Quest 
With your membership you will receive our quarterly newsletter, “Quest”, which will keep you informed about medical research, disability and legal issues, as well as keeping you up-to-date about our many projects.  “Quest” includes original articles by doctors, researchers, and lawyers.

ME/CFS and FMS Brochures
When you become a member, you will receive informative brochures about myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), and fibromyalgia syndrome (FMS).  The information will also be available in the "Members Only" section.

Educational Materials
The National ME/FM Action Network has developed a variety of educational materials to assist our membership.  Please click on Educational Materials under Resources in the menu at the left for further  information.

National Doctors’ Roster
We keep a roster of doctors and other health professionals who diagnose and/or treat ME/CFS and FMS patients.  Please contact our office at 613-829-6667 for help in obtaining a doctor in your area.

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.  Please contact our office at 613-829-6667 for help in obtaining a lawyer in your area.

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 change in the way IMEs are done.  Please click on IME Registry under IME in the menu at the left for the IME Registry Form.