Meet Our 2021 Advocacy Week Partners

Advocacy Week Welcomes Partners from Long COVID and Rare Disease Communities The 5th Annual Solve M.E. Advocacy Week will take place from Sunday, April 18, 2021 to Saturday, April 24, 2021. This year, “ME/CFS & Long COVID Advocacy Day” welcomes our new partners from the Long COVID Alliance and the EveryLife Foundation for Rare Diseases […]

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Why Long-COVID?

The Long COVID Alliance is a coalition of different complex, chronic, disease organizations who have come together to pool our resources. Each group is bringing along their expertise as well as their connections with patient advocates, disease experts, drug developers, and more. The top three symptoms of Long COVID are the top three symptoms of […]

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Ramsay Grant Program 2021 RFA is Open!

Solve M.E. will accept applications to study ME/CFS and Long-Covid from February 22 – April 30, 2021 Through the Ramsay Program, Solve M.E. invests in research studies in ME/CFS or long-COVID with a particular emphasis on engaging young investigators and researchers new to the field. Collaborative proposals (involving 2 or more research groups) and studies […]

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NIH launches database to track neurological symptoms associated with COVID-19

A new database will collect information from clinicians about COVID-19-related neurological symptoms, complications, and outcomes as well as COVID-19 effects on pre-existing neurological conditions. The COVID-19 Neuro Databank/Biobank (NeuroCOVID), which was created and will be maintained by NYU Langone Health, New York City, will be a resource of clinical information as well as biospecimens from […]

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