- Last Updated: 06 December 2018 06 December 2018
Disability and Social Security with ME/CFS, Interview with Robert Robitaille | ME/CFS Alert Episode 100
Robert Robitaille discusses his personal experience fighting for disability benefits for his daughter, Robie who has ME.
Living with ME/CFS: Robie's Story | ME/CFS Alert Episode 99, August 26, 2018
Robie talks about her daily life with ME.
Llewellyn King talks with members of our Association in his ME/CFS Alert video series, recorded on March 24, 2017.
NEW! In this conversation, Libby tells of her long journey from being bedridden with ME to being able to function, albeit at a reduced level from when she got ill. She says that a series of holistic therapies, including a special diet, have been working for her.
Libby's experience with ME | ME/CFS Alert Episode 90, published on June 1, 2017
The work of the Massachusetts CFIDS/ME & FM Association | Episode 86, published on March 29, 2017
ME/CFS Diagnosis, children with ME, and the medical community with Alan Gurwitt, M.D. (Episode 87), published on April 12, 2017
Children with ME, Being an Advocate and Advice for Parents | ME/CFS Alert Episode 88, published on April 23, 2017
More to come...
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.