Rare Disease Day happens once a year, but you can bring awareness to myasthenia gravis any day of the week!

Illuminating the support rare disease patients need 365 days of the year.

Rare Disease Week starts on February 28. Learn how you can advocate for people with MG.

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

Priscilla Forrester’s courageous effort to connect community members and volunteer   

Thinking about the impact of COVID on mental health as an MG patient.

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.

Many colleagues and friends reflect on the life and contributions of Dr. Ted Burns