International ME Awareness Day

ME/CFS is a chronic, complex, neuroimmune disease that profoundly limits the health and productivity of patients. There is no cure, nor are there any FDA-approved drugs or treatments. Symptoms can […]

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 […]

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 […]

In Review: A Year of COVID-19 in the U.S.

This year the one-year anniversary of the first confirmed case of COVID-19 in the United States. It’s difficult to overstate the impact the COVID-19 pandemic has had on the world […]

You helped secure $1.15 billion for research!

This is our biggest victory, yet! Earlier this month, Solve M.E. led the charge for federally funded research into Long-COVID and myalgic encephalomyelitis (ME) — previously known as chronic fatigue […]

November is National Family Caregivers Month


November is National Family Caregivers Month, offering an opportunity to acknowledge the vital contributions made by family caregivers everywhere. In the ME/CFS community, we know the difference a loving caregiver […]