
Long Covid Alliance, Solve M.E. Secure $77k CDC Foundation Grant to Form New Patient Advocacy Coalition
Today, Long COVID Alliance proudly announced it will begin establishing a new Infection Associated Chronic

Today, Long COVID Alliance proudly announced it will begin establishing a new Infection Associated Chronic

The 2nd International ME/CFS Meeting at Charité Fatigue Center was held in Berlin on May

This year, Solve is beginning one of our most ambitious advocacy projects to date —

On May 11, as the Biden administration ended the Public Health Emergency for COVID-19, Congresswoman

To mark World ME Day on May 12, 2023, the World ME Alliance and its

Through our Ramsay Research Grant Program, Solve M.E. invests in research studies into ME/CFS, Long

Many individuals who have had COVID-19 experience long-term symptoms that have a major impact on

In 2019, the National Institutes of Health (NIH) National Advisory Neurological Disorders and Stroke (NANDS)

The US ME/CFS Clinician Coalition has published a consensus letter asking doctors to consider ME/CFS

Solve M.E. funded Dr. David M. Systrom at Brigham and Women’s Hospital in 2017 to

As Advocacy Week in Washington, DC drew to a close last week, Solve M.E. honored

A National Academies of Sciences, Engineering, and Medicine (NASEM) committee will conduct a series of