"supporting patients with myasthenia gravis in the heartland one day at a time"
What We Do
Get to know the MGA
We are Here to Help
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
We recognize the fear and uncertainty of patients with myasthenia gravis during this uncertain time. Please know the MGA is always here to support you. For credible information regarding COVID-19 and myasthenia gravis, please see the video by MGNet and a guide prepared by an international working group of MG experts in response to COVID-19 pandemic here.
Onsite Clinics - Support Groups - Community Events - Resources
Find out the latest information about recent news in the MG community, event changes, and any updates regarding the work conducted at the MGA here.
Keep in Touch
IMPORTANT INFORMATION REGARDING COVID-19:
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.
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!
Welcome to the
Myasthenia Gravis Association
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.