8 Medical Lies and Why I Abandoned Medicine

Shane Ellison, M.Sc.
www.earlytorise.com

 

By education and by trade, I was a drug chemist. My passion for science motivated a successful career in drug design and synthesis – in both academia and industry. As a scientist, I witnessed first-hand the priorities of international pharmaceutical companies (Big Pharma), which ranked wealth first and health a distant second.

In the pharmaceutical industry, making money supercedes science. Science no longer prevails in medicine.  Instead, modern medicine has been democratized. Drug approval is a simple matter of 51% telling the other 49% that a prescription drug is safe and necessary. The outcome: deadly drugs are approved for use among misinformed medical doctors and patients.  Herein lies a story of deceit and a chemist’s abandonment of modern medicine.


My suspicion of modern medicine began while I was employed by Eli Lilly to design a new generation of Hormone Replacement Therapy (HRT) drugs.  Such drugs include tamoxifen and raloxifene. Initially, these drugs were thought to block estrogen receptors (excess estrogen can initiate cancer growth) and thereby halt cancer. As time progressed, though, it was learned that they were also capable of activating estrogen receptors.
The end result was a biochemical environment favorable to cancer growth among users. [1] The Journal of the American Medical Association recognized this trend and stated "our data add to the growing body of evidence that recent long-term use of HRT is associated with an increased risk of breast cancer and that such use may be related particularly to lobular tumors."

The risk of cancer associated with HRT drugs was obscured from doctors by drug companies. This can be seen by the fact that tamoxifen is the gold-standard used by medical doctors to fight cancer among their patients, particularly breast cancer. This explains why medical doctors might not notice its ability to cause cancer – the patient already has it.


At any rate, my task was made clear: Design HRT “knock-offs” that are effective without causing cancer.


My attempt to design safer alternatives was unsuccessful.  And after one year, the project was ended.  However, access to HRT drugs like tamoxifen was not.  They remained on the market.

The fuel driving the continued use of HRT drugs was disinformation via Direct-To-Consumer (DTC) advertising
. Since 1962, monitoring DTC advertising has been the sole responsibility of the Food and Drug Administration (FDA). But in a ghastly conflict of interests, the FDA granted the duty of DTC advertising to the pharmaceutical companies in 1997.  Officially, this was done as a means of “promoting health awareness to ensure health and safe
 

1. Sally, A. et al. Estrogen Plus Progestin and the Incidence of Dementia and Mild Cognitive Impairment in Postmenopausal Women. Journal of the American Medical Association. 2003;289:2651-2662.
Chen CL, Weiss NS, Newcomb P, Barlow W, White E. Hormone replacement therapy in relation to breast cancer. Journal of the American Medical Association. 2002 Feb 13;287(6):734-41. Spurgeon, D. Long Term use of HRT Doubles Cancer Risk. British Medical Journal. 2003 Jul 5;327(7405):9.

Yoneva T. Taniguchi K. Tsunenari T. Saito H. Kanbe Y, Morikaw K, Yamada-Okabe H. Identification of a novel, orally bioavailable estrogen receptor downregulator. Anticancer Drugs. 2005 Aug;16(7):751-6.

Labrie, F. et al. EM-652 (SCH 57068), a third generation SERM acting as pure antiestrogen in the mammary gland and endometrium. The Journal of Steroid Biochemistry and Molecular Biology. 1999 Apr-Jun;69(1-6):51-84.

2. Starfield, Barbara. Is US Health Really the Best in the World? Journal of the American Chemical Society, July 26, 2000-Vol 284, No.4.http://msnbc.msn.com/id/7503122/.

3. There were an estimated 58,000 U.S casualties in the Vietnam War.

4. Moride Y, Haramburu F, Requejo AA, Begaud B. Under-reporting of adverse drug reactions in general practice. British Journal of Clinical Pharmacology, 1997 43: 177-181.

5. Tejal K. Gandhi. et al.. Adverse Drug Events in Ambulatory Care. The New England Journal of Medicine. Volume 348:1556-1564. April 17, 2003. Number 16.

"An important function of the immune system is to protect the body from microbes that cause infections. Recently scientists have discovered a possible microbe connection in many chronic diseases that were previously not considered to be infections. A microbe connection has been identified in such diseases as arteriosclerosis, heart disease, Alzheimer's disease, duodenal ulcers, diabetes, SLE (systemic lupus erythematosus), rheumatoid arthritis, Hashimoto's thyroiditis, multiple sclerosis, most forms of cancer, polycystic ovary disease, some types of inflammatory bowel disease, cerebral palsy and even most major psychiatric diseases. The immune system, which spans the boundaries of all the body's vital systems, could be the key factor in understanding the cause of chronic and degenerative disease."
--
Dan Kenner, Ph.D., LAc.

 

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