(TeaParty.org Exclusive) – We all know that the forced vaccination of children under the age of 12 is on the horizon. It’s only a matter of time before schools all across the country will make the COVID-19 vaccine a requirement for students to continue to attend school in-person.
On Tuesday, an FDA panel gave its recommendation that emergency use authorization should be given for the Pfizer-BioNTech COVID vaccines to be used on children ages 5-11. The panel arrived at this conclusion with a vote of 17-0, with one abstention.
The Roster of the Vaccines and Related Biological Products Advisory Committee discussed the question: “Based on the totality of the scientific evidence available, do the benefits of the Pfizer-BioNTech COVID-19 vaccine when administered as a 2-dose series (10 ug each dose, 3 weeks apart) outweigh its risks for use in children 5-11 years of age?”
Interestingly, however, during the meeting many of the panel members questioned whether or not the risks of the vaccines outweighed the purported benefits. They argued that the data indicates that the risks do, in fact, outweigh the benefits for healthy children while conceding that children who are at a higher risk, such as those with underlying health conditions, should have access to the vaccines.
FDA officials will now make the decision as to whether or not to accept the panels’ recommendation, which we all know they will.
After FDA officials agree to follow the panels’ recommendation, the process will then move to a panel at the CDC which will meet next Tuesday to discuss the same data. Of course, we all know the CDC panel will agree to move the vaccine along and approve it for children ages 5-11.
It’s a wonder they even waste time with these panels and formalities when the approval is imminent and inevitable.
COVID patron saint Dr. Anthony Fauci said Sunday on ABC’s “This Week” that if the CDC approves the vaccines they will likely “be available for children from 5 to 11 within the first week or two of November.”
It will be then that droves of parents will be forced to decide how important it is for their children to remain in public schools.
Committee member Dr. Eric Rubin, editor-in-chief of the New England Journal of Medicine, expressed concern about “a side effect that we can’t measure yet,” along with other members of the panel.
The side effect he was referring to is heart inflammation known as myocarditis but in the end he came to the conclusion that there is no other way forward.
“We’re never going to learn about how safe the vaccine is unless we start giving it,” he said. “That’s just the way it goes.”
FDA Voting Member:
“We’re never gonna learn about how safe the vaccine is until we start giving it.”
Video HT @politicalwilli pic.twitter.com/OMAph49Qow
— Techno Fog (@Techno_Fog) October 26, 2021
“I have had 22 different symptoms the last 9 months since my first dose. “Because of the intentional suppression of these reactions, the injured have been unable to get essential medical care, research for treatment, and there is clearly no recovery plan/financial help”
(1/2) pic.twitter.com/BZECsFjKjq— Read My Pinned Thread (@TimIsThaMan) October 26, 2021
Amazing three minutes of analysis to the FDA during the public comment period for EUA approval on vaccines for children 5 to 11. Listen to it all!
Part 1 pic.twitter.com/fG9VLVXZIt— Justin Hart (@justin_hart) October 26, 2021
Of course! It’d be silly not to unleash the vaccines on children without fully understanding just how at risk they are of developing a condition in which their hearts suffer inflammation. After all, millions of parents are chomping at the bit with excitement to get their children vaccinated with these experimental vaccines.
The quicker we can make guinea pigs out of America’s children the better, apparently.
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