Muscular Dystrophy Association

Help Muscular Dystrophy Association (MDA) transform the lives of children and adults with muscular dystrophy, ALS and 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 neuromuscular disease, MDA works tirelessly on behalf of the muscular dystrophy community.  They have done so for 70 years.

The MDA Kevin Hart Kids Telethon

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 24th 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.

  • The MDA Kevin Hart Kids Telethon

    The MDA Kevin Hart Kids Telethon

  • COVID-19 Won't Stop Us

    COVID-19 Won't Stop Us

  • Never Walk Alone

    Never Walk Alone

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 24th 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.

  • The MDA Kevin Hart Kids Telethon

  • COVID-19 Won't Stop Us

about

For 70 years, the Muscular Dystrophy Association (MDA) has been committed to transforming the lives of children and adults 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. Each year thousands of children and young adults learn vital life skills and gain independence at summer camp, at no cost to families, with virtual programming coming for summer 2020. 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.

questions

For questions, please contact mda@psadirect.com.