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FDA Buries Data on Seriously Injured Child in Pfizer’s Covid-19 Clinical Trial

(by Aaron Siri | – When Stephanie and Patrick de Garay enrolled their 12-year-old child Maddie and her two brothers in Pfizer’s Covid-19 clinical trial, they believed they were doing the right thing.

That decision has turned into a nightmare.  Maddie, a previously healthy, energetic, full of life child, was within 24 hours of her second dose reduced to crippling, scream-inducing pain that landed her in the emergency room where she described feeling like someone was “ripping [her] heart out though [her] neck.”

Over the next several months the nightmare continued, during which Maddie was hospitalized several times and suffered numerous systemic injuries, requires a tube through her nose that carries her food and medicine, and a wheelchair for assistance.

Ms. de Garay documented every detail of Maddie’s injury and reported it to the principal investigator for the Pfizer trial at Cincinnati Children’s Hospital where the vaccine clinical trial was occurring and where Maddie was treated and admitted.  They first tried to treat Maddie as “a mental patient,” telling the family it was psychological and in Maddie’s imagination.  Then they claimed it was unrelated to the vaccine (copy of recording with hospital below), and when that argument failed, Pfizer listed this traumatic adverse event as “functional abdominal pain” when reporting to the FDA.

Ms. de Garay reported what occurred to the CDC and FDA through VAERS in June 2021 but nobody from these agencies sought additional information or followed-up with the de Garays.  Ms. de Garay also reached out to Dr. Nath, a Chief in the NIH’s National Institute of Neurological Disorders and Stroke, responded by stating he was “Sorry to hear of your daughter’s illness” and that “We have certainly heard of a lot of cases of neurological complications form [sic] the vaccine and will be glad to share our experience with them.”  (Copy of this email is below.)  Unfortunately, other than a call arranged by Maddie’s neurologist, there was no follow-up or response from NIH or any other federal health agency.  Even after Ms. de Garay did a press event on June 28, 2021 with Senator Ron Johnson, neither Pfizer nor any health agency reached out in any manner to address Maddie’s injury or obtain any additional information.

This story is extremely troubling.  Pfizer’s clinical trial for children aged 12-15 included only 1,131 children who were vaccinated and at least one of those children suffered a devastating, life-altering injury which, despite incontrovertible proof and the cries of both the victim and her parents, has not been appropriately acknowledged by Pfizer or the FDA.  Putting aside that one serious injury in a small trial should alone raise blaring alarm bells, one must ask: what other serious adverse events have been hidden and ignored by regulators?

For a virus that rarely harms children, the need to assure safety of the Covid-19 vaccine is high.  A study with only 1,131 children is underpowered.  It will not pick up anything but the most common adverse events.  If what Maddie suffered will occur in 1/1,000 children, that would result in 75,000 children in this country suffering this serious injury.  If it happens 1/10,000 children, that is 7,500 suffering this serious injury.  It could be that the cure is worse than the disease.  But that will only be known if there is a properly powered (a.k.a., sized) clinical trial with children. Read Full Article >

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