Friedreich Ataxie Austria (FAU) is an Austrian organization that supports people living with Friedreich’s ataxia, a rare genetic neuromuscular disease. It assists patients with a confirmed or suspected diagnosis, as well as their families and caregivers. The organization provides information about the condition, practical guidance for living with FA, and updates on medical research, treatment options, and rehabilitation. FAU also organizes meetings, support groups, and opportunities for patients to share experiences. Its mission is to improve the quality of life of those affected and to ensure better access to care, knowledge, and a supportive community.