As we head into September, there are plenty of opportunities to connect, learn, and build community with others impacted by myasthenia...

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...

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

What began as a fun way to connect with the community and raise funds for those living with myasthenia gravis has become one of the most...

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...

The Asociación Miastenia de España (AMES)  is a nonprofit organization declared to be of public utility and made up of individuals...

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...

Written by Kathryn Clemens, Community Program Coordinator Last month, I had the opportunity to attend the World Orphan Drug Congress USA...

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

In honor of Autism Awareness Month and Adult Autism Awareness Day on April 18, we wanted to highlight the powerful and deeply personal...

Spring is here, and we’re excited to offer a full lineup of support groups, educational programs, and community gatherings throughout...

Creativity has a unique way of healing, empowering, and connecting us, especially in the face of life’s challenges. For many in the MG...

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

February is packed with opportunities to connect, learn, and support one another in the MG community! Whether you're looking for...