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Madison Lawson is passionate about hair, make-up, and fashion, and the importance of inclusivity in the fashion and beauty industry. Born with spinal muscular atrophy (SMA), she became interested in…

Researchers at Cumberland Pharmaceuticals Inc. are seeking boys and men living with Duchenne muscular dystrophy (DMD) to participate in a phase 2 clinical trial to evaluate the safety, and efficacy of…

When most people think of August, they think of the end of summer and back to school, but did you know that August is also National Make-a-Will month?  Whether you’re…

As the Muscular Dystrophy Association (MDA) continues our commitment to empowering people living with neuromuscular disease, we are excited to share our 2022 blog series: “Quest for Success”. Success looks…

Amy and Shelli It’s an honor to be able to share my thoughts on friendship and what that means to me to celebrate friendship day! For those of you who…

As the days become longer and the fireflies come out to play, it might be hard to start thinking about the new school year right around the corner.  But when…

The Muscular Dystrophy Association (MDA) today announced that the 35th Annual Trans New Hampshire Bike Ride (TNHBR) held on June 25, starting and ending at the Portsmouth Senior Center in Portsmouth,…

Money kept in savings accounts pulls double duty: It’s accessible to address urgent, unexpected expenses, and it’s also a key component of a long-term investment strategy. In the face of…

We’re back! After a 3-year hiatus, advocates are going back to Capitol Hill, but this time virtually. We’re excited to announce that the MDA Advocacy Institute: Virtual Summit and Hill Day will…

As the Muscular Dystrophy Association (MDA) continues our commitment to empowering people living with neuromuscular disease, we are excited to share our 2022 blog series: “Quest for Success”. Success looks…