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THE MERCURY MISCHIEF: As Obama Warns of Hazards, the FDA Approves Mercury Dental Fillings

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The government seems to be speaking out of both sides of its mouth, as the President preaches one thing and the FDA does another. If we are going to have "smarter medicine that really works," we need to get politics, lobbies and cronyism out of science.

President Obama has proposed covering the costs of his new medical plan with "smarter" medicine, meaning the adoption of procedures that eliminate inefficiencies and stress prevention. At a town hall meeting in New Hampshire on August 11, 2009, he gave the example of a diabetic needing to have a foot amputated, at a cost of $30,000 to $50,000. It would have been smarter to counsel the patient on diet and weight loss and monitor his medications before amputation was required. The insurance company would have saved money and the patient would have saved a foot.

The 2008 Obama/Biden Plan for a Healthy America also stressed preventive approaches to disease, including the reduction of toxins to which the body is exposed; and chief among these toxins was mercury. The Plan stated as a fundamental goal:

"Reduce Risks of Mercury Pollution. More than five million women of childbearing age have high levels of toxic mercury in their blood, and approximately 630,000 newborns are born at risk every year. The EPA estimates that every year, more than one in six children could be at risk for developmental disorders because of mercury exposure in the mother's womb."

As a Senator, Obama was responsible for extensive legislation reducing environmental exposure to mercury, including a ban on the export of elemental mercury, and legislation to phase out the use of mercury in the manufacture of chlorine.

Mercury can get into the blood by various routes, and one that has been lately in the news is the mercury found in the thimerosol in vaccines. Another source that made the news in July is the mercury released from dental fillings by chewing. The World Health Organization has stated that between 3-17 micrograms of mercury are released into the body each day by chewing, compared to only 2-5 micrograms from fish and all other environmental sources combined. In 1990, the New England Journal of Medicine published an editorial calling mercury amalgam fillings "possibly the chief source of exposure [to mercury] of a large segment of the U.S. population".

Surprise FDA Ruling

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When mercury amalgam made the news on July 29, 2009, however, it was not to warn of its hazards. Rather, it was to report the FDA's surprise ruling that mercury fillings are safe. The ruling came after years of foot dragging by the FDA and a wave of consumer lawsuits. A growing consumer movement had amassed so much evidence for the dangers posed by mercury dental fillings that when a court finally ordered the FDA to come out with a ruling, the plaintiffs announced, "We won!" But instead of the declaration they expected, the FDA imposed no restrictions on the use of mercury amalgam. Dentists were not even required to inform their patients that "silver" fillings are composed mostly of mercury. The FDA conceded that it did not know if amalgam was harmful to children under six, pregnant women, or nursing mothers, but it took no steps to protect them. It even pulled from its website an existing neurological risk advisory that said, "Dental amalgams contain mercury, which may have neurotoxic effects on the nervous systems of developing children and fetuses."

Consumer advocates were stunned, as the FDA had earlier agreed to strengthen its warnings against mercury amalgam fillings. The evidence against mercury amalgam dental fillings was considered so compelling that Sweden, Norway, and other countries had already banned their use entirely. Degussa, Germany's largest producer of amalgam and the world's largest producer of metals for dentistry, completely shut down its amalgam production after a federal court ruled that dentists who used it faced legal liability. The FDA was expected to follow suit.

Why its unexpected about-face? Charles Brown, of the National Counsel for consumers for Dental Choice, suggests it had to do with a change in personnel. In May 2009, Dr. Margaret Hamburg succeeded to the post of FDA Commissioner. The Wall Street Journal noted that for five years before that, she served on the board of Henry Schein Inc., a $4 billion firm that distributes medical and dental supplies, including vaccines. Brown wrote skeptically:

"Washington is famous for the revolving door -- those in the party out of power take highly paid corporate positions, then return to government to bail out their benefactors. The new FDA Commissioner, Margaret Hamburg, worked in the Clinton Administration, then went out and became a director at the dental products colossus Henry Schein, earning a quarter million dollars a year for the handful of hours it takes to be a director. Corporations do this because they know the other party will return to power, at which time the corporations will call in their chits."

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Science or Politics? The Liability Question

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Ellen Brown is an attorney, founder of the Public Banking Institute, and author of twelve books including the best-selling WEB OF DEBT. In THE PUBLIC BANK SOLUTION, her latest book, she explores successful public banking models historically and (more...)
 

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