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International Mito Patients is a network of national patient organisations involved in mitochondrial disease. The national patient organisations support and advocate for patients, fund research, increase awareness and improve education in their country.

By joining forces, IMP represents a large group of patients, creating a stronger voice on an international level.

IMP is a member of the European Organisation for Rare Diseases (EURODIS), which has international partners such as the National Organisation for Rare Diseases (NORD) and Canadian Organization for Rare Diseases (CORD).

 

© 2020 Int. Mito Patients