Here we go again. The next instance of F.D.A. harassment and control. Any step necessary to suppress pharmaceutical drug competition. Just as blatant as it sounds.
Let’s do whatever possible to look out for our brother, Daniel and his family.
by Brian Shilhavy
For almost 5 years, the FDA has been attacking Daniel Smith of Spokane Washington for selling a mineral supplement that purifies water and has been used in places like Africa by the Red Cross to prevent Malaria. The product is called MMS (Miracle Mineral Solution), and the active ingredient is sodium chlorite, a common mineral that is even used in some municipalities in the U.S. to purify water instead of chlorine.
Daniel Smith will face a trial in less than 30 days, the culmination of close to 5 years of legal battles, that could result in him spending 37 years in prison if convicted.
Why?
Because the FDA has not approved his product for health claims.
Has the product killed anyone? No.
Do FDA approved products kill anyone? Yes.
According to statistics published by medical authorities themselves, FDA prescription drugs are one of the top causes of death in the United States, and probably the #1 cause of death among Americans today.
An older study published by the Journal of the American Medical Association in 1998 stated that 106,000 people died from prescription drugs every year, and the CDC has previously stated that overdoses of FDA-approved prescription opioid pain relievers now exceed deaths involving heroin and cocaine combined.
By contrast, a Government Accounting Office (GAO) report in 2013 found ZERO deaths due to dietary supplements.
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