“Motus Vita” is a society that offers support to people with special needs, uniting those who suffer from neuromuscular diseases (ALS/MND), as well as their family members.

The Foundation’s support is aimed at helping people afflicted by neuromuscular diseases, defending their rights and interests, providing them with opportunities to meet other people, and offering patients themselves with information about these diseases, their treatment methods and options, as well as about the psychological and social problems they entail and means of resolving them.