Health News Articles
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The maker of a drug shown to shorten recovery time for severely ill COVID-19 patients says it will charge $2,340 for a typical treatment course for people covered by government health programs in the United States and other developed countries. Gilead Sciences announced the price Monday for remdesivir, and said the price would be $3,120 for patients with private insurance. The amount that patients pay out of pocket depends on insurance, income and other factors. The price was swiftly criticized; a consumer group called it an outrage because of the amount taxpayers invested toward the drug's development. In 127 poor or middle-income countries, Gilead is allowing generic makers to supply the drug; two countries are doing that for around $600 per treatment course. The drug, given through an IV, interferes with the coronaviruss ability to copy its genetic material. In a U.S. government-led study, remdesivir shortened recovery time by 31% 11 days on average versus 15 days for those given just usual care. Peter Maybarduk, a lawyer at the consumer group Public Citizen, called the price an outrage. Remdesivir should be in the public domain because the drug received at least $70 million in public funding toward its development, he said. The price puts to rest any notion that drug companies will do the right thing because it is a pandemic, Dr. Peter Bach, a health policy expert ... said. The price might have been fine if the company had demonstrated that the treatment saved lives. It didnt.
Note: The March coronavirus package passed in the U.S. "not only omitted language that would have limited drug makers intellectual property rights, it specifically prohibited the federal government from taking any action if it has concerns that the treatments or vaccines developed with public funds are priced too high." While many suffer economically from the virus, big Pharma is raking in big bucks. For more along these lines, see concise summaries of deeply revealing news articles on Big Pharma corruption and the coronavirus from reliable major media sources.
Lately, my country has caught the attention of the media. Swedens response to the pandemic has been singled out as radical, lax and controversial because Sweden has not imposed a broad general lockdown. Sweden is known as a country with a strong welfare model, including public healthcare for all, and has among the worlds highest life expectancies. Some might find it difficult to reconcile this image with our approach to containing COVID-19. Sweden shares the same goals as all other countries to save lives and protect public health. Swedens measures differ from other countries in a few significant ways. We are not shutting down schools for younger children or daycare facilities. We have no regulation that forces citizens to remain in their homes. And we have not ordered the closure of any businesses. Swedish laws on communicable diseases are mostly based on voluntary measures and on individual responsibility. The use of recommendations in public health efforts rather than mandates is a common strategy in Sweden. One example of this is child immunizations. In contrast to the United States, where all 50 states mandate immunizations for children in order to enroll in school ... Swedens child vaccination program is based on recommendations from the authorities and is not a legal requirement. Yet more than 97% of Swedish children are vaccinated. Swedens strategy may not provide all the answers, but we believe the combination of voluntary and mandated measures is not only more sustainable for Sweden than a lockdown strategy but will strengthen the resilience of Swedish society to fight this virus in the long run.
Note: Almost every other major media article criticizes Sweden for its approach, which is supported by more than 80% of Swedes. And almost every news article compares them to other Scandinavian countries, which are doing much better than Sweden, but fails to mention its neighbors France, Belgium, and the UK, which have locked down, and are doing much worse than Sweden. Yet even the New York Times has admitted their economy will fair better than most other countries. For more, see concise summaries of revealing news articles on the coronavirus from media sources.
A woman with COVID-19 at a Solano County hospital the nations first case from an unknown source exposed 121 health workers to the coronavirus, yet only three got the disease, a new study of the February case reveals. All three had been in close contact for about two hours with the patient, and two had no protective gear, according to the report published Tuesday by the Centers for Disease Control and Prevention. Those workers also examined the patient and performed treatments that involved close contact, such as placing her on a breathing machine. The researchers tested just 43 of the 121 workers for the coronavirus because only they had developed a cough or other symptoms similar to those of COVID-19 patients within two weeks after exposure. Across the country, more than 9,200 health workers out of an estimated 18 million have the disease, the CDC reported Tuesday in a separate paper, which notes that the number probably understates the true number of coronavirus infections. Dr. Robert Siegel, an infectious disease expert at Stanford, called the relatively low infection rate from the Solano County patient a hopeful sign. But he added that public health officials should remain vigilant in protecting workers. The results are promising for health care workers. It means that the risk may be less than we thought, Siegel said.
Note: If only three out of 121 got the virus, and those three all had prolonged exposure, how contagious really is it? Explore a ZeroHedge article titled "Whistleblower: How CDC Is Manipulating The COVID-19 Death-Toll." For more along these lines, see concise summaries of deeply revealing news articles on health and the coronavirus pandemic from reliable major media sources.
The Environmental Protection Agency on Thursday announced a sweeping relaxation of environmental rules in response to the coronavirus pandemic, allowing power plants, factories and other facilities to determine for themselves if they are able to meet legal requirements on reporting air and water pollution. The move comes amid an influx of requests from businesses for a relaxation of regulations as they face layoffs, personnel restrictions and other problems related to the coronavirus outbreak. Issued by the E.P.A.s top compliance official, Susan P. Bodine, the policy sets new guidelines for companies to monitor themselves for an undetermined period of time during the outbreak and says that the agency will not issue fines for violations of certain air, water and hazardous-waste-reporting requirements. Companies are normally required to report when their factories discharge certain levels of pollution. The order asks companies to act responsibly if they cannot ... monitor or report the release of hazardous air pollution. Businesses, it said, should minimize the effects and duration of any noncompliance and keep records to report to the agency how Covid-19 restrictions prevented them from meeting pollution rules. Gina McCarthy, who led the E.P.A. under the Obama administration ... called it an open license to pollute. She said that while individual companies might need flexibility, this brazen directive is nothing short of an abject abdication of the E.P.A. mission to protect our well being.
Note: For more along these lines, see concise summaries of deeply revealing news articles on government corruption and the coronavirus pandemic from reliable major media sources.
Just last month, the World Health Organization announced that two of three strains of polio had been eradicated. It's been one of the great success stories of modern medicine. The disease, which, of course, can lead to paralysis, has been reduced to just a handful of cases around the world. But now scientists say there's been a troubling setback. One of the vaccines used to prevent polio has actually been causing some people to get polio. The problem begins with what's called a live vaccine, which has little bits of weakened polio virus in it, given to children around the world. What seems to have gone wrong? The oral polio vaccine that's used primarily in low- and middle-income countries - it's been the workhorse of this global effort to eradicate polio. But it is a live vaccine. It's cheap. It's easy to administer. However, this live vaccine is continued to be used worldwide. And while you're doing that, some of that vaccine has gotten out into the world. And it's mutated. It starts circulating again, just like regular polio. But early on, it's just - it's still a vaccine. It's not dangerous. And then slowly, it sort of regains strength. And they're finding they can actually genetically see this - that scientists can actually trace it back directly to the vaccine. And now these vaccine-linked cases are actually causing more cases of paralysis each year than actual traditional - what scientists call wild polio. In the United States and in Europe ... we're using an injectable vaccine, which is a dead vaccine. It is not a live virus, and it cannot cause polio.
Note: For more along these lines, see concise summaries of deeply revealing news articles on vaccines from reliable major media sources.
The global insulin market is dominated by three companies: Eli Lilly, the French company Sanofi and the Danish firm Novo Nordisk. All three have raised list prices to similar levels. According to IBM Watson Health data, Sanofis popular insulin brand Lantus was $35 a vial when it was introduced in 2001; its now $270. Novo Nordisks Novolog was priced at $40 in 2001, and as of July 2018, its $289. The companies appear to have increased [prices] in lockstep over a number of years, prompting allegations of price fixing. All three companies denied these charges. (In 2010, Mexico fined Eli Lilly and three Mexican companies for price collusion on insulin, an allegation Eli Lilly also denied.) In the United States, a federal prosecutor and at least five state attorneys general are currently investigating the companies pricing practices. There is also another, less known corporate entity in the mix: pharmacy benefit managers (PBMs), which include Express Scripts, OptumRx and CVS Health; all are now named in lawsuits on high insulin prices. These corporate entities are powerful special interests. In 2017, the pharmaceutical and health product industry ... spent nearly $280 million on lobbying, the biggest spender by far of 20 top industries, according to the Center for Responsive Politics. The industry also has a revolving door to government. Alex Azar, the head of the Department of Health and Human Services, was the president of Eli Lillys U.S. division until 2017.
Note: For more along these lines, see concise summaries of deeply revealing news articles on pharmaceutical industry corruption from reliable major media sources.
Spending hours on smartphones and tablet devices has frequently been linked to exacerbating mental wellbeing, but new research claims the damage might start in users as young as two. After just one hour of screen time, children and adolescents may have less curiosity, lower self-control and lower emotional stability, which can lead to an increased risk of anxiety and depression, claims a US study published in the journal Preventive Medicine Reports. The researchers found that those aged 14 to 17 are more at risk for such adverse effects, but noticed the correlations in younger children and toddlers, whose brains are still developing, as well. The study found that nursery school children who used screens frequently were twice as likely to lose their temper. It also claimed that nine per cent of those aged 11 to 13 who spent an hour a day on screens were not curious in learning new things, a figure which rose to 22.6 per cent for those whose screen time was seven hours a day or more. Authors Professor Jean Twenge, of San Diego State University, and Professor Keith Campbell, of the University of Georgia, said: "Half of mental health problems develop by adolescence. "Thus, there is an acute need to identify factors linked to mental health issues that are amenable to intervention in this population, as most antecedents are difficult or impossible to influence. "Compared to these more intractable antecedents of mental health, how children and adolescents spend their leisure time is more amenable to change."
Note: For more along these lines, see concise summaries of deeply revealing news articles on health from reliable major media sources.
[Robert] Rook was allowed to keep his family practice open, so long as hes chaperoned, despite facing multiple criminal charges for rape. Prosecutors subsequently downgraded the charges to more than 20 counts of sexual assault in the second- and third-degree, charges for which Rook says he is innocent. An Associated Press investigation finds that even as Hollywood moguls, elite journalists and politicians have been pushed out of their jobs or resigned amid allegations of sexual misconduct, the world of medicine is more forgiving. Even when doctors are disciplined, their punishment often consists of a short suspension paired with therapy that treats sexually abusive behavior as a symptom of an illness or addiction. The investigation finds that decades of complaints that the physician disciplinary system is too lenient have led to little change in the practices of state medical boards. The #MeToo campaign and the push to increase accountability for sexual misconduct in workplaces don't appear to have sparked a movement toward changing how medical boards deal with physicians who act out sexually against patients or staffers.
Note: For more along these lines, see concise summaries of deeply revealing news articles on sexual abuse scandals and health.
People are developing dementia a decade before they were 20 years ago, perhaps because of environmental factors such as pollution and the stepped-up use of insecticides, a wide-ranging international study has found. The study, which compared 21 Western countries between the years 1989 and 2010, found that the disease is now being regularly diagnosed in people in their late 40s and that death rates are soaring. The study was published in the Surgical Neurology International journal. The problem was particularly acute in the United States, where neurological deaths in men aged over 75 have nearly tripled and in women risen more than fivefold, the leader of the study, Colin Pritchard from Bournemouth University, [said]. Scientists quoted in the study said a combination of environmental factors such as pollution from aircraft and cars as well as widespread use of pesticides could be the culprit. Early-onset dementia used to cover people developing the disease in their late 60s. Now, its meant to mean people much younger than that, the research showed. The study found that deaths caused by neurological disease had risen significantly in adults aged 55 to74, virtually doubling in the over-75s. The sharp increase in death rates from dementia-related diseases cannot simply be blamed on an aging population or stepped-up diagnosis, Pritchard said. The rate of increase in such a short time suggested a silent or even a hidden epidemic, in which environmental factors must play a major part.
Note: For more along these lines, see concise summaries of deeply revealing news articles on health from reliable major media sources.
Promotion of influenza vaccines is one of the most visible and aggressive public health policies today. Twenty years ago, in 1990, 32 million doses of influenza vaccine were available in the United States. Today around 135 million doses of influenza vaccine annually enter the US market, with vaccinations administered in drug stores, supermarkets—even some drive-throughs. This enormous growth has not been fueled by popular demand but instead by a public health campaign that delivers a straightforward ... message: influenza is a serious disease, we are all at risk of complications from influenza, the flu shot is virtually risk free, and vaccination saves lives. Yet across the country, mandatory influenza vaccination policies have cropped up, particularly in healthcare facilities, precisely because not everyone wants the vaccination, and compulsion appears the only way to achieve high vaccination rates. Closer examination of influenza vaccine policies shows that although proponents employ the rhetoric of science, the studies underlying the policy are often of low quality, and do not substantiate officials’ claims. The vaccine might be less beneficial and less safe than has been claimed, and the threat of influenza appears overstated. Since 2000, the concept of who is “at risk” has rapidly expanded, incrementally encompassing greater swathes of the general population. Today, national guidelines call for everyone 6 months of age and older to get vaccinated. Now we are all “at risk.”
Note: Full text available here. For more along these lines, see concise summaries of deeply revealing news articles on vaccines from reliable major media sources.
A US court this week banned three weedkillers widely used in American agriculture, finding that the Environmental Protection Agency (EPA) broke the law in allowing them to be on the market. The ruling is specific to three dicamba-based weedkillers manufactured by Bayer, BASF and Syngenta, which have been blamed for millions of acres of crop damage and harm to endangered species and natural areas across the midwest and south. Discovery documents turned up in the litigation showed the companies knew that their dicamba weedkillers would probably lead to off-target crop damage. This is the second time a federal court has banned these weedkillers since they were introduced for the 2017 growing season. In 2020, the ninth circuit court of appeals issued its own ban, but months later the Trump administration reapproved the weedkilling products. But a federal judge in Arizona ruled on Monday that the EPA made a crucial error in reapproving dicamba, finding the agency did not post it for public notice and comment as required by law. US district judge David Bury wrote ... that it was a “very serious” violation and that if EPA had done a full analysis, it probably would not have made the same decision. Bury wrote that the EPA did not allow many people who are deeply affected by the weedkiller – including specialty farmers, conservation groups and more – to comment. “The evidence has shown that dicamba cannot be used without causing massive and unprecedented harm to farms as well as endangering plants and pollinators,” said George Kimbrell [with] the Center for Food Safety, which litigated the case.
Note: For more along these lines, see concise summaries of deeply revealing news articles on health and government corruption from reliable major media sources.
Federal regulators announced warnings against two major food and beverage industry groups and a dozen nutrition influencers on Wednesday, as part of a broad action to enforce stricter standards for how companies and social media creators disclose paid advertising. The Federal Trade Commission sent warning letters on Monday to American Beverage, a lobbying group whose members include Coca-Cola and PepsiCo, as well as the Canadian Sugar Institute and a dozen health influencers who collectively have over 6 million followers on TikTok and Instagram. The agency flagged nearly three dozen social media posts that it said failed to clearly disclose who was paying the influencers to promote artificial sweeteners or sugary foods. The action follows a months-long investigation by The Examination and The Washington Post that revealed how the food and beverage industry had enlisted popular dietitians to promote industry-friendly messages on social media posts that often failed to disclose the names of sponsors. Social media marketing ... has been described as the Wild West of advertising. Over $6 billion is expected to be spent on influencer marketing in the United States in 2023. The enforcement action is the first the FTC has taken against major food and beverage industry groups for social media marketing. The agency urged the trade groups and nutrition influencers to remove posts or add proper disclosures and noted that future failures could trigger fines of more than $50,000 for each violation.
Note: Read how cereal giant Kellogg used fake experts to sell its sugary cereals. For more along these lines, see concise summaries of deeply revealing news articles on food system corruption from reliable major media sources.
A 2022 investigation by the journal The BMJ declared that FDA oversight of clinical trials, including those for Pfizer and Moderna's mRNA Covid-19 vaccines, was "grossly inadequate," from not conducting enough inspections to failing to alert scientific journals or the public when violations were flagged. But the issues here are not confined to behind the pharmacy counter. Dr. John Abramson, author of the recent book "Sickening: How Big Pharma Broke American Health Care and How We Can Repair It," traces the roots of issue back decades. "In 1992, when what turned out to be effective HIV drugs were stuck in the bottleneck of the FDA, they didn't have enough staff to get them through quickly enough. Many people were dying, and it was a real crisis," he explains. "The solution was that the Prescription Drug User Fee Agreement was passed. The drug companies started to pay a user fee with that was due upon application for new drug approval. And now roughly 65% of the FDA budget for overseeing human products comes from the drug and device companies. This comes with rigid timelines, and as I see from the outside, some degree of influence and obligation to the drug companies that derives from this agreement." The numbers here vary — Forbes puts that budget figure as high as 75%. Another similar conflict of interest that concerns Abramson is what he calls "the revolving door that goes between FDA and the drug industry."
Note: Read about Brook Jackson, a researcher for the Pfizer COVID-19 vaccine trials, who discovered patient safety concerns, data integrity issues, and other significant issues at her site. When she reported it to the FDA, she was fired the same day. For more along these lines, see concise summaries of deeply revealing news articles on government corruption and health from reliable major media sources.
Life insurance actuaries are reporting that many more people are dying – still – than in the years before the pandemic. Among working people 35 to 44 years old, a stunning 34% more died than expected in the last quarter of 2022, with above-average rates in other working-age groups, too. “COVID-19 claims do not fully explain the increase,” a Society of Actuaries report says. There was an extreme and sudden increase in worker mortality in the fall of 2021 even as the nation saw a precipitous drop in COVID-19 deaths. In the third quarter of 2021, deaths among workers ages 35-44 reached a pandemic peak of 101% above ... the three-year pre-COVID baseline. In two other prime working-age groups, mortality was 79% above expected. In the year ending April 30, 2023 ... at least 104,000 more Americans died than expected. In the U.K., 52,427 excess deaths were reported in that period; in Germany, 81,028; France, 17,731; Netherlands, 10,418; and Ireland, 2,640. The actuarial reports can only speculate on the factors causing these deaths, including oft-cited delayed health care, drug overdoses and even weather patterns. But the question remains: What explains this ongoing wave of excess deaths? Life insurance data suggests something happened in the fall of 2021 in workplaces, especially among white-collar workers. These are people whose education, income level and access to health care would predict better outcomes.
Note: Critical care physician Dr. Pierre Kory, one of the co-authors of this article, recently published an in-depth explanation on what he believes is behind the excess death among American youth, and why it wasn’t mentioned in the USA Today article. For more along these lines, see concise summaries of deeply revealing news articles on health from reliable major media sources.
Over 30 million Americans a year use benzodiazepines, or “benzos,” including Xanax, Valium, Ativan and Klonopin. Benzodiazepines are prescribed to treat anxiety disorders, insomnia, muscle spasms, schizophrenia, bipolar disorder, seizures and epilepsy. But this widely used class of drugs is linked to severe side effects and life impacts that can last for years — even after people have stopped taking the drugs — a new study finds. “Patients have been reporting long-term effects from benzodiazepines for over 60 years. I am one of those patients,” Dr. Christy Huff, a cardiologist and co-author of the study, said in a news release. The new research, published in PLOS One, includes a lengthy list of side effects that a majority of benzo users experienced more than a year after they stopped taking the drugs. Those long-lasting symptoms include low energy, difficulty focusing, memory loss, anxiety, insomnia, sensitivity to light and sounds, digestive problems, symptoms triggered by food and drink, muscle weakness and body pain. Alarmingly, users also struggled with severe life impacts: 54.7% reported suicide attempts or suicidal thoughts, for example. Health experts noted numerous other problems with benzos, including an increased risk of suicide and dependence on the drug, among other adverse side effects. Withdrawal from benzos can produce troubling symptoms as soon as within 24 hours, and these adverse effects can last for months.
Note: For more along these lines, see concise summaries of deeply revealing news articles on Big Pharma corruption from reliable major media sources.
New York state on Friday became the first state in the nation to pass legislation restricting neonicotinoid pesticides (neonics) that are toxic to bees and other pollinators and wildlife. The Birds and Bees Protection Act would eliminate 80 to 90% of the neonics used in New York each year by banning applications that are either easily replaceable or do not give an economic boost to farmers. "Every year for the past decade, New York beekeepers have lost more than 40% of their bee colonies–largely due to neonic pesticides," bill sponsor State Senator Brad Hoylman-Sigal said in a statement. "Today, in this landmark victory for our pollinators, economy, and farming industry, New York is working to reverse that trend." The bill ... bans the use of neonics to coat corn, soybean, and wheat seeds as well as for lawns and gardens. Neonics are a class of pesticides that work by attacking the nervous systems of insect pests. A lethal dose will cause paralysis and death, while non-lethal effects include memory, immune, navigation, and fertility problems. They are one of the deadliest pesticides out there, yet they are also the leading insecticide used in the U.S. This is a problem because about 95% of neonics used to coat seeds don't enter the plant at all, but instead spread into the environment via the soil, where they do not break down easily. They also harm the development of birds and mammals; and studies have linked ingredients of neoicotinoid insecticides with adverse human health outcomes as well.
Note: For more along these lines, see concise summaries of deeply revealing news articles on food system corruption and health from reliable major media sources.
A study of military veterans has shown the strongest evidence yet that the widespread chemical trichloroethylene (TCE)–used in spot removers, office products and dry-cleaning–is linked to Parkinson's disease. The research focused on service members who were stationed at Camp Lejeune in North Carolina between 1975 and 1985, when levels of TCE in the base's water reached 70 times higher than the Environmental Protection Agency's limit. After accounting for demographic factors, Camp Lejeune veterans were 70 percent more likely to develop the movement disorder than service members stationed at Camp Pendleton in California, where the water was uncontaminated. The large study, published last week in the journal JAMA Neurology, adds to a handful of smaller, earlier papers that found a link between TCE and Parkinson's. TCE, which can be in liquid or vapor form, has been commonly used since the 1920s, including as an inhaled surgical anesthetic and in several cleaning products. Today, it's primarily used in making refrigerants and degreasing metal equipment. The chemical breaks down slowly and can be detected in the air, water and soil. It's also found in one-third of U.S. drinking water. The Camp Lejeune drinking water was contaminated with TCE and other chemicals from 1953 to 1987, per the study, due to leakage from underground storage tanks, industrial spills, waste disposal sites and a dry-cleaning business.
Note: Internal corporate documents reveal how global chemical giant Syngenta secretly influenced scientific research regarding links between its top-selling weedkiller and Parkinson's disease. For more along these lines, see concise summaries of deeply revealing news articles on health from reliable major media sources.
Antidepressants raise the risk of suicide while also giving people the means to kill themselves, scientists have warned, after discovering thousands of inquests linked to the drugs. Psychologists at the University of East London (UEL) analysed media reports of nearly 8,000 coroners' inquests in England and Wales between 2003 and 2020, in which antidepressants were mentioned. They found the drugs were linked to 2,718 cases of hanging and 2,329 overdoses, of which 933 people had overdosed on antidepressants themselves. A further 2,083 had been struck by a train, tube, lorry or other vehicle, had jumped or fallen to their death, drowned, shot themselves, or been involved in a fire or electrocution. Study author Dr John Read ... said: "Not only do antidepressants not reduce suicidality, but they also actually increase it for many, and for some they provide the mechanism for killing oneself." The research, ... concluded: "If the goal is to prevent suicide then clearly they are not working for thousands of people." Around one in six of the adult population takes antidepressants each year. In 2018, Prof Read surveyed nearly 1,500 people taking antidepressants and found that 50 per cent reported suicidal thoughts after starting the drugs. Recent studies have also called into question the benefits of antidepressants. Last year, University College London (UCL) concluded that depression is not caused by a chemical imbalance of serotonin and argued that life events were a larger factor.
Note: Antidepressants are some of the most commonly prescribed medications, yet their significant risks are often withheld from public debate. Furthermore, an in-depth investigation reveals the glaring conflicts of interest and financial ties to corporate drugmakers that are behind many studies marketing clinical antidepressants as safe.
Over the last decade alone, at least 540 doctors and healthcare practitioners collectively paid the government hundreds of millions of dollars to negotiate their way out of trouble via civil settlements, then continued to practice medicine without restrictions on their licenses despite allegations that included fraud and patient harm, a Reuters investigation found. That figure is the result of the first-ever comprehensive analysis of federal civil settlements and state disciplinary actions. Separately, more than 2,200 hospitals and healthcare companies likewise negotiated civil deals to sidestep prosecution for alleged offenses that included paying bribes, falsifying patients records and billing the government for unnecessary patient care, the Reuters analysis shows. In many of those cases, the physicians, staffers and top brass who purportedly committed those misdeeds were not named publicly by prosecutors or forced to pay settlements themselves. Federal enforcers said they sometimes withhold names of individuals in these situations because of ongoing or planned investigations. The U.S. government collected more than $26.8 billion in healthcare-related civil settlements and judgments from 2013 to 2022, the Reuters analysis found. Victims, meanwhile, received no share of these settlements, which are funneled to a Treasury Department general fund. Consequently, they must pursue their own civil cases in search of restitution for suffering and harm, Reuters found.
Note: For more along these lines, see concise summaries of deeply revealing news articles on corporate corruption and health from reliable major media sources.
I staunchly supported the efforts of the public health authorities when it came to COVID-19. I was with them when they called for lockdowns, vaccines, and boosters. I was wrong. We in the scientific community were wrong. And it cost lives. The scientific community from the CDC to the WHO to the FDA and their representatives, repeatedly overstated the evidence and misled the public about its own views and policies, including on natural vs. artificial immunity, school closures and disease transmission, aerosol spread, mask mandates, and vaccine effectiveness and safety, especially among the young. All of these were scientific mistakes at the time, not in hindsight. Some of these obfuscations continue to the present day. We excluded important parts of the population from policy development and castigated critics, which ... exacerbated longstanding heath and economic disparities. We systematically minimized the downsides of the interventions we imposed–imposed without the input, consent, and recognition of those forced to live with them. In so doing, we violated the autonomy of those who would be most negatively impacted by our policies: the poor, the working class, small business owners, Blacks and Latinos, and children. We severely judged lockdown critics as lazy, backwards, even evil. We believed "misinformation" energized the ignorant. If our public health officials had led with less hubris, the course of the pandemic in the United States might have had a very different outcome, with far fewer lost lives.
Note: The above was written by MD/PhD student Kevin Bass. For more along these lines, see concise summaries of deeply revealing news articles on the coronavirus from reliable major media sources.
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