Health News StoriesExcerpts of Key Health News Stories in Major Media
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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.
There is nothing the state of North Carolina can do, Elaine Riddick says, to make up for forcing her to be sterilized when she was 14 years old. "They cut me open like I was a hog," [she said]. About 7,600 people were sterilized under North Carolina's eugenics program. Roughly 85 percent of the victims were women or girls. Unlike most states, North Carolina ramped up its sterilizations after World War II, despite associations between eugenics and Nazi Germany, which took eugenics to even more horrifying lengths. Around 70 percent of all North Carolina's sterilizations were performed after the war, peaking in the 1950s, according to state records. Nationwide, there were more than 60,000 known victims of sterilization programs, with perhaps another 40,000 sterilized through "unofficial" channels like hospitals or local health departments working on their own initiative. Eugenics was aimed at creating a better society by filtering out people considered undesirable, ranging from criminals to those imprecisely designated as "feeble-minded." People as young as 10 in North Carolina were sterilized for not getting along with schoolmates, being promiscuous or running afoul of local social workers or doctors. "Where did all this come from? This came from doctors, medical practitioners, professors, not guys in pickup trucks wearing white sheets," said Edwin Black, author of the eugenics history War Against the Weak.
It's fraudulent for academics to give their names to medical articles ghostwritten by pharmaceutical industry writers, say two Canadian law professors who call for potential legal sanctions. Studies suggest that industry-driven drug trials and industry-sponsored publications are more likely to downplay a drug's harms and exaggerate a drug's virtues, said Trudo Lemmens, a law professor at the University of Toronto. The integrity of medical research is also harmed by ghostwritten articles, he said. Ghostwriting is part of marketing that can distort the evidence on a drug, Lemmens said. Industry authors are concealed to insert marketing messages and academic experts are recruited as "guest" authors to lend credibility despite not fulfilling criteria for authorship, such as participating in the design of the study, gathering data, analyzing the results and writing up of the findings. Lemmens and his colleague Prof. Simon Stern argue that legal remedies are needed for medical ghostwriting since medical journals, academic institutions and professional disciplinary bodies haven't succeeded in enforcing sanctions against the practice. Ghostwritten publications are used in court to support a manufacturer's arguments about a drug's safety and effectiveness, and academic experts who appear as witnesses for pharmaceutical and medical device companies also boost their credibility with the publications on their CV, Lemmens said.
Note: For a respected doctor's powerful analysis of fraud in the pharmaceutical industry, click here. For lots more from reliable sources on key health issues, click here.
Do drugs really stop working after the date stamped on the bottle? Fifteen years ago, the U.S. military decided to find out. Sitting on a $1 billion stockpile of drugs and facing the daunting process of destroying and replacing its supply every two to three years, the military began a testing program to see if it could extend the life of its inventory. The testing, conducted by the U.S. Food and Drug Administration, ultimately covered more than 100 drugs, prescription and over-the-counter. The results ... show that about 90% of them were safe and effective far past their original expiration date, at least one for 15 years past it. The program's returns have been huge. The military from 1993 through 1998 spent about $3.9 million on testing and saved $263.4 million on drug expense. In light of these results, a former director of the testing program, Francis Flaherty, says he has concluded that expiration dates put on by manufacturers typically have no bearing on whether a drug is usable for longer. "Manufacturers put expiration dates on for marketing, rather than scientific, reasons," says Mr. Flaherty, a pharmacist at the FDA until his retirement last year. "They want turnover." Joel Davis, a former FDA expiration-date compliance chief, says that with a handful of exceptions - notably nitroglycerin, insulin and some liquid antibiotics - most drugs are probably as durable as those the agency has tested for the military. "Most drugs degrade very slowly," he says. "In all likelihood, you can take a product you have at home and keep it for many years." Drug-industry officials ... acknowledge that expiration dates have a commercial dimension.
Note: As the Wall Street Journal charges to view this article at the above link, you can view it free here. For lots more on how the pharmaceutical industry cares more about profits than your health, click here.
A consortium of U.S. organic farmers and seed dealers filed suit against global seed giant Monsanto Co. on [March 29], in a move to protect themselves from what they see as a growing threat in the company's arsenal of genetically modified crops. The Public Patent Foundation filed the suit on behalf of more than 50 organizations challenging the chemical giant's patents on its genetically modified seeds. The group is seeking a ruling that would prohibit Monsanto from suing the farmers or dealers if their organic seed becomes contaminated with Monsanto's patented biotech seed germplasm. Monsanto has filed scores of lawsuits and won judgments against farmers they claimed made use of their seed without paying required royalties. Many farmers have claimed that their fields were inadvertently contaminated without their knowledge, and the issue has been a topic of concern for not only farmers, but also companies that clean and handle seed. "This case asks whether Monsanto has the right to sue organic farmers for patent infringement if Monsanto's genetically modified seed should land on their property," said Dan Ravicher, executive director of PUBPAT. The suit also alleges that Monsanto's GMO seeds do more harm than good and claims the patents on genetically modified seed are invalid because they don't meet the "usefulness" requirement of patent law.
Note: For a powerful, quality documentary revealing the gross abuses of Monsanto which endanger public health, click here.
The number of American children diagnosed with bipolar disorder increased 40-fold in a recent 10-year span, one study found. In Minnesota, spending on powerful antipsychotic drugs to treat bipolar and other disorders in children has risen 17-fold since 2000 and exceeds $6 million annually -- just in one state-funded health program. Now, in a medical reversal with few parallels, psychiatrists are backing away from the diagnosis. While some feel bipolar was once under-diagnosed in children, they worry that thousands of kids have since received the diagnosis in error, due to overzealous doctors, desperate parents, quirks in the health insurance system and aggressive marketing by drug companies. This summer, in a sign of the profession's second thoughts, the manual that psychiatrists use to make diagnoses is being rewritten and field-tested with a new disorder that would replace bipolar in many cases. The profession's about-face could help the next generation of troubled children, but it also raises questions about the harm done to children who shouldn't have received either the diagnosis or the potent drugs used to treat it. While antipsychotics can be lifesavers for patients who truly are bipolar, they come with increased risks of obesity, diabetes, muscle spasms and other serious side effects.
Note: For a powerful analysis of corruption in medicine by a leading medical researcher, click here. For key reports on health from reliable sources, click here.
An international study which debunks research linking cellphones to cancer risks received major funding from wireless manufacturers. The World Health Organization's International Agency for Research on Cancer classified [the] radio frequency emitted by wireless devices as possibly carcinogenic, but a panel of international scientists recently published a study challenging these findings. But in the study's conflict of interest disclaimer, the panel acknowledged it received support from the wireless industry to conduct the research. A number of organizations, including the Mobile Manufacturers' Forum, were cited as sources of funding. Dr. Devra Davis, an American scientist who runs the non-profit education group [Environmental Health Trust] says the new study is "misleading" and "wrong." "It is propaganda," said Davis, who also founded the world's first Center for Environmental Oncology. Davis says cellphone safety is a major public health issue and governments need to move away from the idea of taking action after there are "enough sick people or dead bodies." "The fact that we don't have an epidemic right now is of course what we expect," she said. "It is actually preposterous to imply or they really say that because don't have any increase now, there's no problem. It's really very sad."
Note: For more on the health threats posed by cell phones, click here.
There is an epidemic of cancer today. One in three Americans will be diagnosed with cancer, often before the age of 65. Since 1940, we have seen in Western societies a marked and rapid increase in common types of cancer. In fact, cancer in children and adolescents has been rising by 1 to 1.5 percent a year since the 1960's. And these are cancers for which there is no screening. For most common cancers - prostate, breast, colon, lung - rates are much higher in the West than in Asian countries. Yet Asians who emigrate to the United States catch up with the rates of Americans within one or two generations. While in Asia, Asians are protected not by their genes, but by their lifestyle. We continue to invest 97 percent of our cancer research funds in better treatments and early detection. Only 3 percent is invested in tackling causes. The World Cancer Research Fund published a report in 2007 concluding that a majority of cancer cases in Western societies could be avoided with life-style measures: 40 percent from changes in diet and physical activity (more vegetables and fruits, less sugar, less red meat, regular walking or the equivalent activity 30 minutes six times per week), 30 percent from smoking cessation, and about 10 percent from reduced alcohol consumption. We now even have data about how specific foods such as broccoli and cabbages, garlic and onions, green tea or the spice turmeric directly help kill cancer cells and reduce the growth of new blood vessels they need to develop into tumors.
Note: The author of this article, Dr. David Servan-Schreiber, is a clinical professor of psychiatry at the University of Pittsburgh and a founding board member of Doctors Without Borders, USA, and author of Anticancer - A new way of life. For an excellent, inspiring 10-minute video interview with this doctor, click here.
The food and advertising industries have launched a multi-pronged campaign to squash government efforts to create voluntary nutritional guidelines for foods marketed to children. Calling themselves the Sensible Food Policy Coalition, the nation’s biggest foodmakers, fast-food chains and media companies, including Viacom and Time Warner, are trying to derail standards proposed by four federal agencies. The U.S. Chamber of Commerce has also lent its lobbying muscle to the effort. The guidelines are designed to encourage foodmakers to reduce salt, added sugars and fats in foods and drinks targeted to children. Public-health experts say children, many of whom may lack the critical-thinking skills to understand advertising, are bombarded daily by television ads, Web sites, toy giveaways and cartoon characters promoting junk food. The food and beverage industry spends about $2 billion a year marketing directly to children. The business community has portrayed the government’s guidelines as job-killing government overreach. “We allow companies into our homes to manipulate children to want food that will make them sick,” said Margo Wootan of the Center for Science in the Public Interest.
Note: The "Sensible Food Policy Coalition" is arguing against voluntary guidelines designed to help our children eat more nutritious food. Is that Orwellian doublespeak or what?
What causes autism? Scientists still don't have an answer, but two new studies suggest that conditions in a mom's womb may trigger the developmental disorder. Heredity is considered a major factor that triggers autism spectrum disorders, but scientists have long wondered what roles - if any - environmental factors play. Scientists used California health records to identify 192 pairs of twins - fraternal or identical - where at least one was affected by autism. Using diagnostic techniques that included directly observing the children, the scientists found 77 percent of male identical twins and 50 percent of female identical pairs both had autism. Those findings weren't too surprising, considering identical twins share the same genes. But what surprised researchers were the high rates of autism spectrum disorders they found in pairs of fraternal twins: 31 percent rate for males and 36 percent for females. Fraternal twins, from two fertilized eggs, share no more genetic material than any other siblings. But since they share the same womb, that could play a role, said Dr. John Constantino, professor of psychiatry at the Washington University School of Medicine in St. Louis, who wasn't involved in the new research. Constantino calls the research a "key finding that puts a spotlight on pregnancy as a time when environmental factors might exert their effects."
Note: For major media articles presenting evidence of a link between autism and vaccines, click here.
For all those who've declared the autism-vaccine debate over a new scientific review begs to differ. It considers a host of peer-reviewed, published theories that show possible connections between vaccines and autism. The article in the Journal of Immunotoxicology is entitled "Theoretical aspects of autism: Causes--A review." The author is Helen Ratajczak, surprisingly herself a former senior scientist at a pharmaceutical firm. Ratajczak did what nobody else apparently has bothered to do: she reviewed the body of published science since autism was first described in 1943. Not just one theory suggested by research such as the role of MMR shots, or the mercury preservative thimerosal; but all of them. Ratajczak's article states, in part, that "Documented causes of autism include genetic mutations and/or deletions, viral infections, and encephalitis following vaccination. Therefore, autism is the result of genetic defects and/or inflammation of the brain." The article goes on to discuss many potential vaccine-related culprits, including the increasing number of vaccines given in a short period of time. Ratajczak also looks at a factor that hasn't been widely discussed: human DNA contained in vaccines. Ratajczak reports that about the same time vaccine makers took most thimerosal out of most vaccines (with the exception of flu shots which still widely contain thimerosal), they began making some vaccines using human tissue. Why could human DNA potentially cause brain damage? The way Ratajczak explained it to me: "Because it's human DNA and recipients are humans. That DNA is incorporated into the host DNA. Now it's changed, altered self and body kills it. Where is this most expressed? The neurons of the brain. Now you have body killing the brain cells and it's an ongoing inflammation." We asked Ratajczak how she came to research the controversial topic. She told us that for years while working in the pharmaceutical industry, she was restricted as to what she was allowed to publish. "I'm retired now," she told CBS News. "I can write what I want."
Note: For an excellent report endorsed by dozens of respected doctors and nurses on the serious risks and dangers of vaccines, click here. For other major media articles presenting evidence on the risks and dangers of vaccines, click here.
Physician Janette Sherman, M.D. and epidemiologist Joseph Mangano published a report Monday highlighting a 35% spike in northwest infant mortality after Japan's nuclear meltdown. The report spotlighted data from the CDC's Morbidity and Mortality Weekly Report on infant mortality rates in eight northwest cities, including Seattle, in the 10 weeks after Fukushima's nuclear meltdown. The average number of infant deaths for the region moved from an average of 9.25 in the four weeks before Fukushima' nuclear meltdown, to an average of 12.5 per week in the 10 weeks after. The change represents a 35% increase in the northwest's infant mortality rates. In comparison, the average rates for the entire U.S. rose only 2.3%.
Note: For details of this very important analysis of the CDC's data on US infant mortality after the Fukushima meltdowns, click here and here.
California Sen. Dianne Feinstein renewed a decadelong push [on June 17] to phase out the routine use of antibiotics in livestock, hogs and poultry. Government officials have warned that increasing antibiotic resistance in humans poses a serious public health threat. In the United States, the Food and Drug Administration has confirmed that 80 percent of all antibiotics are given to farm animals in low doses intended to stave off disease in large livestock operations. Many of the antibiotics are the same ones used to treat human diseases. Scientists have linked the practice to rising antibiotic resistance in humans, along with the overprescription of antibiotics by doctors. Feinstein's legislation, opposed by the National Pork Producers Council, would phase out the use of antibiotics considered "medically important" to humans and require new applications for animal antibiotics to prove that they do not endanger human health. The bill would permit antibiotics to treat sick animals. The California Democrat's bill is an identical version of a House bill, HR965, the Preservation of Antibiotics for Medical Treatment Act, by Rep. Louise Slaughter, D-N.Y., a microbiologist on a crusade to eliminate low-dose antibiotic use in livestock.
Note: For key reports on health issues from reliable sources, click here.
Cancer is not one disease. It is many. Yet oncologists have long used the same blunt weapons to fight different types of cancer: cut the tumour out, zap it with radiation or blast it with chemotherapy that kills good cells as well as bad ones. New cancer drugs are changing this. Scientists are now attacking specific mutations that drive specific forms of cancer. A breakthrough came more than a decade ago when Genentech, a Californian biotech firm, launched a drug that attacks breast-cancer cells with too much of a certain protein, HER2. In 2001 Novartis, a Swiss drugmaker, won approval for Gleevec, which treats chronic myeloid leukaemia by attacking another abnormal protein. Other drugs take different tacks. Avastin, introduced in America in 2004 by Genentech, starves tumours by striking the blood vessels that feed them. These new drugs sell well. Last year Gleevec grossed $4.3 billion. Roche’s Herceptin (the HER2 drug) and Avastin did even better: $6 billion and $7.4 billion respectively. The snag, from society’s point of view, is that all these drugs are horribly expensive. Last year biotech drugs accounted for 70% of the increase in pharmaceutical costs in America, according to Medco, a drug-plan manager. Cancer plays a huge role in raising costs.
Note: To see what happens when inexpensive potential cures for cancer are discovered, click here. For key reports on health issues from reliable sources, click here.
Eric Merola's "Burzynski" charts how a Texas medical doctor and biochemist developed Antineoplastons, genetic-targeted medicines, and with them began to treat a wide range of cancers, including difficult-to-treat brain malignancies, with remarkable and continuing success only to bring down the full force of the medical establishment, which has laid assault to him in the most stupefying, devious and costly manner. Stanislaw Burzynski, a Polish immigrant ... eventually won a 14-year struggle – during which he found himself threatened with life imprisonment and astronomical fines for fraud and other violations – to obtain FDA-approved clinical trials of his Antineoplastons, an ordeal that cost Burzynski $2.2 million in legal expenses and the FDA $60 million in taxpayers' money. The film makes the case that big pharmacy holds the FDA in its thrall. Burzynski's Antineoplastons, with their high success rate and lack of side effects, pose a significant threat to the trillion-dollar industry of treating cancer with the traditional methods of surgery, radiation and chemotherapy.
Note: The Los Angeles Times now requires payment to view this article at this link. For the Burzynski clinic website, click here. You can watch part or all of this revealing movie at this link. For another powerful documentary featuring a variety of potential cancer cures that have been suppressed, click here. For excerpts from numerous major media articles with potential cancer cures that are being suppressed, click here.
Cellphones are “possibly carcinogenic” to humans, according to [an international panel of experts] organized by the World Health Organization. But an exhaustive, eight-day review of hundreds of studies concluded that the existing evidence is insufficient to know for sure. And because cellphones are so popular, further research is urgently needed, the experts said. “Possibly carcinogenic” is the WHO’s third-highest rating, falling below “carcinogenic” and “probably carcinogenic”. Other substances that the group has categorized as “possibly carcinogenic” include talcum powder, which has been possibly linked to ovarian cancer, and low-frequency magnetic fields, which are emitted by power lines and appliances and have been possibly associated with childhood leukemia. The cellphone classification marks a departure for the WHO, which previously said there were no risks from exposure to radio frequency electromagnetic fields emitted by the devices. “The conclusion means that there could be some risk, and, therefore, we need to keep a close watch for a link between cellphones and cancer risk,” said Jonathan M. Samet of the University of Southern California, who chaired the WHO’s International Agency for Research on Cancer panel.
Note: Remember how long it took for the evidence to surface that smoking causes cancer. Consider using a wired headset with your cellphone to decrease any cancer risk. Watch a Senate committee meeting on the risks and dangers of cell phones, including greatly increased brain cancer rates. For other safety suggestions, click here. For key articles on health issues from reliable sources, click here.
Mobile phones and computers with wireless internet connections pose a risk to human health and should be banned from schools, a powerful European body has ruled. A Council of Europe committee examined evidence that the technologies have "potentially harmful" effects on humans, and concluded that immediate action was required to protect children. In a report, the committee said it was crucial to avoid repeating the mistakes made when public health officials were slow to recognise the dangers of asbestos, tobacco smoking and lead in petrol. The report also highlighted the potential health risks of cordless telephones and baby monitors, which rely on similar technology and are widely used. Fears have been raised that electromagnetic radiation emitted by wireless devices can cause cancers and affect the developing brain.
Note: Consider using a wired headset with your cellphone to decrease any cancer risk. For other safety suggestions, click here. For key articles on health issues from reliable sources, click here.
The government is conducting armed raids on dairies that sell raw milk, [yet it allows us] to buy food that is so toxic ... it has to carry "safe handling instructions." Factory farms that knowingly produce chicken and eggs teeming with salmonella are not considered a threat to public health, but an impeccably clean organic raw milk dairy is treated like a meth lab. I used to think the "food freedom" activists were being paranoid about this stuff. Not anymore. The federal government is broke, but we're hiring 18,000 food police, to the tune of hundreds of millions of dollars. How does this happen? The former CEO of genetically modified organism powerhouse Monsanto is now our secretary of agriculture and head of food safety. Talk about the fox guarding the henhouse. Tell your representatives to defund the Food Safety Modernization Act of 2010, and buy organic and local. While you still can.
Note: For more on this bizarre development, click here and here.
Pennsylvania Amish farmer Dan Allgyer has become a cause celebre for raw milk drinkers as the target of a Food and Drug Administration campaign - using sting operations and guns-drawn raids usually reserved for terrorists and drug lords - to eliminate unpasteurized milk. Such milk, also known as raw or fresh milk, is legal in California and considered essential to Europe's finest cheeses, creams and butters. Allgyer is the latest to feel the force of a yearslong Food and Drug Administration campaign against raw milk that has focused on tiny farms and consumer co-ops. Raw milk drinkers say cooking milk diminishes its flavor and nutrients. They said similar sterilization standards, if applied across the American diet, would ban sushi, medium-rare steaks, oysters on the shell and most raw fruits and vegetables. The Food Safety and Modernization Act approved by Congress last year and signed by President Obama in January has vastly enhanced the agency's powers. Starting July 3, the agency can confiscate any food at any farm that it deems unsafe or mislabeled. Throughout Europe, uncooked milk is the norm, dispensed in vending machines in Switzerland, Austria, France, Italy, Slovenia and the Netherlands. It is healthy, adherents say, because it contains fat that is not broken down by homogenization and is free of antibiotics and hormones, because cows are raised in small herds on pastures.
We could make faster progress against cancer by changing the way drugs are developed. In the current system, if a promising compound can’t be patented, it is highly unlikely ever to make it to market — no matter how well it performs in the laboratory. The development of new cancer drugs is crippled as a result. The reason for this problem is that bringing a new drug to market is extremely expensive. In 2001, the estimated cost was $802 million; today it is approximately $1 billion. To ensure a healthy return on such staggering investments, drug companies seek to formulate new drugs in a way that guarantees watertight patents. In the meantime, cancer patients miss out on treatments that may be highly effective and less expensive to boot. In 2004, Johns Hopkins researchers discovered that an off-the-shelf compound called 3-bromopyruvate could arrest the growth of liver cancer in rats. The results were dramatic; moreover, the investigators estimated that the cost to treat patients would be around 70 cents per day. Yet, three years later, no major drug company has shown interest in developing this drug. The hormone melatonin, sold as an inexpensive food supplement in the United States, has repeatedly been shown to slow the growth of various cancers when used in conjunction with conventional treatments. Early this year, another readily available industrial chemical, dichloroacetate, was found by researchers at the University of Alberta to shrink tumors in laboratory animals by up to 75 percent. However ... dichloroacetate is not patentable, and the lead researcher is concerned that it may be difficult to find funding from private investors to test the chemical. Potential anticancer drugs should be judged on their scientific merit, not on their patentability.
Note: To explore several cancer cures which have shown dramatic potential, yet are not being studied for lack of funds due to inability to patent the process, click here. Why are these very promising treatments not being fast-tracked as the expensive AIDS drugs were? For a top MD's revealing comments on this, click here. And for why the media won't feature these promising cancer treatments in headlines, click here.
Federal health officials may have only recently called autism a “national health emergency”, but a new study released [on May 11] showed the U.S. has been quietly compensating families with autism for nearly two decades. The report from SafeMinds.org — a group that believes scientific evidence has linked autism to vaccinations – alleges that a fund set up by the U.S. government to compensate those injured by vaccines has paid out claims to dozens of families of autistic kids. The study conducted by the Pace Environmental Law Review revealed that since the late 1980s, the National Vaccine Injury Compensation Program (NVICP) has paid money for 83 cases involving autism out of approximately 1,300 cases of vaccine injury that resulted in childhood brain injury. In that same time period, federal officials have maintained that autism — which now affects an estimated one in 110 individuals — is still “rare” and has publicly conceded to only one vaccine-induced autism case involving nine-year-old Hannah Poling. The study’s authors stand behind the findings and warn they are only “the tip of the iceberg.” Currently, there are over 5,000 vaccine court cases pending that claim autism as a result of vaccine injury.
Note: For more information from major media sources on the dangers of vaccines, click here. And for a fascinating study suggesting that vaccines are much less effective than is publicly acknowledged, click here.
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.