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The Muscular Dystrophy Association is the world’s leading nonprofit health agency dedicated to finding treatments and cures for muscular dystrophy, amyotrophic lateral sclerosis (ALS) and other neuromuscular diseases. MDA funds worldwide research; provides comprehensive health care services and support to MDA families nationwide; and rallies communities to fight back through advocacy, fundraising and local engagement.
MDA annually funds more than 250 research projects around the world. Thanks to MDA-funded research:
- clinical trials of potential therapies are under way in Duchenne and Becker muscular dystrophies, spinal muscular atrophy, ALS and other diseases;
- the largest drug discovery project in ALS to date is being conducted at the ALS Therapy Development Institute;
- optimal care guidelines have been developed for several rare conditions;
- a lifesaving enzyme replacement therapy has been developed for Pompe disease; and
- more new drugs for muscle diseases are planned in the next five years than in the previous 50.
Providing families with support
MDA’s comprehensive services program helps individuals and their families meet the challenges imposed by chronic, progressive muscle diseases through:
- a national network of 200 medical clinics staffed by experts in neuromuscular diseases, including more than 40 clinics designated as MDA/ALS centers;
- local support groups and events for individuals and families;
- assistance locating, obtaining and repairing needed durable medical equipment; and
- online opportunities to connect, share and learn through online communities, social media, care coordination tools and webinars.
Each year, thousands of youngsters ages 6 to 17 attend a free weeklong accessible summer camp session where they get to be "just kids."
Public and professional health education
Online and in print, MDA offers a vast library of information about research, clinical trials, health care and daily living strategies. MDA also regularly convenes international scientific meetings and conferences for researchers and MDA clinic directors.
MDA represents the needs of the neuromuscular disease community in matters of public policy and research advancement, and facilitates involvement in these areas by the people it serves.
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