Story at-a-glance
- In late June 2022, the United States became the first country in the world to grant emergency use authorization (EUA) for Pfizer’s and Moderna’s COVID jabs for toddlers as young as 6 months. The Food and Drug Administration issued the EUA June 17, and the very next day, the Centers for Disease Control and Prevention recommended all toddlers get the shot as soon as possible
- The pediatric EUA was based on extremely weak evidence — and that’s after the FDA lowered its efficacy requirements for the pediatric population, even though they have the lowest risk of COVID and therefore have the least need for the shots
- With this recommendation, the FDA and CDC have evaporated any last vestiges of trust they may have held onto. The reason they authorized COVID jabs for toddlers is because the drug industry needs this age group to be included under the EUA for legal indemnity purposes
- Once the emergency is over, the next phase of liability shielding requires that the shots receive approval by the CDC’s Advisory Committee on Immunization Practices (ACIP). Once the COVID jab is on the childhood vaccination schedule, the vaccine makers are permanently shielded from liability for injuries and deaths that occur in any age group, including adults
- The FDA and CDC have sold out America’s children. Once enough people realize what they’ve done, they and the entire childhood vaccine program will be finished, as no one will trust any of the vaccines on the schedule. Already, only 44% of Americans believe what the CDC says
“Why the Rush for Toddler Vaccines?” asks Wall Street Journal editorial board member Allysia Finley in a July 4, 2022, op-ed.1 Indeed, many are asking that same question, and I’m glad the legacy media’s WSJ had the courage to print it.
Continue reading “The CDC Is Sacrificing Kids for Big Pharma”
