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-- Skip to main content Give Search MDA.org Search About Us I Will Donate Today Our Story About MDA Our Impact MDA History FAQs Our Team MDA Leadership Meet Our Partners -- National Ambassadors Careers Resources Press Room Financials Quest Magazine Art Collection Contact Us Care & Services I Will Donate Today Care Centers About MDA Services MDA Care Centers Meet Your Team Your Visit Family Seminars MDA Engage Events MDA Resource Hub National Resource Center Request Services Community Resources Community Education Outside Organization Programs & Information MDA Summer Camp -- Young Adults Program -- Summer Camp MDA Summer Camp Become a Camp Volunteer Apply for Camp Science & Research I Will Donate Today Our Approach About MDA Research Grants at a Glance Creating a New Therapy What We've Achieved MOVR Data Hub Clinical Trials Finder Tool For Researchers Our Research Program Funding Opportunities Contact our Research Team MDA Annual Conference MDA Venture Philanthropy For Clinicians Clinical Trials Finder Tool MDA Annual Conference Medical Education & Resources Get Involved I Will Donate Today Participate Get Involved Participate in an Event Become a Volunteer Volunteer Resources Advocate Donate Make a Donation Matching Gifts Legacy Gifts Product Donations Partner Become an MDA Partner Meet Our Partners Fire Fighters for MDA Support an ALS event About Neuromuscular Diseases I Will Donate Today About Neuromuscular Diseases Full List of Diseases Amyotrophic Lateral Sclerosis (ALS) Charcot-Marie-Tooth Disease (CMT) Congenital Muscular Dystrophy (CMD) Duchenne Muscular Dystrophy (DMD) Emery-Dreifuss Muscular Dystrophy Endocrine Myopathies Metabolic Diseases of Muscle Mitochondrial Myopathies (MM) Myotonic Dystrophy (DM) Spinal-Bulbar Muscular Atrophy (SBMA) Spinal Muscular Atrophy (SMA) Our Blog Search Donate Search MDA.org Search Close We transform the lives of people living with muscular dystrophy, ALS and related neuromuscular diseases. Donate Now Your browser doesn't support HTML5 video tag. First Name Last Name Email What We Do Since 1950, we've spearheaded efforts to transform the lives of people with muscular dystrophy, ALS, and related neuromuscular diseases. We fund groundbreaking research for promising treatments and provide families with the highest quality care from the best doctors in the country. Innovations in Science We are accelerating the delivery of treatments and cures. Explore the Science Innovations in Care We provide services that help people affected by neuromuscular disease. Experience the Care The freedom to walk, to talk, to run and play. To laugh, to hug, to eat — even breathe. Each day these freedoms are taken away from kids and adults with muscular dystrophy, ALS and related diseases that weaken muscle strength and limit mobility. Together we can change that. About Neuromuscular Diseases City or State or Zip Find MDA in Your Community How You Can Help Whether you’re looking to volunteer at a camp or a local office, organize a group of friends to fundraise, run a marathon, or advocate for the cause, the ways to get involved are endless. Participate in an Event Become a Volunteer Raise Your Voice Ways to Get Involved Latest Stories For the latest happenings in the MDA community and to read inspiring stories, browse the MDA blog. Researchers Look to Treat Genetic Disease at its Source Read More Register Now to Attend MDA’s Public Policy and Advocacy Conference Read More US House Passes Newborn Screening Reauthorization Read More Burn Boot Camp Bands Together for MDA Read More Visit Our Blog Recent News Jan 28, 2020 Announces 2020-2021 National Ambassador Ethan LyBrand from Alabama Ethan's goals are to find a cure for all types of muscular dystrophy, help people get the healthcare they need when they need it and make... Read More Jan 13, 2020 MDA Awards Venture Philanthropy Funding of More Than $1M to AavantiBio to Develop Gene-Targeting Therapy for Friedreich's Ataxia Read More Dec 19, 2019 The Names Steven J. Farella as Chairman and Dr. Donald S. Wood as Vice Chairman of the Board MDA is focused on driving innovations in research and care for people living with neuromuscular diseases. Read More Dec 13, 2019 MDA Celebrates FDA Approval of Vyondys 53 for Treatment of DMD Amenable to Exon 53 Skipping Second approved exon-skipping therapy for Duchenne muscular dystrophy Read More See Recent News Meet Our Partners These friends are helping give strength to MDA families. Meet Them All Join Us Sign up to receive email updates on volunteer opportunities and the impact you’re making for families. First Name Last Name Email MDA Resource Center: We’re Here For You Our trained specialists are here to provide one-on-one support for every part of your journey. Send a message below or call us at 1-833-ASK-MDA1 (1-833-275-6321). If you live outside the U.S., we may be able to connect you to muscular dystrophy groups in your area, but MDA services are only available in the U.S. Request Services Media Careers Donate Contact Us National Office 161 N. Clark, Suite 3550 Chicago, Illinois 60601 800-572-1717 | ResourceCenter@mdausa.org Facebook Twitter YouTube Instagram The (MDA) is a qualified 501(c)(3) tax-exempt organization. ©2020, Inc. All rights reserved. Privacy Policy | Terms of Use | State Fundraising Notices Sign Up for MDA News & Updates First Name Last Name Email The (MDA) is a qualified 501(c)(3) tax-exempt organization. ©2018, Inc. All rights reserved. Privacy Policy | Terms of Use | State Fundraising Notices Facebook Twitter YouTube Instagram...