Living with myasthenia gravis (MG) often means navigating a journey filled with unexpected challenges, unanswered questions, and the...

Navigating a rare disease like myasthenia gravis (MG) can come with more than just physical challenges, emotional and mental well-being...

As we head into the heart of summer, MGA is excited to offer a full calendar of programs and events throughout August designed to...

Whether you're heading into middle school, starting college, or returning to school as an adult, managing Myasthenia Gravis (MG) while...

Living with Myasthenia Gravis (MG) often means juggling high-cost therapies, complex insurance decisions, disability paperwork, and...

As summer heats up, so does our calendar, with plenty of opportunities to learn, connect, and grow with others in the MG community....

Planning a trip when you live with Myasthenia Gravis can feel overwhelming, but with the right preparation, it is possible to travel...

This week’s Friday Feature shines a spotlight on Susie Craig, a tenured professor in Food Safety and Health with Washington State...

The Myasthenia Gravis Association (MGA) is thrilled to announce our first-ever Snowflake Saturday, a multi-location event held on June 7,...

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...

May is full of meaningful opportunities to connect, learn, and engage with the MG community! Whether you prefer virtual events or...

In a world where digital communication often dominates, it’s easy to forget the profound impact a simple handwritten note can have. For...

written by Mckenna Fulton, Community Program Coordinator for the Myasthenia Gravis Association Over three days, I had the incredible...