About the M.E. Society

The M.E. Society of Edmonton (CFS) was started in 1991.
We are a charitable society, which serves people primarily in
Edmonton and northern Alberta Canada. Most members have Myalgic Encephalomyelitis (Chronic Fatigue Syndrome) or the related disorder fibromyalgia. Operated by a volunteer board, the Society was set up to provide support and information to people with CFS and their families, educate the public, especially the medical and legal professions, and to advocate for better treatment and services for people with CFS.

Our Mission Statement

Our mission is to offer moral support, to provide relevant information and to encourage research regarding Myalgic Encephalomyelitis (Chronic Fatigue Syndrome) to sufferers, their families and caregivers.
 

Disclaimer
The M.E. Society of Edmonton (CFS) does not accept the responsibility, legal or otherwise for the opinions in any editorial, or the content of any articles posted on this site. It is recommended that anyone wishing to start treatments suggested in any of the literature on the site do so under close supervision of a qualified and competent doctor.