Solve M.E. serves as a catalyst for critical research into diagnostics, treatments, and cures for ME/CFS, Long Covid, and other post-infection diseases. Through their work with scientific, medical, and pharmaceutical communities, advocacy with government agencies, and alliances with patient groups around the world, they strive to make these “long haul” diseases widely understood, diagnosable, and treatable.
To help researchers identify causes and treatments, Solve M.E. founded the You + ME Registry, a collection of patient-reported data + biological samples from people living with ME/CFS, Long Covid, and healthy volunteers. This large, rich dataset will help researchers around the world uncover treatments and a cure.
Informed patients are empowered patients. Solve M.E. has compiled patient & caregiver resources to help people suffering through these difficult health journeys.
Check out their guides to symptom tracking, finding a doctor, and securing a personal support system.
Solve M.E. is the proud host of the annual Advocacy Month, when patients, scientists, clinicians and caregivers meet with Congress to share their unique stories and call for action. They also provide tools for chronic disease advocates to find current actions, local campaigns, legislative efforts to make a difference in the lives of individuals suffering from post-infection diseases.
Learn more and join their efforts by clicking the link below.
