News StoriesExcerpts of Key News Stories in Major Media
Note: This comprehensive list of news stories is usually updated once a week. Explore our full index to revealing excerpts of key major media news stories on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.
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.
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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."
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Unhealthy food and beverage companies powerfully undermine the eating habits of young people by deploying ubiquitous ads that encourage poor dietary choices and increase the risk of serious disease and premature death, according to a sweeping new study published in Obesity Reviews. The first-of-its-kind summary highlights a clear cumulative pattern: The more high-fat, high-sugar, and salty food ads young people see, the more of those products they consume–and the higher the risk that they may develop obesity, type 2 diabetes, and other diet-related diseases. Companies also disproportionately target adolescents, lower-income communities, and Black and Latino youth with the marketing of health-harming food and beverages. The review summarizes 25 years of scientific evidence and findings from 108 empirical studies and 19 systematic reviews of unhealthy food marketing to adolescents (13-17) and young adults (18-25). One study showed that children who watched just five minutes of food ads ate about 130 more calories that day. Only 19% of studies examined health impacts, but most of those found links between unhealthy food marketing and higher BMI, weight gain, or increased obesity risk–especially from ultra-processed foods and sugary drinks. One U.S. study ... found that children who could recall more food ads chose more food items and consumed more calories after exposure.
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More than 30 percent of American teenagers were considered prediabetic in 2023, according to recent data from the Centers for Disease Control and Prevention (CDC). The CDC calculated there were 8.4 million children between the ages of 12 and 17 who were labeled prediabetic – or those whose blood sugar level may be higher than normal – that year, putting them at risk of developing Type 2 diabetes or other health problems like heart disease and stroke. That translates to 32.7 percent of the total adolescent population in the country. Some diabetes experts have taken issue with the CDC's findings since the organization only released a summary and not any raw data or a peer-reviewed study outlining how it came to its conclusion. The CDC also changed its methodology from a 2020 prediabetes analysis without explaining why. "I am going to be skeptical of data updates until there is transparency and clarity on the source of the data and analysis," [said] Christopher Gardner, a diabetes expert. The CDC's newest findings do align with other data showing that prediabetes is becoming more common among American adolescents. One 2022 study published in JAMA Pediatrics ... found that about 1 in 3 American adolescents were prediabetic and the rate among those ages 12-19 more than doubled between 1999 to 2002. From 2015 to 2018, according to the study, the rate for the condition jumped from 12 percent to 28 percent among that age group.
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Martin Makary, the commissioner of the Food and Drug Administration, and Vinay Prasad, the newly appointed head of the FDA's vaccine division, have unveiled a new policy in which the government will no longer recommend Covid booster shots for healthy Americans ages 64 and younger. In addition, as of today, Covid vaccine manufacturers like Moderna and Pfizer will have to conduct trials to prove that their updated vaccines offer clinical benefits such as fewer symptoms, hospitalizations, or deaths. Previously, pharmaceutical companies only had to show that their updated booster shots produced antibodies. That less rigorous standard will still apply for people 65 and older and the immunocompromised. It is well established that people 65 and older account for the vast majority of Covid deaths, while most children, in particular, show few effects from the virus. The move is one part of what is expected to be further changes in federal Covid vaccine policy. According to The Wall Street Journal, Health and Human Services Secretary Robert F. Kennedy Jr. plans to scrap guidelines recommending routine Covid vaccinations for pregnant women, teenagers, and children. Late last month, in an interview with Phil McGraw (popularly known as Dr. Phil), Kennedy advised parents to "do your own research" before vaccinating their newborns. Less than a quarter of Americans received boosters in recent years.
Note: For more along these lines, read our concise summaries of news articles on COVID vaccine problems.
Certain kinds of gut microbes absorb toxic Pfas "forever chemicals" and help expel them from the body via feces, new first-of-its-kind University of Cambridge research shows. The findings are welcome news as the only options that exist for reducing the level of dangerous Pfas compounds from the body are bloodletting and a cholesterol drug that induces unpleasant side effects. The microbes were found to remove up to 75% of some Pfas from the gut of mice. Several of the study's authors plan to develop probiotic dietary supplements that boost levels of helpful microbes in the human gut, which would likely reduce Pfas levels. "If this could be used in humans to create probiotics that can help remove Pfas from the body then this would be a nicer solution in that it wouldn't have so many side effects," said Anna Lindell, Cambridge doctoral student and a co-author of the study. Pfas are a class of about 15,000 compounds most frequently used to make products water-, stain- and grease-resistant. They have been linked to cancer, birth defects, decreased immunity, high cholesterol, kidney disease and a range of other serious health problems. They are dubbed "forever chemicals" because they do not naturally break down in the environment. The microbes [in the study] largely addressed "long-chain" Pfas, which are larger compounds and more dangerous than smaller "short chains" because they stay in the body longer.
Note: Explore more positive stories like this in our comprehensive healing our bodies and technology for good.
Regenerative agriculture offers a way to move beyond what I call the â€dead Earth assumption' – this mechanistic belief that the Earth is made up of lifeless raw materials meant for extraction. Because that's the foundation of industrial agriculture: all it cares about is how many tons of food it produces, with no regard for soil health, biodiversity or the wellbeing of farmers. Regenerative agriculture, on the other hand, shows us the opposite. It means collaborating with nature and recognizing that we are all living organisms on a living Earth. That is what farming should be about: regenerating the potential of the living soil, the living seeds, the living water, the living insects, and the entire web of life. By embracing this potential, we can also transform the way we relate to nature. Because regeneration writes its own poetry – it brings the Earth back to life again in our minds and, in doing so, our relationship with the Earth is being regenerated as well. Some people say: â€You're naive, because companies will always win.' But I don't think that companies will win, and I will give you a reason why. The first corporation ever created was the East India Company in 1600, but after the revolt of the peasants in 1857, they shut down in 1858. So the first corporation that was created to rule the world, was shut down by peasants. In today's world, meaningful change can happen too, when we unite. It all comes down to nurturing the living soil and the living seed.
Note: The above was written by Vandana Shiva. Explore more positive stories like this on healing social division and healing the Earth.
On July 14, 48 students walked through the doors of the Alice L. Walton School of Medicine in Bentonville, Ark. to become its inaugural class. Named after its founder–the world's richest woman and an heir to the Walmart fortune–the school will train students over the next four years in a radically different way from the method most traditional medical schools use. And that's the point. Instead of drilling young physicians to chase symptom after symptom and perform test after test, Alice Walton wants her school's graduates to keep patients healthy by practicing something that most doctors today don't prioritize: preventive medicine and whole-health principles, which involve caring for (and not just treating) the entire person and all of the factors–from their mental health to their living conditions and lifestyle choices–that contribute to wellbeing. Visually, the school lives up to its acronym: AWSOM. The building, with soaring glass walls, is located on Walton family property and includes not just a wellness studio and gym, but a rooftop park, healing gardens where students can study, growing gardens for producing healthy foods, and a reflection pond. Walton is covering tuition for the first five graduating classes. They will get all the science and disease knowledge they need to manage the â€sick-care' side of things," Walton says. But "I wanted to create a school that really gives doctors the ability to focus on how to keep their patients healthy."
Note: Explore more positive stories like this on healing our bodies.
The United States Department of Justice this week released nearly 11 hours of what it described as "full raw" surveillance footage from a camera positioned near Jeffrey Epstein's prison cell the night before he was found dead. The release was intended to address conspiracy theories about Epstein's apparent suicide in federal custody. But instead of putting those suspicions to rest, it may fuel them further. Metadata embedded in the video ... shows that rather than being a direct export from the prison's surveillance system, the footage was modified. Hany Farid, a professor at UC Berkeley whose research focuses on digital forensics and misinformation, reviewed the metadata at WIRED's request. Farid is a recognized expert in the analysis of digital images. He has testified in numerous court cases involving digital evidence. "If a lawyer brought me this file and asked if it was suitable for court, I'd say no. Go back to the source. Do it right," Farid says. "Do a direct export from the original system–no monkey business." The footage confirms that from the time Epstein was locked in his cell at approximately 8 pm on August 9, 2019. However, the recording includes a notable gap: Approximately one minute of footage is missing, from 11:58:58 pm to 12:00:00 am. The video resumes immediately afterward. It looks suspicious–but not as suspicious as the DOJ refusing to answer basic questions about it.
Note: Followup reporting by Wired indicated that almost 3 minutes were cut before this footage was released. Internal US Bureau of Prison (BOP) documents suggest a possible cover-up, while a 60 Minutes 2020 investigation uncovered compelling evidence that challenges the official suicide ruling in Jeffrey Epstein's death–including suspicious neck fractures, missing surveillance footage, and a series of unexplained security failures. Read our comprehensive Substack investigation covering the connection between Epstein's child sex trafficking ring and intelligence agency sexual blackmail operations.
President Donald Trump's Justice Department scrambled on Tuesday to answer questions after its leadership concluded there was no evidence to support a number of long-held conspiracy theories about the death of accused sex trafficker Jeffrey Epstein and his alleged clientele. The Justice Department's memo on Epstein, released on Monday, concluded that after reviewing more than 300 gigabytes of data, there was "no incriminating client list" nor was there any evidence that Epstein may have blackmailed prominent people. The memo also confirmed prior findings by the FBI which concluded that Epstein died by suicide in his jail cell. A subsequent report by the Justice Department's inspector general later found that the Bureau of Prisons employees who were tasked with guarding Epstein failed to search his cell or check on him in the hours before his suicide. [FBI Director Kash] Patel and FBI Deputy Director Dan Bongino, a former podcaster, both previously made statements before working at the FBI about a so-called client list and often suggested that the government was hiding information about Epstein from the American public.
Note: Could it be that powerful people don't want the full truth about Epstein to be revealed? Read our comprehensive Substack investigation covering the connection between Epstein's child sex trafficking ring and intelligence agency sexual blackmail operations. For more along these lines, read our concise summaries of news articles on Jeffrey Epstein's child sex trafficking ring.
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.
The woman, in her 60s, was losing her eyesight. [She] happened to be taking Elmiron, a drug for a bladder condition called interstitial cystitis. By the end of 2024, hundreds of patients on Elmiron had suffered vision loss or blindness. Others taking the drug were even more unlucky. Dozens of patient deaths associated with Elmiron were reported to the Food and Drug Administration (FDA), and 45 patients were hospitalized with severe colitis. Another problem? There's no good evidence that Elmiron works. When the government approved Elmiron in 1996, the manufacturer provided close to zero data that the drug effectively treated interstitial cystitis. Elmiron is just one of hundreds of drugs that have been approved by the FDA over the last several decades on the basis of flimsy or nonexistent evidence. Drug companies have been allowed to market hundreds of prescription drugs to doctors and sell them to unsuspecting patients despite glaringly inadequate evidence that they offer any benefit and in many cases amid clear signs that they pose a risk of serious, often irreparable harm. From January 2013 until Dec. 31, 2022, the FDA approved 429 drugs, most of which were authorized on the basis of inadequate evidence that they worked, according to a database of government records created for this investigation. In the U.S. alone, an estimated 128,000 people are killed each year by side effects of prescription drugs that are properly prescribed. That number excludes opioid overdoses and is more than deaths from all illegal drugs combined.
Note: This article is also available here. A JAMA study reveals how Big Pharma spends more on ads for low-benefit drugs to push consumer demand for treatments doctors are less likely to prescribe. For more along these lines, read our concise summaries of news articles on government corruption and Big Pharma profiteering.
Ultraprocessed foods, seed oils, herbicides and pesticides, and fluoride: They're all targets of the "Make America Healthy Again" movement, whose chief proponent is US Health and Human Services Secretary Robert F. Kennedy Jr. Now, MAHA Films, a production company dedicated to promoting the movement's values, has released its first documentary. "Toxic Nation: From Fluoride to Seed Oils – How We Got Here, Who Profits, and What You Can Do." [The film] highlights those four food- and environmental-related issues that Kennedy's nonprofit MAHA Action ... says "silently endanger millions of Americans every day." The documentary's release follows the May 22 publication of the first MAHA Commission report, which lays the groundwork for an overhaul of federal policy to reduce the burden of chronic disease on American children. Composing up to 70% of the US food supply, ultraprocessed foods are made with industrial techniques and ingredients never or rarely used in kitchens, or classes of additives whose function is to make the final product palatable or more appealing. Ultraprocessed foods are typically low in fiber; are high in calories, added sugar, refined grains and fats, and sodium; and include additives. The [also] film raises concerns about the herbicide glyphosate, citing previously documented links to cancer. Sources also said glyphosate may cause endocrine disruption and damaged gut microbiomes, with the latter potentially increasing risk for irritable bowel diseases and celiac disease.
Note: Read our latest Substack article on how the US government turns a blind eye to the corporate cartels fueling America's health crisis. For more along these lines, read our concise summaries of news articles on food system corruption and toxic chemicals.
The letters the Food and Drug Administration sends to pharmaceutical companies explaining its decisions on drugs are a treasure trove of valuable information. The FDA has begun making drug decision letters public and is publishing past decision letters retroactively. The historical lack of transparency about FDA decision-making has allowed companies to spin the information to investors and shareholders. For example, if an FDA rejection letter explains that the applicant did not meet agency standards and tells the company to perform a new clinical trial to be reconsidered for approval, the firm might mislead shareholders by saying that the FDA had just asked for a few minor things. A 2015 analysis by the FDA found that drug companies avoided mentioning 85 percent of the agency's concerns about safety and efficacy when announcing publicly that their application had not been approved. In addition, when the FDA calls for a new clinical trial for safety or efficacy, that critical information is not disclosed about 40 percent of the time. As a result, capital can be wasted on futile therapies or companies misrepresenting their regulatory guidance. It is important to point out that when making decision letters public, the FDA will redact any trade secrets and confidential commercial information. At the same time, the deliberations of agency scientists are not the property of the drug's sponsor. The FDA does not belong to the industry; it belongs to the American people.
Note: The above was written by Dr. Marty Makary, the US Commissioner of Food and Drugs. For more along these lines, read our concise summaries of news articles on government corruption and Big Pharma profiteering.
The first report of the Maha Commission made headlines in May when it raised concerns about a "chronic disease crisis" in children. Echoing language that [Robert F.] Kennedy campaigned on, the report argued that "the American diet has shifted dramatically toward ultra-processed foods" and that "nearly 70% of children's calories now come from UPFs, contributing to obesity, diabetes, and other chronic conditions". "The greatest step the United States can take to reverse childhood chronic disease is to put whole foods produced by American farmers and ranchers at the center of healthcare," the report found. It went on to describe the dismal state of nutrition research in the United States: "Government funding for nutrition research through the NIH is only 4-5% of its total budget and in some cases is subject to influence by food industry-aligned researchers." Kennedy has ordered the FDA to explore how to eliminate a policy that allows food companies to decide themselves whether food additives are safe, called the Generally Recognized as Safe (Gras) loophole. "That's a really, really big deal," says Dariush Mozaffarian, a cardiologist and director of the Food is Medicine Institute at the Friedman School of Nutrition Science and Policy at Tufts University. "Ninety-nine per cent of compounds in food were added through this loophole." Several states are also pursuing policies that would limit spending from the Supplemental Nutrition Assistance Program (Snap) on "junk food".
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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."
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Most of us are raised on stories and songs of the family farm, where the barns are rust-red and picturesque, and cute animals gambol happily in a picket-fenced yard. "Little Red Barns," [journalist Will Potter's] second book, is the reportage of his epic, emotionally and physically draining 10-year investigation into American factory farms – also known as CAFOs, "concentrated animal feeding operations" – and the dedicated activists seeking to expose the mass suffering within. Like his first book, "Green Is the New Red" (2011), an exploration of how agencies such as the FBI target environmental and animal rights activists, it's impassioned and deeply researched. The book is a lucid indictment of a food system whose normalization of cruelty on a staggering scale is rivaled only by the tightly controlled, government-sanctioned regime of non-transparency that enables it. Discussing the history of undercover efforts to expose abuses in farm factories – in which the advent of phone cameras and other concealable, portable video equipment in the 2000s played a key role – Potter describes the subsequent rise of "ag-gag" laws, passed to stop reporters and activists from filming such private abuses and making them public. Keep in mind, Potter notes, that the U.S. agriculture lobby spends as much on buying influence with politicians every year as the fossil fuel lobby; in 2023 alone, it spent $177 million.
Note: For more along these lines, read our concise summaries of news articles on food system corruption and factory farming.
European Commission President Ursula von der Leyen defended herself before the European Parliament Monday as she faces a largely symbolic no-confidence vote. Thursday's vote focuses on "Pfizergate" – a 35 billion euro ($38.5 billion) deal with Pfizer for up to 1.8 billion Covid vaccine doses that von der Leyen, head of the EU executive branch, negotiated ... with the company's CEO. The controversy began in March 2021 when von der Leyen bypassed normal EU procedures to negotiate directly with Pfizer CEO Albert Bourla via text. The EU paid substantially more for the vaccines von der Leyen negotiated – 19.50 euros ($21.45) per dose versus 15.50 euros ($17.05) in previous contracts, according to leaked EU documents reported by European media – costing taxpayers billions. The text messages could contain vital information about how this price escalation happened and whether proper competitive procedures were followed. The scandal also involves concerns about the sheer volume of doses purchased. The 1.8 billion dose contract was signed when EU vaccination rates were already climbing, raising questions about whether such quantities were necessary. Critics point out that significant amounts of the vaccine supply now sit unused in warehouses across Europe. The European Court of Auditors published a damning report in September 2022 finding von der Leyen had conducted Pfizer negotiations improperly.
Note: For more along these lines, read our concise summaries of news articles on COVID vaccine problems and government corruption.
Loneliness has become a global public health concern. Countries including Britain and Japan have appointed "ministers of loneliness" to help tackle the problem. In the United States, then-Surgeon General Vivek H. Murthy issued a public health advisory on loneliness, stating that the risk for premature death from loneliness is akin to smoking up to 15 cigarettes a day. What if, instead of trying to "fix" the individual, strategies focused on shaping the environment in a way that facilitates social connection? Recently, researchers have been trying to leverage nature as a way to bring people together and reduce negative feelings about social isolation. They say living in what is known as a "lonelygenic environment" – one dominated by cars and concrete instead of grass and trees – can cause or aggravate loneliness. Even if you live in a lonelygenic environment, experts say, spending just an hour or two in nature per week ... may help people feel less isolated. One proposed approach for tackling loneliness as a public health issue is through social prescribing, where physicians connect their patients with non-medical services in the community similar to how they prescribe medication. Nature comes in many forms. An ongoing study by [Matthew] Browning and his colleagues investigates the amount of time a representative sample of Americans spends outdoors in nature. "What we find is that nature is, for most people ... watching their kids play soccer outside or grilling in the backyard."
Note: What if the negative news overload on America's chronic illness crisis isn't the full story? Check out our Substacks to learn more about the inspiring remedies to the chronic illness and loneliness crisis! Explore more positive stories like this on healing our bodies and mental health.
What started as a grassroots movement in the United States over a decade ago, park prescriptions have become an evidence-based treatment regimen that helps people confront both mental and physical ailments by spending more time outdoors. In fact, at least nine countries now have nature prescription programs in some form. Park prescriptions fall under an area of medicine called "social prescribing," which encourages doctors to consider non-clinical treatments in primary mental and physical healthcare. "Social prescribing is a model of care delivery that enables health professionals to formally prescribe non-clinical community activities – including the arts, movement, nature, and service (volunteering) – to improve patient health, and at minimal patient cost," Social Prescribing USA's website reads. "Social prescribing is designed to address social determinants of health, including social connection. Built on a foundation of health equity and collaboration across sectors, social prescribing is intended to broaden health professional toolkits, rather than to replace pharmacological measures." Studies show that stress hormone levels drop after just 15 minutes outside; spending time in forests reduces inflammation and risks of lung infections; increasing nature time reduces risks of heart disease, high blood pressure, and diabetes; and seniors who live near walkable green spaces live longer.
Note: Read our Substack to learn about social and green prescribing along with other inspiring remedies to the chronic illness crisis ravaging the world. Explore more positive stories like this on healing our bodies and mental health.
Important Note: Explore our full index to revealing excerpts of key major media news stories on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.