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.

On December 9, the U.S. Senate passed a 1-year extension of Medicare payment rates to physicians. The bill previously was passed by the House of Representatives. President Obama is expected to sign the bill into law.

Without the new law, Medicare payments for services to physicians would have decreased approximately 20%. There has been much speculation, had this been the case, that many doctors would have stopped taking Medicare patients.

Periodic reductions in Medicare payments to doctors occur as the result of an older law that prevents medical payments from increasing more than a certain percentage per year. This older law allows medical payments to increase only in line with cost increases in other sectors of the economy. Medical costs generally increase at a faster rate than other costs. However, Congress has, over the years, permitted payments to doctors to reasonably increase in tandem with other medical costs.

Without this extension, in 2011 a 20% reduction would have gone into effect in order to retroactively offset previous increases in order to meet the requirements of the older law. At this very last moment, Congress acted to prevent the 20% decrease and to maintain current reimbursement levels. For at least another year, patients with Medicare generally should be able to maintain their current access to their physicians.

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.