August 8th is Severe ME Day
Each year on August 8, Severe ME Day, we reflect on the tremendous toll this
August 6, 2021
Each year on August 8, Severe ME Day, we reflect on the tremendous toll this
Myalgic encephalomyelitis, also referred to as chronic fatigue syndrome (ME/CFS) is a complex and chronic
Rep. Jamie Raskin’s landmark legislation, H.R. 7057, The Understanding COVID-19 and ME/CFS Subsets Act, will
Watch now! The Congressional Roundtable on Women’s Chronic Illness During a Pandemic Last week, as
Solve M.E. Chief Executive Officer Oved Amitay and Solve M.E. Research Advisory Council Member Dr.
To watch the recording of the 2020 EmPOWER M.E. Roundtable: How to Navigate Disability Insurance
By: Ann Innes This article originally appeared in ME Association I’m Ann Innes, consultant welfare rights adviser
From ProHealth.com: Using A Heart Rate Monitor to Prevent Post-Exertional Malaise in ME/CFS By Suzan
You + ME is a patient registry and biobank for the ME/CFS community. While Solve M.E.
On Thursday, August 30, Solve M.E.’s Chief Scientific Officer Dr. Sadie Whittaker attended the Center
Guest blogger Michael Ottlinger, PhD, addresses the reasonable accommodations that must be made for students with ME/CFS. Read More…
Often those with ME/CFS experience gastrointestinal symptoms. Biomarkers of these symptoms could help to identify subtypes in ME/CFS. Dr. Armin Aledini is using samples from the SolveCFS BioBank™ to look for auto-antibodies against a range of dietary proteins. In this guest blog post he discusses Celiac disease, which is a commonly misdiagnosed condition with symptoms similar to ME/CFS. READ MORE…
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