Donation subscription

5€ for 5 Things

Advance research – from €5 per month

Be part of a movement: with many small contributions, we can do more biomedical research on ME/CFS and Long COVID – for better diagnostics and effective treatment approaches.

  • If we all give €5, we can raise millions.
  • The hurdle is low – anyone can become part of the solution.
  • Giving research means giving hope.

Donate for
ME/CFS-Research

Joerg Heydecke
Joerg Heydecke
Founder and Managing Director
ME/CFS Research Foundation
"If many patients or their relatives and friends invest €5 per month, we can make lasting progress in ME/CFS research and enable urgently needed therapy studies."
Small gesture. Big impact.

Why €5 a month makes all the difference

ME/CFS has 5 letters. We are entering the 5th year of our commitment in 5 areas of work, in which we want to achieve even more in the future!

When thousands participate, it creates a reliable basis for our commitment to more biomedical ME/CFS and Long COVID research.

01
Funding research
02
Networking of researchers
03
Making progress visible
04
Facts for education
05
Fundraising & Awareness

Our research funding strategy

2026 is a key year for ME/CFS research. Before long-term government programmes take effect, we will continue to promote biomedical research that makes diagnostics and therapies tangible during this transitional phase.

Where we will focus our funding in 2026

Disease mechanisms

Deciphering the causes of PEM, pain, cognitive disorders, circulation problems and other symptoms

Biomarkers & Diagnostics

Search for markers for improved diagnosis and measurement of disease severity and type (e.g. autoimmunity)

Medications & Therapies

Testing the effectiveness of active substances and therapies that are approved for other diseases or are being newly developed.

Voices of our supporters

"Many of the studies we are working on would probably never have come about without private funding."

Prof Carmen Scheibenbogen
Prof Carmen ScheibenbogenCharité Berlin

Seeing the ME/CFS Research Foundation advancing research means a great deal to me. It shows me that our fate is not simply being accepted.

Lisa B.
Lisa B.ME/CFS patient

"For us as a family, it is crucial that genuine biomedical research is advanced. The ME/CFS Research Foundation does exactly that – and for that I am grateful."

Sabine Hermisson
Sabine HermissonMother of a seriously ill daughter

"The funding of our research by the ME/CFS Research Foundation complements public funding in important areas."

Prof Uta Behrends, MD
Prof Uta Behrends, MDTU München

FAQ – Frequently asked questions

Further information can be found in our donation FAQ.

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