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 […]
Meet the new members of the Solve M.E. Community Advisory Council
2020-2022 Community Advisory Council Announced Solve M.E. is pleased to announce the inaugural 2020-2022 class of the Community Advisory Council (CAC). Due to overwhelming response to the call for nominations, […]
Advocacy Success! Florida Members of Congress Take Action for ME/CFS
Florida Members of Congress Take Action for ME/CFS Solve M.E. teamed up with local Florida advocates to launch a lightning advocacy action with huge success this week. Congressmen Gus Bilirakis […]
Stunning Findings of New Pediatric ME/CFS Prevalence Study
7-Year Pediatric ME/CFS Prevalence Study Publishes Stunning Findings Last week, the journal Child & Youth Care Forum published the results of a seven-year ME/CFS prevalence study that screened more than 10,000 […]
Big News in ME/CFS Research Funding
CDMRP Funding Announcement Comes Just 24 Days After Congress Opens Potential $350 Million to ME/CFS Researchers ME/CFS researchers can compete for 5 new funding streams and over 100 awards, up […]
Victory! Six Major Federal Wins for ME/CFS
Dear Friends, Throughout 2019, I reported on our advocacy gains for ME/CFS. Thank you for standing with me and our advocacy partners during a particularly turbulent year while we fought […]
Solve M.E. at the Patient-Centered Outcomes Research Institute (PCORI) Annual Meeting in Washington, D.C.
Allison Ramiller (left) before attending the breakout session Patient Perspective: Learnings and Strategies for Partnership in Research (right) that featured PCORI patient partners Sonya Ballentine and Martie Carnie, Al Richmond from Community-Campus Partnerships for […]
Dr. Sadie Whittaker on the NANDS Working Group’s Strategic, Coordinated Approach to ME/CFS
Within any large organization is a system of operating that is best navigated by those who work within it. That’s why the ME/CFS community is lucky to have among its […]
NIH: Genetic explanation uncovered with links to ME/CFS symptoms
Previously unexplained symptoms found associated with multiple copies of a single gene. Big news out of the National Institutes of Health (NIH) today as the scientists at the National Institute […]
