ME/CFS RESEARCH ROADMAP WEBINAR SERIES

Tomorrow’s NINDS ME/CFS Research Roadmap webinar at 11AM ET will focus on how ME/CFS impacts the immune system, current research, knowledge gaps, and future research opportunities.   Register here.   […]

Solve’s New CEO Addresses Community

Dear Solve community, It is with excitement and enthusiasm that I take the helm of Solve at such a critical inflection point for the organization and our disease category.  I’m […]

Introducing Solve’s New CEO Kristin Jacobson

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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, […]