A future beyond ME/CFS
Millions of people live with ME/CFS, many confined to their homes or beds for decades. Research is our best hope, and your donation helps make it possible. Because our administrative costs are already covered, 100% of every donation goes directly to research.
Together for ME/CFS research
Even with a monthly donation of €5, you can help those affected in the long term and support vital research.
IMAGINE GETTING THE FLU. AND NEVER GETTING YOUR LIFE BACK.
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a serious, life-altering disease that can leave people unable to work, study, care for themselves, or even leave their bed. It affects people of all ages and often develops after an infection.
Based on a prevalence of approximately 0.4% to 0.8%, an estimated 32 to 65 million people worldwide are living with ME/CFS. Despite its enormous impact, there are still no approved treatments, and the disease remains dramatically underfunded and underresearched.
Life with ME/CFS
See where your donations go
"We are investigating innate and adaptive immunity to viruses and researching the pathogenesis of diseases."
Prof. Akiko Iwasaki
Our mission: to provide all people affected by ME/CFS with the support they deserve
– and to find a cure.
Keep up to date with the foundation
WE&ME Award: Unraveling Biological Differences in ME/CFS
New ME/CFS Funding from Private Sources Starting in 2027
ME/CFS in Austria: Four former health ministers support a petition calling for the full implementation of the national PAIS action plan
Together, we are building a better future for people with ME/CFS.
Together, we can advance research, accelerate progress, and bring effective treatments and, ultimately, a cure closer. Patients are at the heart of everything we do.
Step by step.
Join our cause
Every donation, no matter the size, fuels critical research and brings us one step closer to a cure.