The Multiple System Atrophy (MSA) Coalition® is a U.S. based 501(c)(3) charity focused primarily on facilitating MSA research that will lead to the discovery of a cure for this rare and fatal neurodegenerative disease. Until a cure is found, the MSA Coalition will also provide patient/caregiver education and emotional support, education for healthcare professionals, and leadership in MSA advocacy activities. The MSA Coalition is led by a group of dedicated volunteers deeply committed to serving the MSA Community. We seek to partner and collaborate with all multiple system atrophy organizations and advocates around the globe to form a strong unified voice. Over $1Million in research funded!
The Multiple System Atrophy Coalition is a beacon of hope for families around the world touched by this rare and devastating illness. They provide emotional support, share information with families and the healthcare community, lead online and local support groups, organize and sponsor conferences and fund research in an effort to find a cure. — Pam
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