Author Archives: wames
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
Dr Anthony Fauci says that post-covid syndrome “is highly suggestive of” ME
#MEAction blog post: Dr. Anthony Fauci says that post-covid syndrome “is highly suggestive of” Myalgic Encephalomyelitis Blog post extract: Terri asked Dr. Anthony Fauci (Director of the National Institute of Allergy and Infectious Diseases and member of the White … Continue reading
NICE Statement about graded exercise therapy in the context of COVID-19
Statement about graded exercise therapy in the context of COVID-19 NICE is aware of concerns about graded exercise therapy (GET) for people who are recovering from COVID-19. NICE’s guideline on ME/CFS (CG53) was published in 2007, many years before … Continue reading
Altered structural brain networks related to adrenergic/muscarinic receptor autoantibodies in CFS
Altered structural brain networks related to adrenergic/muscarinic receptor autoantibodies in Chronic Fatigue Syndrome, by Hiroyuki Fujii, Wakiro Sato, YukioKimura, Hiroshi Matsuda, Miho Ota, Norihide Maikusa, Fumio Suzuki, Keiko Amano Isu Shin, Takashi Yamamura, Harushi Mori, Noriko Sato in Journal of … Continue reading
Achieving symptom relief in patients with ME by targeting the neuro-immune interface & inducing disease tolerance
Achieving symptom relief in patients with Myalgic encephalomyelitis by targeting the neuro-immune interface and inducing disease tolerance, by Lucie ST Rodriguez, Christian Pou, Lakshmikanth Tadepally, Jingdian Zhang, Constantin Habimana Mugabo, Jun Wang, Jaromir Mikes, Axel Olin, Yang Chen, Joanna Rorbach, … Continue reading
Cardiopulmonary responses to exercise in an individual with ME/CFS during long-term treatment with intravenous saline: a case study
Cardiopulmonary responses to exercise in an individual with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome during long-term treatment with intravenous saline: A case study by Todd E Davenport, Michael K Ward, Staci R Stevens, Jared Stevens, Christopher R Snell, J Mark VanNess, in … Continue reading
A demon on my life – a play about ME
A demon on my life – a play about ME A play written by JB Bruno has been premiered online and is now available to watch on YouTube. “A demon on one’s life. What a ripe metaphor for … Continue reading
