Brownstone Institute
Kid Lab Rats
From the Brownstone Institute
BY
” (since [Covid] is universally mild in children), the risk-to-benefit ratio for the [Covid] mRNA injections in children is infinitely bad,” Baker said. “There is no ethical reason whatsoever to continue clinical trials of these products in children, and all such trials should be stopped.” “
Mommy, can I be a Covid lab rat?”
That is a request most parents will never hear and it is a request that very few parents would ever want to hear.
But, unlike the more typical “Can I have a pony?” request, letting your child be a Covid shot test subject is a request that can actually be granted around the nation.
Right now, for example, Pfizer/BioNTech is running an ongoing clinical trial to test the effectiveness of its shots (the shot is not a vaccine as it does not prevent catching the virus or transmitting the virus as typical vaccines do) on kids.
Pfizer has been running radio and other ads looking for test subjects; this is how they describe the study on their “Enrolling Children 6 to 23 months old for a COVID-19 Vaccine Study” website:
This study will help us learn how well our updated COVID-19 vaccine works in babies and toddlers who have not been previously vaccinated and see if the number of recommended doses can potentially be reduced for children under the age of 5. The study vaccine has been authorized by the United States Food and Drug Administration for children at least 6 months of age. It is designed to protect against the newer COVID-19 variant called XBB.1.5.
The company is also running similar trials for older kids and, of course, adults.
Clinical trials for drugs and procedures involving children are not inherently wrong and they are conducted safely around the world almost daily.
But this Covid trial stands out for a number of reasons.
First, the trial only involves kids who have never had a Covid shot before. The likelihood that a parent who has declined to get the shot for their kids in the first place will say “We chose not to get the shots for our kids, but feel free to experiment on them with the stuff we previously declined” is minimal.
In other words, if a parent didn’t feed their kid aluminum foil-flavored ice cream before it is highly unlikely they would feed their kid an experimental version of aluminum foil-flavored ice cream, even if you paid them (the trial comes with certain compensation enticements – Pfizer did not respond to a request for exactly what they are in this trial, though industry averages would indicate the pay would be between a few hundred to a few thousand dollars).
Second, there is the matter of “informed consent.” A trial subject must give permission freely, be told of any risks, and understand the entire situation. Clearly, nine-month-olds cannot do that.
It is perfectly legal for parents to give their “informed consent,” but here we get into the third problem: the risk/benefit question.
For example, during the pandemic (early 2020 to May 2023) there were 41 Covid deaths in California of kids under five. That number does not differentiate between “died with Covid” or “died from Covid;” that is a debate that continues to rage across the country and shall be put aside for the time being.
Every death of a child is a tragedy and this article is not intended to lessen that fact. However, children in general were not at all likely to get, let alone die from, Covid during the pandemic.
During the pandemic, there were about (rolling average) 2.4 million (about 6% of the total population) under-fives in California and there were about 385,000 cases of Covid reported in that age group.
Currently, about 3.2% of California’s under-fives have had the latest shot. That’s on par with the national average. What is interesting is that of the 70,817 kids who have received the shot in the state, 41,224 live in the Bay Area. In other words, the Bay Area has 20% of the state’s population, but 57% of the state’s “vaccinated” toddlers and babies. But do not ever think that politics has had nothing to do with Covid protocols.
During the pandemic, the overall likelihood of a child dying from/with Covid was about 1 in 60,000; for those over 75 – about 6.5% of the population or 2.7 million – there were about 51,000 with/from Covid deaths, or about 1 in 50.
The risk, clearly, is extremely different depending upon age and general state of health.
With a relative risk of being harmed by Covid, the risks of the Covid shot itself must be considered carefully – note: no kid in the study will get a placebo for comparison purposes.
The Covid shots, in the general population, did have significant side-effects and did cause a number of deaths. While these numbers are not broken out by age, in the same time period there were 640 deaths and 89,000 “adverse effects” experienced (much much more than just a sore arm) by Californians.
Also during the same time period, all other vaccines combined caused 66 people to die and 14,000 to have a reportable “adverse effect.” (Note – the numbers are taken from the CDC’s “vaccine adverse event reporting system,” a tool it stood by as an early warning device for decades…that is, until the Covid problem numbers got too high.)
That puts the general odds of something bad happening to a person after they get a Covid shot at about 1 in a 1,000 and some studies have shown it to be 1 in 800. In other words, the risk from the shot appears to outweigh the risk of Covid itself by a factor of 60 times.
Citing the uncertainty of benefit, it should also be noted that the European Union has not cleared the shot at all (with minor exceptions) for the under-fives and were hesitant in allowing them for the under 18s.
Clearly, the risk outweighs the reward, as it were, and it is unclear – because Pfizer did not answer any request for information/comment (see questions below) – if parents are given those figures when making the decision to enroll their kid in an experimental drug program.
Adults calculate risk and reward constantly – from “Can I make that light before it turns red?” to “Should I tease that lion?” But a seven-month old is simply not capable of doing so and while certain clinical trials do hold out serious hope and are important for society at large, a trial such as this for such a limited reward – kids very very very rarely get, let alone suffer seriously, from Covid – seems dubious.
In other words, if you wanted to test a new malaria drug you would not do so on Santa’s elves at the North Pole because there are no mosquitoes there to infect anyone.
According to the Belmont Report, which set baseline standards for human-involved clinical trials in the late 1970s (it was a government reaction to the horror of the CDC’s own “Tuskegee Syphilis Study”) one of the three core standards for justifying clinical trial testing is “beneficence.”
In other words, there is an obligation to protect persons from harm by maximizing anticipated benefits and minimizing possible risk and harm.
That risk/benefit calculation obviously changes in regard to other far more common childhood maladies, making participation in those studies potentially far more “beneficent.”
But in the case of Covid, the question is how are maximal, as it were, are the anticipated benefits?
Very very minimal and that is the problem, said Dr. Clayton Baker, former Clinical Associate Professor of Medical Humanities and Bioethics at the University of Rochester.
“Given the real and well-established risks of harm (including myocarditis and death), and given the functionally zero potential for benefit (since [Covid] is universally mild in children), the risk-to-benefit ratio for the [Covid] mRNA injections in children is infinitely bad,” Baker said. “There is no ethical reason whatsoever to continue clinical trials of these products in children, and all such trials should be stopped.”
Come to think of it, maybe just get the kid the pony instead.
Here’s a link to an on-going kids Covid study with a handy map so you can find a location near you (mostly Bay Area): A Study to Learn About Variant-Adapted COVID-19 RNA Vaccine Candidate(s) in Healthy Children
For clinical trials in general, you can look here for one that you might be interested in taking part in:
For clinical trials just about Covid, you can look here:
As noted above, here are the questions Pfizer did not reply to:
-Exactly how is informed consent handled? I assume a parent/guardian can provide said consent?
-Do (or have) you run trials with previously vaccinated children?
-What child/youth trials have been run in the past and what have been their results?
-What is the compensation amount?
-Have any previous trials shown conclusively that the vaccine ameliorates Covid severity in children?
-When and in what manner did the FDA approve this trial?
-When do you expect to conclude the trial?
-Is this trial aimed at testing a “booster” shot or to cover a new variant?
-Has any child in any trial conducted had a significant and serious reaction requiring hospitalization and/or led to death?
-It appears one of the points of the study is to figure out how to cut the number of doses as well as check effectiveness. Is that correct?
-How many children – nationwide and in California specifically – have signed up for/been through the trial so far?
-What are the differences between trials involving children and those involving adults?
-Will Pfizer conduct trials each time it comes out with new variant vaccine shot?
Republished from the author’s Substack
Brownstone Institute
The Deplorable Ethics of a Preemptive Pardon for Fauci
From the Brownstone Institute
Anthony “I represent science” Fauci can now stand beside Richard “I am not a crook” Nixon in the history books as someone who received the poison pill of a preemptive pardon.
While Nixon was pardoned for specific charges related to Watergate, the exact crimes for which Fauci was pardoned are not specified. Rather, the pardon specifies:
Baseless and politically motivated investigations wreak havoc on the lives, safety, and financial security of targeted individuals and their families. Even when individuals have done nothing wrong – and in fact have done the right things – and will ultimately be exonerated, the mere fact of being investigated and prosecuted can irreparably damage reputations and finances.
In other words, the dying breath of the Biden administration appears to be pardoning Fauci for crimes he didn’t commit, which would seem to make a pardon null and void. The pardon goes further than simply granting clemency for crimes. Clemency usually alleviates the punishment associated with a crime, but here Biden attempts to alleviate the burden of investigations and prosecutions, the likes of which our justice system uses to uncover crimes.
It’s one thing to pardon someone who has been subjected to a fair trial and convicted, to say they have already paid their dues. Gerald Ford, in his pardon of Richard Nixon, admitted that Nixon had already paid the high cost of resigning from the highest office in the land. Nixon’s resignation came as the final chapter of prolonged investigations into his illegal and unpresidential conduct during Watergate, and those investigations provided us the truth we needed to know that Nixon was a crook and move on content that his ignominious reputation was carve d into stone for all of history.
Fauci, meanwhile, has evaded investigations on matters far more serious than Watergate. In 2017, DARPA organized a grant call – the PREEMPT call – aiming to preempt pathogen spillover from wildlife to people. In 2018 a newly formed collaborative group of scientists from the US, Singapore, and Wuhan wrote a grant – the DEFUSE grant – proposing to modify a bat sarbecovirus in Wuhan in a very unusual way. DARPA did not fund the team because their work was too risky for the Department of Defense, but in 2019 Fauci’s NIAID funded this exact set of scientists who never wrote a paper together prior or since. In late 2019, SARS-CoV-2 emerged in Wuhan with the precise modifications proposed in the DEFUSE grant submitted to PREEMPT.
It’s reasonable to be concerned that this line of research funded by Fauci’s NIAID may have caused the pandemic. In fact, if we’re sharp-penciled and honest with our probabilities, it’s likely beyond reasonable doubt that SARS-CoV-2 emerged as a consequence of research proposed in DEFUSE. What we don’t know, however, is whether the research proceeded with US involvement or not.
Congress used its constitutionally-granted investigation and oversight responsibilities to investigate and oversee NIAID in search of answers. In the process of these investigations, they found endless pages of emails with unjustified redactions, evidence that Fauci’s FOIA lady could “make emails disappear,” Fauci’s right-hand-man David Morens aided the DEFUSE authors as they navigated disciplinary measures at NIH and NIAID, and there were significant concerns that NIAID sought to obstruct investigations and destroy federal records.
Such obstructive actions did not inspire confidence in the innocence of Anthony Fauci or the US scientists he funded in 2019. On the contrary, Fauci testified twice under oath saying NIAID did not fund gain-of-function research of concern in Wuhan…but then we discovered a 2018 progress report of research NIAID funded in Wuhan revealing research they funded had enhanced the transmissibility of a bat SARS-related coronavirus 10,000 times higher than the wild virus. That is, indisputably, gain-of-function research of concern. Fauci thus lied to the American public and perjured himself in his testimony to Congress, and Senator Rand Paul (R-KY) has referred Fauci’s perjury charges to the Department of Justice.
What was NIAID trying to preempt with their obstruction of Congressional investigations? What is Biden trying to preempt with his pardon of Fauci? Why do we not have the 2019 NIAID progress report from the PI’s who submitted DEFUSE to PREEMPT and later received funding from NIAID?
It is deplorable for Biden to preemptively pardon Fauci on his last day in office, with so little known about the research NIAID funded in 2019 and voters so clearly eager to learn more. With Nixon’s preemptive pardon, the truth of his wrongdoing was known and all that was left was punishment. With Fauci’s preemptive pardon, the truth is not yet known, NIAID officials in Fauci’s orbit violated federal records laws in their effort to avoid the truth from being known, and Biden didn’t preemptively pardon Fauci to grant clemency and alleviate punishment, but to stop investigations and prosecutions the likes of which could uncover the truth.
I’m not a Constitutional scholar prepared to argue the legality of this maneuver, but I am an ethical human being, a scientist who contributed another grant to the PREEMPT call, and a scientist who helped uncover some of the evidence consistent with a lab origin and quantify the likelihood of a lab origin from research proposed in the DEFUSE grant. Any ethical human being knows that we need to know what caused the pandemic, and to deprive the citizenry of such information from open investigations of NIAID research in 2019 would be to deprive us of critical information we need to self-govern and elect people who manage scientific risks in ways we see fit. As a scientist, there are critical questions about bioattribution that require testing, and the way to test our hypotheses is to uncover the redacted and withheld documents from Fauci’s NIAID in 2019.
The Biden administration’s dying breath was to pardon Anthony Fauci not for the convictions for crimes he didn’t commit (?) but to avoid investigations that could be a reputational and financial burden for Anthony Fauci. A pardon to preempt an investigation is not a pardon; it is obstruction. The Biden administration’s dying breath is to obstruct our pursuit of truth and reconciliation on the ultimate cause of 1 million Americans’ dying breaths.
To remind everyone what we still need to know, it helps to look through the peephole of what we’ve already found to inspire curiosity about what else we’d find if only the peephole could be widened. Below is one of the precious few emails investigative journalists pursuing FOIAs against NIAID have managed to obtain from the critical period when SARS-CoV-2 is believed to have emerged. The email connects DEFUSE PI’s Peter Daszak (EcoHealth Alliance), Ralph Baric (UNC), Linfa Wang (Duke-NUS), Ben Hu (Wuhan Institute of Virology), Shi ZhengLi (Wuhan Institute of Virology) and others in October 2019. The subject line “NIAID SARS-CoV Call – October 30/31” connects these authors to NIAID.
It is approximately in that time range – October/November 2019 – when SARS-CoV-2 is hypothesized to have entered the human population in Wuhan. When it emerged, SARS-CoV-2 was unique among sarbecoviruses in having a furin cleavage site, as proposed by these authors in their 2019 DEFUSE grant. Of all the places the furin cleavage site could be, the furin cleavage site of SARS-CoV-2 was in the S1/S2 junction of the Spike protein, precisely as proposed by these authors.
In order to insert a furin cleavage site in a SARS-CoV, however, the researchers would’ve needed to build a reverse genetic system, i.e. a DNA copy of the virus. SARS-CoV-2 is unique among coronaviruses in having exactly the fingerprint we would expect from reverse genetic systems. There is an unusual even spacing in the cutting/pasting sites for the enzymes BsaI and BsmBI and an anomalous hot-spot of silent mutations in precisely these sites, exactly as researchers at the Wuhan Institute of Virology have done for other coronavirus reverse genetic systems. The odds of such an extreme synthetic-looking pattern occurring in nature are, conservatively, about 1 in 50 billion.
The virus did not emerge in Bangkok, Hanoi, Bago, Kunming, Guangdong, or any of the myriad other places with similar animal trade networks and greater contact rates between people and sarbecovirus reservoirs. No. The virus emerged in Wuhan, the exact place and time one would expect from DEFUSE.
With all the evidence pointing the hounds towards NIAID, it is essential for global health security that we further investigate the research NIAID funded in 2019. It is imperative for our constitutional democracy, for our ability to self-govern, that we learn the truth. The only way to learn the truth is to investigate NIAID, the agency Fauci led for 38 years, the agency that funded gain-of-function research of concern, the agency named in the October 2019 call by DEFUSE PI’s, the agency that funded this exact group in 2019.
A preemptive pardon prior to the discovery of truth is a fancy name for obstruction of justice. The Biden administration’s dying breath must be challenged, and we must allow Congress and the incoming administration to investigate the possibility that Anthony Fauci’s NIAID-supported research caused the Covid-19 pandemic.
Republished from the author’s Substack
Brownstone Institute
It’s Time to Retire ‘Misinformation’
From the Brownstone Institute
By
This article was co-authored with Mary Beth Pfieffer.
In a seismic political shift, Republicans have laid claim to an issue that Democrats left in the gutter—the declining health of Americans. True, it took a Democrat with a famous name to ask why so many people are chronically ill, disabled, and dying younger than in 47 other countries. But the message resonated with the GOP.
We have a proposal in this unfolding milieu. Let’s have a serious, nuanced discussion. Let’s retire labels that have been weaponized against Robert F. Kennedy, Jr., nominated for Health and Human Services Secretary, and many people like him.
Start with discarding threadbare words like “conspiracy theory,” “anti-vax,” and the ever-changing “misinformation.”
These linguistic sleights of hand have been deployed—by government, media, and vested interests—to dismiss policy critics and thwart debate. If post-election developments tell us anything, it is that such scorn may no longer work for a population skeptical of government overreach.
Although RFK has been lambasted for months in the press, he just scored a 47 percent approval rating in a CBS poll.
Americans are asking: Is RFK on to something?
Perhaps, as he contends, a 1986 law that all but absolved vaccine manufacturers from liability has spawned an industry driven more by profit than protection.
Maybe Americans agree with RFK that the FDA, which gets 69 percent of its budget from pharmaceutical companies, is potentially compromised. Maybe Big Pharma, similarly, gets a free pass from the television news media that it generously supports. The US and New Zealand, incidentally, are the only nations on earth that allow “direct-to-consumer” TV ads.
Finally, just maybe there’s a straight line from this unhealthy alliance to the growing list of 80 childhood shots, inevitably approved after cursory industry studies with no placebo controls. The Hepatitis B vaccine trial, for one, monitored the effects on newborns for just five days. Babies are given three doses of this questionably necessary product—intended to prevent a disease spread through sex and drug use.
Pointing out such conflicts and flaws earns critics a label: “anti-vaxxer.”
Misinformation?
If RFK is accused of being extreme or misdirected, consider the Covid-19 axioms that Americans were told by their government.
The first: The pandemic started in animals in Wuhan, China. To think otherwise, Wikipedia states, is a “conspiracy theory,” fueled by “misplaced suspicion” and “anti-Chinese racism.”
Not so fast. In a new 520-page report, a Congressional subcommittee linked the outbreak to risky US-supported virus research at a Wuhan lab at the pandemic epicenter. After 25 hearings, the subcommittee found no evidence of “natural origin.”
Is the report a slam dunk? Maybe not. But neither is an outright dismissal of a lab leak.
The same goes for other pandemic dogma, including the utility of (ineffective) masks, (harmful) lockdowns, (arbitrary) six-foot spacing, and, most prominently, vaccines that millions were coerced to take and that harmed some.
Americans were told, wrongly, that two shots would prevent Covid and stop the spread. Natural immunity from previous infection was ignored to maximize vaccine uptake.
Yet there was scant scientific support for vaccinating babies with little risk, which few other countries did; pregnant women (whose deaths soared 40 percent after the rollout), and healthy adolescents, including some who suffered a heart injury called myocarditis. The CDC calls the condition “rare;” but a new study found 223 times more cases in 2021 than the average for all vaccines in the previous 30 years.
Truth Muzzled?
Beyond this, pandemic decrees were not open to question. Millions of social media posts were removed at the behest of the White House. The ranks grew both of well-funded fact-checkers and retractions of countervailing science.
The FDA, meantime, created a popular and false storyline that the Nobel Prize-winning early-treatment drug ivermectin was for horses, not people, and might cause coma and death. Under pressure from a federal court, the FDA removed its infamous webpage, but not before it cleared the way for unapproved vaccines, possible under the law only if no alternative was available.
An emergency situation can spawn official missteps. But they become insidious when dissent is suppressed and truth is molded to fit a narrative.
The government’s failures of transparency and oversight are why we are at this juncture today. RFK—should he overcome powerful opposition—may have the last word.
The conversation he proposes won’t mean the end of vaccines or of respect for science. It will mean accountability for what happened in Covid and reform of a dysfunctional system that made it possible.
Republished from RealClearHealth
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