Osoba s Prader-Williho syndrómom

The paper deals with the specifics of a person with a rare genetic disorder called Prader-Willi syndrome. It presents the results of qualitative research in the form of a case study of a person with Prader-Willi syndrome. The aim of the paper is to describe the educational opportunities of a person with Prader-Willi syndrome and the extent to which a person with Prader-Willi syndrome influences the functioning of the family. The results of the research show that a person with Prader-Willi syndrome currently has a relatively wide range of educational opportunities, from kindergartens, through primary schools to secondary schools. The birth of a person with Prader-Willi syndrome significantly interferes with the functioning of the family and also has a fundamental impact on the further functioning of the family.