By David Tuller, DrPH
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Medical education in the US has not generally included accurate information about ME/CFS. If medical students learned anything at all about the illness, it is most likely the view that it should be regarded as psychosomatic and that exercise and psychotherapy should be prescribed. The same is true for residencies and fellowships, and for continuing medical education (CME), which physicians must pursue to maintain their licenses.
The Open Medicine Foundation (OMF), whose work was featured in Inside Philanthropy in August, has recently partnered with Lucinda Bateman, a well-known ME/CFS specialist in Salt Lake City, Utah, to expands efforts to promote better medical education. According to OMF, the Medical Education Resource Center (MERC) at Bateman Home Center “is dedicated to educating healthcare professionals to expand their awareness, knowledge, diagnostic, and treatment ability for the benefit of those with multi-system Chronic Complex Diseases (msCCD) such as ME/CFS, FM, post-viral syndromes, and related comorbidities.”
Bateman is the founder and medical director of the BHC and education director of the MERC. Her own medical training, at Johns Hopkins in the late 1980s, coincided with the emergence of “chronic fatigue syndrome” as a clinical entity, so all her learning about the illness essentially occurred on-the-job. We recently spoke by zoom about the lack of medical education in this domain and related issues. (We had some technical issues—specifically, a wobbly signal—which turned out to be because I was having poor reception in one part of my flat. So a couple of sections are glitchy, and I don’t know how to edit them out.)
(Originally posted on Virology Blog.)