As expected the FDA announces today that Pfizer has been granted Biologic License Application approval for their COVID-19 vaccine. [Press release Here] and you can find the Approval Letter at the following LINK HERE. The vaccine will now be known as “Comirnaty”, and is approved for individuals 16 years of age and older.
Unfortunately, questions about which specific vaccine regime has been approved still appear to be in conflict with federal health officials. The initial dose and one booster shot appears to have gained FDA approval.
However, how many booster shots are safe? What effect from multiple vaccination booster shots? Those questions left unanswered.
It is unlikely that many people who have done their research into the issues of efficacy and safety will be swayed by this FDA announcement. There are simply too many unknowns. The approval letter outlines dates for ongoing evaluations of safety, most of those dates are several years from now. The studies and outcomes can reverse the approval; however, the adverse impact ramifications cannot be undone once administered.
Everyone has their own perspective on what is in their best interests. Your personal health decisions should be private and respected. As a reminder of my overall view, I share the prior outline below which has not changed since written.
“This is no small thing, to restore a republic after it has fallen into corruption. I have studied history for years and I cannot recall it ever happening. It may be that our task is impossible. Yet, if we do not try then how will we know it can’t be done? And if we do not try, it most certainly won’t be done. The Founders’ Republic, and the larger war for western civilization, will be lost.”
Our Father, who art in heaven, hallowed be thy Name. Thy kingdom come. THY WILL BE DONE, on earth as it is in heaven. Give us this day our daily bread. And forgive us our trespasses, as we forgive those who trespass against us. And lead us not into temptation, but DELIVER US FROM EVIL.
The Moderna and Pfizer vaccine tests were conducted, as customary, with a control group; a group within the trial who were given a placebo and not the test vaccine. However, during the trial -and after the untested vaccines were given emergency use authorization- the vaccine companies conducting the trial decided to break protocol and notify the control group they were not vaccinated. Almost all the control group were then given the vaccine.



