Photo by Jouko Karanka
Information, networking and support for sufferers of rare diseases
HARSO is a registered association that serves as an umbrella organisation for patient associations supporting people with rare diseases and debilitating conditions. It promotes the activities and collaboration of all organisations and individuals in the field of rare diseases in Finland. We share specialist information and patient experiences of rare diseases and debilitating conditions to improve the position of these patients and their care. HARSO was founded on 21 January 2012. The organisation’s membership consists of more than 20 patient organisations for rare diseases.