An important way to get involved with the MDA community is through the Association’s advocacy program. Based in Washington D.C., the advocacy team monitors and supports programs, legislation and health care policies relevant to people with neuromuscular diseases, such as medical care, insurance, accessibility, transportation, independent living, personal assistance services and research funding.
Sign up to be an MDA Advocate and receive e-updates and up-to-the-minute news on policy issues impacting the MDA community.
MDA’s “Take 5” advocacy initiative encourages everyone to “take five minutes” to contact their elected officials using online tools that provide talking points about important legislation and contact information for elected officials.
MDA’s National Task Force on Public Awareness is a group of volunteers who advise the Association on issues of interest and importance to people with disabilities. The Task Force consists of adults who are leaders in their communities and who are affected by one of the neuromuscular diseases in MDA’s program.
Since MDA began, adults with neuromuscular diseases have been among its leaders as members of the board of directors and advisers. Under their guidance, MDA has educated the public about living with disabilities, and supported efforts to provide people with disabilities with equal rights and opportunities.
National legislation to which MDA lent leadership and support include:
"My ultimate happiness was found in the world of advocacy. I encourage anyone who is thinking about taking on a leadership role in advocacy. It is very rewarding. Receiving help is an art ... Through advocacy I can give back."
— Angela Wrigglesworth, Texas, spinal muscular atrophy
Muscular Dystrophy Association — USA
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The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization.
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