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
February 14, 2020
Florida Members of Congress Take Action for ME/CFS Solve M.E. teamed up with local Florida
7-Year Pediatric ME/CFS Prevalence Study Publishes Stunning Findings Last week, the journal Child & Youth Care
Researchers from DePaul University and Lurie Children’s Hospital screen 10K children, teens in NIH-funded study
CDMRP Funding Announcement Comes Just 24 Days After Congress Opens Potential $350 Million to ME/CFS
Dear Friends, Throughout 2019, I reported on our advocacy gains for ME/CFS. Thank you for
Last week we announced the research teams funded by Solve M.E.’s 2019 Ramsay Grant Program. The Program is designed to attract
Solve M.E. is proud to announce that our inaugural 2020 Community Advisory Council (CAC) will join the
Allison Ramiller (left) before attending the breakout session Patient Perspective: Learnings and Strategies for Partnership in
The Covering Life-saving Investigations Needed in Cancer and Other Life-threatening Conditions through Timely use of
What you Need to Know: The Senate Appropriations Committee included our ME/CFS Advocacy Day request for Defense.
Within any large organization is a system of operating that is best navigated by those
By: Ann Innes This article originally appeared in ME Association I’m Ann Innes, consultant welfare rights adviser