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House Republicans on the subcommittee probing the origin of the Covid-19 virus appear to have inadvertently released a trove of new documents related to their investigation that shed light on deliberations among the scientists who drafted a key paper in February and March of 2020. The paper, published in Nature Medicine on March 17, 2020, was titled "The Proximal Origin of SARS-CoV-2" and played a leading role in creating a public impression of a scientific consensus that the virus had emerged naturally in a Chinese "wet market." The paper was the subject of a hearing on Capitol Hill on Tuesday, which coincided with the release of a report by the subcommittee devoted to the "Proximal Origin" paper. The scientists believed one thing in private – that lab escape was likely – while working to produce a paper saying the opposite in public. Much of Tuesday's hearing focused on a critical few days in early February 2020, beginning with a conference call February 1 that included the eventual authors of the paper and Drs. Anthony Fauci, then head of the National Institute of Allergy and Infectious Diseases, and Francis Collins, then head of its parent agency, the National Institutes of Health. Later minutes showed that the consensus among the experts leaned toward a lab escape. Yet within days, they were circulating a draft – including to Fauci and Collins – that came to the opposite conclusion, the first draft of which had been finished the same day of the conference call.
Note: Read more about the leaked documents that reveal high level covid science manipulation. For more along these lines, see concise summaries of deeply revealing news articles on government corruption and the coronavirus from reliable major media sources.
In 1953, a paper developed for cigarette maker RJ Reynolds detailed possible cancer-causing agents in tobacco, but the document would remain hidden from public view for decades. In the interim, the industry told the public: "We don't accept the idea that there are harmful agents in tobacco." The chemical industry, it seemed, took note. Just a few years later, DuPont scientists found PFAS enlarged lab rats' livers and likely caused birth defects in workers. Still, the company told its employees the cancer-linked compounds are "about as toxic as table salt". Like the tobacco industry before it, the chemical industry managed to keep PFAS's health risks hidden from the public for decades. A new peer-reviewed study dissecting PFAS producers' public relations strategies provides a smoking gun timeline composed of industry studies and comments from DuPont and 3M officials showing they knew the dangers, but publicly insisted the chemicals were safe. Between 1961 and 2006, the authors identified dozens of instances where DuPont or 3M scientists discovered or acknowledged PFAS toxicity internally, but did not publish the findings or report them to the EPA, as required under federal law. DuPont's chief toxicologist in 1961 found rats' livers enlarged at very low doses of exposure, a health impact recognized as "the most sensitive sign of toxicity." The report recommended PFAS be handled "with extreme care" and that "contact with the skin should be strictly avoided."
Note: These chemicals have contaminated 41 percent of US tap water. For more along these lines, see concise summaries of deeply revealing news articles on corruption in science and in the corporate world from reliable major media sources.
The Biological Weapons Convention (BWC) prohibits the production, use, development, stockpiling, or transfer of biological toxins or disease-causing organisms against humans, animals, or plants. More than 180 countries are party to the pact, which came into force in 1975 as the first multilateral treaty to ban an entire class of weapon. And in the years since, the taboo against state use of biological weapons has largely held. Yet a volatile geopolitical environment, combined with the rapid advance and increased access in the ability to edit and engineer pathogens, is straining and testing the nearly 50-year-old BWC as never before. From the BWC's beginnings, critics have said it lacked vital elements, like a verification mechanism to make sure everyone is following it. Global tensions, scientific advances, and the ever-expanding repertoire of what is possible with both biology and chemistry are making those flaws and cracks ever more visible. Some high-profile mishaps linked to the US chemical and biological weapons programs ... along with public anger over the use of herbicides like Agent Orange during the Vietnam War, prompted Congress to pressure the Nixon administration to review the biological and chemical weapons programs. Contagions are hard to control and contain, and the same pathogens that can infect your target can also sicken you and your population. This is also why they tend to be used as a stealth agent of war. "The holy grail that we've struggled with with the Biological Weapons Convention is how do you verify that the countries that have signed up to the treaty are not making biological weapons?" said Kenneth Ward, US special representative to the Biological Weapons Convention.
Note: Watch our latest Mindful News Brief series on the strong evidence that bioweapons research created COVID-19. Learn more about emerging warfare technology in our comprehensive Military-Intelligence Corruption Information Center. For more, see concise summaries of deeply revealing news articles on science corruption from reliable major media sources.
The origin of SARS-CoV-2, the agent that causes the disease COVID-19, remains a mystery. But there are purportedly a few high up in government and scientific communities well aware of its genesis. In "The Truth About Wuhan: How I Uncovered the Biggest Lie in History," Andrew G. Huff, former EcoHealth Alliance vice president and senior scientist, details his coming forward "as a material witness and whistleblower related to SARS-CoV-2." "The Truth About Wuhan" [contains] an insider's view of working for EcoHealth Alliance; a damning critique of models and techniques used to hunt coronaviruses; a reasoned aversion to "gain of function" research; the real COVID-19 timeline; China and U.S. culpability in the virus mayhem; and the multifarious, direct attacks used by the federal government to harass and discredit Mr. Huff. According to the author, "SARS-CoV-2 leaked from the [Wuhan Institute of Virology] laboratory as early as August 2019. The probable cases detected in Italy in 2019 make sense as Italy is one of the most popular tourist destinations of the Chinese. By mid-October 2019 the disease was likely already on every continent except Antarctica. The DoD, along with militaries globally, detected the disease in their countries' service members that attended the Military World Games in Wuhan. Trying to avoid global panic, governments began to implement response plans, which included the U.S. government's mobilization of the mRNA SARS-CoV-2 gene therapy."
Note: Before buying this book, you might read this review and the reviews on Amazon. For more along these lines, see concise summaries of deeply revealing news articles on the coronavirus from reliable major media sources.
New scientific breakthroughs make it increasingly easy to identify dangerous viruses in nature, manipulate them in the lab and synthetically create them from genetic sequences. But some scientists have taken it further, adding "gain of function" mutations that make potential pandemic viruses more transmissible. The National Institutes of Health funded two research groups to increase the transmissibility of an earlier strain of avian influenza that had killed hundreds of people but could not efficiently spread from person to person. Both groups created viral mutants that could transmit in ferrets. The Obama administration was so alarmed that it halted gain-of-function work on potential pandemic influenza viruses in 2014, but the N.I.H. allowed it to restart by 2019. In my view, there is no justification for intentionally making potential pandemic viruses more transmissible. The consequences of an accident could be too horrific, and such engineered viruses are not needed for vaccines anyway. Natural viruses that haven't yet infected humans can also pose a risk if researchers try to find the most dangerous ones and bring them back to the lab for experiments. Suspicions about a lab-accident origin of SARS-CoV-2 have been fueled by the fact that the Wuhan Institute of Virology was involved in Chinese and international efforts to find and experiment with new high-risk coronaviruses. A final category of pandemic risk involves viruses that used to transmit in humans but became extinct long ago – like the 1918 influenza virus.
Note: For more along these lines, see concise summaries of deeply revealing news articles on science corruption and the coronavirus from reliable major media sources.
Twice in the last week, Pennsylvania’s official COVID-19 death count spiked. Then, on Thursday, the number plummeted. The state Department of Health provided several justifications for the fluctuations, citing technical issues, lengthy investigations, and the addition of “probable” deaths. Facing mounting questions about the accuracy of the count, officials on Thursday removed more than 200 probable deaths from the tally. Health Secretary Rachel Levine said the change was made in an effort to be transparent. The state’s coroners – tasked with investigating suspicious deaths – have grown increasingly frustrated by the Health Department’s reluctance to seek their help. “There’s a discrepancy in the numbers,” Charles E. Kiessling Jr., president of the Pennsylvania Coroners Association ... said Thursday. The confusion began Sunday, when Pennsylvania raised its coronavirus death toll to 1,112 – an increase of 276 overnight. On Tuesday, the department reported another spike, from 1,204 to 1,564 deaths.The jump that day, first blamed on a computer glitch, was explained as a “reconciliation” of multiple reporting systems.” Levine also said the “significant increase” included “probable positive” COVID-19 deaths. “We will now be reporting probable deaths related to COVID-19 in addition to confirmed deaths,” she said. Jeffrey Conner, the coroner in Franklin County, said he was blindsided by the department’s news on Tuesday that 10 people had died of COVID-19 in the county. As of Wednesday afternoon, he said, he was aware of only one death. On Thursday, the state’s revised data reported just one death for the county.
Note: For more along these lines, see concise summaries of deeply revealing news articles on the coronavirus from reliable major media sources.
Scientific misconduct does not happen only at Stanford and Harvard. Of the nearly 5,500 retractions we catalogue in 2022, and the thousands of cases we have reported on since launching our watchdog website Retraction Watch in 2010, the vast majority involve researchers at institutions without anywhere near Stanford and Harvard's pedigrees. The number of retractions each year reflects about a tenth of a percent of the papers published in a given year – in other words, one in 1,000. Yet the figure has grown significantly from about 40 retractions in 2000, far outpacing growth in the annual volume of papers published. Retractions have risen sharply in recent years for two main reasons: first, sleuthing, largely by volunteers who comb academic literature for anomalies, and, second, major publishers' (belated) recognition that their business models have made them susceptible to paper mills – scientific chop shops that sell everything from authorships to entire manuscripts to researchers who need to publish lest they perish. These are not merely academic matters. Particularly when it comes to medical research, faker hurts real people. The truth, however, is that the number of retractions in 2022 – 5,500 – is almost definitely a vast undercount of how much misconduct and fraud exists. We estimate that at least 100,000 retractions should occur every year. Journals and publishers ... fail to do their part, finding ways to ignore criticism of what they have published, leaving fatally flawed work flagged.
Note: Back in 2015, the editor-in-chef of The Lancet, one of the most prestigious medical journals in the world, wrote that much of scientific literature, perhaps half, may simply be untrue. According to a revealing article by Nature, a leading science journal, medicine is plagued by untrustworthy clinical trials. Who can we trust? For more along these lines, see concise summaries of deeply revealing news articles on science corruption from reliable major media sources.
Trust in public health has been shattered–half of America has lost faith in the scientific community altogether. Our current government is doubling down on World Health Organization (WHO) decrees that directly circumvent public oversight. The WHO has drafted a new global Pandemic Accord. The U.S. ambassador to the WHO, Pamela Hamamoto, on February 27 imprudently promised "The United States is committed to the Pandemic Accord." This comes immediately after the exposure of yet another disgrace undermining trust in public health institutions. It turned out the February 2020 Lancet article calling the lab origin of the SARS-CoV-2 virus a "conspiracy theory" was itself the true conspiracy, contrived behind closed doors contemporaneously with a March 2020 publication in Nature. If that coordinated media campaign was designed to conceal malfeasance by Drs. Francis Collins and Anthony Fauci–who, as leaders of America's National Institutes of Health, reportedly sent American tax dollars to fund China's dangerous gain-of-function research and circumvent Obama administration-introduced restrictions–we may be witnessing the deadliest cover-up scandal in history. News media are also beginning to acknowledge facts that refute the original reasons behind lockdowns. Despite protestations to the contrary, all signers of the Pandemic Accord clearly relinquish critical autonomy to the WHO. Most ominous is that WHO defines "public health emergency" on its own terms.
Note: For more along these lines, see concise summaries of deeply revealing news articles on government corruption and the coronavirus from reliable major media sources.
The work of a task force commissioned by the Lancet into the origins of covid-19 has folded after concerns about the conflicts of interest of one its members and his ties through a non-profit organisation to the Wuhan Institute of Virology. Task force chair Jeffrey Sachs ... told the Wall Street Journal that he had shut down the scientist led investigation into how the covid-19 pandemic started because of concerns about its links to the EcoHealth Alliance, a non-profit organisation run by task force member Peter Daszak. The decision came as evidence continued to accumulate that Daszak had not always been forthright about his research and his financial ties to the Wuhan Institute of Virology. EcoHealth Alliance has been given millions of dollars in grants by the US federal government to research viruses for pandemic preparedness. The alliance has subcontracted out its research ... to the Wuhan Institute of Virology. Shortly after the pandemic began Daszak led a February 2020 statement in the Lancet alleging that it was a "conspiracy theory" to argue that the pandemic could have started from a laboratory leak in Wuhan. "I have no conflicts of interest," Daszak later told the Washington Post. But Daszak's story began falling apart last November when the non-profit group US Right to Know published emails ... that showed he had orchestrated the Lancet statement without disclosing that he was funding Shi Zhengli through grants from the National Institutes of Health (NIH).
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A small group of scientists and others who believe the novel coronavirus that spawned the pandemic could have originated from a lab leak or accident is calling for an inquiry independent of the World Health Organization's team of independent experts sent to China last month. Officials with the W.H.O. have said in recent interviews that it was "extremely unlikely" but not impossible that the spread of the virus was linked to some lab accident. The open letter ... lists what the signers see as flaws in the joint W.H.O.-China inquiry. The letter emphasized that the team was denied access to some records and did not investigate laboratories in China. Dr. David A. Relman, a professor of medicine and microbiology at Stanford University [said] "the W.H.O. investigation appears to be biased, skewed, and insufficient." Richard Ebright, a molecular biologist at Rutgers University and one of the scientists who signed the letter, said it grew out of a series of online discussions among scientists, policy experts and others who came to be known informally as the Paris group. Many of those who signed the letter were based in France and Dr. Ebright, who has been outspoken about the need to investigate a possible laboratory leak, said such discussion had been less vigorous in the United States. He said that no one in the group thought that the virus had been intentionally created as a weapon, but they were all convinced that an origin in a lab through research or by accidental infection was as likely as a spillover occurring in nature from animals to humans.
Note: Read more about the controversial "gain-of-function" research that took place at the Wuhan Institute of Virology. For more along these lines, see concise summaries of deeply revealing news articles on the coronavirus from reliable major media sources.
Senior officials at the U.S. Centers for Disease Control and Prevention told staffers to avoid using seven words such as science-based and fetus in budget-related documents. The backlash was swift and strident; headlines accused the CDC of censoring scientific ideas. Documents recently obtained via two Freedom of Information Act (FOIA) requests indicate the CDC and other executive branch agencies ... quietly implement organized strategies to control the flow and tone of scientific information to the press and the public. Moreover, these practices have been in place under both the Trump and Obama administrations. The techniques being used are much more subtle ... than mere censorship. Two agencies under the Department of Health and Human Services umbrella have erected obstacles to reporters access to federal scientists. And by striking backroom deals with favored journalists, press officers try to get reporters to cleave to an official narrative. Meanwhile government workers at the FDA, are also portraying a ... press-restraining practice as a boon to journalists. In a so-called close-hold embargo - exposed by Scientific American in 2016 - a few select journalists are given early access to information; in return they agree to hold off on publishing until the agency gives the go-ahead, and to let officials choose whom the reporter may speak with before the embargo expires. Collectively, these practices at the FDA and CDC are staunching the flow of important science and policy decisions to the public.
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More than six years after the FBI crime laboratory was rocked by controversy, the Justice Department has identified about 3,000 criminal cases that could have been affected by flawed science and skewed testimony. Government officials told The Associated Press they are aware of between 100 and 150 cases in which prosecutors have alerted defendants of problems they concluded were material to verdicts. None has resulted in overturned convictions, they said. The identification of cases and prosecutorial reviews are the final stages of a scandal that shook the FBI during the mid-1990s when a senior chemist at the famed crime lab went public with allegations of shoddy work, tainted evidence and skewed testimony. A Justice Department internal investigation concluded in 1997 that 13 lab technicians made scientific errors in cases or slanted testimony to help prosecutors. Several were reprimanded, but none was fired or prosecuted. Some criminal defense lawyers are concerned by the Justice Department's decision to let federal, state and local prosecutors decide whether to notify defendants of problems. "That's like asking the fox to guard the hen house," said former federal prosecutor Neal Sonnett. He is past president of the National Association of Criminal Defense Lawyers. "If there is a possibility that evidence has been tainted, then the Department of Justice or prosecutors should not be the arbiter of whether it's material," Sonnett said.
Note: In 2015, the FBI admitted its scientists used flawed evidence for decades to help prosecutors wrongfully convict defendants. For more along these lines, see concise summaries of deeply revealing news articles on government corruption from reliable major media sources.
A group of whistleblowers has provided evidence that the Environmental Protection Agency has not adequately assessed the health risks posed by several new chemicals on the grounds that they are corrosive. Those harms include cancer, miscarriage, and neurotoxicity, according to the whistleblowers, who work as health assessors in the division. In some cases â₏¦ the risks were calculated, found to be significant, and later deleted from official documents. In March 2020, Gallagher, the human health assessor, found that another chemical presented risks to workers. Information [about the hazards] was included in a version of the assessment. But a month later, a manager in the New Chemicals Division created a new assessment [that] explained: "Risks were not evaluated for workers via repeated dermal exposures because dermal exposures are not considered likely due to the corrosivity of the new chemical substance." According to the whistleblowers, this statement is false. "It is intentionally misleading for EPA to put into a report that we did not calculate risk when we did," said Martin Phillips, a chemist and human health assessor who works in the EPA's Office of Pollution Prevention and Toxics. "It's lying about what we did. It's not just that we did the calculations. We did the calculations and found risks, and then they got rid of them and said that we didn't calculate them. It's fundamentally inaccurate."
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The Environmental Protection Agency's (EPA) internal watchdog has found that top agency officials retaliated against three staffers for expressing different scientific opinions. The employees who were victims of this alleged retaliation thought chemicals should be considered more toxic, while top officials sought to consider them safer, according to the reports from the EPA's inspector general. EPA scientist Sarah Gallagher says she thought the agency should consider the chemical as toxic to fetal development, while another official wanted to classify it as a lower-priority body weight issue. In another case documented in a report finding retaliation against scientist Martin Phillips, a senior science adviser allegedly changed an assessment in a way that removed "reproductive toxicity" as a concern from safety information that goes to people who work with the chemical. In a third report finding retaliation against scientist William Irwin, a manager also allegedly tried to remove evidence of reproductive toxicity. These instances appeared to have a chilling effect that could impact other agency scientists' willingness to stand up to management. "Other assessors noticed how those who disagreed with management were perceived," the reports said. They added that a person whose name was redacted testified that disagreeing or delaying the resolution of backlogged cases could cause management to label an employee "problematic."
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In December of 2002, Sharyl Attkisson, an Emmy-winning investigative reporter for CBS News, had an unsettling interview with smallpox expert Jonathan Tucker. In a post-9/11 world, with fears of terrorists using a long-eradicated disease like smallpox as a bioweapon, the US was preparing to bring back the smallpox inoculation program. But to Tucker, the very idea was "agonizing," writes Attkisson. Why? Because it involved "weighing the risk of a possible terrorist use of smallpox ... against the known risks of the vaccine," Tucker told the author. "A â€toxic' vaccine?" She writes. "Didn't the smallpox vaccine save the world?" But as she soon discovered, it had serious side effects, including a surprisingly high possibility of death. Attkisson witnessed firsthand how deadly the vaccine could be in April of 2003, when a colleague at NBC, journalist David Bloom, died from deep vein thrombosis while on assignment in Iraq. He'd also recently been vaccinated for smallpox, and ... thrombosis was a possible side effect of the inoculation. The majority of scientific studies are funded and even dictated by drug companies. "Studies that could stand to truly solve our most consequential health problems aren't done if they don't ultimately advance a profitable pill or injection," Attkisson writes. "These aren't necessarily drugs designed to make us well, but ones we'll â€need' for life," writes Attkisson. Some [drug companies] hire "ghostwriters" to author studies promoting a new drug, exaggerating benefits and downplaying risks, and then paying a doctor or medical expert to sign their name to it. "We exist largely in an artificial reality brought to you by the makers of the latest pill or injection," she writes. "It's a reality where invisible forces work daily to hype fears about certain illnesses, and exaggerate the supposed benefits of treatments and cures."
Note: Top leaders in the field of medicine and science have spoken out about the rampant corruption and conflicts of interest in those industries. For more along these lines, see concise summaries of deeply revealing news articles on Big Pharma corruption from reliable major media sources.
Nearly half of the AI-based medical devices approved by the US Food and Drug Administration (FDA) have not been trained on real patient data, according to a new study. The study, published in Nature Medicine, finds that 226 of the 521 devices authorised by the FDA lack published clinical validation data. "Although AI device manufacturers boast of the credibility of their technology with FDA authorisation, clearance does not mean that the devices have been properly evaluated for clinical effectiveness using real patient data," says first author Sammy Chouffani El Fassi. The US team of researchers examined the FDA's official "Artificial Intelligence and Machine Learning (AI/ML)-Enabled Medical Devices" database. "Using these hundreds of devices in this database, we wanted to determine what it really means for an AI medical device to be FDA-authorised," says Professor Gail Henderson, a researcher at the University of North Carolina's Department of Social Medicine. Of the 521 devices in this database, just 22 were validated using the "gold standard" – randomised controlled trials, while 43% (226) didn't have any published clinical validation. Some of these devices used "phantom images" instead – computer-generated images that didn't come from real patients. The rest of the devices used retrospective or prospective validation – tests based on patient data from the past or in real-time, respectively.
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A recent audit of Pentagon funding of gain-of-function research outside the US "may have shielded" collaborations with Chinese biotech firms – including at least one linked to Beijing's military, a Republican senator alleged. Sen. Roger Marshall (R-Kan.) pressed Defense Secretary Lloyd Austin for answers about redactions that had concealed the firms – WuXi AppTec, Pharmaron Beijing Co., and Genscript Inc. – from public scrutiny in the audit, according to a letter. "American taxpayers deserve transparency about the programs they are funding, and I am disappointed this OIG report does not provide that accountability," Marshall wrote. According to the Defense Department Office of Inspector General audit, more than $15.5 million in grants between 2014 and 2023 flowed through subrecipients to "contracting research organization[s] in China or other foreign countries for research related to potential enhancement of pathogens of pandemic potential." However, the 20-page audit cited "significant limitations with the adequacy of data" – and said the Pentagon "did not track funding at the level of detail necessary to determine whether the DoD provided funding ... for the gain-of-function experiments. Such research is classified as "offensive biological work" by the Pentagon, which Marshall said "raises questions" about National Institutes of Health (NIH) officials having admitted this year to funding gain-of-function experiments at the ... Wuhan Institute of Virology.
Note: Watch our 15-min Mindful News Brief video on the strong evidence that bioweapons research created COVID-19. For more along these lines, see concise summaries of deeply revealing news articles on COVID-19 and military corruption from reliable major media sources.
For nearly nine years Anthony Fauci's institute concealed plans to engineer a pandemic capable mpox virus with a case fatality rate of up to 15 percent, congressional investigators revealed in a new report. In June 2015, a scientist at the National Institute of Allergy and Infectious Diseases received formal approval from the National Institutes of Health's Institutional Review Board for experiments expected to engineer an mpox virus with high transmissibility and moderate mortality. NIAID – the institute Fauci oversaw for nearly four decades and which underwrites most federally funded gain-of-function research – concealed the project's approval from investigators with the House Committee on Energy and Commerce over the course of a 17 month-long investigation. [The] report describes the obstruction and secrecy around the mpox proposal as a case study in how the institute "oversees and accounts for the monitoring of potentially dangerous gain-of-function research of concern." The revelations land amid global concerns about whether coronavirus gain-of-function research – research that might generate pathogens with increased pathogenicity or transmissibility – may have contributed to the worst pandemic in a century. The committee, in conjunction with the House Committee on Oversight and Reform, is also investigating coronavirus gain-of-function research underwritten by NIAID at the Wuhan Institute of Virology, and faces similar stonewalling in that investigation.
Note: Watch our 15-min Mindful News Brief video on the strong evidence that bioweapons research created COVID-19. For more along these lines, see concise summaries of deeply revealing news articles on COVID and government corruption from reliable major media sources.
Experienced professionals are increasingly scared to openly discuss their views on the treatment of children questioning their gender identity. This was the conclusion drawn by Hilary Cass in her review of gender identity services for children this week, which warned that a toxic debate had resulted in a culture of fear. Her conclusion was echoed by doctors, academic researchers and scientists. Some said they had been deterred from pursuing what they believed to be crucial studies, saying that merely entering the arena would put their reputation at risk. Others spoke of abuse on social media, academic conferences being shut down, biases in publishing and the personal cost of speaking out. Sallie Baxendale, a professor of clinical neuropsychology ... received abuse after publishing a systematic review of studies that investigated the impact of puberty blockers on brain development. Her review found that "critical questions" remained around the nature, extent and permanence of any arrested development of cognitive function linked to the treatment. The paper, which summarised the state of relevant research, was met with an immediate backlash. "I've been accused of being an anti-trans activist, and that now comes up on Google and is never going to go away," Baxendale said. "Imagine what it's like if that is the first thing that comes up when people Google you? Anyone who publishes in this field has got to be prepared for that."
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A robust British review found guidelines for the treatment of children with gender dysphoria ignored standards and are based on flimsy foundations. Pediatrician Hilary Cass' much-anticipated report found no reliable evidence on which to base gender-affirming care for youth; the rationale for blocking puberty in young children remains unclear and muddled and that the use of cross-sex hormones in the under-18s presents numerous unknowns. Cass said published studies suffer from "remarkably weak evidence," that results are "exaggerated or mispresented" by people on both sides of the debate over transgender health care to bolster their own viewpoint. Cass found that there is no solid evidence on the long-term outcomes of any of the interventions. Cass said the toxicity of the debate has been exceptional. "There are few other areas of healthcare where professionals are so afraid to openly discuss their views, where people are vilified on social media and where name-calling echoes the worst bullying behaviour. This must stop," Cass wrote. The systematic review on puberty blockers found no evidence the drugs improve body image or dysphoria. The drugs might temporarily or permanently disrupt adolescent brain maturation, "which could have a significant impact on the young person's ability to make complex risk-laden decisions, as well as having possible longer-term neuropsychological consequences," according to the Cass report.
Note: For more along these lines, see concise summaries of deeply revealing news articles on health and corruption in science from reliable major media sources.
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