You Are Part of An Experiment in Consent and Choice By: Stand for Health Freedom via Green Med Info
As summer melts into fall, informed consent is on the line, with FDA approval of the Pfizer vaccine expected by Labor Day. Full approval will usher in changes that will impact our rights. There is no question about this. The question is, though, what can we do about it?
We have seen sporadic covid vaccine mandates by employers, schools, and governments, but many are holding off. The legal footing for mandates is built on sand but still more solid when vaccines are approved rather than authorized. Vaccine approval will trigger mandates across the country in the U.S. military, entire cities, the federal government, college campuses. Education and employment are already being jeopardized by the jab as condition of access. Pfizer’s impending FDA approval has public and private bodies rushing to use mandates to fortify the castle.
Things are changing rapidly. It’s time to draw our line in the sand.
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What does Full Approval Mean?
Full approval eliminates EUA red tape for covid vaccine use. Under full approval a doctor can use discretion in off-label uses like boosters or administrations to younger children. The FDA will grant no more vaccine EUAs because there is a “safe and effective” product on the market. Approval should trigger an end to the EUAs for Moderna and Janssen vaccines, since there would be an approved alternative.
Former FDA chief scientist Jesse Goodman asserts approval and experimental authorization is “not a huge difference, but it is a real difference.” i Other officials have concurred, “[It] is just a matter of degree.” ii
On one hand, they may be right. The FDA approval for the vaccines will not change anything about the science of it, nor does it appear the integrity of the data will be called into question, and Pfizer shots will continue to be injected under a different legal framework.
But on the other hand, the legal differences are like a tsunami that could wipe out human rights in America.
Our Body and the Law
There is no space more sacred than our bodies. This truth is enshrined in American law.
“No right is held more sacred, or is more carefully guarded by the common law, than the right of every individual to the possession and control of his own person, free from all restraint or interference of others, unless by clear and unquestionable authority of law.” This notion of bodily integrity has been embodied in the requirement that informed consent is generally required for medical treatment.” iii (emphasis added) -Supreme Court Justice William Rehnquist
American citizens hold dear the Constitutionally protected right to make informed choices about medical interventions. These natural laws and human rights have been reaffirmed by our Supreme Court time and time again.
It is on these principles, America’s Frontline Doctors filed a lawsuit praying to halt not only EUAs, but also full approval, citing faulty CDC data about safety and efficacy. Without trustworthy data, Americans cannot truly give informed consent, nor properly exercise their right to refusal.
Most Americans do not know how a drug becomes “safe and effective,” yet that information is crucial to assessing its risks and benefits. Here’s a peek at the process.
