Solve M.E Kicks Off Advocacy Month Highlighting Long Covid’s Widespread Impact, Spotlight on ME/CFS
Advocacy Month 2022 focuses on connecting people with ME/CFS, Long Covid, and other related illnesses—brings together scientists, clinicians, and caregivers to educate Congress and the world As the prevalence and […]
After Vaccination, Health of People with ME/CFS More Likely to Worsen Compared to Controls
In survey, 19% of people with ME/CFS said health worsened after vaccination compared to 4% reported by controls. A recent survey conducted by our You + ME Registry found that the health […]
The Path to Diagnostics for ME/CFS: Can Long Covid Pave a Short-Cut?
By Oved Amitay, President and CEO, Solve M.E. It is often said that there are no biomarkers for ME/CFS. In fact, a number of objective measurable biological differences between people […]
Solve M.E., Long COVID Alliance highlighted in U.S. News & World Report
In her U.S. News & World Report article, “In Long COVID, Advocates Battling Chronic Fatigue Syndrome See Allies, Hope,” journalist Chelsea Cirruzzo examines the ME/CFS and Long COVID connection, and how the […]
Ramsay Grant Program 2021 RFA is Open!
Solve M.E. will accept applications to study ME/CFS and Long Covid from February 22 – April 30, 2021 Through the Ramsay Program, Solve M.E. invests in research studies in […]
NIH launches database to track neurological symptoms associated with COVID-19
A new database will collect information from clinicians about COVID-19-related neurological symptoms, complications, and outcomes as well as COVID-19 effects on pre-existing neurological conditions. The COVID-19 Neuro Databank/Biobank (NeuroCOVID), which […]
