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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.

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To read a specific blog post in full, click on the particular title of interest.

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How Patient Voices Are Shaping the Future of MG Care

We are sharing this on behalf of a partner, Regeneron. No two myasthenia gravis (MG) journeys look exactly alike. Symptoms can begin subtly, be misread or dismissed, and the path to diagnosis and long-term management can feel uncertain for people living with MG and caregivers alike. This variability is exactly why the voices of people with MG are so important. Regeneron, a leading biotechnology company that develops medicines for serious diseases, is taking a listen-first app

November 2025: Programs and Events

As we welcome November, the Myasthenia Gravis Association is excited to bring a month full of opportunities to learn, connect, and celebrate community. From caregiver-focused programs in honor of National Family Caregivers Month to our 65th Annual Meeting & Educational Seminar, there’s something for everyone. Enjoy coffee clubs, support groups, and creative spaces designed to foster connection and empowerment across our MG community. Take a look below to find the events that

Celebrate 65 Years of Connection, Education, and Empowerment: MGA’s 65th Annual Meeting & Educational Seminar

Join the Myasthenia Gravis Association for our 65th Annual Meeting & Educational Seminar, a day filled with learning, inspiration, and community. Whether you attend in Kansas City or online, this event is designed to inform, empower, and bring together those living with myasthenia gravis, their families, and the professionals who support them. This year’s program features two incredible keynote speakers, a Neurology Q&A panel with leading MG specialists, and opportunities to

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© 2020 | Myasthenia Gravis Association | MGA Digest

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