Dr. Jay Goes to Washington: Reforming Science from the Inside at NIH | Uncommon Knowledge
Dr. Jay Goes to Washington: Reforming Science from the Inside at NIH | Uncommon Knowledge
https://www.youtube.com/watch?v=K4Cs7Q3qmOE
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Champion of Truth
Dr. Jay Goes to Washington: Reforming Science from the Inside at NIH | Uncommon Knowledge
https://www.youtube.com/watch?v=K4Cs7Q3qmOE
“Vaccine “skeptic” David Geier has reportedly been hired by the U.S. Department of Health and Human Services (HHS) as a data analyst to oversee a new study probing the possible links between vaccinations and autism.
High-quality research and transparency are not likely outcomes from a project headed by Geier. Geier and his physician father, Mark, have published in a variety of obscure journal articles claiming that vaccines cause autism. Based on those sketchy publications, they began hiring themselves out as “expert witnesses” in hundreds of vaccine-related lawsuits. Mark Geier was stripped of his medical license by the Maryland Board of Physicians over dosing autistic children with his home-brewed treatments.
The Geiers asserted that their research had found that tiny amounts of ethyl mercury preservative (thimerosal) in some vaccines was the culprit behind the rise in autism diagnoses. Interestingly, thimerosal has never been used in the measles-mumps-rubella (MMR) vaccine that has most widely been blamed for causing autism. However, excepting seasonal flu vaccines, thimerosal in the U.S. was removed from any other vaccines in 1999. Amusingly, the Geiers took note of that fact and published an article in 2006 claiming that autism rates were subsequently declining. As it happens, the rate of autism diagnoses has increased since then. Evidently tiny amounts of mercury in vaccines has nothing to do with autism.
In any case, the claim that vaccines cause autism has been comprehensively debunked.
“The problem with the Geiers’ research is that they start with the answers and work backwards,” said Dr. Steven Black, director of the Kaiser Permanente Vaccine Study Center in Oakland, California, in 2005. “They are doing voodoo science.”
By applying his methodology in his new study of the putative relationship between autism and vaccines, Geier will doubtlessly and transparently get the answers that our new secretary of Health and Human Services thinks he already knows.”
https://reason.com/2025/04/03/rfk-jr-hires-a-vaccine-skeptic-to-find-the-cause-of-autism/
The 3 Myths Supporting NIH Funding
https://reason.com/2025/04/01/the-3-myths-supporting-nih-funding/
The Trump-Musk attack on Academia and DEI is doing more harm than good.
https://www.youtube.com/watch?v=pXx5Ziwh6is
“”The DEA’s attempt to classify DOI, a compound of great significance to both psychedelic and fundamental serotonin research, as a Schedule I substance exemplifies an administrative agency overstepping its bounds,” Rush says. “The government admits DOI is not being diverted for use outside of scientific research yet insists on placing this substance in such a restricted class that it will disrupt virtually all current research.”
SSDP describes the two compounds as “essential research chemicals in pre-clinical psychiatry and neurobiology,” noting that their unscheduled status has made them accessible as tools for studying serotonin receptors. It says DOI, in particular, has been “a cornerstone in neuroscience research” due to its selectivity for the 5-HT2A serotonin receptor, crucial for understanding the therapeutic effects of psychedelics. Scientists have used DOI to “map the localization of an important serotonin receptor in the brain critical in learning, memory, and psychiatric disease,” SSDP notes, and DOI studies “have shown encouraging results in managing pain and reducing opioid cravings.””
https://reason.com/2024/11/09/a-psychedelic-ban-would-disrupt-important-research/
“Prior to COVID-19, Fauci had long supported funding pandemic research that other scientists found risky, if not downright dangerous.
In 2005, as NIAID director, he praised researchers who’d used a grant from his agency to resurrect the virus that had caused the Spanish flu pandemic. Better understanding that virus would help prevent future diseases, he argued. “The certain benefits to be obtained by a robust and responsible research agenda aimed at developing the means to detect, prevent and treat [future pandemics] far outweigh any theoretical risks,” he said in an October 2005 statement co-authored with then–CDC Director Julie Gerberding.
This wasn’t a universal opinion at the NIAID. The agency’s chief scientist described this approach to pandemic prevention as “looking for a gas leak with a lighted match.”
Fauci would continue to praise and fund this kind of research. In 2011, researchers at the University of Wisconsin and at Erasmus University Medical Center in the Netherlands managed to manipulate the virus H5N1 (which had been responsible for a 2004 bird flu epidemic in Asia) to transmit between mammals, a “gain of function” for a virus that had heretofore only been able to pass from infected birds to humans. One of the researchers involved in the work would say the enhanced pathogen they’d created was “very, very bad news” and “probably one of the most dangerous viruses you can make.” Fauci was more sanguine, telling The New York Times that “there is always a risk. But I believe the benefits are greater than the risks.””
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“In 2014, there was a series of embarrassing safety lapses at U.S. government labs, highlighting this risk.
Dozens of CDC employees were potentially exposed to live anthrax samples shipped by mistake to labs not equipped to handle them. At another CDC lab, a less dangerous version of bird flu was accidentally contaminated with deadly H5N1. Vials of smallpox capable of infecting people were stashed in a cabinet at an NIH lab, where they’d apparently been sitting for decades. None of these incidents were direct results of gain-of-function research. But they heightened the concern that researchers working to enhance deadly pathogens might do so in unsafe settings.”
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“In 2021, Fauci said the NIH “has not ever and does not now fund gain-of-function research in the Wuhan Institute of Virology.” That wasn’t true. What EcoHealth was doing in Wuhan clearly met the widely understood definition of gain-of-function research.
In his June 2024 testimony, Fauci dodged accusations that he lied by saying that while EcoHealth’s work might have met a generic definition of gain-of-function research, it didn’t meet the precise definition established in the P3CO framework.
Fauci said that every time he mentioned gain-of-function research, “the definition that I use is not my personal definition; it is a codified, regulatory and operative definition.” That definition, he said, “had nothing to do with me.”
On the contrary, regulatory definitions had quite a bit to do with Fauci. They were designed with the expectation that he and his fellow public health bureaucrats would use discretion and good judgment when making decisions. The relevant regulatory language included lots of “likelys and highlys and reasonably anticipated,” says Gerald Epstein, a former director at the White House Office of Science and Technology Policy who wrote the P3CO policy. “These words are inherently subjective. You can’t not be. You’ve got to be making judgment calls on something that does not yet exist.” Those subjective definitions gave Fauci and his NIAID underlings considerable room to decide what research required additional review.”
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“We probably won’t ever definitively discover the origins of COVID-19.”
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“Chinese officials obstructed any investigation into the Wuhan Institute of Virology. In September 2019, the Associated Press reported, the institute took its database of viruses offline. It also hasn’t made public lab notebooks and other materials that might shed light on exactly what kinds of work it was doing in the lead-up to the pandemic. In late 2019, the Chinese government also exterminated animals and disinfected the Wuhan wet market. If COVID did leap from animal to human in the Wuhan market, as many natural origin proponents argue, that evidence is gone.
What we’re left with is studying the structure of the SARS-CoV-2 virus itself and whatever information can be gleaned from the U.S.-funded research that went on at Wuhan leading up to the pandemic.
On both fronts, Fauci, his underlings at the NIAID, and NIAID-funded scientists involved with work at Wuhan have worked to conceal information and discredit notions that COVID might have leaked from a lab.
In late January 2020, Fauci’s aides flagged the NIAID’s support of EcoHealth’s Wuhan research in emails to their boss. A few weeks later, Fauci and Daszak would go on Newt Gingrich’s podcast to dismiss the idea that COVID-19 came from the Wuhan lab, calling such arguments “conspiracy theories.”
Both men also worked to shape the discourse behind the scenes away from any focus on a lab leak. Daszak organized a group letter of scientists in The Lancet, the U.K.’s top medical journal, declaring that they “stand together to strongly condemn conspiracy theories suggesting that COVID-19 does not have a natural origin.” Daszak did not disclose his relationship to the Wuhan lab when organizing this letter; The Lancet’s editor would eventually concede that this was improper.
In testimony to the House coronavirus subcommittee in May 2024, Daszak would claim the “conspiracy theories” mentioned in the Lancet letter referred only to such wild early pandemic notions that COVID had pieces of HIV or snake DNA inserted into it. He said a word limit prevented him from being more precise.
Fauci, meanwhile, would help corral virologists into publishing the widely cited “proximal origin” paper in early 2020. In the paper, the authors flatly declared that “we do not believe any type of laboratory-leak scenario is plausible.”
Yet troves of private messages and emails released by the House subcommittee’s investigation show that the authors privately expressed far more openness to a lab leak theory.
One of the paper’s authors, Scripps Research evolutionary biologist Kristian Andersen, privately rated a lab leak as “highly likely.” But Andersen had a pending $8.9 million grant application with the NIAID as the paper was drafted. That grant was later approved. In an email, one of the paper’s authors, Edward Holmes, references “pressure from on high” during the drafting process.
The authors of the proximal origin paper say they merely had their minds changed while drafting the paper. They were just following the scientific method.”
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“Fauci’s best defense is that he ran a sprawling agency that doled out billions of dollars in grants. Even the most detail-obsessed administrator couldn’t possibly keep track of every single program and project. And U.S. officials had limited control over what happened in the distant, opaque Wuhan lab.
But even if that’s true, it’s an admission of administrative negligence, since the oversight protocols weren’t followed. It also implies a dramatic failure of the risky research that Fauci championed for pandemic prevention. As Ridley says, the pandemic “occurred with the very viruses that there was the most attention paid to, in the very area where there was the most research going on, where there was the biggest program looking for potential pandemic pathogens, and yet they failed to see this one coming.” At a minimum, gain-of-function research didn’t protect the public from the pandemic.
Meanwhile, the more direct case against Fauci is strong: Not only was he an ardent supporter of research widely believed to be risky, but he manipulated bureaucratic protocols in order to avoid scrutiny of that research, then responded evasively when called to account for his actions. At least one of the programs born out of Fauci’s risky research crusade was pursuing exactly the type of viral enhancements that were present in COVID-19, and that research was conducted at the Wuhan virology lab in the very same city where the virus originated. Lab leak proponents cite the virus’s transmissibility as evidence for a Wuhan leak: After all, EcoHealth was trying to create pathogens primed to spread rapidly in humans.
The evidence is not fully conclusive. But it seems reasonably likely that Fauci pushed for what his peers repeatedly said was dangerous research, that some of that dangerous research produced a deadly viral pathogen that escaped the lab, and that Fauci helped cover up evidence and arguments for its origins.”
https://reason.com/2024/09/14/faucis-pandemic/
“As earlier threatened, the Food and Drug Administration (FDA) has just issued new rules that will significantly slow down the development of new diagnostic tests. Specifically, the agency requires that all laboratory-developed tests (LDTs) be submitted to its regulators before the tests can be offered to patients and physicians. As I explained earlier, LDTs are in vitro diagnostic (IVD) tests for clinical use that are designed, manufactured, and performed by individual laboratories. They can diagnose illnesses and guide treatments by detecting relevant biomarkers in saliva, blood, or tissues; the tests can identify small molecules, proteins, RNA, DNA, cells, and pathogens. For example, some assess the risks of developing Alzheimer’s disease or guide the treatment of breast cancer.”
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” “Laboratory developed testing services are not medical devices and subjecting them to medical device regulation will harm patient access to needed testing and compromise innovations that drive personalized medicine,” said American Clinical Laboratory Association President Susan Van Meter in a statement. “The rule will limit access to scores of critical tests, increase health care costs, and undermine innovation in new diagnostics.””
https://reason.com/2024/04/29/fda-once-again-stands-athwart-biomedical-innovation-yelling-stop/
“the World Health Organization’s International Agency for Research on Cancer (IARC) declared aspartame as “possibly carcinogenic.” Another WHO committee, the Joint FAO/WHO Expert Committee on Food Additives (JECFA), independently assessed the ingredient, too, but maintained its existing recommendation — suggesting not that people cut the substance entirely out of their diets but that they limit their daily aspartame consumption to about 40 mg per kilogram (or about 2.2 pounds) of body weight. Diet soda contains about 200 mg of aspartame per 12-ounce can. By that measure, an adult weighing 60 kg, or roughly 132 pounds, would need to drink about 12 cans of diet soda a day to exceed the JECFA’s recommendation, assuming they had nothing else containing aspartame.
Making matters more confounding, the Food and Drug Administration had yet another take. It told Vox in an email that it had reviewed the information used in WHO’s assessment and “identified significant shortcomings” in the studies the agency relied on. “Aspartame is one of the most studied food additives in the human food supply,” the agency added.”
“The new study includes Exxon’s graphs, models, projections and publications that show it understood how its business would affect the planet, according to the researchers Geoffrey Supran of the University of Miami, Stefan Rahmstorf of the University of Potsdam and Naomi Oreskes of Harvard University. Oreskes previously co-authored the book “Merchants of Doubt,” which detailed the efforts of a small number of scientific researchers who worked to undermine the public’s acceptance of climate science.
“All told, ExxonMobil was aware of contemporary climate science, contributed to that science, and predicted future global warming correctly,” the researchers wrote. “ExxonMobil accurately foresaw the threat of human-caused global warming, both prior and parallel to orchestrating lobbying and propaganda campaigns to delay climate action.”
Exxon spokesperson Todd Spitler rebutted the claims and said the company supports addressing climate change.”
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“Exxon’s models aligned with the best science between 1970 and 1990, the paper found. Exxon projected 0.2 degrees Celsius (0.36 Fahrenheit) of warming every decade with a 0.04-degree C margin of error. That figure is close to the 0.19 degrees C rise and 0.03-degree C margin of error derived from 18 government and academic models.
Under one metric, Exxon proved more precise than famed NASA climate scientist James Hansen, who first brought global warming to Congress’ attention in 1988.
“It has been established that, for many years, Exxon’s public affairs strategy was — as a 1988 internal memo put it — to ‘emphasize the uncertainty in scientific conclusions regarding the potential enhanced greenhouse effect,’” the report said. “However, our analysis shows that in their reports and briefings to management, ExxonMobil’s own scientists did not particularly emphasize uncertainty.””
“Right now, the majority of published scientific findings — and the vast majority of prestigious new research — is hidden behind paywalls. Most of the top scientific publications charge readers high fees for access, with prices that are rising faster than inflation. An annual membership with Nature costs $199, Science starts at $79 per year, and The Lancet charges $227. And these are only a few of the hundreds of journals where new research appears.
This money goes to publishers, not to the academics who actually write scientific papers.”
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“in a bid to tear down the paywall and make science more accessible to all, the White House last month announced new guidelines requiring that all taxpayer-funded research, including data used for a study, be made public at no cost by the end of 2025.
The Biden plan is one of the biggest wins yet for the “open science” movement. In practice, it often refers to publishing the papers that describe new scientific findings immediately and without paywalls. It can also include publicly sharing full datasets and code used for analysis.”
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“Freeing research largely paid for by taxpayer money can seem like a no-brainer, but over time, the potential downsides of open science efforts like the Plan S mandate have become more apparent. While pay-to-publish but free-to-read platforms bring more research to the public, they can add barriers for researchers and worsen some existing inequalities in academia. Scientific publishing will remain a for-profit industry and a highly lucrative one for publishers. Shifting the fees onto authors doesn’t change this.
Many of the newly founded open-access journals drop the fees entirely, but even if they’re not trying to make a profit, they still need to cover their operating costs. They fall back on ad revenue, individual donations or philanthropic grants, corporate sponsorship, and even crowdfunding.
But open-access platforms often lack the prestige of well-known top journals like Nature. Scientists early in their careers — as well as those at less wealthy universities in low-income countries — often rely on precarious, short-term grant funding to carry out their research. Their career depends on putting out an impressive publication record, which is already an uphill battle.
The established journals are reluctant to commit to open access, since submission fees may deter potential researchers from sending in their work. And if journals don’t charge submission fees or reader subscriptions, they’ll have to turn to other sources of income, which may be unsustainable in the long run.”