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Wednesday, Nov 27th

Last update08:48:04 AM GMT

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FDA Threatens to Seize All Natural Products that Dare to Mention H1N1 Swine Flu

In an effort to censor any online text that might inform consumers of the ability of natural products to protect consumers from H1N1 influenza A, the FDA is now sending out a round of warning letters, threatening to "take enforcement action... such as seizure or injunction for violations of the FFDC Act without further notice."

The message is crystal clear: No product may be described as protecting against or preventing H1N1 infections unless it is approved by the FDA. And which products has the FDA approved? Tamiflu (the anti-viral drug that most people will never have access to), and soon the new H1N1 vaccine that's being manufactured at a cost of one billion dollars (paid to Big Pharma by the taxpayers). This vaccine, of course, will be utterly useless because H1N1 will undoubtedly mutate between now and the time the vaccine is ready, rendering the vaccine useless.

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Green tea could delay prostate cancer: U.S. study

Active compounds in green tea may slow down the progression of prostate cancer, researchers reported on Friday.

Capsules made using green tea extracts called polyphenols lowered levels of proteins that tumors use to grow, the researchers found.

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Cancer boost from whole carrots

The anti-cancer properties of carrots are more potent if the vegetable is not cut up before cooking, research shows.

Scientists found "boiled before cut" carrots contained 25% more of the anti-cancer compound falcarinol than those chopped up first.

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Swine Flu Vaccination Poses Serious Threat to Your Health

It looks like governments around the world will either force these vaccinations on the public or launch a massive propaganda campaign to trick you into submitting to a jab. If they attempt to force these untested and essentially experimental vaccinations on you, cite the Nuremberg Code, which states: “The voluntary consent of the human subject is essential.” No experimental vaccine should be “conducted where there is an a priori reason to believe that death or disabling injury will occur, except, perhaps, in those experiments where the experimental physicians also serve as a subjects.

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A Stem-Cell Therapy for Blindness

An experimental therapy using human embryonic stem cells to treat degenerative eye diseases has proved safe and effective in animal studies, and may begin early human trials in the next few months if it receives approval from the Food and Drug Administration. If granted approval, the therapy will be the second embryonic-stem-cell-based treatment to progress to human trials, and it will provide a test case for further applications of stem cells.

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Lilly Sold Drug for Dementia Knowing It Didn’t Help, Files Show

Eli Lilly & Co. urged doctors to prescribe Zyprexa for elderly patients with dementia, an unapproved use for the antipsychotic, even though the drugmaker had evidence the medicine didn’t work for such patients, according to unsealed internal company documents.

In 1999, four years after Lilly sent study results to the U.S. Food and Drug Administration showing Zyprexa didn’t alleviate dementia symptoms in older patients, it began marketing the drug to those very people, according to documents unsealed in insurer suits against the company for overpayment.

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Lobbyists Spend Millions Fighting Over Obama's Universal Health Care Plan

The most lucrative job in Washington these days just might be health care lobbyist -- as prominent interest groups announce plans to pour millions of dollars into fighting over President Obama's efforts to create a universal health care system.

The White House has sought to curtail the role of lobbyists, but the heated public debate over Obama's health plan has made them very much a part of the legislative process.

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