What is Muscular Dystrophy (MS)?
Muscular dystrophy is a group of genetic conditions that cause the muscles to gradually weaken over time. Because there are more than 30 different types, the condition can look very different from one person to another, some forms begin in infancy, others appear in childhood or adulthood, and the rate of progression can vary. What all types share is that the genes responsible for keeping muscles healthy don’t work as they should, leading to muscle fibers that break down more easily and become weaker over the years. Depending on the type, muscular dystrophy may affect the muscles used for movement, breathing, swallowing, or even the heart. Some people experience mild symptoms and remain active for many years, while others face more significant challenges early in life. Although there is no cure yet, treatments such as therapy, medications, and supportive care can help maintain mobility, manage symptoms, and improve quality of life.
