Lived Experience Taskforce Applications Now Open!
We are thrilled to announce that we are now accepting applications for our Lived Experience Task Force (LET). We are actively seeking community partners who are: Partners affected by myalgic […]
Exciting Changes at Solve!
Dear Friend, I joined Solve as CEO in 2020, when we embarked on a strategy that connected ME/CFS with Long Covid, which was just emerging at that time as a […]
Solve M.E. Ramsay Grant Program Updates Empower Patients
Through our Ramsay Research Grant Program, Solve M.E. invests in research studies into ME/CFS, Long Covid, and other post-infection diseases with a particular emphasis on engaging young investigators and propelling […]
Thank you! Your support fuels big plans!
What a way to close out 2022! We are so grateful for your generosity throughout the year, and especially during our recent year-end campaign. Thank you for helping us surpass […]
Solve M.E. Engages New Community Partners Through Lived Experience Taskforce (LET)
Building on our commitment to centering the crucial voices from our community in the leadership and decision-making at Solve M.E., we are transforming our Community Advisory Council (2019 – 2022) […]
