Chronic Illnesses in Women: ME/CFS and Migraine

Online

Join us for this event in which ME/CFS & migraine comorbid communities collaborate to bring together patients, researchers, and doctors to discuss ME/CFS, migraine disorders, and their impact on women's […]

Implications of ME/CFS Case Definitions for Long Covid

Online

Our friends at the U.S. Action Working Group are hosting Dr. Leonard Jason, Professor of Psychology DePaul University, for a special webinar event. Leonard Jason’s talk will cover the content […]

ME/CFS: NO problem?

Online

Nitric oxide (NO) – a gas produced by cells lining the blood vessels (endothelial cells) – helps to promote the widening of blood vessels (vasodilation) and is involved in the […]

Long Covid: Research, Policy and Economic Impact (Session II)

Online

Solve Long Covid Initiative, in partnership with the Global Interdependence Center, is conducting a year-long webinar and conference series exploring the pandemic’s long-term healthcare, policy, and economic impact, specifically the […]

CDMRP for ME/CFS: Navigating the Grant Application Process

The FY22 Defense Appropriation provides funding to support therapeutic research related to medical threats, and treatments for Service Members in current and future battlefield settings. The managing agent for the […]

Advocacy Month Kickoff

Online

We are kicking off Advocacy Month with a keynote address by disability advocate Jessica Kellgren-Fozard and a discussion about the importance of sharing our stories and raising our voices to […]

Remote Congressional Meeting Training

Online

Join the Solve M.E. Advocacy team for a training session outlining best practices for your congressional meetings! Register here.

House Action Day

Online

Participants who register to participate in meetings with their elected officials will receive personalized meeting links via email or the advocacy portal. Register is closed, but advocates wishing to participate […]

House Action Day 2

Online

Participants who register to participate in meetings with their elected officials will receive personalized meeting links via email or the advocacy portal. Register is closed, but advocates wishing to participate […]

World ME Day

Solve M.E. is proud to be a partner in the first-ever World ME Day, May 12, 2022. We're joining ME/CFS organizations around the world to campaign together and raise awareness […]

World Premiere: Long Haul Voices

In honor of World ME Day, Solve M.E. is releasing the first episode of the series Long Haul Voices: Living with Long Covid and ME/CFS worldwide. Long Haul Voices seeks […]

Long COVID & Fatiguing Illness Recovery Program ECHO

Online

History of ME/CFS Lucinda Bateman, MD Medical Director, Provider, & Research expert in the diagnosis and treatment of ME/CFS. Founder and Chief Medical Officer of the Bateman Horne Center of […]

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