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Every cent of your donation goes toward research.

Thank you for your interest in helping those affected and researching diseases such as ME/CFS! Your donation will enable research projects to be launched and advanced.

Account information for direct donations to the WE&ME Foundation

  • Recipient: We & Me Foundation
  • IBAN: AT95 2011 1842 5439 4200
  • BIC: GIBAATWWXXX
Ein schwarz-weißer QR-Code mit einem quadratischen Muster. Der Code enthält Bankkonto-Informationen, bestehend aus schwarzen und weißen Modulen, die in einem Raster auf weißem Hintergrund angeordnet sind, mit drei größeren Quadraten in drei Ecken zur Ausrichtung.
Donate and Support Now!
Donate and Support Now! 100% of your donation funds our mission.
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Tax advantages in Austria

As an Austrian citizen, your donation is tax-deductible as a special expense (private individuals) or as a business expense (companies) in accordance with § 4a Z 3 or 4 EStG (tax code) (registration number ZG 18163). We report to the tax office annually in February for the entire previous year.

If you are donating as an individual, we need your full name and date of birth for the automatic deduction of your donation. Please include both in the reference field of your transfer.

Schwarzer Text auf weißem Hintergrund lautet: IHRE SPENDE IST STEUERLICH ABSETZBAR Reg. Nr. ZG 18163 innerhalb eines schwarzen rechteckigen Rahmens.
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GUARDIANS4ME Exchange Energy

guardians 4 me guardians 4 me

Guardians4ME is a WE&ME program that offers volunteers the opportunity to support the millions of ME/CFS patients.

  • Twenty million people currently remain unheard and unseen. Let’s join forces and give them a voice.
  • You can sponsor an ME/CFS patient, whether you know someone personally or choose to help one of the countless people who are currently overlooked and underserved by society.
  • Your skills, your choice. You can contribute by writing a patient’s story, creating content, managing social media, shooting videos, or any other skill you possess.

We strongly support those affected by ME/CFS

Guardians4ME

Guardians

Laura Karasinski

Laura Karasinski

Laura, a creative person with many talents, actively contributes to Guardians4ME by photographing portraits of our team. She has a long-standing friendship with Christoph, and thanks to her generous donation of time and talent, we have benefited from her creative output. This has allowed us to focus on building the WE&ME Foundation.

Julia Scheve, BSc

Julia Scheve, BSc

Julia is a management consultant and fitness trainer based in Vienna. She witnessed her best friend Christoph deteriorate due to ME/CFS and now supports the WE&ME Foundation by helping to raise awareness of this illness.

Eine lächelnde Frau mit langen blonden Haaren steht neben einem Banner der WE & ME Foundation und hält Informationsmaterial, das den Gemeinsamen Geist hervorhebt, draußen in der Nähe eines Holzgebäudes mit grün umrahmten Fenstern.

Kathrin Fuchs

My name is Kathrin, and my support for the WE&ME Foundation is deeply personal. Christoph has been one of my closest friends since our school days. His fate and the fight against ME/CFS therefore affect me directly. As someone who works in the pharmaceutical industry, I know from experience that even the smallest building block can contribute to something really big. This knowledge motivates me to support the foundation’s work so that research and education can make decisive progress. That’s why I stand firmly by Christoph and the foundation.

Awareness for ME/CFS

Everyone can make a difference

ME/CFS is a serious, often invisible illness. Many sufferers lose their normal lives—their jobs, their education, their social contacts. This makes it all the more important that we take notice, talk about it, and raise awareness of the illness.

Awareness doesn’t have to be big or perfectly organized. It starts with compassion—and with the desire not to look away.

Sometimes it comes through music, through involvement in a school, through a sporting challenge or a run, through an event in a club, or through an initiative among friends. Sometimes it grows into a larger evening event like the charity gala “Zeit zum Hinschauen” (Time to Look). And sometimes it simply manifests itself in people coming to a demonstration and showing their presence.

Even in moments of farewell, many families send a strong message by asking for donations for ME/CFS at funerals.

All these gestures—quiet or visible, small or large—give those affected a voice. Awareness means working together to make visible what has been overlooked for too long. Together, we can create hope and advance research.

People who are severely affected often lie in darkened rooms due to their sensitivity to light and noise and require round-the-clock care. They mainly suffer from extreme stress intolerance, which makes even small activities such as brushing their teeth a torture.

There are currently no recognized therapies or cures. That is why we are committed to raising awareness, providing information, and promoting research. With your donation, we want to be a ray of hope in the dark realm of this disease.

Donate and Support Now!
Donate and Support Now! 100% of your donation funds our mission.
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We are fighting for research, awareness and a cure for ME/CFS

Stories of people affected

Life with ME/CFS

A young woman sits cross-legged on a bed in a room lit in blue-green light. Behind her is a sign that reads “Hello MTV welcome to my crib” and a poster of a woman with the inscription ALBERTINA modern The 80s. The atmosphere is relaxed and artistic.
Styria: Ill since 2022 following a coronavirus infection
Two people embrace in a dimly lit room; one person wears an eye mask and stands next to a bed, while the other leans against it for support. The blue lighting creates a calm, serene atmosphere.
Lower Austria: Fell ill in 2018 after a viral infection (pathogen unclear)
Image of Kornelia Spahn
Lower Austria: Suffering from ME/CFS since 2022 after infection with Epstein-Barr virus and COVID-19
Image of Martin Privec
Upper Austria: Ill since 2017 following an Epstein-Barr infection (“Pfeiffer’s glandular fever”)
A man wearing glasses stands with his arms crossed in a dimly lit room, looking thoughtfully at a brass trumpet on a windowsill. Nearby are white curtains and a green leafy plant.
Vienna: Ill since 2023 following a coronavirus infection
THE BROKEN DREAMS OF A YOUNG WOMAN

Together, we are on the path to a better life for ME/CFS patients.

Unfortunately, this takes time and does not happen overnight. ME/CFS patients do not simply wake up one day and return to their normal lives.

But there is hope, and we are here to fight for those who can no longer do so themselves. By funding more research and raising awareness, we will achieve our goal.

Step by step.

Join our cause

Every donation, no matter the size, fuels critical research and brings us one step closer to a cure.

Donate and Support Now!
Donate and Support Now! 100% of your donation funds our mission.
Donate Now
Schwarzer Text auf weißem Hintergrund lautet: IHRE SPENDE IST STEUERLICH ABSETZBAR Reg. Nr. ZG 18163 innerhalb eines schwarzen rechteckigen Rahmens.
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