These five muscular dystrophy patients are inspiring the entire community with their stories and their outlook on life.
In this inspiring video from MDA, we meet Jimmy Valdes and his wife, Julie. Originally from Queens, New York, 47-year-old Jimmy was diagnosed with spinal muscular dystrophy (SMA) in 1971 at 2 years old. Watch the video to learn more about their amazing love story.
This video from Muscular Dystrophy WA shares Laura’s story. Laura is a 22-year-old university student from Western Australia who has Emery-Dreifuss muscular dystrophy. She’s studying for a Bachelor of criminology and justice with the hope of one day working with criminal offenders on parole.
In this episode of Muscle Owl Talks from Muscle Owl, host Peter Duffy meets Jon Hastie, a Duchenne muscular dystrophy patient who made the film A Life Worth Living. Jon talks about the film and his charity DMD Pathfinders and what it’s like to be an adult with Duchenne.
This MDA video — a part of its Live Unlimited initiative — is all about Haley Frieler. Haley was diagnosed with spinal muscular atrophy at 2 years old and has spent her life in a wheelchair. She hasn’t let her SMA get in the way of achieving her goal of working in the fashion industry, as she says “if there’s a will, there’s a way!”.
This video from Muscular Dystrophy Queensland follows several patients who have different forms of degenerative muscular conditions.
Muscular Dystrophy News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.
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