Karolina PODOLSKA
MD, Internal medicine clinician, General Faculty Hospital in Prague, Board member, World Duchenne Organization and Parent Project Czech Republic
Dr Karolina Podolska has been involved with rare diseases, particularly with Duchenne Muscular Dystrophy for ten years. In the past five years she has developed a system of transition of care from pediatric to adult for patients with Duchenne and is building a center of care for adults with dystrophinopaties in the Czech Republic. She also works for Czech Ministry of Health in a project which aims to improve the system of care for patients with rare diseases in all ERN centers. She has joined the JARDIN project (Joint Action on integration of ERNs into national healthcare systems) as the main contact person for the Czech Republic.