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 […]
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 […]