The NATIONAL ME/FM ACTION NETWORK became a Canadian charitable organization on June 18, 1993 dedicated to Myalgic Encephalomyelitis, also known as Chronic Fatigue Syndrome (ME/CFS) and Fibromyalgia (FM) through support, advocacy, education and research.
Read MoreThe network works hard to raise issues regarding ME/CFS and FM with federal government officials and politicians. Through direct contact with government administrators, we continue to advocate for better awareness, education, health care, disability support and equitable research funding.
Through our website we offer educational resources for patients, the medical community and educators. We offer documents online and in print containing information on ME/CFS and FM, best medical practices, assistance for disability applications and a guide to educating young people with ME/CFS and FM.