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Save Homeopathy & Natural Compounding!

Mainstream Medicine has failed the REAL epidemic: Chronic Disease

Just a quick note that if you struggle with the zip code finder at the bottom of this page, just copy the below text, find your U.S. Rep and both Senators and paste into an email to all 3 politicians.


    Government’s exploitation of COVID-19 fear to abuse Americans has collapsed whatever remaining trust ever even existed in institutions such as the government, media, big business, and health authorities. And with mainstream medicine’s failure to stem the real epidemic – chronic illness – families are increasingly demanding more natural treatments to gain health. Government should not, therefore, be persecuting alternative-health approaches like traditional homeopathy or pharmacy compounding.  Please support Representative Griffith’s bill - when reintroduced - to protect compounding, and urge Congress to overturn – or withhold Appropriations for –  the latest homeopathy guidance from the U.S. Food and Drug Administration (FDA).

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FIRST, Homeopathy has been successfully and safely used for more than 200 years. In fact, a century ago, many hospitals operated not under the mainstream-medical-school regime called allopathy (relying on chemical medicine to treat disease symptoms, not causes), but rather on a more natural approach called homeopathy – treating the body as a whole and promoting treatments that elicit the body’s own self-healing mechanisms. President Abraham Lincoln found superior outcomes via homeopathic hospitals, while homeopathic flu treatments during the Spanish Influenza epidemic of 1918-1919 (which killed some 20 million worldwide) were greatly successful. The death rate for those patients treated with allopathic drugs was 30%, compared to a death rate of only 1.5% for those treated with homeopathy. In other words, homeopathy was 98% successful.

Homeopathic remedies are like allopathic drugs in one sense, in that they occasionally fail or become contaminated – in which case the FDA  has an already-existing power under the Federal Food, Drug and Cosmetic Act of 1938, to recall products dangerous to the public for fraudulent labeling or improper manufacturing processes. The FDA codified this approach in 1988 but then withdrew it in 2019 in favor of pre-approval, which will smother the homeopath market by redefining them all as “unapproved, new drugs.”

Not only is it too expensive to gain FDA approval for natural, unpatentable treatments, but it also is impossible. That’s because natural substances are not patentable, and homeopathy is not applicable to mass testing – since its therapies are individualized based upon each person’s unique situation.  

It is unsurprising that the FDA – funded as it is by Pharma user fees – is attacking Pharma’s competitors.  Among other things, homeopathy is popular for allergies, arthritis, and pain – each a billion-dollar market for Pharma. Outrageously, large pharmacy chains now face lawsuits for selling homeopathic products on a shelf located “too close” to Pharma alternatives. FDA’s guidance is targeting homeopathic products first that use, not oral or topical application, but rather injection – and those for more serious health problems. Hence, the persecution, for example, of mistletoe injections, an increasingly popular cancer treatment alternative. Please withhold funds in the Appropriations bill from FDA’s homeopathy pre-approval guidance.