I’ve long avoided chicken and beef when eating in restaurants. I’ve just assumed the meat comes from animals loaded with antibiotics and other things I’d rather not know about. We’re learning more about those “other things.”

The latest tidbit comes from the U.S. Food and Drug Administration proudly announcing that a Pfizer subsidiary will discontinue a parasite-controlling drug that’s been routinely fed to commercially-raised chickens since the 1940s, well over 60 years.

Why? Michael Taylor, the deputy commissioner, stated: “FDA detected increased levels of inorganic arsenic in the livers of chickens treated with 3-Nitro, raising concerns of a very low but completely avoidable exposure to a carcinogen.” Better late than never, right? And now we understand better the source of the arsenic in the chicken litter being used in GMO corn fed to cattle that Ken Conrad discusses following my previous post.

It’s hard to know what to say to the absurdity of the FDA allowing a carcinogen in our food for decades, while going after producers of raw milk, health-giving herbs and, most recently, even a maker of elderberry juice.  The reaction of the seller of elderberry juice in the video is instructive–it’s typical of small producers set upon by the FDA…they’ve made changes to their promotion to tone down any health claims, but can’t figure out what the FDA continues to be concerned about because the FDA won’t explain its objections.

A backlash to such actions is definitely developing and expanding. The Maine legislature, in one of its final acts of the current session, just passed a food sovereignty resolution. It’s not a law, but it sends a strong message of defiance:

“RESOLVED: That We, the Members of the One Hundred and Twenty-fifth Legislature now assembled in the First Regular Session, on behalf of the people we represent, and in recognition of our State’s proud agricultural heritage, take this opportunity to oppose any federal statute, law or regulation that attempts to threaten our basic human right to save seed and grow, process, consume and exchange food and farm products within the State of Maine.”

Those legislators are going to find themselves with a lot of opposing to do, since the U.S. Food and Drug Administration is on the march to begin implementing the Food Safety Modernization Act, and its new regulations covering farmers and food producers, beginning next month.
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Also on the state front, there will be hearings next Tuesday in Massachusetts on two proposed pieces of legislation designed to improve access to raw milk. One would allow milk to be transported from dairy farms to customers, and the other would explicitly legalize herdshare arrangements, which aren’t covered by existing laws.

Here’s an updated table of pending state legislation affecting raw milk.
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Lessons to be learned from the European E.coli pathogen causing illness? Get ready for this drumbeat to grow louder, from David Acheson, a former associate commissioner of the FDA and now a consultant: “Perhaps it’s time to ask ourselves why interventions, such as high pressure treatment or irradiation are not being evaluated and used more? Clearly consumers need to have a choice, and products have to be labeled appropriately, but as US consumers look at over 470 people in the EU with a life-threatening foodborne illness that is unquestionably a life-altering event they may wish to have the option of irradiated or high pressure treated food more readily available in the local supermarket than it is today. Offering such options in grocery stores would provide the consumer with the ability to make choices and have a role in determining the safety of the food they serve their family.”

Funny how these food safety types advocate for “choice” when it fits their agenda. And you know how long the choice will last–till the treated food gets a toe-hold, at which time Acheson and colleagues will push for “eliminating the risk” by getting rid of the untreated foods.