Solve M.E.’s Appropriations Efforts for 2024
At Solve M.E., our mission is to drive research and advocacy efforts for Myalgic Encephalomyelitis/Chronic
June 6, 2024
At Solve M.E., our mission is to drive research and advocacy efforts for Myalgic Encephalomyelitis/Chronic
The National Academies of Sciences, Engineering, and Medicine (NASEM), a nongovernmental institution that advises federal
In an effort to move the ME/CFS field toward translational studies and clinical trials, the
In the wake of the Long Covid pandemic, the need for empowered patient advocates and
In Cort Johnson’s latest piece for Health Rising, experts confirm that the fastest change for
Solve community member Rebecca Groble Hull successfully advocated for Evanston, Illinois Mayor Daniel Bliss to
May 12 is World ME Day! This date coincides with the birthday of Florence Nightingale
Dr. Sonya Marshall-Gradisnik and her team have been developing a new way to treat patients
Solve President & CEO and World ME Alliance co-chair Emily Taylor will be among the
Solve Advocacy Efforts Yield Another Victory! CDMRP Program at Department of Defense Announces $13.1M Grant for
In honor and recognition of May as ME Awareness Month, Solve is launching our inaugural
Solve M.E. is pleased to announce that Emily Taylor, Vice President of Advocacy and Engagement,