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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.

Be a Member

Thank you for becoming a member and your continued support. Your tax-deductible contribution will allow the Association to provide patient services, public and health care education, and advocacy.

Please fill out the information in the form below. If you wish to pay by check, check the box on this page. If you wish to pay conveniently and securely online using your credit card, you will enter your credit card information via PayPal on the next page.

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Members Receive our Newsletter

The e-newsletter brings you ME/CFS & FM related news including information about events, conferences, lectures, recent articles, new research findings and more. Your email address will be used only for the purpose of sending you news about ME/CFS & FM and other communications from the Massachusetts ME/CFS & FM Association. You may unsubscribe at any time.

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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.