COVID-19
There are no licensed COVID shots for kids under 12 – but CDC wants babies to get 3 Pfizer shots by 9 months
From LifeSiteNews
By and
“This is an insult to people’s intelligence,” she said, “I pray that parents will have the good sense to say no to these dangerous and unnecessary shots for babies.”
Nine-month-old babies must receive multiple doses of an unlicensed mRNA COVID-19 vaccine to be considered “up to date” with their COVID-19 vaccination, according to the Centers for Disease Control and Prevention (CDC).
The CDC’s updated guidance, issued August 30, states that children – as young as 6 months old – should get either two doses of the 2024-2025 Moderna vaccine or three doses of the 2024-2025 Pfizer-BioNTech vaccine.
If getting the new Pfizer shot, the baby is supposed to receive the first dose at 6 months, the second dose three weeks later and the third dose at least eight weeks after the second dose – meaning, that by 9 months old, babies are supposed to have received three Pfizer shots.
If getting the latest Moderna shot, the CDC recommends babies get the first dose at age 6 months and the second dose a month later.
The latest Pfizer and Moderna COVID-19 shots for children under 12 are unlicensed in the U.S. The U.S. Food and Drug Administration (FDA) has granted only emergency use authorization (EUA) for the vaccines.
Children’s Health Defense (CHD) CEO Mary Holland told The Defender, “The earlier COVID shots have been proven unsafe and ineffective. Now we’re asked to believe that newer versions are miraculously safe and effective?”
“This is an insult to people’s intelligence,” she said, “I pray that parents will have the good sense to say no to these dangerous and unnecessary shots for babies.”
As of July 28, 37,814 deaths following COVID-19 vaccination had been reported to VAERS, the Vaccine Adverse Event Reporting System, run by the FDA and CDC.
Of those, 187 reports were for children and teens under 18. Nearly 13,000 reports listed the age as “unknown.”
VAERS analyst and expert Albert Benavides recently told The Defender he believes VAERS is “throttling” and underreporting deaths of all ages following COVID-19 vaccination.
Meanwhile, the CDC continues to tell the public that COVID-19 vaccines are “safe and effective.”
CDC ‘absolutely misleading’ public on safety of EUA vaccines
Holland said the CDC is “absolutely misleading” the public by asserting that COVID-19 EUA vaccines are safe and effective because EUA vaccines are not held to the same safety or efficacy standards as licensed vaccines.
“By law,” she explained, “EUA products ‘may be effective,’ and they have not undergone the safety testing required to permit licensing.”
“This is one more horrific example of the CDC putting profits before people and acting as an unethical arm of Big Pharma’s marketing operation,” Holland added.
CHD Chief Scientific Officer Brian Hooker agreed. “It is criminal that these untested vaccines are being recommended to infants and children, especially given the fraudulent tactics to market them to an unsuspecting public,” Hooker told The Defender.
There’s no licensed COVID vaccine for kids under 12
There are still no licensed COVID-19 vaccines available for children under 12, Hooker said – so all COVID-19 vaccines given to young kids are EUA products.
The FDA’s website on EUA for medical products states that EUA vaccines only have to meet the standard of “may be effective” as long as if, “based on the totality of the scientific evidence, it is reasonable to believe that the product may be effective for the specified use.”
“The ‘may be effective’ standard for EUAs provides for a lower level of evidence than the ‘effectiveness’ standard that FDA uses for product approvals,” the website states.
Before a vaccine can be fully licensed, the vaccine maker typically is required to conduct numerous clinical trials to demonstrate that the product is safe. However, the safety requirements for EUA are more flexible.
According to the FDA:
The amount and type(s) of safety information that FDA recommends be submitted as part of a request for an EUA will differ depending upon a number of factors, including whether the product is approved for another indication and, in the case of an unapproved product, the product’s stage of development.
Despite this, the first statement on the CDC’s “6 Things to Know about COVID-19 Vaccination for Children” says, “COVID-19 vaccination for children is safe.”
Risks outweigh benefits for kids
Hooker said the CDC’s actions are especially problematic as, historically, the meaning of “safe” has been interpreted by regulatory authorities as meaning that the benefits of a drug outweigh its risks.
“With the risk to children of dying from a COVID-19 infection being statistically zero, it is unclear if there is any benefit,” he said.
Meanwhile, the CDC still claims that “while adverse reactions are rare, the benefits of COVID-19 vaccination outweigh the known risks of COVID-19 and possible severe complications.”
Pfizer fact sheet more forthcoming about risks
For licensed vaccines, the CDC typically provides an official vaccine information statement (VIS) that describes the vaccine’s risks and potential benefits.
According to the CDC website, “Federal law requires that healthcare staff provide a VIS to a patient, parent, or legal representative before each dose of certain vaccines.”
However, for EUA COVID-19 vaccines, the CDC directs people to “fact sheets” – produced by the vaccine manufacturer, not the CDC, and authorized by the FDA – which detail the product’s risks and benefits.
There is no federal law requiring healthcare providers to share these fact sheets with patients, or parents of minors, before a COVID-19 vaccination.
“Pfizer’s own ‘fact sheet’ for its latest COVID-19 vaccine appears to give a more accurate picture [of the vaccine’s risks] than the CDC’s own websites,” Hooker said. “Shouldn’t the CDC be more a watchdog than Pfizer?”
For example, Pfizer’s fact sheet states, “A product authorized for emergency use has not undergone the same type of review by FDA as an FDA-approved product.”
The Pfizer fact sheet also acknowledges that its vaccine “may not protect everyone” and that reported side effects associated with the Pfizer vaccines include myocarditis and pericarditis.
Hooker pointed out that research has shown that vaccine-induced myocarditis, inflammation of the heart, and pericarditis, inflammation of the tissue surrounding the heart, can be fatal.
He urged parents to “read between the lines” when assessing the CDC’s COVID-19 vaccination recommendation for babies and children.
“Most of all,” he added, “use common sense to decide if the CDC’s and the FDA’s logic is sound.”
This article was originally published by The Defender – Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
COVID-19
US medical center refusing COVID shots for employees but still promoting to public
Exert from Medical Musings by Dr. Pierre Kory
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Major Covid mRNA policy reversals and awakenings occurred this week within a major U.S health system, a large U.S state, a South American country, and in the UK. The dominoes are starting to fall.
This week a nurse reached out with disturbing descriptions of some major changes she has witnessed inside the Ohio State University Medical Center (OSUMC) system.
OSUMC s a large and comprehensive healthcare organization, with a significant presence in Ohio and a strong focus on research, education, and patient care. It is a massive institution with over 23,000 employees, including:
- Over 2,000 physicians
- More than 1,000 residents and fellows
- Nearly 5,000 nurses
Lets start off with this screenshot of a webpage from OSUMC’s website which provides information to the public as to where they can get Covid-19 vaccines. Check out the highlighted sentence at the bottom of the page:
Wait, what? Ohio State is suddenly no longer offering the Covid-19 vaccine to any of their employees but they are happily offering to inject them into the public? How can such a policy be justified? Why was this change in policy done and why was it done so quietly?
Let’s get this straight. Ohio State’s leadership is now making an institutional decision that employees should not be offerred access to any Covid-19 mRNA vaccine. I am (pretending to be) confused. I mean, if the vaccines could protect patients from being infected by staff members and they were safe to give to staff members, why wouldn’t you do everything possible (like a mandate) to ensure they receive them?
The only possible reason for the action above is that either OSUMC leadership recently discovered that the vaccines: a) do not work or b) are not safe. I think you would agree that, of the two possible answers, the only one that makes sense to explain this abrupt change in policy is B) they are not safe. I say this because if they were safe but instead just didn’t really work very well, Ohio State would not have the incentive to divorce themselves so abruptly and strongly from the recommendations of our benevolent federal government. I believe such an action would pretty quickly and negatively impact federal research funding by the NIH. It is my belief that agency’s money kept the nations 126 major academic medical centers in line throughout Covid, as those CEO’s and Deans are well aware that NIH retaliation in terms of rejecting grant funding if they “dissent” is real and happens (inflated reimbursements from the gov’t was another one of course).
I asked the brave browser AI, “why is Ohio State Medical Center no longer offering Covid-19 vaccines to its employees?” Two sentences jumped out:
- “Based on the provided search results, it appears that Ohio State Medical Center did offer COVID-19 vaccines to its employees at one point.”
- “Without further information or clarification from Ohio State Medical Center, it’s difficult to provide a definitive answer on why they may not be offering COVID-19 vaccines to their employees.”
So it must be the case that Ohio State leadership somehow found themselves a stronger financial disincentive to subjecting employees to Covid-19 vaccine injection. Where would such a disincentive come from? Answer: lawsuits. I also suspect that fear of worsening staff shortages from disability and/or death further disrupting operations played a role as well (as you will learn below).
This new policy action (taken very quietly) is absolutely dam breaking to me in terms of progress towards the truth about the mRNA platform getting out to the public. It is also appears ethically reprehensible, i.e. the institution made the decision to keep jabbing the public with a toxic and lethal vaccine while becoming aware that same vaccine is either exposing them to unmanageable legal risks and/or is disrupting their operations by negatively impacting the health of their workforce. Welcome to dystopia.
COVID-19
Trial for Freedom Convoy leaders ends, verdict may take 6 months
From LifeSiteNews
In her concluding statements last Friday in an Ottawa courthouse, presiding judge Heather Perkins-McVey said that she does ‘not know’ when a decision will be rendered in the Freedom Convoy leaders’ trial.
The trial for Freedom Convoy leaders Tamara Lich and Chris Barber, which was supposed to have been only 16 days long, has now concluded after over a year, with the presiding judge observing that determining a verdict, which could take up to six months, will be “daunting” task.
In her concluding statements last Friday in an Ottawa courthouse, presiding judge Heather Perkins-McVey said that she does “not know” when she will “be in a position to give my decision,” adding that coming up with a verdict will be “a little daunting.”
The judge has promised that on November 26, she will be providing an update as to when a decision could be forthcoming.
The trial has been ongoing for over one year and began on September 3, 2023. As reported by LifeSiteNews, both Lich and Barber face a possible 10-year prison sentence for their role in the 2022 Freedom Convoy.
In an X post on Friday, Lich shared her thoughts on the trial finally wrapping up.
“Well, that’s a wrap to the Longest Mischief Trial of All Time,” she wrote.
Well, that’s a wrap to the Longest Mischief Trial of All Time. Check in date Nov 26 to hopefully set a date for the verdict.
The crown really disappointed me today. His remarks about the Event That Shall Not Be Named being nothing more than a weekend party are indicative of…
— Tamara Lich (@LichTamara) September 13, 2024
“The Crown really disappointed me today. His remarks about the Event That Shall Not Be Named (Freedom Convoy) being nothing more than a weekend party are indicative of a level of smugness and elitism that I can never and will never understand,” added Lich.
Both Lich and Barber had attended the hearings in person, travelling from their homes in Alberta and Saskatchewan respectively. Last Friday, however, they attended via video.
Lich and Barber face multiple charges from the 2022 protests, including mischief, counseling mischief, counseling intimidation, and obstructing police. In Canada, anyone charged with mischief could face a potential jail sentence of up to 10 years.
The Crown prosecution has held steadfast to the notion that Lich and Barber somehow influenced the protesters’ actions through their words as part of a co-conspiracy. This claim has been rejected by the defense as weak.
It has also been asserted “that the absence of violence or peaceful nature of the protest didn’t make it lawful, emphasizing that the onus was on the Crown to prove the protest’s unlawfulness.”
The reality is that Lich and Barber collaborated with police on many occasions so that the protest remained law abiding.
The Democracy Fund, which is crowdfunding Lich’s legal costs, noted in one of its last legal updates of the trial that it expected the Crown would try to prove the leaders were “co-conspirators,” meaning that accusations placed against one leader automatically apply to the other.
As reported by LifeSiteNews at the time, despite the non-violent nature of the protest and the charges, Lich was jailed for weeks before she was granted bail.
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