We are

"People helping people help themselves".

through

EDUCATION     ADVOCACY     SUPPORT     RESEARCH

QUEST
With your membership you will receive our newsletter, "Quest", which will keep you informed about medical medical research, disability and legal issues, as well as keeping you up-to-date about our projects and other news.  "Quest" includes original articles by doctors, researchers, and lawyers.  There is a one year lag between the time a newsletter is published and when it is posted on our website in consideration to our membership.

ME/CFS and FMS Brochures
You will receive informative brochures about myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and fibromyalgia syndrome (FMS).

Educational Materials
The National ME/FM Action Network has developed numerous educational materials to assist our membership.

National Doctors' Roster
We have a roster of doctors and other health professionals who diagnose and/or treat ME/CFS and FMS patients.

National Lawyers' Roster
We keep a roster of lawyers and legal advocates who are knowledgeable about ME/CFS and FMS and represent patients with these illnesses.

Independent Medical Examination (IME) Registry
A registry of disability applicants, who have attended IMEs arranged by insurance companies, CPP and WSIB, is being developed to give us a data bank of fair and unfair reports.  This information will be used to make appropriate recommendations for changes in the the way IMEs are done.  All names are kept strictly confidential and reports are given numbers.
  
Please Help Us Help You!
Our projects benefit all sufferers of these illnesses.  We need your support!  

Membership Fee
$25.00 per year, which includes our newsletter.

To become a member and/or give a donation to help support the important work being done, please complete our Membership Application.