Welcome to ORDI’s Neuromuscular Club Session – Edition 40! In this session, we explore Myotonic Dystrophy Type 1 (DM1)—a multisystem genetic disorder that affects muscles, the heart, the endocrine system, and more. This educational session focuses on: ✔ What is Myotonic Dystrophy Type 1? ✔ Common signs and symptoms ✔ Genetic causes and inheritance ✔ Diagnosis & available management options ✔ Long-term care considerations for patients and caregivers At ORDI, our mission is to spread awareness, support families, and improve access to early diagnosis and care for rare neuromuscular diseases in India. 👉 Subscribe for more awareness sessions, patient stories, and expert discussions. 👉 Join us in building a stronger rare disease community! #RareDiseases #ORDI #NeuromuscularClub #MyotonicDystrophy #DM1 #NeuromuscularDisorders #GeneticDisorders #RareDiseaseAwareness #MuscularDystrophy #HealthcareIndia
