Author Archives: wames
Plasma proteomic profiling suggests an association between antigen driven clonal B cell expansion & ME/CFS
Plasma proteomic profiling suggests an association between antigen driven clonal B cell expansion and ME/CFS, by Milica Milivojevic, Xiaoyu Che, Lucinda Bateman, Aaron Cheng, Benjamin A Garcia, Mady Hornig, Manuel Huber, Nancy G Klimas,Bohyun Lee, Hyoungjoo Lee, Susan Levine, Jose G … Continue reading
Coronavirus: why are some people experiencing long-term fatigue?
The Conversation blog post: Coronavirus: why are some people experiencing long-term fatigue?, by Prof Frances Williams, 16 July 2020 People who have been seriously unwell and treated on intensive care units can expect to take some months to recover … Continue reading
‘I need to start listening to what my body is telling me’: Does mindfulness-based cognitive therapy help people with CFS?
‘I need to start listening to what my body is telling me.’: Does mindfulness-based cognitive therapy help people with Chronic Fatigue Syndrome? by Bridie O’Dowd & Gemma M Griffith in Human arenas 2020, July 16 [https://doi.org/10.1007/s42087-020-00123-9] Research abstract: Mindfulness-Based Cognitive … Continue reading
Cognitive function declines following orthostatic stress in adults with ME/CFS
Cognitive Function declines following orthostatic stress in adults with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), by C Linda M C van Campen, Peter C Rowe, Freek W A Verheugt, Frans C Visser in Front Neurosci. 2020 Jun 26;14:688. [doi.org/10.3389/fnins.2020.00688] Research … Continue reading
Severe ME in children
Severe ME in children, by Nigel Speight in Healthcare Vol 8, #3 p 211, July 14, 2020 [This article belongs to the Special Issue ME/CFS] Guideline abstract The current problem regarding Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome (ME/CFS) is the … Continue reading
Health Care responsibility & compassion-visiting the housebound patient severely affected by ME/CFS
Health Care responsibility and compassion-visiting the housebound patient severely affected by ME/CFS, by Caroline Kingdon, Dionysius Giotas, Luis Nacul and Eliana Lacerda in Healthcare 2020, 8(3), 197 [doi.org/10.3390/healthcare8030197] [This article belongs to the Special Issue ME/CFS – the Severely and … Continue reading
WAMES Facebook interruption
Apologies, if you follow WAMES on Facebook. We are currently unable to access the site to post. The reason is unclear. Bear with us as we seek a solution. We will continue to post on this blog and twitter.
Environmental accommodations for university students affected by ME/CFS
Environmental accommodations for university students affected by myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), by Lily Chu, Lynn R Fuentes, Olena M Marshall and Arthur A. Mirin in Work pp. 1-12, 2020[DOI: 10.3233/WOR-203176] Research abstract: Background: Today, 24% of college and … Continue reading
Two-Day cardiopulmonary exercise testing in females with a severe grade of ME/CFS: comparison with patients with mild & moderate disease
Two-Day cardiopulmonary exercise testing in females with a severe grade of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: comparison with patients with mild and moderate disease, by C (Linda) MC van Campen, Peter C Rowe and Frans C Visser in Healthcare 2020, 8(3), … Continue reading
“That’s why they don’t believe you, you don’t look sick!”: creating medical credibility & patient visibility for ME/CFS through television
“That’s why they don’t believe you, you don’t look sick!”: creating medical credibility and patient visibility for ME/CFS through television, by Giada Da Ros Article abstract: Since the end of the 20th century, the Myalgic Encephalomyelitis / Chronic Fatigue Syndrome … Continue reading
