Nyheim Hines 2022

Nyheim Hines, running back for the Indianapolis Colts, was 14 years old when his mother was diagnosed with muscular dystrophy. Ethan, who turns 13 in 2022, was diagnosed with muscular dystrophy when he was just 2 years old.

With over 150 Care Centers across the United States, the Muscular Dystrophy Association (MDA) helps Nyheim’s mom and kids like Ethan to live their lives to the fullest.

Air this new public service announcement and help MDA provide care to adults and kids living with neuromuscular disease in your community.

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Nyheim Hines 2021

Nyheim Hines, running back for the Indianapolis Colts, was 14 years old when his mom was diagnosed with muscular dystrophy. Throughout her illness, Muscular Dystrophy Association (MDA) has been there for her, and millions of others like her, with support and resources needed to keep her cheering Nyheim on from the sidelines.

With over 150 Care Centers across the United States, MDA is the leading organization in research and care for kids and adults living with muscular dystrophy, ALS and neuromuscular diseases. Nyheim supports MDA and hopes he can count on your support to air their new public service announcement to educate your audiences.

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COVID-19 Won't Stop Us

COVID-19 Won’t Stop Us highlights the life-saving care that Muscular Dystrophy Association is providing to one of the most vulnerable communities at this time, children and adults with neuromuscular diseases. This community is particularly at risk from COVID-19 due to their significant muscle deterioration that can lead to reduced function of respiratory and cardiac function. Additionally, those with neuromuscular diseases are facing increasing isolation from care givers and assistance they desperately rely on.

Muscular Dystrophy Association is on the frontline protecting communities across the United States during the COVID-19 pandemic. MDA is working with care centers to share new treatment guidelines, best practices for telemedicine and providing additional education and support to families.

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Never Walk Alone

Never Walk Alone highlights the life-saving care that Muscular Dystrophy Association is providing to one of the most vulnerable communities at this time, children and adults with neuromuscular diseases. This community is particularly at risk from COVID-19 due to their significant muscle deterioration that can lead to reduced function of respiratory and cardiac function. Additionally, those with neuromuscular diseases are facing increasing isolation from care givers and assistance they desperately rely on.

Muscular Dystrophy Association is on the frontline protecting communities across the United States during the COVID-19 pandemic. MDA is working with care centers to share new treatment guidelines, best practices for telemedicine and providing additional education and support to families.

• HD :60 Play Download

The MDA Kevin Hart Kids Telethon

This year is the 70th Anniversary of Muscular Dystrophy Association and we are fighting harder than ever to provide our community with opportunities to live fulfilling, independent lives. COVID-19 has disrupted critical research as well as services we provide to those living with neuromuscular diseases so we need your help more than ever.  On October 24^th we are taking a stand by introducing the MDA Kevin Hart Kids Telethon to increase awareness of our mission and highlight the life changing work MDA is doing on the front lines. Learn more at thetelethon.org.

Help make a difference in the lives of those children living with neuromuscular disease.

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