Health Media Articles
Below are key excerpts of revealing news articles on health from reliable news media sources. If any link fails to function, a paywall blocks full access, or the article is no longer available, try these digital tools.
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Dr Maria Abreu is on the cutting edge of one of the biggest health tragedies in a generation. Over the past decade, the Miami gastroenterologist has diagnosed an increasing number of young people with colon cancer - once considered an old person's disease. Dr Abreu [said] she believes two additives that became common in the 1970s ... are seldom talked about in relation to the colon cancer crisis. The first is high-fructose corn syrup, a liquid sweetener uniquely common to the United States and not used in other countries. High fructose corn syrup was introduced in the 1970s as a bid to stabilize food prices. At the time, President Richard Nixon authorized subsidizing corn crops. High-fructose corn syrup ... became cheaper to produce than sugar. The other ingredient is emulsifiers, which is used to give foods a creamy texture and found in healthy foods such as low-fat yogurts, cottage cheese, and peanut butter. Dr Abreu said these ingredients wreak havoc on the microbiome, a network of healthy bacteria in our guts, [reducing] our ability to protect the digestive tract from pathogens that irritate our cells and create inflammation. Chronic inflammation can also lead to inflammatory bowel conditions like Crohn's disease and ulcerative colitis, which Dr Abreu said 'significantly' raises the risk of colon cancer. The introduction of high-fructose corn syrup and emulsifiers in the 1970s and 80s could explain why so many adults in their 40s are getting colon cancer. Researchers from the University of Missouri-Kansas City [found that] the rate of colorectal cancers grew 500 percent among children ages 10 to 14 and 333 percent among teenagers aged 15 to 19 years. Rates rose by 71 percent among people 30 to 34 to seven cases per 100,000 people.
Note: Big Food profits immensely as American youth face a growing health crisis, with close to 30% prediabetic, one in six youth obese, and over half of children facing a chronic illness. Nearly 40% of conventional baby food contains toxic pesticides. Yet what if the negative news overload on America’s chronic illness crisis isn’t the full story? Check out our Substack article to learn more about the inspiring remedies to the chronic illness crisis!
Former New York City Mayor’s Office Senior Advisor for Public Health Jay Varma admitted to pushing monkeypox drug TPOXX despite the low risk of the disease to the general public, according to undercover video shared by podcaster Steven Crowder. Varma helped guide former NYC Mayor Bill de Blasio’s response to COVID-19, including crucial decisions about public schools and issuing a vaccine mandate for healthcare workers. He was exposed last week for having admitted to hosting large nude gatherings during the pandemic while urging city residents to remain isolated. In the new clip shared by Crowder, Varma revealed the risk of monkeypox to the general U.S. population is "very low," and it is mainly a concern for gay men who have unprotected sex. Despite this, Varma said he was pushing to receive FDA approval for TPOXX, otherwise known as Tecovirimat. “We want the Food and Drug Administration, the FDA, to approve our drug specifically for monkeypox,” he said. Varma added the news cycle was a key component of his push to get approval for the drug. “We also need to keep up the people’s belief that the [TPOXX] drug works,” Varma said. “So, that’s why spinning it in the media is helpful. Basically what we’re trying to get the media to say is ‘oh, the drug didn’t work because it was designed the wrong way, so they’re going to do another study and it’ll probably work,’” he added. “That’s what we want the story to be.”
Note: Back in 2022, Dr. Jay Varma appeared on a talk show, warning that he feared "monkeypox could become permanently entrenched." For more along these lines, see concise summaries of deeply revealing news articles on health and government corruption from reliable major media sources.
The city’s ex-COVID czar got the boot from his job at a pharmaceutical firm Monday — a week after he was caught bragging about hosting sex parties and attending an underground rave at the height of the pandemic. Dr. Jay Varma was serving as a senior health adviser to then-Mayor Bill de Blasio during COVID-19 when he and his wife put on the sex- and drug-fueled debauchery and attended a packed Wall Street rave, according to secretly recorded conversations the doctor had with a woman. “Varma boasted about harassing people into submission over the vaccine mandate and admitted to participating in illegal sex parties, all while he, former Health Commissioner Dr. David Chokshi, and then-Mayor Bill de Blasio imposed draconian measures that shut down the entire city,” [city Councilman Bob Holden] said. Varma’s seamy chats ... were made public last week. Michael Kane of Teachers for Choice said, “What disgusts me the most was hearing Varma say having drug-fueled group sex orgies was necessary for him to be his ‘authentic self’ because COVID had him ‘pent up.'” Varma said at one point, “My wife and I had one with our friends in August [2020] of like that first summer.” “So we rented a hotel ... we all took, like, you know, molly [MDMA] and like it was like eight or nine or us, eight to 10 of us were in a room and everybody had a blast because everybody was like so pent up.”
Note: For more along these lines, see concise summaries of deeply revealing news articles on health and government 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.
[Don] Poldermans was a prolific medical researcher at Erasmus Medical Center in the Netherlands, where he analyzed the standards of care for cardiac events after surgery, publishing a series of definitive studies from 1999 until the early 2010s. One crucial question he studied: Should you give patients a beta blocker, which lowers blood pressure, before certain surgeries? Poldermans’s research said yes. European medical guidelines (and to a lesser extent US guidelines) recommended it accordingly. The problem? Poldermans’s data was reportedly fake. A 2012 inquiry by Erasmus Medical School, his employer, into allegations of misconduct found that he “used patient data without written permission, used fictitious data and ... submitted to conferences [reports] which included knowingly unreliable data.” Poldermans admitted the allegations and apologized. After the revelations, a new meta-analysis was published in 2014, evaluating whether to use beta blockers before non-cardiac surgery. It found that a course of beta blockers made it 27 percent more likely that someone would die within 30 days of their surgery. Millions of surgeries were conducted across the US and Europe during the years from 2009 to 2013 when those misguided guidelines were in place. One provocative analysis ... estimated that there were 800,000 deaths compared to if the best practices had been established five years sooner.
Note: For more along these lines, see concise summaries of deeply revealing news articles on corruption in science and in Big Pharma 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.
Note: For more along these lines, see concise summaries of deeply revealing news articles on health and artificial intelligence from reliable major media sources.
Almost two-thirds of supermarket baby food is unhealthy while nearly all baby food labels contain misleading marketing claims designed to "trick" parents. Those are the conclusions of an eyebrow-raising study in which researchers at Australia's George Institute for Global Health analyzed 651 foods marketed for children ages 6 months to 36 months at 10 supermarket chains in the United States. The study ... found that 60% of the foods failed to meet nutritional standards set by the World Health Organization. In addition, 70% of the baby food failed to meet protein requirements, 44% exceeded total sugar recommendations, 25% failed to meet calorie recommendations, and 20% exceeded recommended sodium limits set by the WHO. The most concerning products were snack foods and pouches. "Research shows 50% of the sugar consumed from infant foods comes from pouches, and we found those were some of the worst offenders,” said Dr. Elizabeth Dunford, senior study author. Sales of such convenient baby food pouches soared 900% in the U.S. in the past 13 years. Consumption of processed foods in early childhood can set lifelong habits of poor eating that could lead to obesity, diabetes, and some cancers. The study also found that 99.4% of the baby food analyzed had misleading marketing claims on the labels that violated the WHO's promotional guidelines. On average, products contained four misleading marketing claims; some had as many as eleven.
Note: Big Food profits immensely as American youth face a growing health crisis, with close to 30% prediabetic, one in six youth obese, and over half of children facing a chronic illness. Nearly 40% of conventional baby food contains toxic pesticides. For more along these lines, explore concise summaries of news articles on food system corruption from reliable major media sources.
The internet can be misused. It is understandable that those in the Senate might seek a government solution to protect children. The Kids Online Safety Act, known as KOSA, would impose an unprecedented duty of care on internet platforms to mitigate certain harms associated with mental health. As currently written, the bill is far too vague, and many of its key provisions are completely undefined. The bill empowers the Federal Trade Commission (FTC) to regulate content that might affect mental health, yet KOSA does not explicitly define the term "mental health disorder." Instead, it references the fifth edition of the Diagnostic and Statistical Manual of Mental Health Disorders…or "the most current successor edition." Even more concerning, the definition could change without any input from Congress. The sponsors of this bill will tell you that they have no desire to regulate content. In truth, this bill opens the door to nearly limitless content regulation, as people can and will argue that almost any piece of content could contribute to some form of mental health disorder. Anxiety and eating disorders are two of the undefined harms that this bill expects internet platforms to prevent and mitigate. Should we silence discussions about gun rights because it might cause some people anxiety? Could pro-life discussions cause anxiety in teenage mothers considering abortion? What about violent images from war? They are going to censor themselves, and users, rather than risk liability. This bill does not merely regulate the internet; it threatens to silence important and diverse discussions that are essential to a free society. [This] task is entrusted to a newly established speech police. The ACLU brought more than 300 high school students to Capitol Hill to urge Congress to vote no on KOSA.
Note: This article was written by Kentucky Senator Rand Paul. For more along these lines, see concise summaries of deeply revealing news articles on censorship and mental health from reliable major media sources.
The 43,000 tons of radioactive waste and soil came from a top-secret initiative: The Manhattan Project, which built the atomic bombs America dropped on Japan in 1945. In 1973, that waste ended up in an unlined landfill in Bridgeton, Missouri, a St. Louis suburb. Workers spread it to cover trash and construction debris. In 1990, the U.S. Environmental Protection Agency declared the West Lake Landfill one of the nation’s most contaminated sites requiring cleanup. [In 2012], residents mobilized, spotlighting stories of children dying from cancer. And they pressed waste-management giant Republic Services, the dump’s owner, to remove the radioactive waste. In refuting neighbors’ complaints, Republic tapped an unlikely ally that U.S. corporations have leaned on for decades: a federal health agency set up to protect people from environmental hazards just like the West Lake dump. A 2015 report by that small bureaucracy, the Agency for Toxic Substances and Disease Registry (ATSDR) ... declared that the landfill posed no health risk to the community. Deborah Mitchell grew up ... less than a mile from the dump. She lost both parents to cancer and battled the disease herself. Dozens of neighbors have similar stories. Three cancer researchers told Reuters the number of cases in the neighborhood is worrisome. “You just feel like you’re being gaslighted by your own government,” Mitchell said of the ATSDR’s role.
Note: For more along these lines, see concise summaries of deeply revealing news articles on government corruption and toxic chemicals from reliable major media sources.
What if your entire economy was based on one product? For all intents and purposes, Denmark quite literally runs on Ozempic, a diabetes medication that is now widely used by consumers to lose weight. Worldwide sales have increased by over 60% in the past year alone. In the United States, which is one of its largest markets, prescriptions for Ozempic and similar drugs quadrupled between 2020 and 2022. At the end of 2023, Novo became the largest company in Europe. And its rise has eclipsed the Danish economy, creating a lot of value on the one hand, but an imbalanced economy on the other. You might have heard of "petrostates," countries where fossil fuel extraction dominates the economy. By that measure, you might call Denmark a pharmastate, because Novo now dominates the Danish economy. Nearly 1 out of every 5 Danish jobs created last year was at Novo. And that's just directly. If you also include the jobs that Novo has created indirectly — like, for example, at its suppliers, or from all the newly wealthy Novo employees spending their money at shops and restaurants — nearly half of all private-sector nonfarm jobs created in Denmark can be traced back to Novo. Novo Nordisk's meteoric trajectory raises a question about economic growth that's much bigger than just Denmark: Namely, what are the risks of having one giant company driving your entire economy? And crucially, what happens if that company's fortunes take a turn for the worse?
Note: The makers of these weight-loss drugs could be hit with over 10,000 lawsuits over severe adverse events from these drugs. It is now estimated that 1 in 8 adults in the US have taken Ozempic or another weight-loss drug. For more along these lines, see concise summaries of deeply revealing news articles on Big Pharma profiteering from reliable major media sources.
Pesticides may cause cancer on a level equivalent to smoking cigarettes, a new study has found. The widespread use of pesticides may lead to hundreds of thousands of additional cancer cases in major corn-producing states like Iowa, Illinois, Indiana, Missouri and Ohio — even for Americans who don’t work on farms, according to findings published ... in Frontiers in Cancer Control and Society. In February, scientists from the Endocrine Society and the International Pollutants Elimination Network raised concerns that there was no safe level of exposure to many common pesticides. Research ... has tended to focus on specific pesticides, regions or cohorts of the population (like farm workers) — which obscures the fact that pesticides are used across the country, and that those exposed to any of them tend to be exposed to many of them, creating a greater compound risk. The researchers found a difference of 154,000 cancer cases per year, adjusted for population, between the area with the lowest pesticide use — the Great Plains — and that with the highest, the corn belt of the inner Midwest, where hundreds of millions of pounds of glyphosate are applied each year across millions of acres. When it came to individual cancers, pesticide use seemed to have the strongest association with blood cancers like leukemia or non-Hodgkin lymphoma. Half again as many cases of the latter appeared to be “caused by pesticides compared to smoking,” the researchers wrote.
Note: For more along these lines, see concise summaries of deeply revealing news articles on health and food system corruption from reliable major media sources.
A new study found the amount of pesticides used on farms was strongly associated with the incidence of many cancers — not only for farmers and their families, but for entire communities. The just-released analysis showed that “agricultural pesticides can increase your risk for some cancers just as much as smoking,” says co-author Isain Zapata. Living in places with high pesticide use increased the risk of colon and pancreatic cancers by more than 80 percent. Pesticides are currently an integral part of the country’s industrialized agricultural system. About a million pounds of pesticides are used each year, across nearly every state in the country. These chemicals make their way through the food system: a pesticide linked to infertility, for example, is widely found in household staples like Cheerios. When a pesticide is first registered with federal regulators, the vast majority of the information available about it is science conducted by the company who made it. “The presumption in the U.S. is in favor of the safety of the chemical,” Burd says. Elsewhere, like the European Union, “chemicals are not presumed safe, they adopt a much more precautionary approach.” There’s also a revolving door between the [Environmental Protection Agency] and the industry it regulates. Alexandra Dunn, the former assistant administrator for the Office of Chemical Safety and Pollution Prevention, for example, is now running CropLife America, the pesticide industry’s leading lobbying group. She’s only the latest; since 1974, all of the office’s directors went on to work for pesticide companies.
Note: For more along these lines, see concise summaries of deeply revealing news articles on toxic chemicals and food system corruption from reliable major media sources.
Dr. Kate Mulligan is the Senior Director of the Canadian Institute for Social Prescribing (CISP), a new national hub created to support health care providers and social services professionals to connect people to non-clinical supports and community resources. Mulligan ... led one of Canada’s first social prescribing projects. "They have a conversation with someone with expertise [like a doctor] to determine a plan, and get support to follow through on something non-clinical that benefits their health. It should be happening systematically, as a regular part of our health system," [said Mulligan]. Someone experiencing food insecurity or an illness like diabetes can be prescribed fresh foods. That could mean a voucher for your local farmers’ market, a food box delivery to your home or a credit card that you can spend at the regular grocery store. Social prescribing also means making sure the provided food is culturally appropriate ... thinking about possible connections to include and benefit local farmers. A small community largely inhabited by retirees — lots of people ending up living alone without a strong support network — implemented social prescribing. An older man was diagnosed with depression after his wife died. He kept going for primary care, but really what he was experiencing was unsupported grief. Through social prescribing, he was connected with a fishing rod and a fishing buddy. This is like a $20 intervention. Within a fairly short time, he got off his medication and reconnected with other services too — built friendships, got connected to other community offerings. The health centre started developing their own services, like grief support cooking classes for older grieving widows.
Note: Explore more positive stories like this about healing our bodies and healing social division.
Being overweight or obese is a serious, common, and costly chronic disease. More than two in five U.S. adults have obesity. By 2030, nearly one of two adults in the U.S. are projected to be obese. More than 108 million U.S. adults live with obesity and more than 1 billion people are obese around the world. Obesity accounted for nearly $173 billion in medical expenditures in 2019. Recent news that weight loss medications, including GLP-1 receptor agonists like Ozempic and others, are revolutionizing obesity medicine. Some patients lose up to 20 percent of their initial body weight in a year or two on these drugs. Yet a recent lawsuit challenging a top brand heightens concerns about this relatively new class of drugs. More than half of graduating medical students report that the time dedicated to clinical nutrition instruction is insufficient. In a striking study of 115 medical doctors, the majority of participants (65.2 percent) demonstrated inadequate nutrition knowledge, with 30.4 percent of those scoring low having a high self-perception of their nutrition knowledge. The important role of medical doctors in addressing nutrition in clinical practice has been acknowledged by multiple authoritative professional bodies. Ironically, most doctors often lack the knowledge to help a patient eat healthy and to realize the importance of food to wellness. In a contested space filled with commercial interests and influencers, it is critical for a doctor to be a reliable source of evidence-based nutrition.
Note: For more along these lines, see concise summaries of deeply revealing news articles on health and food system 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.
Vaccine adverse effects are real. I know it makes some people uncomfortable to acknowledge this, but alongside the benefits of vaccines, there are cases of profound harm. Recently, the New York Times covered my story: “Thousands Believe COVID Vaccines Harmed Them. Is Anyone Listening?” Sadly, no one is listening yet, and very few people are willing to help. I am a research nurse practitioner who has dedicated my professional career to community health and clinical research, including vaccines. My beliefs are firmly rooted in science. Three years ago, when the COVID-19 vaccine emerged, I stepped forward to receive it. What followed was unexpected and devastating. Within hours I developed tingling along my right arm, which over days radiated across my body. A neurologist and colleague recommended that I proceed with a second dose. With the vaccine mandate from my employer at the top of my mind, I proceeded, against my own medical judgment. After the second dose, my condition rapidly worsened. I developed positional tachycardia, wildly fluctuating blood pressures, internal tremors, electrical zap sensations on my legs, intense right-sided headaches, abdominal pain and severe tinnitus. I struggle to live with all of this and more to this day. Medical gaslighting, coupled with the absence of legal recourse or adequate compensation, compounds the challenges we endure. When I reach out for help, my pleas often fall on deaf ears, or I am disparaged as a misinformed “anti-vaxxer.”
Note: This article was written by Shaun Barcavage, a nurse practitioner in New York City. Explore our nuanced, uncensored investigation about this important issue. For more along these lines, see concise summaries of deeply revealing news articles on COVID vaccine problems from reliable major media sources.
Jonathan Haidt is a man with a mission ... to alert us to the harms that social media and modern parenting are doing to our children. His latest book, The Anxious Generation: How the Great Rewiring of Childhood Is Causing an Epidemic of Mental Illness ... writes of a “tidal wave” of increases in mental illness and distress beginning around 2012. Young adolescent girls are hit hardest, but boys are in pain, too. He sees two factors that have caused this. The first is the decline of play-based childhood caused by overanxious parenting, which allows children fewer opportunities for unsupervised play and restricts their movement. The second factor is the ubiquity of smartphones and the social media apps that thrive upon them. The result is the “great rewiring of childhood” of his book’s subtitle and an epidemic of mental illness and distress. You don’t have to be a statistician to know that ... Instagram is toxic for some – perhaps many – teenage girls. Ever since Frances Haugen’s revelations, we have known that Facebook itself knew that 13% of British teenage girls said that their suicidal thoughts became more frequent after starting on Instagram. And the company’s own researchers found that 32% of teen girls said that when they felt bad about their bodies, Instagram made them feel worse. These findings might not meet the exacting standards of the best scientific research, but they tell you what you need to know.
Note: For more along these lines, see concise summaries of deeply revealing news articles on Big Tech and mental health from reliable major media sources.
Late last year, the U.S. Food and Drug Administration (FDA) quietly introduced a regulation that may be one of the most important shifts in how [clinical research organizations, universities large and small, pharma companies, and multi-billion dollar corporations] conduct future medical and public health research. A bedrock of ethical research design is the universal requirement of informed consent for any medical procedure, treatment, or intervention. These measures have generally been strengthened since the Nuremberg Trials, formally adopted across the U.S. government through the institutional review board (IRB) system. An IRB is a committee of specialists and administrators at each institution that oversees research design and assures the protection of research subjects. At its core, the new FDA rule change allows any IRB to broadly assume the FDA's own exemption power, dubiously granted under the 21st Century Cures Act of 2016, to grant exemptions to informed consent requirements based on "minimal risk." Based on vague guidelines, it effectively gives thousands of IRB committees the unilateral ability to determine that researchers need not obtain true informed consent from research participants. The relaxed standards could facilitate the quick approval of controversial research projects. The Gates Foundation-backed Oxitec program is currently releasing millions of genetically modified mosquitos in the Florida Keys. Another application of the relaxed standards is to government-funded studies of online posts designed to identify "misinformation." Entities like the Stanford Internet Observatory have laundered government demands for censorship of speech—even true speech—in online settings like Facebook and X (formerly Twitter). The literal purpose of this research is to harm its research subjects by censoring their speech and labeling them as purveyors of misinformation. In 2021, a conservative journalist sued Stanford University for slandering him via this research project, which never sought his informed consent to be a subject of their study. Under the new FDA rule, IRBs everywhere would feel no compunction to require it.
Note: Read about the shocking history of human experimentation. See a disturbing timeline of corporate and government experiments that treated people like guinea pigs. For more, see concise summaries of deeply revealing news articles on corruption in science from reliable major media sources.
Dr. Robert Lufkin, a physician and father of two young children, has been diagnosed with four chronic diseases — the same ones that claimed his father’s life. Inspired by his own medical struggles, Lufkin decided to write a book exposing what he calls “medical lies” that contribute to the risk of chronic disease in the US – some of which he says he himself once taught as a professor at UCLA and USC. His own diagnoses, Lufkin said, “woke him up” to the flaws in the medical system. The doctor noted that ... a “new class of diseases” has posed a challenge. These include obesity, diabetes, hypertension, cancer, cardiovascular disease, Alzheimer’s disease and even mental illness, Lufkin said. “Up to 80% of our resources are now spent on these chronic diseases.” The tools that were so effective in the 20th century — “the pills and surgeries” — might save lives in the moment. But they only address the symptoms of these chronic diseases — not their root causes. “There’s a common metabolic cause that underlies most of these diseases,” Lufkin said. Ten percent of American adults have type 2 diabetes, and about 38% have prediabetes. The diabetes lie declares that the best way to treat type 2 diabetes is with insulin. However, it will also raise the body’s overall insulin levels, worsening insulin resistance, the underlying cause of type 2 diabetes. Additionally, elevated insulin levels drive other chronic diseases. There are also financial incentives. In 2013, sales of insulin and other diabetes drugs reached $23 billion, according to data from IMS Health, a drug market research firm. That was more than the combined revenue of the National Football League, Major League Baseball and the National Basketball Association.
Note: For more along these lines, see concise summaries of deeply revealing news articles on health from reliable major media sources.
Kansas on Monday sued Pfizer Inc., accusing the pharmaceutical giant of misrepresenting the safety of its Covid-19 vaccine and violating the state’s consumer protection law. The lawsuit was filed by state Attorney General Kris Kobach in Kansas District Court, Thomas County. The suit alleges the drugmaker misled the public when it said it had a safe and effective Covid-19 vaccine. “Pfizer said its COVID-19 vaccine was safe even though it knew its COVID-19 vaccine was connected to serious adverse events, including myocarditis and pericarditis, failed pregnancies, and deaths,” the state wrote in the complaint. The company administered more than 3.5 million vaccine doses in Kansas as of Feb. 7, 2024, according to the lawsuit. The complaint also said Pfizer maintained its own adverse events database, separate from the federal Vaccine Adverse Event Reporting System (VAERS), a national early warning system managed by the Food and Drug Administration and Centers for Disease Control and Prevention to detect possible safety problems in US-licensed vaccines. Pfizer’s database contained cases of adverse events reported spontaneously to Pfizer, cases reported by the health authorities, and cases published in the medical literature, according to the suit. “Pfizer’s adverse events database contained more adverse event data than VAERS because it included both information in VAERS and information not in VAERS,” Kobach wrote.
Note: For more along these lines, see concise summaries of news articles on COVID vaccines from reliable major media sources.
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