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CDC Recommends COVID Boosters After FDA Advisory Panel Voted Not to Approve Them
By: David Deschesne
Fort Fairfield Journal, October 6, 2021
U.S. Centers for Disease Control and Prevention Director, Rochelle Walensky recently confirmed the suspicion that the entire COVID narrative and gene therapy program never had anything to do with a virus, or public health. By endorsing the CDC’s Advisory Committee on Immunization Practices’ (ACIP) recommendation for a booster shot for ages 16-65 after an 18 member vaccine advisory panel for the US FDA voted 16-2 against recommending the vaccines for that age group, Walensky has shown the COVID industrial complex is more about an agenda, an agenda that has nothing to do with saving lives or stopping a virus.
The CDC did not approve anything. They merely recommended booster shots—despite the FDA advisory panel’s vote against them. The CDC’s verbiage in their recommendation is replete with words such as “should” and “may” which makes them mere suggestions—not approval, or mandates.1
What’s lost on most people is the CDC does not have any authority to actually approve any drug or vaccine. That job falls entirely on the FDA (which has approved one deadly and dangerous drug after another for years).
Even the CDC’s own website admits as much by stating, “The U.S. Food and Drug Administration’s (FDA’s) Center for Biologics Evaluation and Research (CBER) is responsible for regulating vaccines in the United States.”2
The CDC further states that vaccines are monitored for safety in the Vaccine Adverse Event Reporting System which is co-sponsored by both the CDC and FDA. Intriguingly, that VAERS database now lists over 15,000 deaths attributed to the experimental ‘vaccines’3 and more than 700,000 serious adverse events [editor: as of the time of this writing, over 15,000. The database is updated weekly and as of December 17 had topped 20,000]. Yet, neither government organization seems interested in acknowledging that data in their decision-making process. Certainly, the left wing media has refused to report those numbers.
As of this writing, the FDA has not acted on their advisory committee’s recommendations. However, people are advised to consider how their lives will be impacted by life-altering side effects when they won’t be able to sue the vaccine manufacturers for damages.
Some of the more serious side effects of the experimental gene therapies are: blood clotting, heart attacks, stroke, myocarditis (heart inflammation), neuropathy, Bell’s Palsy, miscarriage in pregnant women (1,500+ so far this year), and paralysis.
While many people may argue that they have received the vaccine and suffered no serious side effects (yet), those who have suffered are doing so at a statistical rate much higher than has ever been allowed for any other vaccine or drug in the history of the FDA. Also, because these drugs have never been used before, it is not known what the long-term side effects will be two, five or ten years out. Only time will tell.
The recent push to get everyone “vaccinated” with the experimental drugs is a concerted effort to virtually eliminate any sizable control group from the public (those who haven’t received any of the drugs) so there will be nobody left to compare to when analyzing the rates of those side effects between those who received the drugs and those who haven’t.
notes
1. https://www.cdc.gov/media/releases/2021/p0924-booster-recommendations-.html
2. https://www.cdc.gov/vaccines/basics/test-approve.html
3. https://medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=AGE&EVENTS=ON&VAX=COVID19&DIED=Yes