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StopDuchenne Poland supports people living with rare neuromuscular diseases, particularly Duchenne and Becker muscular dystrophy. The foundation provides assistance related to health improvement, care, rehabilitation, education, and daily functioning for patients and their families. It offers information on medical care, legal and administrative
matters, and access to projects such as cardiology care and PFRON-funded support. StopDuchenne Poland organizes scientific and educational conferences, including events for World Duchenne Awareness Day, as well as information campaigns and school lectures about Duchenne muscular dystrophy and clinical trials. The organization promotes knowledge about rare diseases and clinical research, works to counteract social exclusion, and cooperates with other patient organizations and medical institutions.