As a child in Iran, Dr. Fatemeh Khani Habibabadi was always interested in the world around her. Now her research in autoimmune neurological disorders is making a difference for people with MG.

Miss Kingston Audrey Getman shares her MG story.

Traveling with an illness like myasthenia gravis can be challenging, but with some planning and the right tricks up your sleeve, you can enjoy your trip safely.

See photos and watch session recordings from our first in-person patient conference since 2019.

MGFA’s Meridith O’Connor talks with Dr. Jonathan Strober, director of the Neuromuscular Clinic at Benioff Children’s Hospital.

The struggle seronegative myasthenia gravis patients face for diagnosis and treatment.

Hear from patients about why they are attending the MGFA National Patient Conference in 2023.

Danny DeBerry and his CAR T-Cell Therapy story.

Melissa Edmonds offers a nurse’s perspective on managing MG.

Elyse Bruce’s book “Fantastic Things” helps children relate to and understand myasthenia.