Muscular Dystrophy Association
Muscular Dystrophy Association (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS, and related neuromuscular diseases. For over 70 years, MDA has led the way in accelerating research, advancing care, and advocating for the support of our families. MDA’s mission is to empower the people we serve to live longer, more independent lives.
MDA supports many types, including Duchenne, Becker, limb-girdle, and facioscapulohumeral (FSHD).
Learn more at https://www.mda.org/disease
06/05/2026
In recognition of MG Awareness Month, MDA is spotlighting the voices and journeys of people living with myasthenia gravis all month long.
What happens when a nurse who cared for myasthenia gravis patients discovers she has the condition herself?
Tina Vassar shares her 30+ year voyage with generalized myasthenia gravis, from years of unexplained symptoms and diagnosis challenges to finding strength, community, and hope.✨
"At first, I felt like I was in a dinghy in an open ocean without a compass. Now, I have a compass and a community."
🔗 Read her full post story: https://mdaquest.org/mda-ambassador-guest-blog-my-myasthenia-gravis-voyage/
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