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To stay connected with MDA Care Specialists and receive the latest updates on MDA news and events, it is important that you ensure that your contact information is up to…

In a note to his younger self, Zach Jorgenson shares how his experience at MDA Summer Camp impacted his life.

Nicole Lahoud, a high school teacher, offers unique insight into the value of structuring a classroom to meet the needs of everyone.

Creating true economic independence is part of a new MDA advocacy initiative called Ensuring Economic Independence.

Researchers at Newcastle University are seeking adults living with general pain or with myotonic dystrophy (DM) to participate in a survey.

Hiker Skye Lemmen raised funds for MDA while trekking the Pacific Crest Trail When Skye Lemmen, of Grand Rapids, Michigan, decided to hike the Pacific Crest Trail, she knew she…

Most neuromuscular diseases are genetic disorders, we share how genetic neuromuscular diseases are inherited.

PJ’s Protocol outlines procedures that healthcare providers should follow for patients who depend on corticosteroids.

Research advances and the promise of better therapeutics on the horizon offer hope for people living with Duchenne muscular dystrophy.

How to establish and maintain good relationships with personal care attendants Anyone who lives with a neuromuscular disease that affects mobility knows that it often takes a village of caregivers…