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Big Pharma Desperate to Get COVID Shots on Childhood Schedule Before ‘Emergency’ Ends

By  Dr. Joseph Mercola

Once the COVID-19 vaccine 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.

Story at a glance:

  • The rate of COVID-19-associated hospitalization among children aged 5 to 11 is just 0.0008%. In real-world terms, that’s so close to zero you basically cannot lower it any further.
  • Despite that, the vaccine advisory panel — the Vaccines and Related Biological Products Advisory Committee (VRBPAC) — of the U.S. Food and Drug Administration (FDA) on June 15 unanimously approved granting Emergency Use Authorization (EUA) to Pfizer’s and Moderna’s COVID shots for infants and young children.
  • Pfizer’s EUA is for a three-dose regimen (3-microgram shots) for children 6 months to 5 years old; Moderna’s EUA is for a two-dose regimen (25-microgram shots) for children 6 months to 6 years.
  • In granting this EUA, the FDA again ignored injury and death data and swept medical ethics aside.
  • The drug companies need this last remaining age group to be included under the EUA, because once the emergency is finally declared “over,” the next phase of liability shielding requires that the shots receive approval by the CDC’s Advisory Committee on Immunization Practices. Once the vaccine 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.

Statistics show the rate of COVID-19-associated hospitalization among children aged 5 to 11 is 0.0008%. 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.

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.

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. 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, on June 15, the FDA’s vaccine advisory panel — the VRBPAC — unanimously approved (21-0) to grant EUA to both Pfizer’s and Moderna’s COVID shots for infants and young children.

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 published 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.”

[…]

Via https://childrenshealthdefense.org/defender/big-pharma-covid-vaccine-child-immunization-schedule-cola/

3 thoughts on “Big Pharma Desperate to Get COVID Shots on Childhood Schedule Before ‘Emergency’ Ends

  1. Pingback: Big Pharma Desperate to Get COVID Shots on Childhood Schedule Before ‘Emergency’ Ends – The Free

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