Muscular Dystrophy Association
Help Muscular Dystrophy Association (MDA) transform the lives of children and adults with muscular dystrophy, ALS, and over 43 related neuromuscular diseases through innovations in science and innovations in care by airing their public service announcement (PSA) with your community. As the largest and longest-established organization for children and adults with muscular dystrophy, ALS, and related neuromuscular diseases, MDA works tirelessly on behalf of over 300,000 families nationwide. They have done so for 70 years.
Nyheim Hines
Nyheim Hines
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.
- Campaign Overview Download
COVID-19 Won't Stop Us
COVID-19 Won't Stop Us
Never Walk Alone
Never Walk Alone
The MDA Kevin Hart Kids Telethon
The MDA Kevin Hart Kids Telethon
Nyheim Hines
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.
- Campaign Overview Download
about
For 70 years, the Muscular Dystrophy Association (MDA) has been committed to transforming the lives of people living with muscular dystrophy, ALS, and related neuromuscular diseases. We do this through innovations in science and innovations in care. As the largest source of funding for neuromuscular disease research outside of the federal government, MDA has committed more than $1 billion since our inception to accelerate the discovery of therapies and cures. Research we have supported is directly linked to life-changing therapies across multiple neuromuscular diseases. MDA’s MOVR is the first and only data hub that aggregates clinical, genetic, and patient-reported data for multiple neuromuscular diseases to improve health outcomes and accelerate drug development. MDA supports the largest network of multidisciplinary clinics providing best-in-class care at more than 150 of the nation’s top medical institutions. Our Resource Center serves the community with one-on-one specialized support, and we offer educational conferences, events, and materials for families and healthcare providers. MDA Advocacy supports equal access for our community, and each year thousands of children and young adults learn vital life skills and gain independence at summer camp and through recreational programs, at no cost to families. During the COVID-19 pandemic, MDA continues to produce virtual events and programming to support our community when in-person events and activities are not possible. MDA’s COVID-19 guidelines and virtual events are posted at mda.org/COVID19. For more information, visit mda.org.
questions
For questions, please contact mda@psadirect.com.