Health Media ArticlesExcerpts of Key Health Media Articles in Major Media
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Note: Explore our full index to key excerpts of revealing major media news articles on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.
Traditional antidepressants like Prozac work on a group of chemical messengers in the brain called the serotonin system. Researchers once thought that a lack of serotonin was the cause of depression, and that these drugs worked simply by boosting serotonin levels. Recent research suggests a more complicated explanation. Serotonin drugs work by stimulating the birth of new neurons, which eventually form new connections in the brain. Ketamine, in contrast, activates a different chemical system in the brain – the glutamate system. Researcher Ron Duman at Yale thinks ketamine rapidly increases the communication among existing neurons by creating new connections. This is a quicker process than waiting for new neurons to form and accomplishes the same goal of enhancing brain circuit activity. Ketamine has been used for decades as an anesthetic. It also has become a wildly popular but illegal club drug known as "Special K." Mental health researchers got interested in ketamine because of reports that it could make depression vanish almost instantly. Carlos Zarate ... does ketamine research at the NIH. Zarate says patients typically say, "'I feel that something's lifted or feel that I've never been depressed in my life. I feel I can work. I feel I can contribute to society.' And it was a different experience from feeling high. This was feeling that something has been removed."
Note: For many inspiring potential treatment breakthroughs in health issues, click here.
The symptoms of the bizarre illness known as Morgellons are enough to make your skin crawl. For patients who say they are suffering from the condition, that sensation is all too real. Sufferers report feeling that bugs are crawling all over their skin or just under it. They have fatigue and painful sores. They also say that they’ve pulled “fibers” and other solid materials ... through their skin, leaving lesions, according to new research by the Centers for Disease Control and Prevention (CDC). The new study — a $600,000 project launched in 2008 in response to a massive swell of interest and inquiries about the condition from lawmakers and patients — sought to determine how common Morgellons is. The new findings suggest that their symptoms may exist only in their minds. CDC researchers took skin biopsies and urine and blood samples to look for infectious diseases, including bacteria or fungus, that could explain the illness. There were none. They looked for environmental causes too, and couldn’t find any. Although the CDC report concluded that no medical explanation for Morgellons can be found, the paper “confirms what anybody who has ever seen a patient with this knows, which is that these patients are suffering greatly and their suffering is real; they shouldn’t be dismissed,” Jason Reichenberg, director of dermatology at the University of Texas Southwestern-Austin, told USA Today.
Note: Remember that the Feds also insisted Lyme disease was a delusion for many years. For a list of FAQ on Morgellons, click here. For more on this intriguing phenomenon, click here and here.
California's ban on the sale of pork from "downer" pigs, those that were too feeble to walk before being slaughtered, can't be enforced because a less stringent federal law regulates slaughterhouse inspections, the U.S. Supreme Court ruled unanimously [on January 23]. State lawmakers enacted the ban in 2008 after a Humane Society video showed immobile cows being kicked, dragged, shocked and rammed with forklifts at a warehouse in San Bernardino County. Advocates said meat from those animals was more likely to be diseased. Federal law forbids the sale of meat from animals suffering from serious diseases, a ban that recent regulations extended to cattle that were unable to walk. But federal law allows meat sales from downer pigs and other nonambulatory animals, like sheep and goats, that pass federal inspection. Court challenges from meat processors and packers prevented the California law from taking effect. A federal appeals court upheld the California statute in 2010, but the Obama administration joined the National Meat Association in a successful Supreme Court appeal. The ruling dismayed the Humane Society of the United States, which has unsuccessfully lobbied Congress and the U.S. Department of Agriculture for nationwide rules like California's. "The meat industry has the USDA and Congress in its tight grips," said the society's president, Wayne Pacelle.
Note: For lots more from major media sources on corporate and government corruption, click here and here.
New research finds that chemicals commonly found in non-stick cookware, microwave popcorn bags and other manufactured goods may make childhood vaccines less effective, perhaps making it easier for certain diseases to spread through the population. A study published [in] the Journal of the American Medical Association suggests that exposure to perfluorinated compounds, called PFCs, before and after birth may lower a child's ability to make disease-fighting antibodies for tetanus and diphtheria later in life. Researchers studied nearly 600 children and their mothers from the Faroe Islands, a small nation in the North Atlantic between Iceland and Scotland. The study found that higher levels of PFCs in both mothers and children meant lower numbers of disease-fighting antibodies in the children. Study author Philippe Grandjean said very few chemicals are known to have such an effect on the body's immune system. "The PFCs make the immune system more sluggish, so that it doesn't respond as vigorously against micro-organisms as it should," Grandjean said. "If vaccinations don't work, there may be an increased risk of epidemics." The study authors said the marine diet of Faroese people may have influenced the levels of PFCs in the children in the study, since the chemical is commonly found throughout the environment, even in polar bears that live far from pollution sources. But exposure to the chemicals is also high in the United States. In 2004, the Centers for Disease Control and Prevention tested the blood of more than 2,000 Americans and found certain types of PFCs in nearly 98 percent of them.
Note: For more on major problems with many vaccines, see the deeply revealing reports from reliable major media sources available here.
The first genetically engineered animal may be about to enter the food supply. This is also the moment for consumers to demand to know what's in their food. Consumers Union, the advocacy arm of Consumer Reports, believes that genetically engineered fish should not be allowed into the food supply unless it is proved safe for humans and the environment. At the very least, it should be labeled. One of the most critical issues before the [Food and Drug Administration] is the potential for genetically engineered fish to cause consumers to experience increased allergic responses. Unfortunately, the FDA allowed AquaBounty Technologies, the company developing the genetically engineered salmon, to declare that there was no increase in allergy-causing potential in their AquAdvantage salmon, based on data from just six engineered fish - even when the data suggested the genetic engineering process itself did increase the allergy-causing potential. Public opinion clearly and consistently supports mandatory labeling. Our polling found that 95 percent of the public wants labeling of genetically engineered animals, while other polls found that only 35 percent of the public said that they would be willing to eat seafood that has been genetically engineered. Consumers sent nearly 400,000 comments to the FDA demanding the agency reject genetically engineered salmon, or at least require that it be labeled.
Note: For an excellent overview of the threats to health from genetically-modified foods, click here.
BASF, the German chemical giant, is to pull out of genetically modified [GM] plant development in Europe and relocate it to the US, where political and consumer resistance to GM crops is not so entrenched. The headquarters of BASF Plant Science will move from Limburgerhof in south-west Germany to Raleigh, North Carolina, and two smaller sites in Germany and Sweden will close. The company will transfer some GM crop development to the US but stop work on crops targeted at the European market – four varieties of potato and one of wheat. The decision ... signals the end of GM crop development for European farmers. Bayer, BASF’s German competitor, is working on GM cotton and rice in Ghent, Belgium – but not for European markets. “This is another nail in the coffin for genetically modified foods in Europe,” said Adrian Bebb of Friends of the Earth. BASF battled for some 13 years before the European Union approved in 2010 cultivation of its Amflora potato, which was intended to provide high-quality starch for industrial customers. However, German test sites had to be put under constant guard and activists still succeeded in destroying potato fields.
Note: The European public is well aware of the serious threats of GM food, yet the U.S. public, thanks to a controlled media, knows very little about this. For an excellent overview of the threats to health from genetically-modified foods, click here. For key articles from major media sources on these risks, click here.
In the fight against maternal mortality in the developing world, a rugged, portable “Solar Suitcase” is providing reliable electricity to clinics in 17 countries where healthcare workers previously struggled to provide emergency obstetric care by the light of candles, flashlights and mobile phones. The Solar Suitcase powers medical LED lights, headlamps, mobile phones, computers and medical devices. Healthcare workers using the Solar Suitcase report greater facility and ease in conducting nighttime procedures. Improved lighting allows health workers to identify and treat complications such as obstetric lacerations and hemorrhage, nurses to locate and administer intravenous medication, and emergency Caesarean sections to be performed 24 hours a day. Solar-powered mobile phones allow on-call doctors to be alerted when obstetric emergencies require surgery. With augmentation, the solar suitcase powers blood bank refrigeration, permitting life-saving transfusions to occur without delay. An estimated 358,000 maternal deaths occur worldwide. Reducing childbirth deaths depends, in part, on providing adequate emergency obstetric care. However, a lack of health facility power translates to an inability to perform life-saving care.
Insurance companies spent millions of dollars trying to defeat the U.S. health care overhaul, saying it would raise costs and disrupt coverage. Instead, profit margins at the companies widened to levels not seen since before the recession, a Bloomberg Government study shows. Insurers led by WellPoint ... recorded their highest combined quarterly net income of the past decade after the law was signed in 2010, said Peter Gosselin, the study author. "The industry that was the loudest, most persistent critic of this law, the industry whose analysts and executives predicted it would suffer immensely because of the law, has thrived," Gosselin said. Health insurers contributed $86.2 million to the U.S. Chamber of Commerce to oppose the law after Obama administration officials criticized the [corporations'] plans for enriching themselves by raising customer premiums. Companies are changing their business focus to gain from provisions in the law that will expand the size of Medicaid, the $401 billion government health plan for the poor.
Note: Is it surprising that health insurance companies are raking in big profits from the new health care legislation?
Medicines to treat attention deficit hyperactivity disorder are in such short supply that hundreds of patients complain daily to the Food and Drug Administration (FDA) that they are unable to find a pharmacy with enough pills to fill their prescriptions. The shortages are a result of a troubled partnership between drug manufacturers and the Drug Enforcement Administration (DEA), with companies trying to maximize their profits and drug-enforcement agents trying to minimize abuse by people. Shortages, particularly of cheaper generics, have become so endemic that some patients say they worry almost constantly about availability. The DEA sets manufacturing quotas that are designed to control supplies and thwart abuse. Every year, the DEA ... allots portions of the expected demand to various companies. How each manufacturer divides its quota among its own ADHD medicines — preparing some as high-priced brands and others as cheaper generics — is left up to the company. Officials at the FDA say the shortages are a result of overly strict quotas set by the DEA, which, for its part, questions whether there really are shortages or whether manufacturers are simply choosing to make more of the expensive pills than the generics, creating supply and demand imbalances.
Note: This curious story reveals an astonishing level of government manipulation of the manufacturing and availability of medications, and corporations appear to go along with it because it keeps profits high. For lots more on government and corportate corruption from reliable sources, click here and here.
Scientists agreed not to publish certain details of research showing how lethal bird flu can be made contagious after a U.S. biosecurity panel asked that it be kept secret for security reasons. The study at Erasmus Medical Center in Rotterdam described the genetic changes needed to make the H5N1 avian influenza strain spread easily among ferrets and potentially people. The research is under review for publication in the journal Science. It was commissioned by the U.S. National Institutes of Health, the center said yesterday in a statement on its website. Knowing the genetic sequence of a deadly, infectious strain may enable the virus to be recreated through reverse engineering. The censorship was requested by the National Science Advisory Board for Biosecurity, which was created in the aftermath of the 2001 anthrax attacks and advises the U.S. Department of Health and Human Services. The panel called for certain data to be kept secret after determining that the risks of publishing it outweigh the benefits, the Erasmus Medical Center said. The researchers have reservations about this recommendation but will observe it, the center said in the statement.
Note: For key major media reports revealing manipulation around both the avian and swine flus, click here. For solid evidence that Lyme disease originated in a secret government germ laboratory, click here.
Attempts to censor details of controversial influenza experiments that created a highly infectious form of bird-flu virus are unlikely to stop the information from leaking out, according to scientists familiar with the research. The US Government has asked the editors of two scientific journals to refrain from publishing key parts of research on the H5N1 strain of bird-flu in order to prevent the information falling into the hands of terrorists intent on recreating the same flu strain for use as a bioweapon. However, scientists yesterday condemned the move. Some said that the decision comes too late because the information has already been shared widely among flu researchers, while others argued that the move could obstruct attempts to find new vaccines and drugs against an infectious form of human H5N1 if it appeared naturally. Professor Richard Ebright, a molecular biologist at Rutgers University in Piscataway, New Jersey, said that the research, which was funded by the US Government, should never have been done without first assessing the risks and benefits. The work posed risks that outweighed benefits and that were clearly foreseeable before the work was performed, Professor Ebright said. The work should have been reviewed at the national or international level before being performed, and should have been restricted at a national or international level before being performed, he said.
Note: For key major media reports revealing manipulation around both the avian and swine flus, click here. For solid evidence that Lyme disease originated in a secret government germ laboratory, click here.
A deadly strain of bird flu with the potential to infect and kill millions of people has been created in a laboratory by European scientists – who now want to publish full details of how they did it. Some scientists are questioning whether the research should ever have been undertaken in a university laboratory, instead of at a military facility. For the first time the researchers have been able to mutate the H5N1 strain of avian influenza so that it can be transmitted easily through the air in coughs and sneezes. Until now, it was thought that H5N1 bird flu could only be transmitted between humans via very close physical contact. Dutch scientists carried out the controversial research to discover how easy it was to genetically mutate H5N1 into a highly infectious "airborne" strain of human flu. They believe that the knowledge gained will be vital for the development of new vaccines and drugs. But critics say the scientists have endangered the world by creating a highly dangerous form of flu which could escape from the laboratory. The H5N1 strain of avian influenza has killed hundreds of millions of birds since it first appeared in 1996, but has so far infected only about 600 people who came into direct contact with infected poultry. What makes H5N1 so dangerous, though, is that it has killed about 60 per cent of those it has infected, making it one of the most lethal known forms of influenza in modern history – a deadliness moderated only by its inability (so far) to spread easily through airborne water droplets.
Note: For key major media reports revealing manipulation around both the avian and swine flus, click here. For solid evidence that Lyme disease originated in a secret government germ laboratory, click here.
An estimated 14,000 excess deaths in the United States are linked to the radioactive fallout from the disaster at the Fukushima nuclear reactors in Japan, according to a major new article in the December 2011 edition of the International Journal of Health Services. This is the first peer-reviewed study published in a medical journal documenting the health hazards of Fukushima. Authors Joseph Mangano and Janette Sherman note that their estimate of 14,000 excess U.S. deaths in the 14 weeks after the Fukushima meltdowns is comparable to the 16,500 excess deaths in the 17 weeks after the Chernobyl meltdown in 1986. The rise in reported deaths after Fukushima was largest among U.S. infants under age one. The 2010-2011 increase for infant deaths in the spring was 1.8 percent, compared to a decrease of 8.37 percent in the preceding 14 weeks. The IJHS article [is] available online ... at http://www.radiation.org. Internist and toxicologist Janette Sherman, MD, said: "Based on our continuing research, the actual death count [in the US] may be as high as 18,000, with influenza and pneumonia, which were up five-fold in the period in question as a cause of death. Deaths are seen across all ages, but we continue to find that infants are hardest hit because their tissues are rapidly multiplying, they have undeveloped immune systems, and the doses of radioisotopes are proportionally greater than for adults."
Note: To read the report (in pdf format) on excess mortality in the US already caused by the Fukushima meltdowns, click here.
Sometimes, not trying to fix something is precisely what's needed to fix it. It's a hard strategy to follow because we have penchant for being proactive. If there's a problem, we feel better when we attack it aggressively. But consider the idea that we might spend a lot of time, effort, and money solving problems that can't, in fact, be solved with time, effort, and money. In 2009, Americans spent about $3.6 billion on over-the-counter cold, cough, and throat remedies, according to the New York Times. And yet, the article concluded, there's very little evidence that any of those medicines do anything to cure, or even shorten the duration of, a cold. And some remedies, like taking antibiotics, bring along side effects that risk making some people worse. In other words, the best strategy for coping with the common cold is to do nothing. So how do we know whether to do something or nothing? "When many cures are offered for a disease," wrote Chekhov, "it means the disease is not curable." If past experience or data suggests that multiple solutions are possible but none are reliably successful, nothing may be the best strategy. Also, if you've tried two or three solutions and none of them have worked, perhaps it's time to try nothing.
Note: The article at the New York Times link in the summary above is well worth reading to understand the effectiveness, or lack thereof, of many treatments for the common cold.
The federal government has not done enough to oversee the treatment of America's foster children with powerful mind-altering drugs, according to a Government Accountability Office (GAO) report. The GAO's report, based on a two-year-long investigation, looked at five states - Florida, Massachusetts, Michigan, Oregon and Texas. Thousands of foster children were being prescribed psychiatric medications at doses higher than the maximum levels approved by the Food and Drug Administration (FDA) in these five states alone. And hundreds of foster children received five or more psychiatric drugs at the same time despite absolutely no evidence supporting the simultaneous use or safety of this. Overall, the GAO ... found that more than one-fourth of foster children were prescribed at least one psychiatric drug, [and] were prescribed psychotropic drugs at rates up to nearly five times higher than non-foster children. The chances of a foster child compared to a non-foster child being given five or more psychiatric drugs at the same time were alarming. In Texas, foster children were 53 times more likely to be prescribed five or more psychiatric medications at the same time than non-foster children. Foster children were also more than nine times more likely than non-foster children to be prescribed drugs for which there was no FDA-recommended dose for their age. For ... those less than 1 year old, foster children were nearly twice as likely to be prescribed a psychiatric drug compared to non-foster children.
Note: For more along these lines, see concise summaries of deeply revealing news articles on corruption in government and in the pharmaceutical industry.
Silver amalgam fillings, which have plugged American cavities for more than 150 years, have lost their luster over the last couple of decades thanks to the rise of more attractive tooth-colored fillings and concerns about the environmental and health impact of their chief ingredient: mercury. Although use of amalgam fillings has dropped 30 percent in the last decade, according to the American Dental Association, these fillings are still sitting in hundreds of millions of mouths, and dentists continue to fill some 50 million teeth with amalgam each year — especially in children. Mercury, a known neurotoxin, makes up 50 percent (in weight) of amalgam fillings, which also contain silver, copper and tin. For some dentists, toxicologists and advocates, the fact that mercury has been shown to hurt the neurological system, kidneys and other organs is reason enough to keep it out of people's mouths. "When you plant a neurotoxin two inches from the brain, can you say no one is ever harmed from that?" said Charlie Brown, director of Consumers for Dental Choice. His group advocates that dentists be required to disclose the mercury content of amalgam fillings to patients. The buildup of mercury from vapors 24 hours a day, over a lifetime, is the greatest concern, said Boyd Haley, retired professor emeritus at the University of Kentucky. Eighty percent of mercury vapor stays in body tissue for days, months, even years, because the body doesn't have a good system for excreting it, he said.
Note: For an informative article by Dr. Mercola showing that there is no reason to put mercury in your mouth and plenty of risk, click here.
If you’re a parent (or know one) ... you might have already made up your mind about the connection between vaccination and disease. A new documentary, The Greater Good, adds perspective to the issue, asking how much of a good thing a person can take until it’s not all that good any more. “It is an advocacy film,” says The Greater Good producer Chris Pilaro. The filmmakers chose to follow three families whose lives were adversely affected by vaccines because, as director-producer Kendall Nelson says, “Historically, those stories were really not being told.” One thread follows young Jordan King, who before being vaccinated was a “normal,” happy toddler. After being vaccinated... he ended up diagnosed with autism. After her youngest child died after receiving vaccinations, Stephanie Christner, a doctor, dedicated her life to finding connections between vaccination and disease. The most persuasive story is that of Gabi Swank, a teenage girl who saw ads on MTV for the cervical cancer vaccine Gardasil and insisted that her mom get her on it. After taking the drug, Gabi experienced a dramatic decline in her health and her family paid a deep financial and emotional cost. Despite her upbeat demeanor and refusal to be perceived as a victim, Gabi’s story is a tragic one. Idaho-based filmmakers Nelson and Pilaro ... gained the co-operation of the Centers for Disease Control and Prevention and the Food and Drug Administration and proceeded to interview medical experts, pharmaceutical representatives and lawmakers on opposite sides of the issue. What’s clear after watching the film is not that vaccinations are necessarily bad, but that every child is different and each will have a different response to them. But it’s a hard case to make when your doctor is following state law.
Note: Did you know the government has never done a study comparing the health of vaccinated and non-vaccinated children? Watch a video of the CDC's chief of vaccinations making excuses for why they won't do a study. For more on this, see concise summaries of deeply revealing vaccines news articles from reliable major media sources.
In the wake of an ABC News investigation into alleged unsanitary and inhumane practices at one of the nation's largest egg farms, animal rights activists are calling for an end to the egg industry's widespread use of so-called "battery cages," in which birds live six to a cage in long stacks of wire cages. "The battery cage system is inherently cruel," said Nathan Runkle of Mercy for Animals, who estimated that 95 percent of the hens used in egg production are kept in battery cages. He urged the industry to adopt more humane methods of egg production, and urged McDonald's, the nation's largest egg buyer, to stop buying eggs from battery cage farms. Undercover video shot by a Mercy for Animals activist who worked at one of the nation's largest egg producers, Sparboe Farms, shows the battery cages in use. "Scott," the activist who made the tape, said that the five to seven birds were kept in each cage, with their beaks cut at an early cage so they wouldn't peck each other, and that each bird lived its life in an area smaller than a standard sheet of paper. He said the birds "can't fully spread their wings, they can't walk around. There were [dead] birds that were left in the cages that were decomposing for weeks or months at a time," claimed Scott. Until the ABC News investigation and the FDA's warning, McDonald's drew all its eggs for restaurants west of the Mississippi River from Sparboe. Just before the ABC News report aired, McDonald's announced that it would no longer get its eggs from Sparboe Farms. Activists, however, are now asking why McDonald's won't stop buying eggs from any producer that uses battery cages.
Note: To watch a video of this sad scene, click here. To learn how this report resulted in both McDonald's and Target canceling their contracts with Sparboe Farms, click here.
The European Commission adopted new rules Nov. 14 regarding X-ray, or backscatter, body scanners at all airports in Europe. A press release ordered members of the European Union to remove X-ray scanners from its airports to avoid risking “citizens’ health and safety.” The news [brings] into question the continued use of the very same X-ray scanners in U.S. airports. While the Transportation Security Administration also employs millimeter-wave scanners in U.S. airports, X-ray scanners are the ones that have received more criticism from public-safety advocates. While ... the amount of radiation exposure from X-ray machines is very low, several studies have shown that a small number of cancer cases could result from scanning millions of passengers every year. Some critics of the scanners say that any small amount of cancer is too much to tolerate. Although the TSA doesn’t show signs of budging on the use of X-ray scanners, Europe will instead use machines that rely on radio frequency waves, which have not been linked to cancer.
Note: For key reports from reliable sources on government and corporate threats to privacy, click here.
Over the last year, the Obama administration has aggressively pushed a $433-million plan to buy an experimental smallpox drug, despite uncertainty over whether it is needed or will work. Senior officials have taken unusual steps to secure the contract for New York-based Siga Technologies Inc., whose controlling shareholder is billionaire Ronald O. Perelman, one of the world's richest men. Siga ... was the only company asked to submit a proposal. The contract calls for Siga to deliver 1.7 million doses of the drug for the nation's biodefense stockpile. The price of approximately $255 per dose is well above what the government's specialists had earlier said was reasonable. Once feared for its grotesque pustules and 30% death rate, smallpox was eradicated worldwide as of 1978 and is known to exist only in the locked freezers of a Russian scientific institute and the U.S. government. There is no credible evidence that any other country or a terrorist group possesses smallpox. If there were an attack, the government could draw on $1 billion worth of smallpox vaccine it already owns to inoculate the entire U.S. population and quickly treat people exposed to the virus. The vaccine, which costs the government $3 per dose, can reliably prevent death when given within four days of exposure.
Note: This is pure and blatant corruption to pad the pockers of Siga and those involved. For key reports from reliable sources on government corruption, click here. For more on corrupt drug companies, click here.
Important Note: Explore our full index to key excerpts of revealing major media news articles on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.