Essential Info about CM8

The effectiveness of CM8 is built upon a basic fundamental scientific fact. Swiss Albino Mice are “immune” from the ravages of arthritis. In nature, they do not contract it at any age. It is also already well known that there is a known toxin called mycobacterium butyricum, or Freund’s adjuvant. When injected , this toxin is known to cause animals to become arthritic. However, when forcibly injected with this synthetic version of arthritis, (known as Freunds adjuvant), Swiss Albino mice still could not contract arthritis. Rats, on the other hand, ARE susceptible to adjuvant-induced arthritis when injected. Through testing, it was discovered that rats who were first treated by injection of cetyl myristoleate could not subsequently contract arthritis when injected with Freunds adjuvant, making them virtually immune to arthritis, much like the Swiss Albino Mice. This discovery was published in PubMed.gov, the official publication of the US National Library of Medicine and the National Institutes of Health.

CM8 Quick Fact..

Similar compounds such as cetyl myristate and cetyl elaidate (the trans-isomer of cetyl oleate, proved to be virtually ineffective in the same tests

CM8 Quick Fact..

The discoverer of cetyl myritsoleate, Dr. Harry Diehl, was an expert in sugar synthesis, and it was his method of sugar synthesis that was used to prepare the oral polio vaccine that was later developed by Dr. Jonas Salk. In the 50’s, 60’s and 70’s, Polyomyrelitis was a contagious, historically devastating disease, and in 1952, nearly 60,000 cases with more than 3000 deaths were reported in the USA. By 1979, occurences of polio thru natural infection was completely eradicated and eliminated from the United States, thanks to Dr. Salk’s vaccine. In 1977, Dr. Salk received the Presidential Medal of Freedom from President Jimmy Carter.

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By a strange twist of fate, Dr. Diehl contracted arthritis in his later years. Since his discovery had not yet been widely accepted by the drug companies, he mixed himself up a batch of CM8, from which he self medicated until his eventual death in 1999, at the age of 89.

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Like everything else, cetyl myristoleate does not work 100% of the time. Failure to work can be associated with failure to follow the proper dosage or dietary recommendations, failure to take a sufficient amount of CM8, failure of the liver to uptake and respond to the CM8, and misdiagnosis in which the condition is not really an arthritis-type condition.

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Contraindication & Toxicity studies have been performed on cetyl myristoleate and the lack of toxicity is evident. Test results deemed CM8 a non-toxic material in accordance with Federal Regulations. Mega-doses were given to test animals with no ill effects. Moreover, subsequent necropsy of these test animals showed no effects whatsoever on their internal organs.

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Cetyl myristoleate exists in nature in sperm whale oil, and in a small gland in the male beaver. At this time no other sources in nature are knwon to contain CM8. While the first amounts of CM8 for experimentation were extracted from mice, Dr. Diehl quickly developed a methiod for making cetyl myristoleate in the lab by the esterification of myristoleic acid.

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Since its introduction into the US marketplace in 1999, CM8 has become the fastest growing all natural anti inflammatory compound in the USA, and it continues to grow exponentially each year.