The Massachusetts ME/CFS & FM Association, a 501(c)3 founded in 1985, exists to meet the needs of patients with ME (Myalgic Encephalomyelitis), CFS (Chronic Fatigue Syndrome) or FM (Fibromyalgia), their families and loved ones. The Massachusetts ME/CFS & FM Association works to educate health-care providers and the general public regarding these severely-disabling physical illnesses. We also support patients and their families and advocate for more effective treatment and research.
- Last Updated: 20 July 2019 20 July 2019
Support the MassMECFS Half Marathon Team!
Leah (your Association President) and her friends, Liz and Holly, are running the Boston Athletic Association Half Marathon on Sunday, October 13th, 2019 as a fundraiser for the Massachusetts ME/CFS & FM Association. Please support our team and give now! Your donations enable our work to improve health care and support services for people affected by ME/CFS in Massachusetts.
Are you a healthy ally who likes to run? Join our team! You'll get camaraderie, training runs along the Charles River, and a free T-shirt. You can register for the BAA Half Marathon here. Then use the Contact Us form to let us know.
Notice about names
The Massachusetts ME/CFS & FM Association would like to clarify the use of the various acronyms for Chronic Fatigue Syndrome (CFS), Chronic Fatigue & Immune Dysfunction Syndrome (CFIDS) and Myalgic Encephalomyelitis (ME) on this site. When we generate our own articles on the illness, we will refer to it as ME/CFS, the term now generally used in the United States. When we are reporting on someone else’s report, we will use the term they use. The National Institutes of Health (NIH) and other federal agencies, including the CDC, are currently using ME/CFS.
Massachusetts ME/CFS & FM Association changed its name in July, 2018, to reflect this consensus.