(Jun. 28, 2022) — Statistics show the rate of COVID-19 associated hospitalization among children aged 5 to 11 is 0.0008%.1 In real-world terms, that’s so close to zero you basically cannot lower it any further. Yet, despite such reassuring data, children in this age group are urged to get two to three doses of the COVID jab, even though side effects of the injection could harm them for life, or kill them.
As noted by the Vaccine Safety Research Foundation in the video below, myocarditis — one of the recognized effects of the COVID jab — “has a mortality rate of 25% to 56% within three to 10 years, owing to progressive heart failure and sudden cardiac death.”
Sudden cardiac death is what the media and public health agencies are now glibly referring to as “sudden adult death syndrome” or SADS. The older and more appropriate description for SADS is “sudden arrhythmic death syndrome,” but they don’t even want to use the word “arrhythmic” anymore, as that tells you what the death is really caused by, and many are now aware that the jab can cause heart inflammation.
By avoiding the word “arrhythmic,” it’s easier for them to pretend as though people are dying for no apparent reason, and certainly not because of the COVID shots. Still, real-world facts tell us that SADS didn’t take off until after the shots were rolled out, and the vast majority of young healthy people who suddenly die for no apparent reason have been jabbed.2
Also, understand that if your child or you are injured by the shot, you cannot sue the drug company for damages and, so far, the U.S. government has rejected all but one of the claims filed with the Countermeasures Injury Compensation Program (CICP).3 At the current pace of about 18 claims a month, it would take 38 years just to get through the current backlog, Reuters has noted.4 Basically, many may die before their case even gets through review.
COVID Jab Authorization Granted for Babies
As if the situation were not bad enough already, June 15, 2022, the U.S. Food and Drug Administration’s vaccine advisory panel — the Vaccines and Related Biological Products Advisory Committee (VRBPAC) — unanimously approved (21-0) to grant Emergency Use Authorization (EUA) to both Pfizer’s and Moderna’s COVID shots for infants and young children.5
Pfizer’s EUA is for a three-dose regimen (3-microgram shots) for children 6 months to 5 years old, while Moderna’s EUA is for a two-dose regimen (25-microgram shots) for children 6 months to 6 years.
In the video at the top of the page, Steve Kirsch, president of the Vaccine Safety Research Foundation, interviews reporter Toby Rogers, who endured the entire nine-hour day of the recent VRBPAC meeting.
The day before that meeting, June 14, Rogers published6 a written summary of Pfizer’s trial on young children, which he referred to as “an embarrassment.” “Any VRBPAC member who votes Aye on this junk science application should be removed from his/her job,” he wrote. Apparently, they all need to go.
In the interview, Rogers laments the fact that the VRBPAC members remain “locked in their information bubble” and won’t allow any conflicting data to influence their preconceived biases.
As noted by Rogers, they have a sacred duty to protect public health, and they’re being flippant about it. They’re ignoring data, they’re ignoring the pleas of the vaccine injured, they’re ignoring serious questions, they’re ignoring everything except the flimsiest bits and pieces upon which their narrative is built. Rogers called the experience “heartbreaking.”
VRBPAC Refuses to Answer Lawmakers’ Questions
The VRBPAC members aren’t even swayed by concerns from lawmakers. They simply ignore their questions too. As reported by The Defender:7
“The Vaccines and Related Biological Products Advisory Committee (VRBPAC) ignored pleas from experts, the vaccine injured and a congressman representing 17 other lawmakers to halt authorization until questions about the safety and efficacy of COVID-19 vaccines for the nation’s youngest children could be properly addressed …
Rep. Louie Gohmert (R-Texas) said there are many unanswered questions … ‘I’m deeply concerned that the push to vaccinate these children is nothing more than a dystopian experiment with unknown consequences,’ Gohmert told the committee. ‘Some of us have outlined these questions in a letter8 to VRBPAC but have not received any answers, and I pose some of them here.’ Gohmert said:
‘Number 1, why has the FDA refused to release the hundreds of thousands of pages of data from preapproval manufacturer studies, post-approval adverse events data and other post-approval manufacturer data?
Number 2, what is the cardiac risk factor in administrating these COVID vaccines to children?
Number 3, world-renowned immunologists have raised concerns about potential antibody-dependent enhancement, or ADE, resulting from COVID vaccines, and since ADE was a problem in prior unrelated respiratory vaccine trials, we need to know what studies, if any, the FDA has that it’s used regarding ADE from COVID vaccines in children 5 and under or any age group. Can the FDA affirm there’s no risk of ADE for vaccinated children?
Number 4, if widely approved among children 5 and under, how many lives, if any, does FDA estimate will be saved next year? Given the injuries reported in the FDA’s VAERS [Vaccine Adverse Event Reporting System] system, how will FDA evaluate serious vaccine injuries versus serious COVID outcomes?
Number 5, is it possible the proposed COVID vaccines in young children could create increased risk in future novel COVID variants?
Number 6, why has the FDA recently lowered the efficacy bar for COVID vaccines for youngest children? This change significantly lowers the expected benefits from any COVID vaccination for young children and it’s of particular concern given that over 70% of that age cohort already is seropositive.’
Gohmert said these questions and 13 other questions posed by lawmakers are critical and deserve answers from the FDA and VRBPAC prior to any EUA with the ‘accompanied protection for liability for all harm done.'”
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