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Welcome to the

Myasthenia Gravis Association

Support the MGA

The MGA has a rich history of people and places that make the organization what it is today. Now more than ever, the MGA is comprised of a committed staff, a dedicated board of directors, and an expert medical advisory committee, all working towards improving the lives of those with myasthenia gravis.

Resources regarding medical conditions are vast and complex, often times leaving patients feeling stressed and overwhelmed. Our goal is to provide you with the most relevant information so that you can be your own advocate and stay informed. Check out our resources page to learn about best practices and other helpful information regarding MG.

The Myasthenia Gravis Association (MGA) is dedicated to supporting patients, families, friends, and communities impacted by myasthenia gravis.

Together, we strive to build a supportive community for those affected by myasthenia gravis by increasing public awareness, providing educational opportunities, and fostering meaningful connections with one another.

Research within the MG community is growing, and we want you to be the first to know about it. Learn about current and upcoming clinical trials and other research studies that may benefit you.

The MGA works diligently to ensure patients with MG are being supported and cared for through awareness efforts, education, and member services. Learn about the programs and services we provide here.

Interested in attending our events or looking for ways to become more involved? We host a variety of opportunities that are both fun and informative! Click the links below to learn about opportunities that support the work of the MGA.

The MGA is growing each and every day. Help us shine light on myasthenia gravis by donating today.

What We Do 

COVID continues to plague many of our service areas, thus; the board has put a policy in place to protect the health and safety of our community. The following policy reflects our current decision-making process on in-person programming:

"In areas where there is a high level of COVID-19 transmission per the CDC, in-person support group meetings will be suspended until the risk level returns to low or medium. The MGA will try to make decisions a week in advance when able. Please check the calendar online and your email for any updates."

Get to know the MGA

We are Here to Help


Get Involved

Our quarterly newsletters are here to build camaraderie and confirm that there is a community of support. Read up on our latest newsletter and feel free to explore our archive.

Stay Up to Date

Stay connected with the MGA. You can find us on all social media outlets and can directly contact us with any questions or concerns you may have using this form.

Our blog is designed to highlight the people, places, and perspectives that impact the MG community. Browse articles written by patients, physicians, our team, and others here!

Onsite Clinics - Support Groups - Community Events - Resources

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