Magdalena was born with an open back (spina bifida) and other deformities in 2020, in the middle of the coronavirus pandemic. She was only allowed to return home to her family and brother after several operations. Since then, the life of the little family has naturally been shaped by Magdalena's illness. Magdalena is developing very well, is already very independent and has a great zest for life in her home town. In order for Magdalena to continue to grow up and live in her familiar surroundings of Zell am Moos, many therapies and rehabilitation stays are still necessary.
We hope that Magdalena will continue to develop so well and pass on her joy of life to others with her cheerful laughter.