Announcing the Solve Long Covid Initiative
Dear friend, With an onslaught of Covid-19 cases from the Omicron variant looming, identifying treatments for Long Covid has become even more imperative. Since the beginning of the pandemic, Solve […]
After Vaccination, Health of People with ME/CFS More Likely to Worsen Compared to Controls
In survey, 19% of people with ME/CFS said health worsened after vaccination compared to 4% reported by controls. A recent survey conducted by our You + ME Registry found that the health […]
Our Strategic Commitment, Critical Initiatives and Growing Team
Dear Solve community members, As summer evolves into autumn, I write to share news about our continuing evolution and growth. In the last several months, we deepened our strategic commitment […]
Introducing Solve M.E. Advocacy Month!
We are so excited to announce that next year’s Solve M.E. 2022 Advocacy Week will be bigger and better than ever — and will now be Advocacy Month! For Advocacy […]
The Clinical Treatment Act is Delivering Results
After three years of advocacy, Solve M.E. scored a concrete legislative victory with the passage of The Clinical Treatment Act. This covers clinical trial costs for qualifying 74.8M Medicaid participants — […]
A Win for All of Us
Now that our government has narrowly avoided a shutdown, I’d love to share some insights about next year’s federal budget and how we are helping to shape it today. A […]
Solve M.E./UCLA Announce Pilot Funding for ME/CFS Research
Second year of Solve/UCLA partnership September 2021–Solve M.E. is again partnering with the University of California, Los Angeles (UCLA) Iris Cantor Women’s Health Center to fund ME/CFS research through their Annual Health […]
Measures of General Pediatric Quality of Life
Child Health Questionnaire (CHQ), DISABKIDS Chronic Generic Measure (DCGM), KINDL-R, Pediatric Quality of Life Inventory (PedsQL) 4.0 Generic Core Scales, and Quality of My Life Questionnaire (QoML) Authors: STEPHANIE E. […]
ME/CFS Symptom Checklist
Myalgic encephalomyelitis, also referred to as chronic fatigue syndrome (ME/CFS) is a complex and chronic disease that can have a serious impact on one’s quality of life. Patients can experience […]
Advocacy Director Emily Taylor On Sharing the Success of ME/CFS Advocacy Week
During Solve M.E.’s ME/CFS Advocacy Day 2018, 102 people with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and their loved ones joined us in the largest Capitol Hill action for the disease […]
2021 Advocacy Week Report: Our Biggest Ever — You Made It Happen!
The 5th Annual ME/CFS Advocacy Week hosted by the Solve ME/CFS Initiative (Solve M.E.). Advocacy Week took place from Sunday, April 18, 2021 to Saturday, April 24, 2021. This year, […]
Solve M.E. Partners with UCLA on ME/CFS Research on Brain Stimulation
We’re excited to announce that Solve M.E. has partnered with the University of California, Los Angeles (UCLA) Iris Cantor Women’s Health Center to expand ME/CFS research through their Annual Health Pilot Program—the first […]
