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Expert Advice for Preparing for Medical Emergencies with NMD
Julianne Meiser, MSS, LCSW, an Outpatient Social Worker in the Division of Neurology at the
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Starting corticosteroids earlier helps improve motor function in DMD
Starting daily corticosteroids earlier in young children with Duchenne muscular dystrophy (DMD) helps them move
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A tribute to a friend who taught us how to love, lead, and show up for others
Last Saturday, I lost a dear friend of mine, Timothy Chan, who had Duchenne muscular
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Patient-led group launches network of clinics to improve LGMD care
Patient-led nonprofit The Speak Foundation has announced the launch of the LGMD Centers of Excellence,
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Clinical Research Alert: Phase 3 Study of Omaveloxolone in Children and Teenagers with Friedreich Ataxia (FA)
Researchers at Biogen are seeking pediatric FA patients to participate in a phase 3 clinical
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Navigating disability benefits for muscular dystrophy
When the progressive muscle weakness of muscular dystrophy (MD) begins to interfere with your employment,
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To me, a wheelchair is a symbol of improved function, not disability
Everyone recognizes the blue and white signs featuring a figure in a wheelchair that adorn
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Beyond Approval: Why Drug Development Doesn’t End at FDA Sign-Off
For many neuromuscular community members — and clinicians — who are waiting for a new
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When school is out, my sons with DMD get into their summer groove
This past winter in rural Nebraska was mild, with no real snow and only a
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How MDA Summer Camp Influenced the Direction of My Life
Bio: Rebecca Hume is a Senior Specialist Writer for Quest Media. She graduated from Slippery
