The TREAT Long Covid Act is Back!
On May 11, as the Biden administration ended the Public Health Emergency for COVID-19, Congresswoman Ayanna Pressley (MA-07), alongside Representatives Don Beyer (VA-08) and Lisa Blunt Rochester (D-DE), reintroduced the […]
Solve M.E. Ramsay Grant Program Updates Empower Patients
Through our Ramsay Research Grant Program, Solve M.E. invests in research studies into ME/CFS, Long Covid, and other post-infection diseases with a particular emphasis on engaging young investigators and propelling […]
NIH ME/CFS Telebriefing
NIH’s next ME/CFS Advocacy Call will be held on May 1, 2023 from 12:00 – 1:00 pm ET. The webinar will include updates from NIH on ME/CFS-related research activities and […]
Understand, Diagnose, Treat: ME/CFS Conference 2023, hosted by Charité Fatigue Center
2nd International Meeting of the CFC – Charité Fatigue Center ME/CFS Conference 2023 – Understand, Diagnose, Treat Date: Thursday, May 11, 2023, 9 a.m. to 6 p.m. and Friday, May […]
Long Covid After One Year: The Good News & the Bad News
“Mild Covid-19 disease does not lead to serious or chronic long term morbidity in the vast majority of patients” was the headline in most media coverage of an important study […]
An Evolving Landscape: Long Covid’s Impact on ME/CFS
It’s hard to believe that we’re well into the third year of the COVID-19 pandemic, which coincidentally overlaps with my time as Solve M.E.’s President and CEO. In this time […]
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 […]
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) […]
Solve Ramsay Grant Scientists Among Those Awarded Nearly $5 Million for Biomedical Research
This week the Patient-Led Research Collaborative (PLRC) announced $4.8 million in biomedical research awards for Long Covid and associated conditions. Nine research projects in Long Covid, ME/CFS, dysautonomia, and associated […]
Challenges in Ensuring Equity In the Study and Treatment of ME/CFS and Long Covid
Co-presented by Peter Rowe, MD (Professor of Pediatrics, Director, Johns Hopkins Children’s Center Chronic Fatigue Clinic) and Camille Broussard, MD, MPH (Assistant Professor in the Division of Adolescent and Young […]
RECOVER Study of Paxlovid to Treat Long Covid Begins January 2023, Has Implications for ME/CFS
The National Institutes of Health (NIH) announced that the use of Paxlovid to treat Long Covid will be the first treatment to be studied by its $1 billion RECOVER Initiative. […]
Fiona Lowenstein, Dona Kim Murphey and The Long Covid Survival Guide
For people living with Long Covid, navigating the uncharted territory of this new chronic illness can be challenging. With over two hundred unique symptoms, and with doctors continuing to work […]
