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STOP LEGISLATION TO REGULATE FOOD SUPPLEMENTS LIKE DANGEROUS DRUGS

 

On December 6th, the AER bill (calling for regulation of food supplements) PASSED the Senate on the consent calendar and was sent over to the House. A CHANCE STILL EXISTS THAT it could be heard or tacked on to another bill. It is all happening very fast.

You would take a stand AGAINST this bill if you believe:

  • You value the right to choose dietary supplements and nutrients as a part of your personal health protocol
  • Dietary supplements are nutrients
  • The Dietary Supplement Health and Education Act is ALREADY IN PLACE to regulate food supplements and there is no need to regulate them as risky drugs (and create a regulatory burden that would make it cost prohibitive to produce them)
  • You want supplements to continue to be treated as foods and not synthetic medicines
  • That the government has the burden to show harm before they put more onerous regulations on food supplements

Our "Two Cents":

The pharmaceutical industry has a vested interest in eliminating/regulating food supplements that provide safe, natural, inexpensive alternatives to prescription drugs and their multitude of side effects. This bill is driven and backed by the multi-billion dollar pharmaceutical industry which kills an estimated 200,000 Americans per year according to the Journal of the American Medical Association (the most prestigious medical journal in the world).  This number does not include the hundreds of thousands who suffer illness or serious injury from drug side-effects. Recently, MSNBC highlighted that 700,000 people per year are rushed to the ER due to side-effects of commonly used drugs.

Comparatively, prior to its ban, Americans took more than two billion doses annually of the  supposedly deadly supplement, ephedra, yet the American Association of Poison Control Centers documents only one death per year from wrongful use of ephedra.  (If the media frenzy has caused you to think differently about ephedra, consider this... even though the U.S. Government Accounting Office (GAO) audit of the FDA's case against ephedra concluded that the synthetic pharmaceutical drug "ephedrine", and not ephedra, resulted in the reported adverse effects, ephedra was still banned by the FDA banned in 2006.) 

The pharmaceutical industry recognizes it cannot profit from natural remedies because they cannot patent a substance that is found in nature. They also recognize that consumers are becoming more educated about the side effects, limitations and dangers of pharmaceutical drugs. We are choosing natural remedies to accomplish better health outcomes and that threatens Big Pharma pocket books.  We believe this bill is intended to squelch the competitive risk that natural remedies and whole food supplements present to the pharmaceutical industry.  

We also believe that the FDA should be dealing with the travesty of deaths and serious side effects caused by prescription drugs and leave dietary supplements to exist within already over-rigorous regulatory structure.  As pointed out by Shane Ellison, author of the very informative book, Health Myths Exposed, "An estimated 90% of American Adults are nutrient deficient.  We are not dying from supplements but instead, from lack of supplement use.  Most Americans deny proper diet and nutritional supplementation and instead embrace FDA approved drugs to stay healthy.  Looking at the health of our nation, this model is clearly not working."





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