Latest Post
Laughing Despite (and, Sometimes, Because of!) Myasthenia Gravis: An Interview with Jane Marla Robbins
An actor and author living with MG shares how humor helps her cope
LATEST FROM THE MGFA INSIDER BLOG
Rare Disease Week – Advocacy at Home and on the Hill
Rare Disease Week starts on February 28. Learn how you can advocate
for people with MG.
MG patients discuss finding community at the MGFA Patient Conference
Hear from patients about why they are attending the MGFA National
Patient Conference in 2023.
Let’s Be Courageous, Together
Priscilla Forrester’s courageous effort to connect
community members and volunteer
Thinking About the Mental Health of Those Impacted by COVID-19 – A Time to Begin Healing
Thinking about the impact of COVID on mental health as an MG
patient.
Can Car T-Cell Therapy Effectively Treat Myasthenia Gravis?
Danny DeBerry and his CAR T-Cell Therapy story.
Managing MG: A Nurse’s Perspective
Melissa Edmonds offers a nurse’s perspective on
managing MG.
Novelist Helps Readers Understand Myasthenia Gravis
Elyse Bruce’s book “Fantastic
Things” helps children relate to and understand myasthenia.
Thank You Dr. Ted Burns for Your Years of Dedication to the MG Community
Many colleagues and friends reflect on the life and contributions of
Dr. Ted Burns
MY MG Story: Felicia Jeffries
Felicia Jeffries is a strong voice for MG patients and their complex
journeys
MG Expert Series: Patient Reported Experiences as reported by an International MG Patient Council
New treatment discoveries based on BeatMG study helps researchers
learn valuable lessons about MG