Introducing Solve’s New CEO Kristin Jacobson

john-nicols

Dear friends, It is with great enthusiasm that I announce that Kristin Jacobson, a fierce patient advocate and member of Solve’s Board of Directors, will lead our organization as our […]

Patient advocate by choice: Solve M.E.’s Oved Amitay

This article by Charlotte Kilpatrick  originally appeared on VaccineNation.org. Although the World Vaccine Congress West Coast is a few months away, we and our speakers are already gearing up and preparing a […]

Solve Appropriations Efforts Are Going Strong!

Last month, we shared big appropriations wins for our ME/CFS and Long Covid community members via the FY24 Department of Defense Appropriations Report from the House of Representatives, which included […]

Big Appropriations Wins for MECFS & Long Covid

Congressionally Directed Medical Research Programs (CDMRP) provide funding to support therapeutic research related to medical threats, and treatments for service members in current and future battlefield settings. In recent years, […]

Solve Honors Dr. Peter Rowe

As Advocacy Week in Washington, DC drew to a close last week, Solve M.E. honored Dr. Peter Rowe for his work as a medical provider, researcher, educator, and advocate for […]

Effects of Long Covid and ME/CFS on Sleep

Many individuals who have had COVID-19 experience long-term symptoms that have a major impact on their lives. One of the most common symptoms is sleep disturbance. After more than six […]

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