Sleep and Myasthenia Gravis: Webinar Recap

Find tools and advice to help you prepare for the worst.

In this vlog, Cary asks her husband Zack some questions about his experience as an MG caregiver.

“We want to find a way to give back to an organization that’s been tremendously helpful to us.” 

Read an excerpt from this new ebook, full of humorous and honest tales about life with myasthenia gravis.

Dr. Heather Finlay-Morreale, a medical doctor who lives with MG, shares tips for preparing for your doctor’s appointment and making the most of the time you have with your provider.

In February the MGFA and the MG Community lost a dedicated volunteer and champion advocate of patients and caregivers. Friends and staff remember his legacy.

Get to know the main character of the newest Spiderman film

Knowing your antibody status helps you manage your myasthenia gravis.

How the MG Friends program makes a difference – for patients and volunteers.