The FDA Calls One of the Body’s Basic Healing Functions a “Disease”
Why? To make sure Big Pharma gets a monopoly on new drugs connected to it!

Why? To make sure Big Pharma gets a monopoly on new drugs connected to it!

“I certify that this compounded variation produces ‘a significant difference from the marketed drug version.’ ”
If Congress’s initial, knee-jerk reaction to the 2012 New England Compounding Center (NECC) meningitis tragedy had become law, you would have had to add this federally mandated disclaimer to every prescription you wrote for a compounded drug. It seems Congress, influenced by pharmaceutical industry lobbying dollars, wanted to reward the FDA’s failure to shut down grossly negligent compounding manufacturers—but did so by granting the agency vast new powers.

“We found that FDA focused on perfecting their legal reasons for inaction,” a Senate committee wrote, “instead of protecting families.” Action Alert!

The FDA and the FTC won’t allow reasonable, science-based claims about foods and supplements, but they let mega-companies like Coke run wild. Action Alert!

But the battle to protect health speech goes on both in Europe and America.

Are regular mammograms doing more harm than good? Let’s take a look at the science.
The FDA’s ignorance of vitamin E could create serious risks for consumers. This is on top of other parts of the FDA’s proposed new labeling rules that aim to ban the natural form of folate (vitamin B9), and result in less potent supplements. URGENT Action Alerts!

Click here to donate! On and off Capitol Hill, ANH-USA defends consumer access to dietary supplements, truly healthful foods, and natural health treatments and practitioners. We proactively stop attempts to limit your access to natural health, before you feel their affects. Right now, we’re working to: Stop FDA’s proposed ban on folate, a necessary-to-life B-9 vitamin, […]

If you missed our urgent Action Alert on the attempt to ban folate from dietary supplements, please take action now!