http://www.cfids-cab.org/MESA/ccpc.html

National ME/FM Action Network

http://www.nightingale.ca/   

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

http://www.ourfm-cfidsworld.org/

http://www.mefmaction.net/   

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

http://www.fms-help.com/letter.htm

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

http://www.ncubator.ca/index.html

Jody’s 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.

http://www.meao-cfs.on.ca/splash.shtml

Web site of The Myalgic Encephalomyelitis Association of Ontario.

http://www.mefmaction.net/default.aspx?page=meofficialrecognitionon

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!

http://www.cfids-cab.org/MESA/index.html   

This illness is to fatigue what a nuclear bomb is to a match. It’s an absurd mischaracterization."

http://www.nightingale.ca/nightd.html   

Clinical and Scientific Basis of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome

http://www.cfids-cab.org/MESA/subsets.html   

The Need for Research-based Subsets

http://www.co-cure.org/cccd.htm   

Canadian Expert Consensus Panel Clinical Case Definition for ME/CFS

http://www.cfids-cab.org/MESA/subsets.html

The Need for Research-based Subsets

http://www.gao.gov/new.items/he00098.pdf

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

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