DOMINIE'S UPDATES
 
After years of writing a monthly FMS/CFIDS newsletter (see www.fms-help.com/newsletters.htm for archives), I finally quit in October 2005 to have more personal time.  However,  I continued to receive amazing research articles from readers and also concerned emails asking how I was doing.   So, from time to time, I send out updates to my mailing list (to join, send an email to dom@fms-help.com and ask to be placed on the list)Below are some of the updates I have sent (so far)--

 
October 13, 2005 - Amy's insomnia
October 18, 2005 - reduce stress
March 4, 2006  - bumper stickers for ladies
March 25, 2006 - open letter to "normals"
April 4, 2006 - adrenal insufficiency; epsom salt baths
April 5, 2006 - epsom salt bath warning; urinary frequency; bladder problems
April 24, 2006 - stealth viruses; genetic cause discovered for CFIDS
May 2, 2006 - can't travel due to FMS/CFIDS; Fibromyalgia Awareness Day - May 12, 2006
May 3, 2006 - Fibro & Fatigue Clinic; military vaccinations and CFIDS
May 10, 2006 - sleep CD; L-arginine
May 12, 2006 - mold exposure, chest tightness and breathing problems
May 21, 2006 - bad doctors; explaining your illness; magnetics; Cymbalta
May 25, 2006 - mold recovery; sick building; Fibromyalgia & Fatigue survey
May 26, 2006 - worst doctor I ever encountered; new book about fibromyalgia
June 1, 2006 - animal viruses cause CFS; get your life back from fibromyalgia
June 6, 2006 - Stat-1 protein deficiency and central nervous system; MSG and sleep loss = fat!
June 16, 2006 - 2 new pages on my website
July 4, 2006 - autonomic nervous system, dopamine, circadian rhythm, broken bodyclock related to fibromyalgia
July 13, 2006 - dealing with people who are skeptical of fibromyalgia
July 20, 2006 - letter from a man whose wife has fibromyalgia
July 27, 2006 - relationship suggestions for people who have fibromyalgia
August 3, 2006 - essential oils help me with fibro fog and sleep (AND it helps my hyperactive dog calm down!)
August 8, 2006 - rename CFS to M.E. (myalgic encephalomyelitis); CDC traveling exhibit to educate people about CFS
 
 

DISCLAIMER: I am not a medical doctor. I am a fibromyalgia/chronic fatigue syndrome survivor. The purpose of this website is not to diagnose or cure any disease or malady, but is presented as food for thought.  This information cannot take the place of professional medical advice. Any attempt to diagnose and treat an illness should come under the direction of a physician. No guarantees are made regarding any of the information in this website.


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