MGFA offers many educational and informative materials to help you live with MG. Receive an email with our MGFA Digital Patient Pack with links to webinars, educational materials, support groups, and research information. Complete the online form in this link and you will receive the email with an added option for a hard copy version. You can also reach out to the MGFA at mgfa@myasthenia.org
Living with myasthenia gravis and navigating your disease journey
Whether you have recently received your myasthenia gravis (MG) diagnosis or you have been living with MG for years, you may find yourself wondering how to live your best life possible. Adjusting to life with MG may require you to do some things differently. Arming yourself with the latest information from MG experts and hearing other people’s stories may help guide you on your MG journey.
MGFA offers many educational and informative materials to help you live with MG.
Please visit the links on the right side of this page in the gray sidebar to access a number of resources provided by the MGFA or continue to scroll down to learn more.
Start with our Wellness and What's New in Research Webinar Series
The MGFA Wellness Webinars introduces many qualified and experienced presenters to help you focus on your own health and wellness while living with MG. The What’s New in MG Research Webinars feature medical professionals and academic leaders showcasing new discoveries, research, and information about the latest progress.
Register for upcoming wellness series events
Register for upcoming research series events
Learn more from our YouTube channel
Check out the MGFA YouTube page to view many types of videos including conferences, speaking sessions, patient stories, scientific presentations, and many more. Watch Now.
Find MG Support Groups
Are you looking to connect with others who share common life experiences? Support groups offer fellowship, resources, educational programming, and a chance to get to know others in the same boat. Share your story, learn from local professionals, and build your MG community. In addition to regional support groups, there are specialty support groups for young adults, seronegative (antibody negative) MG patients, caregivers, and Spanish speakers. Learn more about support groups.
Find an MG Friend – Or Become an MG Friend Yourself
Are you or someone you know looking for phone support to help manage myasthenia gravis? MG Friends are here to support you! Our free peer-to-peer phone support program helps to ensure that everyone in the community gets the information they need and knows they are not alone. MG Friends provides the opportunity for a person with questions and concerns to connect to someone else with MG— no matter where they live. Connect Now.
Managing your MG
Managing your MG symptoms and learning “tips and tricks” for going about your daily routines can improve your quality of life. Read about ways to manage your symptoms and live better with MG or how to manage an MG crisis.
Other resources to support you
MGFA Online Community
MGFA National Patient Conference
Patient and Caregiver Resources and Assistance
The MGFA Insiders Blog