An organisation for people with a neuromuscular disease called muscular dystrophy. We provide information about research and life for people with this condition. We also provide social and legal assistance to our members. We organize rehabilitation and educational courses as well as domestic and foreign convalescent stays.

Accompanying and long-term cooperation between volunteers and blind people. Offer counselling, book publishing and cultural activities.

We operate a civic association. We offer help to families with children affected by Rett syndrome. We organize meetings, lectures and conferences. We participate in the publication of information materials about the sysdrome, cooperate with other supporting bodies, recommend specialists, etc.

We help and support member organisations to promote the interests of patients. We offer unique research and focus on improving the quality and accessibility of health services, including digital medicine.

Activities of a civic association supporting wheelchair users after spinal cord injury.