Tag Archives: Mary Dimmock
ME/CFS: what every family physician needs to know
Article extract: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: what every family physician needs to know, by Mary Dimmock, Susan Levine, MD, and Terri L. Wilder, MSW in Family Doctor (journal of New York State Academy of Family Physicians) Winter 2018 6:3 pp 23-25 The onset … Continue reading
Help secure the World Health Organisation’s classification of ME & CFS
ME action blog post: Help secure the World Health Organisation’s classification of ME & CFS Important call to action! We need all hands on deck for a simple, but important task. The World Health Organisation (WHO) is reviewing its International … Continue reading
Estimating the disease burden of ME/CFS in the US
Article abstract: At the National Institutes of Health (NIH), burden of disease is an important factor in funding decisions along with such factors as scientific opportunity, the quality of the science, and the interest of researchers. Recent studies have quantified the … Continue reading
US report says there’s (almost) no evidence CBT/GET work in ME/CFS
Health rising blog, by Cort Johnson, 18 August 2016: Federal Report Says There’s (Almost) No Evidence CBT/GET Work in Chronic Fatigue Syndrome (ME/CFS) This has a been good week for advocacy. It’s shown that smart advocacy works. Twice advocates went … Continue reading
Video interview with parent Mary Dimmock about her son and rituximab
Episode 78 of Llewellyn King’s ME/CFS Alert videos interviews Mary Dimmock, whose son has ME and who is receiving RITUXAN (rituximab) treatment privately. (24 mins)
