Researching ME/CFS: highlight notice The Medical Research Council (MRC) invites applications from researchers that address 1 or more of the research areas identified by the ME/CFS Priority Setting Partnership…
Researchers need to increase study sizes and apply strict diagnostic criteria Polish researchers report that the difficulties with diagnosing ME/CFS and ensuring all research participants have the same condition,…
Hidden from Sight: Why the complexity of ME/CFS needs to be recognised by policy makers, by Tomruk Ustunkaya and Richard Machin, by People, Place and Policy Vol 15, #2, pp. 91-99, November…
mapMECFS – an interactive data portal … providing access to research results across many biological disciplines from studies that are focused on advancing our understanding of Myalgic Encephalomyelitis / Chronic…
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: when suffering is multiplied, by Anthony L Komaroff in Healthcare 2021, 9(7), 919 [doi.org/10.3390/healthcare9070919] 20 July 2021 (This article belongs to the Special Issue ME/CFS – the Severely…
ME Research UK blog post: All in your head? Brain research in ME/CFS, 8 February 2021 Following last week’s introduction to the brain, here is an overview of some…
Potential causal factors of CFS/ME: a concise and systematic scoping review of factors researched, by in Journal of Translional Medicine vol 18, no: 484 (2020) 14 December 2020 Review…
European Parliament Press Release: Myalgic Encephalomyelitis: MEPs call for more funds for research into complex illness 18 June 2020 An estimate of 2 million Europeans affected by the disease ME/CFS…
European ME Coalition Press Release: Scientists call for more European research on ME/CFS, 10 June 2020 More than one hundred scientists have signed an open letter calling for more…
The concept of ‘illness without disease’ impedes understanding of chronic fatigue syndrome: a response to Sharpe and Greco, by Steven Lubet, David Tuller in BMJ Medical Humanities. Published Online First:…