Muscular Dystrophy Association

Highly Engaged Employees

The Muscular Dystrophy Association is a prominent non-profit organization established in 1950, dedicated to combating muscular dystrophy, ALS, and related neuromuscular diseases. Operating within the charitable organizations and foundations sector, the entity focuses on driving innovation through comprehensive research funding, medical services, and community support. By providing essential resources and educational programming, the organization empowers patients and families while advancing the search for effective treatments and cures.

With a robust operational footprint, the Muscular Dystrophy Association maintains 32 locations and supports a workforce of 500-1,000 employees. The organization delivers critical services, including durable medical equipment support, clinical care coordination, and inclusive summer camp experiences for individuals living with neuromuscular conditions. Meet Muscular Dystrophy Association's team to learn about the leadership and professional staff driving these community-focused initiatives and operational programs across North America.

The organization demonstrates significant market presence, competing with entities like the ALS Association and the National Multiple Sclerosis Society. With annual revenue reaching $142.7M, the association leverages diverse funding streams to sustain its mission-critical activities. Explore financial highlights for detailed metrics regarding their fiscal performance, funding history, and resource allocation strategies. This financial stability enables the continued development of digital technology platforms and virtual care solutions designed to improve patient outcomes and quality of life.