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.

This conference, sponsored by the International Association for CFS/ME, brought together over 200 clinicians and researchers from 20 countries. The conference was held September 22-25 in Ottawa, Ontario, Canada.

Dr. Charles Lapp highlights what he found to be most important and interesting of the presentations. Read Dr. Lapp's summary.

Dr. Rosamund Vallings presents a brief summary of every paper presented in the plenary sessions, with a topic index. Read Dr. Vallings' summary.

Dr. Anthony Komaroff presented highlights of the conference from his perspective.  Read a summary.

View videos of the 13 presentations given on the Patient Day.

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.