The true story of FDA terrorism
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Η πραγματική ιστορία τρομοκρατίας του FDA |
Presented by Dale Humpherys, July 2002
Towsend Letter for Doctors and Patients
Posted here with permission of the author
Recent figures released by the MS Society estimate the annual cost of MS in the US at $10 billion, higher than the cost of asthma (about $5 billion) and all infectious diseases (nearly $8 billion) despite a much higher incidence of those conditions. More than 400,000 Americans have MS and this country and Canada have one of the highest national rates in the world. It's been described as a "high-risk area" for the disease.
The cost of four medications "approved" for treatment for MS range from $12,300 to $21,000 a year and now approach $1 billion annually. All four are said to "lessen the frequency and severity" of MS attacks and slow the progression of disability, but none reverse or cure the disease.
However, there is a safe and inexpensive cure for MS which costs less than $100 per month. I and many others have recovered completely and returned to a productive life using this treatment. Among them is Paul Ferrari 650-344-6236 in California and his father who contracted ALS and lived for 20 years on this treatment — the average life span for a victim of this disease is 3 or 4 years. There are now an estimated 500 patients in the US and Canada using this therapy and almost all are recovering. The treatment requires a simple daily injection given by the patient of vitamin B1, 200 to 400 mg and 2 cc of liver extract weekly.
In an article published in the Feb./March 2000 edition of the Townsend Letter my story is told in full. In the October 2001 edition of this medical journal I also tell of the efforts of the FDA to specifically target this treatment by stopping production of liver extract injectables at Merit, Phyne and Swartz Labs. This has been continuing for 3 years and will ultimately result in this treatment being unavailable.
We must take steps to stop this FDA/Pharmaceutical Monolithic display of greed and exploitation of a helpless minority for profit. This can be accomplished. I am asking all patients who feel they are benefiting from this treatment to write me telling of their progress and also get their doctors to do the same. Give me your name, address, telephone or fax number and your doctor's name, address, telephone or fax number. If we unite we have been assured of support in Washington, DC and together we can stop the FDA/Pharmaceutical greed machine from taking away this treatment. This will require the help and cooperation of all to accomplish. It is sad in a free society to see such despotic oppression of an ill minority which requires a desperate response to enable us to keep, restore and maintain our health. But it is this or the wheelchair. Is there a choice?
We ask that you also make copies of this letter and send them to your Senator, Congressperson and all segments of society and government connected with health care. Send copies also to everyone you know who has MS whether they are on this treatment or not. Many MS victims still have not heard of this treatment.
We received substantial help and coverage from Dr. Collin of this journal and Dr. Hoffer of the Orthomolecular Journal in 2000. Prior to that it was largely Canadian media reports.
For those unfamiliar with my history, I was diagnosed with MS in 1973 after 2 severe attacks which forced me to discontinue working and spend most of my time in bed, and able to walk only short distance. I was told by my doctors I would soon be in a wheelchair. After hearing Dr. F.R. Klenner was treating MS with success I went to Reidsville, North Carolina and began treatment. I began to recover and was well enough after 6 months to return to work as a teacher, although it was 2 years before I became symptom-free. I have enjoyed good health since, and at the age of 75 I am still working and looking after a 5-acre farm.
Dale Humpherys #103- 9905 5th St., Sidney, B.C. V8L 2X6
email:dalehms at gmail dot com
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