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 […]
National Institutes of Health Conferences Demonstrate ME/CFS Progress: How Far We’ve Come and How Far We Need to Go
Solve M.E.’s Chief Scientific Officer, Dr. Sadie Whittaker, introducing a clinician panel discussion with Solve M.E. Research Advisory Council members Tony Komaroff (moderator), Dr. Lucinda Bateman, Dr. Susan Levine, Dr. […]
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 […]