Misko was born on January 25, 2007. A year later it turned out that he suffers from a progressive muscle dystrophy of genetic origins (DMD), which is considered an incurable disease by current scientific standards. The aim of our foundation is to make Misko’s life as “ordinary” as possible, while we search for a possible cure together with the parents.

Our foundation would like to raise the funds necessary for Misko to receive the best possible care available. Through Misko’s case, we would also like to provide helpful guidance to all families with children diagnosed with incurable diseases. In addition, our goal is to provide information, best practice examples and useful advice to parents with children facing the same disease.

Through Misko's example, the foundation aims to demonstrate how to reach the best results throughout the progression of the disease and what impasses to avoid. We document the events of Misko's life and publish them regularly both online and in print. Our organization has also committed itself to advising parents of children affected by DMD and to finding the experts who can help us in this either by working directly for the foundation or by serving as advisors.