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Canada :

National ME/FM Action Network   

Nightingale Research Foundation Dedicated to the study and treatment of M.E. / CFS

Our FM/CFS World Inc. is a nonprofit organization maintained by sufferers of Fibromyalgia and Chronic Fatigue Immune Deficiency Syndrome. Our Mission is to improve the quality of life for fellow sufferers, while increasing public, governmental and medical awareness of these diseases.
We append the mission statement to include: fundraising efforts to send donations to help in the Research for the Cause, Treatment and Cure of FM/CFIDS.   

The Welcome to the Web Site for The National ME/FM Action Network. Ottawa Canada

I am trying to get national recognition for the pain sufferers of FMS/CFIDS.   We need patients who are willing to write about their experience with this disorder

Jodyís Blog ( Canada) -A life with Chronic Fatigue Syndrome is a fragile life indeed. Needs lots of protection and nurturing. But though we may be ill and often isolated, it helps to keep in mind that none of us are alone.

Web site of The Myalgic Encephalomyelitis Association of Ontario.

This means that no one in Ontario who suffers from ME/CFS can ever again be told by a doctor that ME/CFS does not exist. If they do, tell them to look up Diagnostic Code 795. 'Chronic Fatigue Syndrome' has been given the OHIP Diagnostic Code 795 by the Ontario Medical Association as a Neurological Illness!   

This illness is to fatigue what a nuclear bomb is to a match. Itís an absurd mischaracterization."   

Clinical and Scientific Basis of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome   

The Need for Research-based Subsets   

Canadian Expert Consensus Panel Clinical Case Definition for ME/CFS

The Need for Research-based Subsets

CFS CDC and NIH Research activities are diverse, but Agency Coordination is limited






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