Welcome to the WE&ME Foundation.
OUR STORY
Welcome to the WE&ME Foundation. The WE&ME Foundation (formerly the TEMPI Foundation) was founded in 2020 by the Ströck family and is based in Vienna, Austria, where the family is known for its “Ströck” bakeries, which have been delighting customers with their baked goods for generations. The Ströck family’s journey has been profoundly shaped by the impact of ME/CFS, which has defined the nature and purpose of the WE&ME Foundation with unwavering determination. Two brothers, Christoph and Philipp Ströck, both of whom are affected by ME/CFS, lead the foundation’s mission. Christoph, the younger brother, was diagnosed in 2016 after years of illness, and his condition worsened due to misconceptions about ME/CFS. In 2018, Philipp, the older brother, was also diagnosed. The family learned firsthand that there are very few doctors who are knowledgeable about the diagnosis and treatment of ME/CFS. Over the years, the Ströck family became aware of the extent of the shortcomings in social security and support for the millions of ME/CFS patients.
The ongoing shortage of qualified professionals in this field has left patients to fend for themselves when it comes to diagnosis and the necessary support—a situation that often leads to an irreversible deterioration in their health. In many cases, they are unable to return to work, which leads to a lack of social support. The situation in which patients and their families find themselves—on top of the reality of this cruel disease—is completely unacceptable. Originally self-funded, the foundation is now working to raise funds for research and raise awareness of the disease in order to improve the situation for patients and their families. The Ströck family and the dedicated WE&ME team are committed to funding groundbreaking research that unravels the complexity of ME/CFS and brings us closer to effective treatments and a cure. We hope that our tireless commitment is reflected in every initiative we undertake to alleviate the burdens associated with ME/CFS. Join us on this journey to make a tangible difference in the lives of those affected by ME/CFS. Together, we can make progress and bring about positive change.
We are committed to ensuring that people with ME/CFS are recognized, taken seriously, and well cared for. That is why we support education and research with the goal of making effective treatments and a cure possible.
We envision a future in which every person with ME/CFS is diagnosed early and has access to effective treatments and a cure.
Demand
- Implementation of competence centers in all federal states with patient care in addition to the reference center as a knowledge hub.
- Demand for improved social security. Improved education and training for doctors and medical staff.
- Demand for research funding from the public sector.
UNITED BY A SINGLE GOAL.
Board of Directors
FOUNDATION TEAM
Scientific Advisory Board
Medical Advisory Board
Patient Advisory Board
Our work in review
Financial Report 2022
Financial Report 2020
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.