Massachusetts ME/CFS & FM Association

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history

The Massachusetts ME/CFS & FM Association is a 501c3 non-profit organization founded in 1985. They support patients with ME/CFS and Fibromyalgia and their families and advocate for more effective treatment and research, as well as, work to educate health-care providers and the general public regarding these often severely-disabling physical illnesses.[1] It is one of the oldest voluntary associations in the United States for patients with Myalgic Encephalomyelitis (ME), Chronic Fatigue Syndrome (CFS or CFIDS) and Fibromyalgia (FM). Bonnie Gorman, RN founded the group.[2]

Resources available throught their website are: Downloadable copy of IACFS/ME Primer - 2014 Edition The Massachusetts CFIDS/ME & FM Disability Handbook; a Newsletter; a designated phone line for patient's questions; a Support Group Leaders Operational Manual; and links to educational videos and websites.

The association frequently works with the Chronic Fatigue Syndrome Advisory Committee, the committee that advises Health and Human Services regarding ME/CFS, often having a member of the Massachusetts ME/CFS & FM Association as a committee member or by providing testimony.

Name change[edit | edit source]

"Legally named Massachusetts C. F. I. D. S. Association, the organization has updated its “doing business as” name periodically, adding Fibromyalgia (“& FM”) in the early 1990s, changing “CFIDS” to “CFIDS/ME” in 2008, and “CFIDS/ME” to “ME/CFS” in 2018."[3]

Contact info[edit | edit source]

P.O. Box 690305
Quincy, MA 02269
Info Line: 617-471-5559

Talks and interviews[edit | edit source]

Online presence[edit | edit source]

See also[edit | edit source]

References[edit | edit source]