Help the Muscular Dystrophy Association during 5 On Your Side's Show of Strength 2022
5:52
Help the Muscular Dystrophy Association during 5 On Your Side's Show of Strength 2022
Aug 15, 2022
ksdk.com
We’re celebrating 75 years of progress! 🎉 The Muscular Dystrophy Association has been at the forefront of breakthroughs in research, care, and advocacy for neuromuscular diseases since 1950. 💙💛 Watch our new PSA, Legacy. Impact. Momentum. – and see how YOU have been part of this incredible journey. Together, we can create a future without neuromuscular disease. Visit MDA75.org to learn more. https://www.mda.org/press-releases/2025/mda-launches-75th-anniversary-campaign-and-premieres-new-psa-t
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We’re celebrating 75 years of progress! 🎉 The Muscular Dystrophy Association has been at the forefront of breakthroughs in research, care, and advocacy for neuromuscular diseases since 1950. 💙💛 Watch our new PSA, Legacy. Impact. Momentum. – and see how YOU have been part of this incredible journey. Together, we can create a future without neuromuscular disease. Visit MDA75.org to learn more. https://www.mda.org/press-releases/2025/mda-launches-75th-anniversary-campaign-and-premieres-new-psa-t
1.5K viewsJan 28, 2025
FacebookMuscular Dystrophy Association
How to help the Muscular Dystrophy Association during 5 On Your Side's Show of Strength
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How to help the Muscular Dystrophy Association during 5 On Your Side's Show of Strength
Aug 19, 2021
ksdk.com
Today, on World Health Day, the Muscular Dystrophy Association reaffirms our commitment to ensuring that every person we serve who lives with a neuromuscular disease—has equitable access to healthcare. We believe that access to lifesaving treatments, specialized care, and groundbreaking research is not a privilege but a right. Together, we are driving real change, but there is more work to be done. Join us in making a difference: MDA.org/Advocacy | Muscular Dystrophy Association
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Today, on World Health Day, the Muscular Dystrophy Association reaffirms our commitment to ensuring that every person we serve who lives with a neuromuscular disease—has equitable access to healthcare. We believe that access to lifesaving treatments, specialized care, and groundbreaking research is not a privilege but a right. Together, we are driving real change, but there is more work to be done. Join us in making a difference: MDA.org/Advocacy | Muscular Dystrophy Association
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Buy MDA Shamrocks at a retailer near you and support families with muscular dystrophy live longer and grow stronger. | Muscular Dystrophy Association
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Buy MDA Shamrocks at a retailer near you and support families with muscular dystrophy live longer and grow stronger. | Muscular Dystrophy Association
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The Muscular Dystrophy Association is proud to share that the recently passed FAA reauthorization law includes significant reforms aimed at improving the air travel experience for passengers with disabilities. These changes will help provide a safer and more dignified air travel experience, making air travel more inclusive for everyone. To celebrate this milestone, MDA reconnected with advocates Mindy Henderson and Madison Lawson to get their thoughts on what this legislation means for accessibl
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The Muscular Dystrophy Association is proud to share that the recently passed FAA reauthorization law includes significant reforms aimed at improving the air travel experience for passengers with disabilities. These changes will help provide a safer and more dignified air travel experience, making air travel more inclusive for everyone. To celebrate this milestone, MDA reconnected with advocates Mindy Henderson and Madison Lawson to get their thoughts on what this legislation means for accessibl
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FacebookMuscular Dystrophy Association
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Until July 31, create a live unlimited image and $1 will be donated to help kids and adults with muscular dystrophy and ALS. | Muscular Dystrophy Association
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Muscular dystrophy, ALS, and other types of neuromuscular disease take away the freedom to move. Now, COVID-19 threatens to take away the vital services that MDA families depend on. | Muscular Dystrophy Association
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Muscular dystrophy, ALS, and other types of neuromuscular disease take away the freedom to move. Now, COVID-19 threatens to take away the vital services that MDA families depend on. | Muscular Dystrophy Association
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Our commitment to accelerating research helped deliver new breakthroughs that are transforming countless lives. In 2020, help us move faster toward cures. | Muscular Dystrophy Association
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