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Note: Explore our full index to revealing excerpts of key major media news articles on dozens of engaging topics. And read excerpts from 20 of the most revealing news articles ever published.

It's hard to talk about the dangers of cell-phone radiation without sounding like a conspiracy theorist. This is especially true in the United States, where non-industry-funded studies are rare, where legislation protecting the wireless industry from legal challenges has long been in place, and where our lives have been so thoroughly integrated with wireless technology that to suggest it might be a problem ... is like saying our shoes might be killing us. Except our shoes don't send microwaves directly into our brains. And cell phones do - a fact that has increasingly alarmed the rest of the world. There are multiple reports, mostly out of Europe's premier research institutions, of cell-phone and PDA use being linked to "brain aging," brain damage, early-onset Alzheimer's, senility, DNA damage, and even sperm die-offs. In September 2007, the European Union's environmental watchdog, the European Environment Agency, warned that cell-phone technology "could lead to a health crisis similar to those caused by asbestos, smoking, and lead in petrol." In the U.S., there's been very little resistance to the march of the cell towers. In fact, in Congress there's been almost nothing but support. The Telecommunications Act of 1996 ... was the result, in part, of nearly $50 million in political contributions and lobbying largesse from the telecom industry. A rider known as Section 704 ... specifically prohibits citizens and local governments from stopping placement of a cell tower due to health concerns.

Note: For more along these lines, see concise summaries of deeply revealing news articles on wireless technology risks from reliable major media sources.

For 40 years the United States Public Health Service has conducted a study in which human beings with syphilis, who were induced to serve as guinea pigs, have gone without medical treatment for the disease and a few have died of its late effects, even though an effective therapy, was eventually discovered. The study was conducted to determine from autopsies what the disease does to the human body. It is too late to treat the syphilis in any surviving participants. The experiment, called the Tuskegee Study, began in 1932 with about 600 black men mostly poor and uneducated, from Tuskegee, Ala., an area that had the highest syphilis rate in the nation at the time. Four hundred of the group had syphilis and never received deliberate treatment for the Venereal Infection. A control group of 200 had no syphilis and did not receive any specific therapy. As Incentives to enter the Program, the men were promised free transportation to and from hospitals, free hot lunches, free medicine for any disease other than syphilis and free burial after autopsies were performed. The Tuskegee Study began 10 years before penicillin was found to be a cure for syphilis and 15 years before the drug became widely available. Yet, even after penicillin became common, and while its use probably could have helped or saved a number of the experiment subjects, the drug was denied them. Senator William Proxmire ... called the study "a moral and ethical nightmare."

Note: Read more about the disturbing history of government and industry experiments on human guinea pigs. For more along these lines, see concise summaries of deeply revealing news articles on government corruption from reliable major media sources.

The Environmental Protection Agency announced Wednesday its proposed decision to reregister dicamba, a herbicide widely used on soybean and cotton farms that has been banned twice by federal courts. The EPA originally approved dicamba's use on genetically engineered soybeans and cotton in 2016. Environmental groups sued the EPA over dicamba in 2020 because of its potential drift away from the intended target, especially during warmer temperatures, and harm neighboring crops, nearby ecosystems and rural communities. The U.S. Court of Appeals for the 9th Circuit ruled against the EPA and said the agency "understated the amount of dicamba damage." The court determined that dicamba "caused substantial and undisputed damage" that tore the "social fabric of the farming communities." After the court vacated the herbicide's registration, the EPA re-registered it months later, and was again challenged by environmental groups. A second federal court vacated that registration in 2024 and prohibited the sale of the herbicide. The popularity of dicamba, which was first introduced in 1967, arose from a need to find solutions to Roundup-resistant weeds, also known as "superweeds." Monsanto ... began selling genetically engineered seeds that could survive being doused by dicamba and Roundup in 2016. Between 2016 and 2019, dicamba use across the country nearly quadrupled to an estimated 31 million pounds a year.

Note: For more along these lines, read our concise summaries of news articles on government corruption and toxic chemicals.

In the last decade, private equity firms have been quietly taking control of dental care from behind the scenes, largely through secondary business organizations that push dental practices to cut costs and, in some cases, encourage unnecessary and irreversible dental procedures. In 2024, the dental industry witnessed 161 private equity deals – the highest number of any health care industry, as tracked by the watchdog organization, Private Equity Stakeholder Project. The data reveals that these investment firms are increasingly acquiring dental practices or inserting themselves into clinic management roles, where they then cut corners on patient care. The dental industry is an especially alluring target for private equity firms because it's comprised of thousands of independent clinics, offering investors a fragmented industry to consolidate and streamline. Between 2011 and 2019, private equity firms bought up $4.4 billion worth of dental practices. Dentists at ClearChoice Dental Implant Centers – a dental chain owned by Aspen Dental, one of the largest dental service organizations – were allegedly extracting healthy teeth from patients and replacing them with expensive implants. Experts have warned in various lawsuits against the implant center that this irreversible procedure exposes patients to excessive costs and surgery complications, plus a greater risk of future dental problems like infections and bone loss.

Note: BlackRock and Vanguard manage over $11 trillion and $8 trillion respectively–an unprecedented concentration of financial power. We hear outrage about billionaires and oligarchs, but rarely about private equity firms, who are backed by both political parties and are drastically reshaping our economy, contributing to environmental destruction, and extracting wealth from communities in the US and all over the world. For more along these lines, read our concise summaries of news articles on health and financial industry corruption.

Since 2000, the food and chemical industry has greenlighted nearly 99% of food chemicals introduced onto the market without federal safety review. This problematic situation happened through companies exploiting a loophole in food chemicals laws allowing them to decide which chemicals are safe to consume. Since 2000, food and chemical companies have petitioned the FDA only 10 times to approve a new substance. By contrast, they have added 863 chemicals, through the "generally recognized as safe," or GRAS, loophole. That's 98.8% of new food chemicals. The loophole lets those companies – not the FDA – decide when a substance is safe. The GRAS loophole was intended to apply narrowly to common ingredients like sugar, vinegar and baking soda. But as EWG's analysis shows, the loophole – not FDA safety review – has become the main way new chemicals are allowed into food. A GRAS determination shows a company believes "the substance is generally recognized, among qualified experts, as having been adequately shown to be safe under the conditions of its intended use." The company can submit a notice to the FDA about its conclusion, through a process that is entirely voluntary. Even Michael Taylor, a former FDA deputy commissioner for food, admitted in 2014 that the FDA "simply do[es] not have the information to vouch for the safety of many of these chemicals."

Note: For more along these lines, read our concise summaries of news articles on food system corruption and toxic chemicals.

In our first hearing of this Congress titled, "The Corruption of Science and Federal Health Agencies: How Health Officials Downplayed and Hid Myocarditis and Other Adverse Events Associated with the COVID-19 Injections," I asked Dr. Joel Wallskog, an orthopedic surgeon injured by the Covid injections, to describe how those suffering from Covid injection injuries felt. His one-word answer: "Abandoned." The passage of the National Childhood Vaccine Injury Act of 1986 ... led to blanket immunity for vaccines through subsequent regulation. An explosion in the number of vaccine doses on the childhood schedule was the result. Prior to 1986, there were 3 routine vaccines totaling 7 injections. Today the CDC's Maternal and Child & Adolescent vaccine schedules include 19 vaccines requiring 76 injections with 94 total doses of antigen. In August 1997, the FDA ... issued draft guidance to allow pharmaceutical companies to advertise directly to consumers beyond print media into TV and radio. According to one estimate, drug companies spent $10 billion on direct-to-consumer advertising in 2024. That amount of spending has paid off handsomely for Big Pharma and its ability to control the narrative and suppress stories of drug and vaccine injuries. But to understand the true reality we face, there is nothing like hearing from those who have suffered the adverse events that are rarely acknowledged by the medical establishment, federal health agencies, and the corporate media.

Note: Watch the full Senate hearing video and read all statements from mothers and scientists who testified at hearing here. For video clips of witness testimonies, click here. Our well-researched and nuanced Substack reveals the undeniable evidence that COVID vaccine injuries and deaths were covered-up and censored. For more along these lines, read our concise summaries of news articles on COVID vaccine problems and Big Pharma corruption.

Dozens of companies that make ice cream and frozen dairy desserts announced on Monday that they would remove artificial food dyes from their products by 2028, marking yet another voluntary move away from such food coloring within the food industry. It comes in response to a mission set forth by Health and Human Services Secretary Robert F. Kennedy Jr. to remove the artificial additives. In April, Food and Drug Administration Commissioner Marty Makary said the agency would move to eliminate several synthetic dyes by the end of next year. That includes Green 3, Red 40, Yellow 5, Yellow 6, Blue 1, and Blue 2. Red 3 was set to be banned in food by 2027 because it caused cancer in laboratory rats; the FDA called for that deadline to move up. Artificial dyes are used widely in U.S. foods. In Canada and in Europe – where synthetic colors are required to carry warning labels – manufacturers mostly use natural substitutes. Several states, including California and West Virginia, have passed laws restricting the use of artificial colors in foods. Health advocates have long called for the removal of artificial dyes from foods, citing mixed studies indicating they can cause neurobehavioral problems, including hyperactivity and attention issues, in some children. The FDA has maintained that the approved dyes are safe and that "the totality of scientific evidence shows that most children have no adverse effects when consuming foods containing color additives."

Note: For more along these lines, read our concise summaries of news articles on food system corruption.

The number of American children diagnosed with A.D.H.D. more than doubled in the early 1990s, from fewer than a million patients in 1990 to more than two million in 1993, almost two-thirds of whom were prescribed Ritalin. Despite Ritalin's rapid growth, no one knew exactly how the medication worked or whether it really was the best way to treat children's attention issues. The diagnosis rate ... kept rising, hitting 5.5 percent of American children in 1997, then 6.6 percent in 2000. Last year, the Centers for Disease Control and Prevention reported that 11.4 percent of American children had been diagnosed with A.D.H.D., a record high. That figure includes 15.5 percent of American adolescents, 21 percent of 14-year-old boys and 23 percent of 17-year-old boys. From 2012 to 2022, the total number of prescriptions for stimulants to treat A.D.H.D. increased in the United States by 58 percent. For a significant percentage of people diagnosed with A.D.H.D., [clinical psychologist Joel] Nigg says, "there's nothing neurobiologically notable about them. Instead, their symptoms are situational or conditional. They may have had a hard life, or they have a lack of social support, or they're in the wrong niche in life." Amphetamines can be powerfully addictive, and last year, a study in The American Journal of Psychiatry found that even a medium-strength daily dose of Adderall more than tripled a patient's likelihood of developing psychosis or mania. [UC Irvine research psychologist James Swanson] acknowledges that medication can often produce short-term improvements in children's behavior. But, he says, "there is no long-term effect. The only long-term effect that I know of has been the suppression of growth."

Note: We recommend reading the full article to explore the complex rise in ADHD diagnoses–and the growing concerns around stimulant medications. According to the scientists interviewed in this article, stimulants neither treat the root causes of ADHD nor improve academic achievement or long-term success. For more along these lines, read our concise summaries of news articles on mental health.

On July 2022, Morgan-Rose Hart, an aspiring vet with a passion for wildlife, died after she was found unresponsive at a mental health unit in Essex. Her death was one of four involving a hi-tech patient monitoring system called Oxevision which has been rolled out in nearly half of mental health trusts across England. Oxevision's system can measure a patient's pulse rate and breathing without the need for a person to enter the room, or disturb a patient at night, as well as momentarily relaying CCTV footage when required. Oxehealth, the company behind Oxevision, has agreements with 25 NHS mental health trusts, according to its latest accounts, which reported revenues of about Ł4.7m in ... 2023. But it is claimed in some cases staff rely too heavily on the infra-red camera system to monitor vulnerable patients, instead of making physical checks. There are also concerns that the system – which can glow red from the corner of the room – may worsen the distress of patients in a mental health crisis who may have heightened sensitivity to surveillance or control. Sophina, who has experience of being monitored by Oxevision while a patient ... said: "I think it was something about the camera and it always being on, and it's right above your bed. "It's the first thing you see when you open your eyes, the last thing when you go to sleep. I was just in a constant state of hypervigilance. I was completely traumatised. I still felt too scared to sleep properly."

Note: For more along these lines, read our concise summaries of news articles on Big Tech and mental health.

Is President Trump pushing gender-confused kids to commit suicide? This shocking claim hit mainstream and social media within minutes of the president's Jan. 28 executive order banning federal funding for child sex-change treatments. The way the argument goes, if kids can't get puberty blockers, cross-sex hormones and surgeries, their mental health will deteriorate to the point of no return. But as I've seen while working with more than 1,000 such kids, there are deeper reasons why they're so unhappy – and giving them powerful experimental drugs and irreversible surgeries is more likely to worsen their condition. From 2018 to 2022, I worked as a case manager for the Washington University Transgender Center at St. Louis Children's Hospital. As kids kept coming back for follow-up check-ins and treatment – almost every kid who begins puberty blockers goes on to receive cross-sex hormones – I realized something was very wrong. When my colleagues and I asked about their mental health, they usually reported that it was the same or better. But as soon as we dug deeper, it became clear that the real answer was no – that their mental anguish was worsening. We ignored or explained away co-morbidities like autism, depression and bipolar disorder while using every new development or difficulty in a kid's life to justify continuing down the sex-change road. In my experience, kids typically find the "treatment brings happiness" mantra of their doctors, nurses and case managers hard to see through. Some literally couldn't look themselves in the mirror, even if they physically looked the part of a boy-turned-girl or vice-versa. While activists insist that kids simply "know who they are," reality is more complicated.

Note: This article was written by Jamie Reed, a queer woman married to a trans man. Many transgender medical care experiences can indeed be life-changing and even life-saving, yet not all experiences align with the mainstream narratives. Reed isn't the only whistleblower who's worked in the field of youth transgender medicine. Even advocates who publicly promote gender medicine for kids question its ethics behind closed doors. Watch our nuanced 25-minute Mindful News Brief on the controversy surrounding youth gender medicine. For more along these lines, read our concise summaries of news articles on transgender medicine.

The payment scheme for people injured by vaccines has cost taxpayers more to run than it has paid out to victims, official figures suggest, fuelling calls for "urgent reform". The Government has spent more than Ł25 million since Nov 1 2021 on medically assessing thousands of claims that vaccinations have left people seriously disabled. It is more than the total Ł23.6 million that since that date has been paid out to 197 victims, with each claim worth Ł120,000. The Vaccine Damage Payment Scheme (VDPS) was established in 1979 and pays tax-free cash to those deemed to have suffered life-changing injuries as a result of certain vaccinations – including those against Covid-19. It awards a one-off Ł120,000 tax-free payment to people who have been severely injured, or to the families of those who have died, as a result of a vaccination. The scheme has been heavily criticised for being too slow to assess cases. Victims also claim that the payouts are insufficient and that the threshold claimants must meet to qualify for a payout is too harsh a measure. Kate Scott, whose husband was left with permanent brain damage after taking the AstraZeneca vaccine against Covid-19, criticised the imbalance between the money the scheme costs to run and the sums paid out. Public hearings for the fourth module of the Covid-19 inquiry started in London on Tuesday. It will hear issues around vaccine safety from families of those who suffered side effects from Covid jabs.

Note: The Vaccine Adverse Event Reporting System (VAERS) is a voluntary government reporting system that only captures a portion of the actual injuries. Vaccine adverse event numbers are made publicly available, and currently show 38,264 COVID Vaccine Reported Deaths and 1,658,330 COVID Vaccine Adverse Event Reports. Our Substack dives into the complex world of COVID vaccines with nuance and uncensored investigation.

Campaigners have accused Facebook parent Meta of inflicting "potentially lifelong trauma" on hundreds of content moderators in Kenya, after more than 140 were diagnosed with PTSD and other mental health conditions. The diagnoses were made by Dr. Ian Kanyanya, the head of mental health services at Kenyatta National hospital in Kenya's capital Nairobi, and filed with the city's employment and labor relations court on December 4. Content moderators help tech companies weed out disturbing content on their platforms and are routinely managed by third party firms, often in developing countries. For years, critics have voiced concerns about the impact this work can have on moderators' mental well-being. Kanyanya said the moderators he assessed encountered "extremely graphic content on a daily basis which included videos of gruesome murders, self-harm, suicides, attempted suicides, sexual violence, explicit sexual content, child physical and sexual abuse ... just to name a few." Of the 144 content moderators who volunteered to undergo psychological assessments – out of 185 involved in the legal claim – 81% were classed as suffering from "severe" PTSD, according to Kanyanya. The class action grew out of a previous suit launched in 2022 by a former Facebook moderator, which alleged that the employee was unlawfully fired by Samasource Kenya after organizing protests against unfair working conditions.

Note: Watch our new video on the risks and promises of emerging technologies. For more along these lines, read our concise summaries of news articles on Big Tech and mental health.

Too many people are being prescribed antidepressants to deal with stressful life events or social problems, according to a growing chorus of doctors and researchers. More than 14% of Australians are currently taking antidepressants, one of the highest rates in the world. Dr Matt Fisher, who researches wellbeing and the impact of stress, says while he has heard health workers talk about this "as a good thing, because it means more people are getting access to help", he doesn't see it as a success story. Fisher ... is concerned Australia's high use of antidepressants "constitutes a failed attempt to medicate away what are, in fact, social problems". He says while "antidepressants may be of benefit to some people suffering persistent psychosocial distress," they should not be the default, first response. Chronic stress, where people are exposed to an ongoing, recurrent stressor without any easy or accessible way to resolve it – increasing the risk of isolation, exclusion, humiliation and harm – is a significant driver of mental distress in Australia. The common causes of chronic stress include things such as being in debt, having a low income, poor working conditions, or being exposed to racism or domestic violence. "Governments evade the problem by persisting with individualised, medicalised, drug-based strategies," he says. "These strategies aren't reducing high rates of mental distress, sometimes do harm, and marginalise attention on social causes."

Note: The UK's medicines regulator is launching a review of over 30 commonly prescribed antidepressants, including Prozac, amid rising concerns about links to suicide, self-harm, and long-term side effects like persistent sexual dysfunction–especially in children. Our latest Substack, Lonely World, Failing Systems: Inspiring Stories Reveal What Sustains Us, dives into the loneliness crisis exacerbated by the digital world and polarizing media narratives, along with inspiring solutions and remedies that remind us of the true democratic values that bring us all together.

A health department in Idaho has voted to halt its COVID-19 vaccination program, joining the growing number of regional governments pushing back against federal vaccination recommendations. Board members at Southwest District Health, outside of Boise, questioned the vaccine's safety during their Oct. 22 meeting and narrowly voted to stop providing the shot in the six counties they serve. Health departments in Texas, Florida and Michigan ... have also pushed back against the COVID-19 vaccine. Last year, Texas policymakers banned health departments and other organizations funded by the state government from using funds to promote their vaccination efforts. The Florida Department of Health issued guidance in September warning Floridians not to get mRNA COVID-19 shots. In Michigan, commissioners in Ottawa County turned down a $900,000 grant for their health department in September. Joe Moss, chair of the commission, said at the time he was "opposed to accepting any COVID grants." The [Idaho] board's physician representative, Dr. John Tribble, questioned the vaccine's safety and cited COVID-19's "diminishing risk" as a reason for the agency's decision to discontinue the shot. "We weighed the risks versus the benefits for all individuals considering the shots," Tribble wrote. "We could not, in good faith, continue to offer a pharmaceutical product that does more harm than good."

Note: The Vaccine Adverse Event Reporting System (VAERS) is a voluntary government reporting system that only captures a portion of the actual injuries. Vaccine adverse event numbers are made publicly available, and currently show 38,068 COVID Vaccine Reported Deaths and 1,652,230 COVID Vaccine Adverse Event Reports. Our Substack dives into the complex world of COVID vaccines with nuance and uncensored investigation.

An ex-FDA employee has revealed what he claims is the most harmful breakfast cereal on the US market. Dr. Darin Detwiler, who previously served as a food safety expert for the agency, [said] that Kellogg's Froot Loops is the worst of the bunch, pointing out that the rainbow rings are "heavily processed and contain high levels of added sugars, artificial dyes and preservatives, which are linked to health concerns." Given the laundry list of bad-for-you ingredients in the bagged cereal, Detwiler says excess sugar is the least odious. A 1-cup serving of Froot Loops contains 12.35 grams of sugar, nearly half of the recommended daily allowance for children. However ... that serving size is unrealistic as most kids eat more than the recommended single cup. The bright red hue found in Froot Loops comes courtesy of Red 40, a controversial additive linked to a slew of health problems. A 2022 study yielded "alarming" results about the effects of Red 40 – sometimes called Allura red – on the human digestive tract. Researchers from McMaster University ... claimed the synthetic dye could potentially trigger irritable bowel syndrome and Crohn's disease after observing the biomarkers of damage in the gut cells of mice. The good doctor's revelation comes as more than 1,000 cereal lovers and health activists marched on Kellogg's Michigan headquarters on Tuesday, demanding the end of "harmful additives" being injected into US batches of products like Froot Loops and Apple Jacks.

Note: Big Food profits immensely as American youth face a growing health crisis. Read our latest Substack for a deep dive into who's behind the chronic disease epidemic that's threatening the future of humanity. For more along these lines, explore summaries of news articles on health and food system corruption from reliable major media sources.

The pharmaceutical industry, as a whole and by its nature, is conflicted and significantly driven by the mighty dollar, rather than altruism. A 2020 peer-reviewed article published in the Journal of the American Medical Association outlines the extent of the problem. The group studied both the type of illegal activity and financial penalties imposed on pharma companies between the years 2003 and 2016. Of the companies studied, 85 percent (22 of 26) had received financial penalties for illegal activities with a total combined dollar value of $33 billion. The illegal activities included manufacturing and distributing adulterated drugs, misleading marketing, failure to disclose negative information about a product (i.e. significant side effects including death), bribery to foreign officials, fraudulently delaying market entry of competitors, pricing and financial violations, and kickbacks. The highest penalties were awarded to Schering-Plough, GlaxoSmithKline (GSK), Allergan, and Wyeth. The biggest overall fines have been paid by GSK (almost $10 billion), Pfizer ($2.9 billion), Johnson & Johnson ($2.6 billion), and other familiar names including AstraZeneca, Novartis, Merck, Eli Lilly, Schering-Plough, Sanofi Aventis, and Wyeth. Five US states – Texas, Kansas, Mississippi, Louisiana, and Utah – are taking Pfizer to court for withholding information, and misleading and deceiving the public through statements made in marketing its Covid-19 injection.

Note: For more along these lines, see concise summaries of deeply revealing news articles on Big Pharma corruption from reliable major media sources.

Toxic PFAS "forever chemicals" used in lithium ion batteries essential to the clean energy transition present a dangerous source of chemical pollution that new research finds threatens the environment and human health. The multipronged, peer-reviewed study zeroed in on a little-researched and unregulated subclass of PFAS called bis-FASI that are used in lithium ion batteries. Researchers found alarming levels of the chemicals in the environment near manufacturing plants, noted their presence in remote areas around the world, found they appear to be toxic to living organisms, and discovered that waste from batteries disposed of in landfills was a major pollution source. PFAS are a class of about 16,000 human-made compounds most often used to make products resistant to water, stains and heat. They are called "forever chemicals" because they do not naturally break down and have been found to accumulate in humans. The chemicals are linked to cancer, birth defects, liver disease, thyroid disease, plummeting sperm counts and a range of other serious health problems. The paper notes that few end-of-life standards for PFAS battery waste exist, and the vast majority ends up in municipal dumps where it can leach into waterways, accumulate locally or be transported long distances. It looked at the presence of the chemicals in historical leachate samples and found none in those from prior to the mid-1990s, when the chemical class was commercialized.

Note: For more along these lines, see concise summaries of deeply revealing news articles on toxic chemicals from reliable major media sources.

After 30 years as one of England's top pediatricians, Dr. Hilary Cass ... took on a project that would throw her into an international fire: reviewing England's treatment guidelines for the rapidly rising number of children with gender distress, known as dysphoria. Staff members who said they felt pressure to approve children for puberty-blocking drugs had filed whistle-blower complaints. Over the next four years, Dr. Cass commissioned systematic reviews of scientific studies on youth gender treatments and international guidelines of care. She also met with young patients and their families, transgender adults, people who had detransitioned, advocacy groups and clinicians. Her final report, published last month, concluded that the evidence supporting the use of puberty-blocking drugs and other hormonal medications in adolescents was "remarkably weak." On her recommendation, the N.H.S. will no longer prescribe puberty blockers outside of clinical trials. Dr. Cass also recommended that testosterone and estrogen, which allow young people to develop the physical characteristics of the opposite sex, be prescribed with "extreme caution." "We have to stop just seeing these young people through the lens of their gender and see them as whole people, and address the much broader range of challenges that they have ... I've spoken to young adults where it was the wrong decision, where they have regret, where they've detransitioned. The critical issue is trying to work out how we can best predict who's going to thrive and who's not going to do well," [said Dr. Cass]. "Medicine should never be politically driven. It should be driven by evidence and ethics and shared decision-making with patients and listening to patients' voices. Once it becomes politicized, then that's seriously concerning, as you know well from the abortion situation in the United States."

Note: We believe that everyone has a right to exist and express themselves the way they want. Yet when it comes to transgender medicine, research suggests significant health concerns. Why aren't we openly discussing this so that people (especially children) can make informed choices about their bodies? Explore our concise summaries of important news articles on transgender medicine.

The toxicity of the culture war over youth gender medicine is well known to most of us. What's less well understood is how that poisonous climate affects the very cohort being argued about – and those who care for them. The Cass Review, led by Dr. Hilary Cass, examines the events and evidence (or lack thereof) that led to the closing of the UK's only public youth gender clinic, the Gender Identity Development Services. Social justice/civil rights framing has made it harder to reckon with what Cass calls the "exponential rise" in adolescent patients starting around 2014. Once it was mostly natal males who transitioned, but now it is mostly natal females, many of whom had no history of gender distress but did suffer from other mental health issues. As for the evidence about how to treat these patients and others who have sought care, Cass concludes: "The reality is that we have no good evidence on the long-term outcomes of interventions to manage gender-related distress." Individual studies may make claims about the efficacy of social transition, puberty blockers, or hormones, but they are too biased and low quality to draw conclusions from. As for the claim that these interventions prevent suicide, Cass reports that "the evidence found did not support this conclusion." Perhaps most important, Cass notes that "clinicians have told us they are unable to determine with any certainty which children and young people will go on to have an enduring trans identity."

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.

Forever chemicals, also known as per- and polyfluoroalkyl substances (PFAS), are a pervasive group of compounds that have been linked to a number of cancers and other illnesses. The toxic substances have become widespread in the air, soil and water via industrial discharge and are found in a number of common household items, from cookware to dental floss to stain-resistant furniture. And many of the products in which they have been detected – including waterproof makeup, workout leggings and period products – are primarily marketed toward women. In May 2022, a team of researchers at the Massachusetts-based Silent Spring Institute published a study ... looking at the presence of PFAS in underwear and several other consumer items. Among those products was menstrual underwear. Research released in August ... also found indicators of PFAS in some period products, including wrappers for several pads and some tampons and outer layers of menstrual underwear. A 2021 study ... tested 231 makeup products and found that 63 percent of the foundations, 58 percent of the eye products, 55 percent of the lip products and 47 percent of the mascaras it looked at contained high levels of fluorine. The Environmental Working Group has identified 300 cosmetic products from 50 different popular brands that contain PFAS in its Skin Deep database. The advocacy organization found that 200 of these products contain PTFE, which is also used in Teflon pans.

Note: For more along these lines, see concise summaries of deeply revealing news articles on health and corporate corruption from reliable major media sources.

Important Note: Explore our full index to revealing excerpts of key major media news articles on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.