The Myasthenia Gravis – Face To Face Association is a patient organization that supports people living with myasthenia gravis and their families. It brings together patients with different forms of the condition, regardless of age or stage of treatment. The association focuses on education about myasthenia gravis, its symptoms, diagnosis, and available therapies, while also helping patients cope with the daily challenges of the disease. It provides informational and emotional support, facilitates contact between patients, organizes meetings and educational activities, and cooperates with medical specialists. Its goal is to improve patients’ quality of life, raise public awareness, and strengthen the voice of people living with myasthenia gravis.