Victory! Six Major Federal Wins for ME/CFS
Dear Friends, Throughout 2019, I reported on our advocacy gains for ME/CFS. Thank you for
January 14, 2020
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.
Thanks to another strong turnout from the ME/CFS advocacy community, 14 Senators and 28 Congressional
Today, without any prior notice to committee members of the public, the Department of Health
May 12 is ME/CFS Awareness Day May 12, 2018 marks the 198th birthday of Florence
This week, Solve M.E. staff and Board of Directors traveled to Washington D.C. and got
This week, the Trump administration released its fiscal year 2019 budget proposal. Ideally, this proposed
Lucinda Bateman, MD, specializes in the diagnosis and management of unexplained chronic fatigue, ME/CFS and fibromyalgia. Having served on the IOM committee that produced the recent report, Beyond ME/CFS: Redefining an Illness, she brings an in-depth, well-informed opinion to the conversation surrounding the IOM report on ME/CFS, the new diagnostic criteria and the proposed name, Systemic Exertion Intolerance Disease (SEID). READ MORE…