Webinar Recap: How the Patient Advocate Foundation Helps Individuals Navigate Cost, Coverage & Care
Living with Myasthenia Gravis (MG)Â often means juggling high-cost therapies, complex insurance decisions, disability paperwork, and...
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Hello and welcome to the MGA blog, The MGA Digest.
The MGA Digest is a blog curated by the Myasthenia Gravis Association.
For more information regarding our organization, please visit our website.
To read a specific blog post in full, click on the particular title of interest.
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July 2025: Programs and Events
As summer heats up, so does our calendar, with plenty of opportunities to learn, connect, and grow with others in the MG community....
Friday Feature: Meet Dawn of Dawn’s Doggie Delights | How One Woman Turned Her Love for Dogs into a Heartfelt Business—While Living with MG
Dawn has been living with myasthenia gravis (MG) since 2002. Over the years, she’s learned how to adapt her pace, listen to her body, and...
Reflecting on the World Orphan Drug Congress USA 2025: A Glimpse into the Future of Rare Disease Treatment
Written by Kathryn Clemens, Community Program Coordinator Last month, I had the opportunity to attend the World Orphan Drug Congress USA...
May 2025: Programs and Events
May is full of meaningful opportunities to connect, learn, and engage with the MG community! Whether you prefer virtual events or...
Rare Disease Week: Advocating for Change in Healthcare Policy
written by Mckenna Fulton, Community Program Coordinator for the Myasthenia Gravis Association Over three days, I had the incredible...
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