About MDA
The Muscular Dystrophy Association (MDA) is a voluntary health agency striving to find the cures, causes, and treatments for 43 different neuromuscular diseases. The Association’s programs are funded almost entirely by individual private contributors. MDA seeks no government grants, United Way funding or fees from those it serves.
Funds raised at Live Ride for MDA will stay in Alaska to help fund services such as clinic visits, medical examinations, flu shots, assistance with the purchase of wheelchairs and leg braces, a week long summer camp for children aged 6-21, and support groups for MDA clients and families.

MDA supports more research on neuromuscular diseases than any other private-sector organization in the world. MDA scientists are in the forefront of gene therapy research and have uncovered the genetic defects responsible for several forms of muscular dystrophy, Charcot-Marie-Tooth disease, a form of amyotrophic lateral sclerosis (ALS, or Lou Gehrig’s disease), childhood spinal muscular atrophy, and several other neuromuscular conditions.
You can contact MDA Alaska at 907-276-2131 or use our handy contact form. To find out more about MDA and their activities visit http://www.mda.org