After Vaccination, Health of People with Long Covid More Likely to Improve or Worsen Compared to Controls
In survey, 30% of people with Long Covid said health improved after vaccination and 28% said health worsened, compared to 4% and 7%, respectively, reported by controls December 21, 2021–With […]
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 […]
Solve M.E./UCLA Announce Pilot Funding for ME/CFS Research
Second year of Solve/UCLA partnership September 2021–Solve M.E. is again partnering with the University of California, Los Angeles (UCLA) Iris Cantor Women’s Health Center to fund ME/CFS research through their Annual Health […]
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 […]
Postdoctoral Fellowship to Foster Trans-Atlantic ME/CFS Research Collaboration
Solve ME partners with Action for ME on two-year research fellowship focused on identifying molecular drivers of ME/CFS May 2021–Solve M.E. and Action for ME are excited to share that […]
You + ME Registry Partners with Emerge Australia to Open Australian ME/CFS Registry
World’s largest ME/CFS data repository expands to Australia in initiative to open worldwide. April 2021 — We are pleased to share that the You + ME Registry and Biobank, […]
You + ME Registry Reaches New Milestone: 2,000 Registrations
We’re thrilled to announce that enrollment in the You + ME Registry has reached 2,000 participants! This would not have been possible without the support of this amazing community. Together, […]
You + ME has joined the world’s biggest study of ME/CFS
We are excited to announce we’re partnering with our UK colleagues Action for ME and Professor Chris Ponting of the Medical Research Council Human Genetics Unit at the University of […]
Solve M.E. Advocacy Director Emily Taylor Answers All Your Questions About H.R. 7057 in this Q&A and Town Hall!
Hi Solve M.E. Community! In case we haven’t met before, my name is Emily Taylor, and I’m the Director of Advocacy and Community Relations at Solve M.E. Over the […]
Your Advocacy In Action Part 1: ME/CFS Senate Resolution Introduced
Your ME/CFS Advocacy Week actions continue to make a difference! Senator Ed Markey, a longtime champion for people with ME/CFS and people with disabilities, introduced S. Res 633, Supporting the […]
The Solve M.E. Spring 2020 Chronicle is available online now!
The electronic version of our flagship research and advocacy journal, The Chronicle, has arrived! It answers the question “Could Improved Testing for Orthostatic Intolerance Lead to Better Care?” and includes a look […]
Leveraging the You + M.E. Registry to Study COVID-19
While COVID-19 has changed where we work, it has not stopped how hard we work on behalf of the ME/CFS community. Following several months of development, user testing and partnership […]
