The MDA Live Unlimited Initiative

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by Wendy Henderson |

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This MDA video–a part of its Live Unlimited initiative– is all about Haley Frieler. Haley was diagnosed with spinal muscular atrophy at two 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!”.

MDA Team Momentum to beat muscular dystrophy at BMW Dallas marathon. Discover more here.

The Muscular Dystrophy Association’s Live Unlimited initiative aims to raise awareness and funds for muscular dystrophy, SMA and ALS, by allowing people to showcase what they can do with their lives if they refuse to believe the word “can’t.”

Find out what it’s like to live with a muscle degenerative disease such as muscular dystrophy.

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.