The foundation was created to support the founders' daughter, Sofina, who suffers from spinal muscular atrophy (SMA). The mission of the fund is to provide for the special needs of children with the same diagnosis.
We are a family trying to support Michalka, who suffers from a rare genetic disease. We offer information about her story and needs. Any help, whether financial or by organizing events, is very valuable to us. Our goal is to provide quality care and life for Míška. Thank you for your support.
We are a family trying to live a full life with the challenges of butterfly wing disease. We offer help and support to other families in similar situations. Our programs include charity events and activities that raise awareness of the disease and bring hope.
Our foundation supports young talents who want to study and grow. We offer financial support and the opportunity to get involved in projects in the region. Join us and change the future of the Pardubice Region.