Muscular Dystrophy Association

The Muscular Dystrophy Association (MDA) is the leading nonprofit organization dedicated to advancing research, care, and advocacy for individuals affected by muscular dystrophy, ALS, and related neuromuscular diseases. With over 70 years of commitment, MDA empowers families and individuals to live longer, more independent lives through a comprehensive array of services. MDA operates specialized care centers providing tailored support from diagnosis onward, alongside community education and resources like workshops and webinars.

Their innovative programs include MDA Summer Camp, where children can explore and thrive in a supportive environment, as well as volunteer opportunities that encourage community involvement. MDA is at the forefront of groundbreaking research, funding studies to discover new treatments and potential cures. Their advocacy efforts ensure that people with disabilities can access critical resources such as voter rights information.

Through its mission to connect, support, and empower, MDA continues to impact the lives of those within the neuromuscular disease community significantly. Visit MDA. org to learn more about their initiatives and how to get involved