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

As autumn settles in and the air turns crisp, many people with Myasthenia Gravis (MG) notice subtle changes in how their muscles feel. While heat sensitivity is often a big topic in the MG community, cold weather can bring its own set of challenges. Cooler temperatures can affect how our muscles and nerves work, sometimes making daily activities feel a bit tougher. Let’s take a closer look at why that happens and what you can do to stay warm, comfortable, and safe this season

Written by Blaise Huck Hello, my name is Blaise Huck, and my mom was diagnosed with MG when I was in high school. She started off with...

Did you know September 21 is National Converse Day? It’s the perfect time to celebrate creativity, individuality, and the stories behind...

The Myasthenia Gravis Association recently hosted an enlightening webinar featuring Dr. James Howard, Professor of Neurology and Medicine...

Written by Manley Lavender Unknowingly my journey started the evening of my 50th surprise birthday party planned by my wife and family. I...

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

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...

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...

In May 2025, the Myasthenia Gravis Association hosted an expert webinar featuring Dr. Henry Kaminski from George Washington University....

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

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...