The Massachusetts ME/CFS & FM Association, or MassME, provides information, connection, and support to those with ME/CFS, fibromyalgia and, more recently, Long COVID. For forty years MassME has been a leading voice in advocating for knowledge, research, and clinical care.
All funds raised will support our ongoing programs, particularly those that provide direct patient support and counseling. Please donate and help us support those with ME/CFS and Long COVID, and their families.
About ME/CFS and Long COVID
ME/CFS and Long COVID are complex, serious, and debilitating illnesses which affect multiple systems of the body. People living with these illnesses experience profound exhaustion, post-exertional malaise, sleep disorder, autonomic dysfunction, neurological and flu-like symptoms, and cognitive problems such as difficulty thinking, processing, and remembering. Research is ongoing, but there are currently no FDA-approved treatments, and no cure.
