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.

Invisible Disabilities: Long COVID and Other Post-Infectious Chronic Illnesses -- Videos

 

This program was presented on September 15th, 2021, by the Health and Disability Partnership at the Massachusetts Department of Public Health, with the Massachusetts ME/CFS & FM Association.

View the videos for this event.

Imagine getting sick with a common cold or flu, or even an insect bite, and then never getting better. We present a diverse panel of people with post-infectious chronic illnesses, including Long COVID and Post-Lyme Disease, joined by a person with ME/CFS. Their personal stories are followed by a presentation from the former Medical Director of the Bureau of Infectious Disease and Laboratory Sciences, at the Massachusetts Department of Public Health: Alfred DeMaria, M.D. addresses the similarities between Long COVID, Post-Lyme, and ME/CFS.


 

Job Posting

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Advances in our Understanding of ME/CFS and the Effects of Long COVID

Announcing Our 2021 Annual Meeting

Annual Event Flyer 2021. Advances in our Understanding of ME/CFS and the Effects of Long COVID with NIH Researchers, Saturday, October 23 from 12:30 pm to 4 pm.

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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.