use authorized vaccine product candidate to all members of the US Military, mandate administration of said product to airline personnel, mandate administration to federal employees and contractors, mandate administration to hospital employees, and attempting to mandate administration to private sector employees. There is no clause concerning Hope as an indicator of efficacy or effectiveness in the Emergency Use Authorization statute 21 U.S. Code § 360bbb–3.
Just to reinforce the point, the US Constitution does not mention regulation of public health or medical practice as a Federal Government role or responsibility, and therefore the right to manage public health and medical practice practices vests with the States, not with unelected federal bureaucrats such as Dr. Birx and her mentor Dr. Fauci.
There must be accountability and restitution for the damages incurred to those who were mandated by the US Federal Government to receive the unlicensed, Emergency Use Authorized products.
Suffice to say, Hope concerning effectiveness of a vaccine using previously untested genetic modification technology is not sufficient justification for federal action to block early treatment options, mandate administration of unlicensed Emergency Use authorized vaccine product candidate to all members of the US Military, mandate administration of said product to airline personnel, mandate administration to federal employees and contractors, mandate administration to hospital employees, and attempting to mandate administration to private sector employees. There is no clause concerning Hope as an indicator of efficacy or effectiveness in the Emergency Use Authorization statute 21 U.S. Code § 360bbb–3.
Just to reinforce the point, the US Constitution does not mention regulation of public health or medical practice as a Federal Government role or responsibility, and therefore the right to manage public health and medical practice practices vests with the States, not with unelected federal bureaucrats such as Dr. Birx and her mentor Dr. Fauci.
There must be accountability and restitution for the damages incurred to those who were mandated by the US Federal Government to receive the unlicensed, Emergency Use Authorized products.