Watch Now! The Congressional Roundtable on Women’s Chronic Illness During a Pandemic
Watch now! The Congressional Roundtable on Women’s Chronic Illness During a Pandemic Last week, as part of our collaboration with the Congressional Bipartisan Women’s Caucus, Miles for Migraine, and the […]
ME/CFS and COVID-19 Long-Haulers: Read Our Op-Ed in The Guardian
Solve M.E. Chief Executive Officer Oved Amitay and Solve M.E. Research Advisory Council Member Dr. Anthony L. Komaroff (Professor of Medicine at Harvard Medical School and Senior Physician at Brigham […]
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 […]
Together, We’re Sponsoring an Historic ME/CFS Legislation!
Four Years of Advocacy has paid off! We’re Proud to have Authored and Initiated the First Ever Legislation for ME/CFS Research Funding, H.R. 7057, The Understanding COVID-19 Subsets and ME/CFS Act […]
Senate Advocacy Action: $60m for ME/CFS Research
Tell Your Senator to SUPPORT INCREASED FUNDING FOR POST-VIRAL-DISEASE RESEARCH INTO ME/CFS! Thanks to your hard work during ME/CFS Advocacy Week, the U.S. Senate is currently circulating our request to include […]
Solve M.E. Funded Study Shows Evidence of Pathogen-driven Connection to Energy Production Problems in ME/CFS
Findings from International Research Group Published in ImmunoHorizons Show HHV-6 Connection to Energy Production Problems in ME/CFS In 2016, Bhupesh Prusty, PhD, a scientist at Julius Maximilians University of Würzburg in Germany, […]
ME/CFS Advocacy Day 2020 Was the Biggest Ever! Help Us Say Thank You
251 Meetings – That’s 47% of Congress! Thanks to the hard work of our advocacy community, Solve ME/CFS Advocacy Day was a wild success! Across the country you called for […]
ME/CFS Advocacy Week Continues: Can You Hear M.E. Now?
Can you hear M.E. Now? Call Congress Today! We connected with over 47% of congress yesterday. But we’re not done yet! Today we’re focusing on phone calls to […]
Watch now! The 2020 EmPOWER M.E. Roundtable: How to Navigate Disability Insurance with ME/CFS!
To watch the recording of the 2020 EmPOWER M.E. Roundtable: How to Navigate Disability Insurance with ME/CFS, visit our YouTube channel or click the video below. You can view and download the slides […]
We’re not done, yet! ME/CFS Advocacy Week Ends April 26!
Looking for a way to make your social media account stand out? We’ve created ME/CFS GIPHY stickers to use on Instagram stories and Twitter, which we think is really easy […]
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 […]
Solve ME/CFS Advocacy Week ONLINE Schedule is here!
Full Schedule of ME/CFS Advocacy Week Online Events and Actions now available This year our ME/CFS Advocacy Week will take place online from April 19 to April 26, 2020. Stay home, […]
