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Excerpts 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.

Some 10,000 US researchers have signed a statement protesting about political interference in the scientific process. The statement, which includes the backing of 52 Nobel Laureates, demands a restoration of scientific integrity in government policy. According to the American Union of Concerned Scientists, data is being misrepresented for political reasons. It claims scientists working for federal agencies have been asked to change data to fit policy initiatives. The Union has released an "A to Z" guide that ... documents dozens of recent allegations involving censorship and political interference in federal science. Campaigners say that in recent years the White House has been able to censor the work of agencies like the Environmental Protection Agency and the Food and Drug Administration because a Republican congress has been loath to stand up for scientific integrity. Michael Halpern from the UCS said the statement of objection to political interference had been supported by researchers regardless of their political views. "This science statement that has now been signed by the 10,000 scientists is signed by science advisers to both Republican and Democratic administrations dating back to President Eisenhower, stating that this is not business as usual and calling for this practice to stop."

Wireless networks — known as wi-fi or wLAN (wireless local area network) — are increasingly used in schools, offices and other public places to connect computers and laptops to the internet using radiofrequency transmitters with no need for complex cabling. In future, whole town centres will be transformed into wi-fi “hot spots.” It has taken the public a while to wake up to the idea that wireless transmitters could be less than benign. The groundswell of concern is mounting, with some people blaming everything from headaches to cancer on exposure to radio-frequency fields. A number of schools have dismantled their wireless networks after lobbying from worried parents, and others are under pressure to follow suit. In Austria the public health department of Salzburg has advised schools and kindergartens not to use wLAN or cordless phones. Lakehead University in Ontario, Canada, which has 7,400 students, has removed wi-fi because of what its Vice-Chancellor, Dr Fred Gilbert, calls “the weight of evidence demonstrating behavioural effects and physiological impacts at the tissue, cellular and cell level”. Some experts have also expressed concerns. In September, 30 scientists from all over the world signed a resolution calling for a “full and independent review of the scientific evidence that points to hazards from current electromagnetic field exposure conditions worldwide.”

Note: For many highly important articles from reliable sources on major health issues, click here.

One hundred years ago, companies were free to follow their own rules. The publication of Upton Sinclair’s novel “The Jungle” in 1906 — with its descriptions of rat-infested slaughterhouses and rancid meat — created public outrage over food safety. Even though the book was written by a socialist agitator, a Republican president, Theodore Roosevelt, eagerly read it. After confirming Sinclair’s claims, Roosevelt battled the drug companies, the big food processors and the meatpacking companies to protect American consumers from irresponsible corporate behavior. Over the past 40 years, the industrialization and centralization of our food system has greatly magnified the potential for big outbreaks. As a result, a little contamination can go a long way. The Taco Bell distribution center in New Jersey now being investigated as a possible source of E. coli supplies more than 1,100 restaurants in the Northeast. Since 2000, the fast-food and meatpacking industries have given about four-fifths of their political donations to Republican candidates for national office. In return, these industries have effectively been given control of the agencies created to regulate them. The current chief of staff at the Agriculture Department used to be the beef industry’s chief lobbyist. The person who headed the Food and Drug Administration until recently used to be an executive at the National Food Processors Association. Cutbacks in staff and budgets have reduced the number of food-safety inspections conducted by the F.D.A. to about 3,400 a year — from 35,000 in the 1970s.

Note: If you care about the health of our nation's food supply, write your political and media representatives encouraging the passage of the Safe Food Act mentioned in this article, which by the way, was written by the author of the most excellent book, Fast Food America.

The scientist who first linked smoking to lung cancer was [later] paid by a chemicals firm while investigating cancer risks in the industry. Professor Sir Richard Doll held a consultancy post with US firm Monsanto for more than 20 years. The BBC has seen private letters which show that Sir Richard ... received a US$1,500-a-day consultancy fee from Monsanto in the mid-1980s. During that time he investigated the potential cancer causing properties of the powerful herbicide Agent Orange, made by the company. Sir Richard [argued] that there was no evidence that Agent Orange caused cancer. Professor Lennart Hardell, of the Oncology Department at University Hospital Orebro, Sweden, has also studied the potential hazards posed by Agent Orange. He was one of the scientists whose work was dismissed by Sir Richard. He said: "It's quite OK to have contacts with industry, but you should be fair and say 'well, I'm [working] as a consultant for Monsanto." Further documents obtained by The Guardian newspaper allegedly show that Sir Richard was also paid a Ł15,000 fee by the Chemical Manufacturers Association, and chemicals companies Dow Chemicals and ICI for a review of vinyl chloride, used in plastics, which largely cleared the chemical of any link with cancers apart from liver cancer. Sir Richard's views on the chemical were used by the manufacturers' trade association to defend it for more than a decade.

Japan has again been forced to confront its wartime conduct after a former doctor in the country's imperial navy admitted he had conducted experiments on Filipino prisoners during the second world war. Akira Makino, 84, said in an interview with the Kyodo news agency that he had performed surgery and amputations on dozens of prisoners of war before they were executed in the Philippines. Mr Makino is one of several former Japanese soldiers who decided to reveal the truth about their country's use of human guinea pigs before they die. Unit 731, the imperial Japanese army's notorious germ warfare unit, killed thousands of Chinese civilians and Allied PoWs at its sprawling complex in Harbin, northern China. The victims ... were injected with typhus, cholera and other diseases. They died during the experiments or were executed to prevent them from talking about their experiences. As the end of the war approached, the unit destroyed evidence of their activities. The extent of their activities only came to light following testimony from repentant former doctors, soldiers and nurses. US authorities secretly granted unit officials immunity from prosecution in return for access to years of research into biological weapons. Several former Unit 731 officials went on to enjoy prominent careers in medicine, academia and business. Mr Makino ... said he remained haunted by memories of the experiments. "We should not repeat that misery again," he said. "I want to tell the truth about the war."

Note: Explore a list depicting the rampant use of humans as guinea pigs in government, military, and medical experiments over the last century.

The Department of Agriculture declared safe for human consumption yesterday an experimental variety of genetically engineered rice found to have contaminated the U.S. rice supply this summer. The move ... to deregulate the special long-grain rice, LL601, was seen as a legal boon to its creator, Bayer CropScience. The company applied for approval shortly after the widespread contamination was disclosed in August and now faces a class-action lawsuit filed by hundreds of farmers in Arkansas and Missouri. The experimental rice ... escaped from Bayer's test plots after the company dropped the project in 2001. The resulting contamination, once it became public, prompted countries around the world to block rice imports from the United States, sending rice futures plummeting and farmers into fits. In approving the rice, the USDA allowed Bayer to take a regulatory shortcut and skip many of the usual safety tests. Joseph Mendelson, legal director of the nonprofit Center for Food Safety, said the quick approval shows that the USDA is more concerned about the fortunes of the biotechnology industry than about consumers' health. "USDA is telling agricultural biotechnology companies that it doesn't matter if you're negligent, if you break the rules, if you contaminate the food supply with untested genetically engineered crops, we'll bail you out," Mendelson said in a statement. Officials in Europe, where genetically altered rice is derisively dubbed "Frankenfood," made clear as recently as last week that European countries will not accept any U.S. rice, he said.

Note: For reliable information on the deception and dangers of GM (Genetically Modified) food, click here.

Hoping to prevent Congress from letting the government negotiate lower drug prices for millions of older Americans on Medicare, the pharmaceutical companies have been recruiting Democratic lobbyists [and] lining up allies in the Bush administration and Congress. Many drug company lobbyists concede that the House is likely to pass a bill intended to drive down drug prices, but they are determined to block such legislation in the Senate. If that strategy fails, they are counting on President Bush to veto any bill that passes. With 49 Republicans in the Senate next year, the industry is confident that it can round up the 34 votes normally needed to uphold a veto. They began developing strategy last week at a meeting of the board of the Pharmaceutical Research and Manufacturers of America. Billy Tauzin, president of that group [and] a former congressman...met with Senator Byron L. Dorgan, a North Dakota Democrat who has been trying for six years to allow drug imports from Canada. The industry vehemently opposes such legislation. The 2003 Medicare law prohibits the federal government from negotiating drug prices or establishing a list of preferred drugs. Drug makers have not set a budget for their campaign. They and their trade groups already spend some $100 million a year on lobbying in Washington. Representative Frank Pallone Jr., Democrat of New Jersey [said] “The 2003 Medicare law was essentially written by the drug industry.” Drug companies may be open to some changes in the Medicare drug benefit, but they say they cannot accept any form of price negotiation.

Note: For lots of verifiable information on the power of the drug industry to corrupt Congress, click here.

Poor people are needlessly dying because drug companies and the governments of rich countries are blocking the developing world from obtaining affordable medicines. Five years to the day after the Doha declaration - a groundbreaking deal to give poor countries access to cheap drugs - was signed at the World Trade Organisation, Oxfam says things are worse. The charity accuses the US, which champions the interests of its giant pharmaceutical companies, of bullying developing countries into not using the measures in the Doha declaration and the EU of standing by and doing nothing. Doha technically allows poor countries to buy cheap copies of desperately needed drugs, but the US is accused of trying to prevent countries such as Thailand and India, which have manufacturing capacity, [from] making and selling cheap generic versions so as to preserve the monopolies of the drug giants. "Rich countries have broken the spirit of the Doha declaration," said Celine Charveriat, head of Oxfam's Make Trade Fair campaign. "The declaration said the right things but needed political action to work and that hasn't happened. In fact, we've actually gone backwards. Many people are dying or suffering needlessly." The US has pursued its own free trade agreements with developing countries, tying them into much tighter observance of patent rights than anticipated at Doha. "The USA has also pressured countries for greater patent protection through threats of trade sanctions," the report says.

The Bush administration said on Sunday that it would strenuously oppose one of the Democrats’ top priorities for the new Congress: legislation authorizing the government to negotiate with drug companies to secure lower drug prices for Medicare beneficiaries. In an interview, Michael O. Leavitt, the secretary of health and human services, said he saw no prospect of compromise on the issue. Dozens of plans are available in every state. They charge different premiums and co-payments and cover different drugs. The 2003 Medicare law explicitly prohibits the federal government from negotiating drug prices or establishing a list of preferred drugs. Representative Nancy Pelosi, the California Democrat who is in line to become the House speaker, has said the House will take up legislation to repeal that ban in its first 100 hours under Democratic control. Senate Democrats have expressed a similar desire. The eight Democrats newly elected to the Senate all say Medicare should have the power to negotiate with drug makers.

Note: To understand how the drug companies have become the most powerful lobby in government and will compromise our health for their profits, read what a top MD has to say by clicking here.

Federal health officials have decided to forgo gathering detailed data on whether children in 22 big cities are receiving recommended immunizations and instead will survey teenagers, who are the target of several new vaccines. The decision is drawing protests from local health officials, who say the soon-to-be-lost information is essential to their efforts to make sure that infants and toddlers, many from poor families, are protected against childhood infections. Each year, the CDC contracts a polling company to get data on vaccination rates in various age, demographic and income groups nationwide. "We need to know if the new vaccine has helped, or had no change, or hurt [coverage], and we cannot really make those judgments without the NIS data," [one health official] said. CDC officials said they are redirecting about $3 million to survey adolescents. The only way to pay for the 22-city sampling would be to use money now used to help states buy vaccine, they added. The decision comes at a time when the government is spending record amounts on public health. The CDC's budget has risen 42 percent since 2001 and is now $8.73 billion.

Note: This unusual decision makes sense if you consider that the powerful pharmaceutical industry doesn't want tracking on toddler vaccinations, as it may show what they have long denied -- that there is a link between autism and childhood vaccinations. The mercury-derivative Thimerosal was largely taken out of childhood vaccinations just a few years ago. The much-awaited data needed to prove or disprove a link will now be more difficult to obtain.

Federal health officials won’t put new restrictions on the use of a mercury-based preservative in vaccines and other medicines. A group called the Coalition for Mercury-free Drugs petitioned the Food and Drug Administration in 2004 seeking the restrictions on thimerosal, citing concerns that the preservative is linked to autism. The FDA rejected the petition. Thimerosal, about 50 percent mercury by weight, has been used since the 1930s to kill microbes in vaccines. There have been suspicions that thimerosal causes autism. However, studies that tracked thousands of children consistently have found no association between the brain disorder and the mercury-based preservative. Critics contend the studies are flawed. Since 2001, all vaccines given to children 6 and younger have been either thimerosal-free or contained only trace amounts of the preservative. Thimerosal has been phased out of some, but not all, adult vaccines as well. Most doses of the flu vaccine still contain thimerosal. There also are minute amounts of mercury, as thimerosal or phenylmercuric acetate, in roughly 45 eye ointments, nasal sprays and nasal solutions, the FDA said.

Note: Why are they still using mercury in flu shots when it is not necessary? Heavy metals are well known to be toxic to the human body. The studies mentioned above are almost entirely funded by pharmaceutical interests and government bodies working with them. For lots more on this major cover-up, click here.

After an avalanche of panicked inquiries from patients across the country who claim to have been stricken with a mysterious skin disease, the federal Centers for Disease Control and Prevention is preparing to begin a full investigation. The patients ... describe symptoms that include sores that are slow to heal, a sensation of things crawling through their skin, joint pain and persistent fatigue. Many say they believe they have Morgellons disease, a diagnosis that has received wide attention on the Internet but is viewed skeptically by some doctors. Morgellons disease joins a growing list of symptom clusters that public health officials have been forced to examine closely in part because of the organizing power and unprecedented reach of the Internet. Morgellons was brought to public attention by ... Mary Leitao, who in 2001 created a Web site describing the mysterious sores and bizarre threadlike extrusions that afflicted her young son. She said she had tried for years to find a medical explanation for his illness. Ultimately, she said, doctors accused her of staging it. After creating the Web site...she was inundated with e-mail messages from people who said they also had the disease. Many of the people who visit her site have been told by doctors that their symptoms are delusional. Several mothers...told her that they had lost custody of their children after doctors decided the youngsters’ symptoms were contrived. Doctors themselves are divided over whether Morgellons is a medical or a psychiatric illness. The patients are clearly suffering from something; it is just not clear what that something is. “I think it’s a real disease,” said Dr. Rafael Stricker, a physician in San Francisco who sees many patients claiming to have Morgellons. Many patients also test positive for Lyme disease.

Several government doctors say drug maker Eli Lilly & Co. subtly orchestrated medical guidelines for treatment of an often lethal blood infection, hoping to boost sales of a drug whose value is being debated. “This company is trying to insinuate its drug into many aspects of patient care that industry really shouldn’t be involved in,” said Dr. Naomi O’Grady, a critical care specialist at the National Institutes of Health. Three of her NIH colleagues claim in Thursday’s New England Journal of Medicine that Lilly worked through medical societies to influence standards for treating the blood infection, sepsis. Ultimately, Xigris was incorporated into the guidelines. Both the guidelines committee and a larger information campaign on sepsis were heavily funded by [Lilly]. Dr. Phil Dellinger, who helped lead the guidelines committee, said...“We’ve been catching grief because we’ve been taking a lot of Lilly money — and we’re appreciative of Lilly giving it.” The U.S. Food and Drug Administration approved Xigris in 2001, despite an evenly split vote by its advisory committee. The lead author of Thursday’s journal article, Dr. Peter Q. Eichacker, voted against approval. Some critics are unhappy that the drug, which works only for the sickest patients, was approved on the basis of a single experiment. Academic officials acknowledged in the published guidelines that Lilly gave more than 90 percent of $861,000 in grants for the campaign and medical recommendations. O’Grady, of NIH, said a panel of disease experts that she headed refused to endorse the sepsis guidelines largely because Lilly “convened the whole panel.”

Note: For lots more on how the powerful pharmaceutical industry endangers our lives, click here.

Three years after the Food and Drug Administration first hinted that it might permit the sale of milk and meat from cloned animals...the agency is poised to endorse marketing of the mass-produced animals for public consumption. The decision...is based largely on new data indicating that milk and meat from cloned livestock and their offspring pose no unique risks to consumers. On Thursday, advocacy groups filed a petition asking the FDA to regulate cloned farm animals one type at a time, much as it regulates new drugs, a change that would drastically slow marketing approval. "The available science shows that cloning presents serious food safety risks, animal welfare concerns and unresolved ethical issues that require strict oversight," the petition states. "The government talks about being science-based, and that's great, but I think there is another pillar here: the question of whether we really want to do this," said Carol Tucker Foreman, director of food policy at the Consumer Federation of America. Each clone is a genetic replica of the animal that donated the cell from which it was grown. It was October 2003 when the FDA released its first draft document concluding that clones and their offspring are safe to eat. But an agency advisory panel and the National Academies, while generally supportive, raised flags, citing a paucity of safety data. Clonal meat or milk would be impossible to authenticate, since there is no way to distinguish them from conventional products. "That you can go online today to any number of different Web sites and purchase semen from cloned bulls tells you there are cloned sires out there fathering calves in the food supply."

Note: For an ABC article on this, click here. If you believe that government agencies are unbiased on matters of public health, I most highly urge you to read our summary at http://www.WantToKnow.info/deception10pg

Witold Bialokur...can run 10 kilometers, or 6.2 miles, in less than 44 minutes. While Mr. Bialokur’s performance would be the envy of most young men, he is not young. Mr. Bialokur is 71. It is one of the persistent mysteries of aging, researchers say. Why would one person, like Mr. Bialokur, remain so hale and hearty while another, who had seemed just as healthy, start to weaken and slow down? Rigorous studies are now showing that seeing, or hearing, gloomy nostrums about what it is like to be old can make people walk more slowly, hear and remember less well, and even affect their cardiovascular systems. Positive images of aging have the opposite effects. The constant message that old people are expected to be slow and weak and forgetful is not a reason for the full-blown frailty syndrome. But it may help push people along that path.

Schizophrenia patients do as well, or perhaps even better, on older psychiatric drugs compared with newer and far costlier medications, according to a study published yesterday that overturns conventional wisdom about antipsychotic drugs, which cost the United States $10 billion a year. The results are causing consternation. The researchers who conducted the trial were so certain they would find exactly the opposite that they went back to make sure the research data had not been recorded backward. The study was requested by Britain's National Health Service to determine whether the newer drugs -- which can cost 10 times as much as the older ones -- are worth the difference in price. While the researchers had expected a difference of five points on a quality-of-life scale -- showing the newer drugs were better -- the study found that patients' quality of life was slightly better when they took the older drugs. There has been a surge in prescriptions of the newer antipsychotic drugs in recent years, including among children. In an editorial accompanying the British study, the lead researcher in the U.S. trial asked how an entire medical field could have been misled into thinking that the expensive drugs, such as Zyprexa, Risperdal and Seroquel, were much better.

Note: Those who have read our two-page health cover-up summary know very well how the entire medical field could have been misled. For those who haven't seen it: http://www.WantToKnow.info/healthcoverup

Top officials at the Centers for Disease Control and Prevention received premium bonuses in recent years at the expense of scientists and others who perform much of the agency's scientific work. Those inside the office of the centers' director, Dr. Julie L. Gerberding, have benefited the most. From 2002 through mid-2006, William H. Gimson III, the agency's chief operating officer, received bonuses totaling $147,863. Before Dr. Gerberding's appointment, members of the C.D.C. director's inner circle rarely received premium bonuses. Because bonus money is limited...the growing share of premium bonuses for Dr. Gerberding's closest advisers has meant less money is available for some scientists and other workers. In addition to those within Dr. Gerberding's inner circle, the increase in large cash awards within the centers has mostly benefited employees in the agency's financial, computer and human resources departments -- not its scientists. Soon after arriving at the centers, Dr. Gerberding began a comprehensive reorganization of the agency. In its wake, many of the agency's senior scientists and leaders either left or have announced that they are planning to leave. The Washington Post and The Atlanta Journal-Constitution have reported on the turmoil at the centers in articles quoting disgruntled former senior scientists who said the changes had undermined the agency.

Note: Could it be that these bonuses are meant to keep top officials in line the the CDC's strong bias towards to pharmaceutical companies? For more vital information on this: http://www.WantToKnow.info/healthcoverup.

We have always been told there is no recovery from persistent vegetative state - doctors can only make a sufferer's last days as painless as possible. But is that really the truth? Across three continents, severely brain-damaged patients are awake and talking after taking ... a sleeping pill. Brain-damaged patients are reporting remarkable improvements after taking a pill that should make them fall asleep but that, instead, appears to be waking up cells in their brains that were thought to have been dead. No one yet knows exactly how a sleeping pill could wake up the seemingly dead brain cells, but [researchers] have a hypothesis. After the brain has suffered severe trauma, a chemical known as Gaba (gamma amino butyric acid) closes down brain functions in order to conserve energy and help cells survive. However, in such a long-term dormant state, the receptors in the brain cells that respond to Gaba become hypersensitive, and as Gaba is a depressant, it causes a persistent vegetative state. It is thought that during this process the receptors are in some way changed or deformed so that they respond to zolpidem differently from normal receptors, thus breaking the hold of Gaba. This could mean that instead of sending patients to sleep as usual, it makes dormant areas of the brain function again and some comatose patients wake up.

Note: For lots more on key health issues from reliable sources, click here.

Most of the federal scientists who improperly accepted personal money from drug or biotechnology companies walked away with reprimands or were allowed to retire unscathed. Only two of the 44 scientists found to have violated rules governing private consulting deals are being investigated for possible criminal activity, and they remain on the government payroll. NIH spokesman John Burklow said his agency wanted eight others reviewed for possible crimes, but those cases were rejected by the investigating office at the U.S. Health and Human Services Department. The two still outstanding...both committed "serious misconduct," so grave that they would be fired if they were civilians, NIH internal ethics reports contend. [A Congressional] subcommittee is expected to question NIH officials about documents showing it approved several taxpayer-paid trips for [Dr. Trey] Sunderland to attend conferences and events in places like Hawaii and Toronto, even after recommending his firing. Of the 44 alleged offenders...the majority received reprimands or warnings for failing to properly obtain approvals for their outside consulting work. NIH ethics reports allege...two scientists had unauthorized, unreported deals with drug companies -- Sunderland earning more than $600,000 over eight years for consulting and speeches and [Dr. Thomas] Walsh more than $100,000 in five years -- and that their consulting improperly overlapped with government duties.

Note: The Los Angeles Times later reported that Dr. Sunderland was the first NIH scientist in 14 years to be found guily of conflict of interest laws. For more vital information on major collusion between government and the pharmaceutical companies: http://www.WantToKnow.info/healthcoverup.

In 1972, the Tuskegee experiments on black people shocked the world. Now, a new report reveals that the official inquiry was a cover-up. The [syphilis] "trial," conducted between 1932 and 1972, involved 400 black sharecroppers. The Tuskegee "volunteers" were not to be treated, either with Salvarsan or even antibiotics after their discovery. Ignorant of the true goal of the trial, the participants were destined to be living, and dying, examples of the terrible course of the untreated illness. Tuskegee, after its exposure in the media in 1972, thus became a byword in America for racist medical experimentation. Soon after the Tuskegee revelations, fault was admitted, apologies made. Yet in time, historians of medicine, sociologists and social anthropologists began to play down the scandal. Tuskegee, they argued, was an understandable error, given the absence of viable antidotes in the 1930s. But renewed outrage over Tuskegee is about to explode with an investigation entitled Medical Apartheid, to be published in the US early next year. The public-health historian Harriet Washington will reveal ... that the Tuskegee trial was even more inhumane and morally degenerate than previously suspected. The role of Nurse Eunice Rivers became crucial. Above all, her task, aided by the study's doctors, was to ensure that the syphilitic men would receive no treatment, despite the extraordinary advances in treatment from the 1940s onwards. "By 1955," according to Washington, "nearly one-third of the autopsied men had died directly of syphilis and many of the survivors were suffering its deadliest complications."

Note: For lots more on the history humans used as guinea pigs in experiments by government: http://www.WantToKnow.info/humanguineapigs and http://www.WantToKnow.info/mindcontrollers10pg#human

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.