Story at-a-glance
- Without strong evidence to support their decisions, the FDA has begun a campaign to use an emergency use authorization (EUA) that will subject the most vulnerable to unnecessary risks from a genetic experiment
- The FDA has also proposed a “Future Framework” to approve all future COVID formulations without clinical trials if they are “biologically similar”; there is still time to take action against the proposal
- The FDA amended the Pfizer EUA to allow a booster shot in children ages 5 to 11 based on a study of 400 children. The EUA they propose for children 6 months to under 5 years is based on 10 children, a number which even outspoken vaccine advocate Dr. Paul Offit finds difficult to comment on
- Approval of the shot in children is critical to protecting the pharmaceutical industry’s financial interests. Once fully licensed, the company is liable for injuries so the shot must be added to the children’s vaccine schedule to allow the government to mandate the shot
- Surveys show many pediatricians are willing to refuse treatment if a family refuses vaccination and state legislatures are changing the rules, so parents are not informed. Over 17,000 doctors and scientists believe healthy children should not be force vaccinated and offer this evidence to parents
This short video is a poignant illustration of the children who have been injured or killed by the mRNA jab. Some have died, while others are living in chronic pain, with seizures, tics and an inability to walk or eat independently.
Continue reading “Tell the FDA to Get Their #HandsOffOurChildren”
