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 […]
Using a Heart Rate Monitor to Prevent Post-Exertional Malaise in ME/CFS & Long Covid
This article was first published on ProHealth.com and is reprinted on SolveME.org with permission of ProHealth and the author Suzan Jackson. Though originally written for individuals with ME/CFS managing PEM, members […]
Guest Blog: How People With Long Covid Can Qualify For Social Security Disability Benefits
Elizabeth Van Arsdall is a recent graduate of Colby College living in Boston and a native of Washington, D.C. Like so many others, Elizabeth has seen firsthand the effects of Covid […]
Solve M.E. CEO Oved Amitay On Potential EBV Vaccine Candidate
Originally published by Solve M.E. CEO Oved Amitay in a LinkedIn post. Very encouraging to learn today that top experts from OPKO Health, Inc. and ModeX Therapeutics Inc team up with Merck to develop Epstein-BarrVirus Vaccine Candidate. […]
CDC Responds to Solve M.E. Comments on Draft Review of Diagnosis and Treatment of ME/CFS
In 2018, the Centers for Disease Control and Prevention (CDC) announced it was soliciting bids to create evidence-based treatment guidelines for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). In 2019, the CDC […]
Kevin Timms, PhD, Joins Ramsay Researchers Class of 2022!
We’re excited to share that Kevin Timms, PhD, is joining our Ramsay Class of 2022! Solve’s Ramsay Research Grant Program attracts new scientists to the field of ME/CFS and Long […]
Watch now! “Long Covid: What Will it Take to Accelerate Therapeutic Progress?”
Solve M.E. and BIO co-hosted a timely and informative event examining the emerging research in Long Covid and the existing body of data in other post-infection diseases such as ME/CFS. […]
FDA to Host Patient-Focused Drug Development Public Meeting for Long Covid
The US Food and Drug Administration (FDA) is hosting a virtual public meeting on Patient-Focused Drug Development for Long Covid on Tuesday, April 25th, 2023, from 10 a.m. to 4:00 p.m. […]
Announcing the 2023 World ME Day Campaign
We’re joining our peer organizations at the World ME Alliance again for World ME Day 2023. This year’s theme focuses on the hallmark symptom of ME/CFS: post-exertional malaise. The goal […]
Letter for Medical Providers on Caring for People with Severe and Very Severe ME/CFS
Are you or a loved one bedbound or homebound as a result of severe or very severe ME/CFS, perhaps following COVID? Do you struggle to do basic activities like taking […]
Join Us For Solve M.E. Advocacy Week!
We are so excited to announce that next year’s Solve M.E. 2023 Advocacy Week will take place both virtually and in person throughout the week of April 17th to April […]
Solve M.E. Engages New Community Partners Through Lived Experience Taskforce (LET)
Building on our commitment to centering the crucial voices from our community in the leadership and decision-making at Solve M.E., we are transforming our Community Advisory Council (2019 – 2022) […]
