Muscular Dystrophy Association

The Muscular Dystrophy Association (MDA), founded in 1950, is a prominent non-profit organization dedicated to combating muscular dystrophy, ALS, and related neuromuscular diseases. Operating within the Charitable Organizations & Foundations and Organizations industries, MDA focuses on funding critical research, providing comprehensive medical and community services, and educating health professionals and the public. Its mission drives innovation in treatment and aims for cures, leveraging digital technology and offering programs like summer camps and durable medical equipment services. The organization's product offerings span advocacy, disease research, and patient support, reflecting a commitment to improving lives through scientific advancement and direct care.

With a significant operational footprint, the MDA maintains 55 locations and employs between 500-1,000 individuals. This scale enables the organization to deliver widespread support and services across North America and beyond. The team's expertise is crucial in navigating complex medical landscapes and advocating for patient needs. Meet Muscular Dystrophy Association's team to understand the leadership and personnel driving these vital initiatives. Their work encompasses a broad range of activities from research coordination to direct patient assistance, underscoring the organization's comprehensive approach to tackling rare diseases.

Financially, the Muscular Dystrophy Association reported a revenue of $142.7M. The organization has also secured funding, including a $5.0M debt financing in May 2020. MDA operates within a competitive landscape featuring organizations like the National Multiple Sclerosis Society, ALS Association, and March of Dimes, all focused on various health-related causes. This financial and competitive context highlights MDA's strategic positioning and operational capacity. Explore financial highlights for a detailedView more...