FDA Violates Free Speech to Limit Supplement Access.

The FDA is trampling free speech to limit
your access to supplements. But ANH-USA
has a bold new legal strategy.

Will you join us in this historic battle?

Did you know that if a supplement company “Likes” a customer’s Facebook post, it magically transforms nutritional supplements into drugs? The same thing happens if a supplement’s website links to a scientific article!

As recently as this week, the FDA has made attacks like these to expand the agency’s definition of “disease claim.” Why? By saying a supplement makes a disease claim, the FDA can call it a “drug”—and then remove it from the market!

This also has scary implications for the government regulation of Internet searches and speech. If supplement companies start deleting customer comments out of fear of FDA action, then the FDA has effectively limited consumer speech by using the company as a censorship puppet.

The FDA is pushing your First Amendment rights
closer and closer to the edge. Will you push back,
before it’s too late?

It doesn’t stop there: the FDA has something called its Evidence-Based Review System. It’s just a backdoor tactic to require prohibitively expensive studies—as in hundreds of millions of dollars—if companies want to make any claim about the science behind their supplements. Because natural products can’t be patented, supplement companies can never recoup these astronomical costs. Only Big Pharma and their blockbuster drugs can afford to “pay-to-play:”

We’ve had enough. How about you?

Here’s our plan: ANH-USA will submit multiple petitions—strategically supported by our ongoing legal activities—to address, from various angles, FDA’s egregious First Amendment violations. If we win, we ALL win. If the petitions are denied, we’re ready to pursue further litigation.

Immediate action is critical. Unfortunately, this is an expensive project. This is why we need your help!

Our goal is to raise $40,000 by June 14, so we can
kick off our FDA petitions to defend free speech
and supplement access.

Please make a tax-deductible gift today!
Any amount—even just a few dollars—
makes a huge difference.

The FDA’s actions leave consumers in the dark about the dietary supplements they are buying for themselves and their families. This can be a matter of safety—for you and the ones you love.

The FDA is halfway down the slippery slope of taking away consumer access to supplements. Will you join us in saying, “Enough is enough!”?

To Slay a Genetically Modified Monster


Copyright © 2012 by W.R.McAfee, Sr. All rights reserved.

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Or, why California’s Proposition 37 is important to the rest of the world

A landmark independent study by Canadian doctors published in the peer-reviewed journal Reproductive Toxicology this May found that toxins from soil bacterium that had been engineered into genetically modified (GM or GMO) Bt corn to kill pests was present in the bloodstream of 93 percent of pregnant women as well as in 80 percent of their fetal cord blood.
It was the first human clinical trial of genetically modified food; though humanity has been eating it for almost 16 years.
During the interim, manufacturers of GMOs refused to allow independent labs in the US to test their “patented seeds” to see if they posed a danger for consumption or whether or not they could cause cancer or trigger unknown or long-term health problems for adults; or harm fetuses, newborns, and children. . .unless researchers signed an agreement allowing the manufacturer to review and approve the results of the study.

European countries ran independent lab tests on animals fed GMOs anyway.
The results weren’t pretty

Rubber stamped by the FDA, GMO seed manufacturers and Big Agra began feeding Americans unlabeled GMO food during the 1990s.  Groundwork for this scheme was laid during the 1970s and continues to date.
Politically appointed personnel connected to the biotech industry were quietly placed at the FDA, USDA, and other key positions in Washington by elected shills slathered with campaign donations from the biotech industry and Monsanto—the world’s largest GM seed manufacturer—to facilitate the introduction of GMO food into the world.
GMOs were subsequently declared “. . .essentially equivalent to natural food . . .” or words to that effect . . . and Monsanto was given the green light to release its genetically modified seed into national and world food markets.
GMOs and their derivatives quickly found their way into 80-85% of what America ate.

With no labeling.

Thus America became Monsanto’s fiat lab for genetically modified food; their long-term clinical study. That’s why GMO-seed manufacturers quietly dumped the lion’s share of their toxic seeds into North America, Latin America, and India ; selling it to farmers as an agricultural Valhalla; “a green revolution”; knowing full well possible dangers could develop from the consumption of this food; all the while keeping the public beneath its toadstool.

It’s also why GMOs haven’t been labeled! in the United States. Other nations, once they realized the potential dangers of GM food, put labels on the food and Monsanto’s markets dried up because grocers refused to carry it when consumers refused to buy it.

Here’s an accurate one hour documentary on the implications of this for humanity .

Why weren’t Americans told about GMO food?