Paul Offit admits on video there are no benefits of the new booster shots
Watch this video where one of the world's most respected vaccinologists admits that there are no benefits to the boosters. He's not taking the boosters. Why should you?
Dr. Paul Offit, MD is the Director of the Vaccine Education Center and practices medicine in the Infectious Disease department at the Children’s Hospital of Philadelphia and he also sits on the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC).
Check out this 1 minute video where Dr. Offit talks about the new bivalent booster and the “scant evidence” and that the “fix was in:”
The background
Several months ago, VRBPAC voted to approve a COVID vaccine novel booster formula that combined the mRNA instructions that targeted BA.4 & BA.5 - the two Omicron strains which circulated last spring and early summer.
There were no human clinical trials conducted on this booster. It was not tested on people. It was tested on just 8 mice. There is no long term data on what happened to the mice after injection. All the mice were challenged with Omicron and every mouse was infected showing that the vaccine had zero protection against getting the virus. The mice were sacrificed shortly thereafter because we don’t want to know the long term effects. Don’t ask, don’t tell.
You will not find a bigger proponent of vaccines in general and the COVID vaccines specifically, in American medicine, than Dr. Paul Offit. He voted YES to give the COVID vaccines to all children, even babies as young as 6-months.
Why did Paul Offit vote No on the boosters
Yet when VRBPAC recently voted on the novel COVID booster, Dr. Offit voted no, because (in his own words) “HELL NO was not a choice!”
How? Why? What happened?
First, there was no trial to show that there are any clinical benefits at all. And any clinical benefits must be weighed against the risks.
Secondly, according to Offit, once you have your initial injection, you’re already protected against severe disease so there is no additional benefit to a booster. In this MedPage Today interview, Offit explains:
The question is, does it matter? Because still it looks like you're protected against severe illness, so does it really matter to get that third dose? I would argue 'no.'
Thirdly, the FDA doesn’t really want the outside committee members to actually review the scientific data. They just want them to vote yes so it looks like outside experts reviewed the data. The FDA provides hundreds of pages of material just days before the meeting giving the members an inadequate amount of time to review the data before voting on it. It’s just another example of sham science: the panel is simply there to rubber stamp what the White House and FDA want to do; they are not there to protect the public.
Why is the government advocating for three or more doses when there is no evidence of a benefit?
The reason for three or more doses is because the press and the public health officials want you to get it. The science doesn’t support it. But science doesn’t matter. This is about compliance with orders, not protecting your health (or the health of others since even Pfizer admits that the vaccine doesn’t protect against transmission).
In the MedPage Today interview, Offit admitted this:
I think this is now a three-dose vaccine for the most part, because that's the way the press and the public have handled it, it's the way public administrators have handled it.
In short, the booster was created to give the public the perception that the government is doing something to protect them.
Even pro-vaccine doctors like Martin Makary, MD are reposting this important video.
Watch the Offit video. Share. Spread the word.
Summary
You can never unvaccinate yourself.
Before you consent to take any vaccine, demand to see at least one all-cause mortality and morbidity study vs. placebo with at least a 12 month follow-up that are independently managed by multiple organizations with no financial ties to the vaccine manufacturers.
Currently, there aren’t any vaccines where such a study is available. Now you would think that if any vaccine had a true cost-benefit, such studies would exist, wouldn’t you?
The Texas State legislators have sent a request to the FDA for emergency use authorization of flu testing in doctors offices and points of care regardless of CLIA status. If the FDA were to authorize this as an emergency use, we could immediately start testing sick children and adults as soon as their symptoms start so that we may apply therapeutics like Tamiflu and Xofluza more immediately. Can Paul Offit help? As we all know a bad flu season is going to be way more impactful than the winter Covid surge on hospitalization and death.
Maybe people saw this post and put pressure on Dr. Offit, but according to this post by Dr. Marc Siegel of Fox news, this is what Dr. Offit had to say about putting the booster on the children's vaccine schedule:
"On Thursday morning I heard from Dr. Paul Offit, head of the Vaccine Education Center at the Children’s Hospital of Philadelphia and a member of the FDA’s Advisory Committee on vaccines about the CDC decision to add the COVID-19 vaccine to their suggested schedule of regular vaccines for children. Offit agrees with the CDC on this, despite his previous criticisms of overly vigorous booster requirements without the approval of his advisory committee."
https://www.foxnews.com/opinion/covid-vaccine-belongs-cdc-list-kids-scheduled-vaccines
Horrible.