Rainbow at shoreline

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.

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Thank you for donating to the Massachussetts ME/CFS & FM Association. Your contributions are greatly appreciated and enable the Association to provide patient services, public and health care provider education, advocacy and outreach. Monthly giving sustains our on-going support group programs.

Please fill out the information in the form below. If you choose to pay online, you may use your existing PayPal account or pay as a guest using your credit card. If you prefer, you can mail a check to:

Massachusetts ME/CFS & FM Association
P.O. BOX 690305
QUINCY, MA 02269-0305

Our EIN/Tax ID: 04-3014644

Contribution Amount

Angel - $ 1,000.00

Patron - $ 500.00

Benefactor - $ 300.00

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Contributor - $ 50.00

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Members receive free admission to our events and receive our email newsletter, in addition to supporting our efforts in patient services, education and advocacy.

The Massachusetts ME/CFS & FM Association is a volunteer, patient-centered organization. All of our income is used to provide essential services. We thank you for your support.

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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.