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The FDA Does What?!

From: Liz S
Sent: Tuesday, June 05, 2012 2:35 PM
To: Lloyd wright
Subject: fwd: The FDA does what?


I am a mom of 4 kids, and I just want the best for them.
So I purchased natural raw foods in local markets and from Amish farmers who traveled down from Pennsylvania.
At least I used to until armed FDA agents stormed into my neighborhood and raided natural food sellers.
They even posed as moms to catch these "criminals."
You see, the FDA thinks they know better than me what’s good for my children, and that’s just plain wrong.

Please take a look at Senator Paul’s email below and sign the petition supporting his amendment to end the FDA’s armed raids.


phase II clinical trial SOC and Boceprevir - Join the Suit

Lloyd Wright,
An email friend referred your site. I am currently in a federal law suit for permanent injury sustained from my participation in a clinical trial of PegIntron / Rebetol / Boceprevir. I suffer multi-system sarcoidosis with occular, renal and pulmonary involvement caused by PegIntron and Rebetol treatment.

7 VITAL Actions for 2011

So Many Threats, So Little Time! 
Here's a List of Vital
Actions for 2011
Forward them to All Your Contacts
So They Can Do the Same.

Vitamin C & The Rise of Tyranny

Not content to kill 100,000 Americans each year with deadly Big Pharma drugs while censoring the truth about the healing effects of herbs, nutritional supplements and natural medicines, the FDA has now set out to deny Americans access to yet another lifesaving medicine known simply as vitamin C.

Senator McCain Files New Bill That Attacks Your Access to Supplements and Repeals Key Sections of the Dietary Supplement Health

This is a Full Court Press From Those Who Want to Implement CODEX.
It MUST BE FOUGHT NOW!  Click Here and Get on Board

Track This Bill HERE

McCain’s bill is called The Dietary Supplement Safety Act (DSSA). It would repeal key sections of the Dietary Supplement Health and Education Act (DSHEA). DSHEA protects supplements if 1) they are food products that have been in the food supply and not chemically altered or 2) if they were sold as supplements prior to 1994, the year that DSHEA was passed. If a supplement fits one of these two descriptions, the Food and Drug Administration (FDA) cannot arbitrarily ban it or reclassify it as a drug.

These protections are far from perfect. They discourage companies from developing new forms of supplements. New supplements may be arbitrarily banned by the FDA or adopted by drug companies in a way that precludes their further sale as supplements.

McCain’s bill would wipe out even the minimal protections contained in DSHEA. It would give the FDA full discretion and power to compile a discreet list of supplements allowed to remain on the market while banning all others.  

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