Latest Post
My MG Story: Victoria Discusses Life and Work with Myasthenia Gravis
Nine years ago, Victoria woke up with MG symptoms. She shares her experience with diagnosis and treatment in a small town.
LATEST FROM THE MGFA INSIDER BLOG
Rare Disease Week: Highlighting Seronegative MG, a “Rare-of-the-Rare” Disease
The struggle seronegative myasthenia gravis patients face for
diagnosis and treatment.
How to Be an Advocate for Yourself and Others with Myasthenia Gravis
Rare Disease Day happens once a year, but you can bring awareness to
myasthenia gravis any day of the week!
When Every Day is Rare Disease Day
Illuminating the support rare disease patients need 365 days of the
year.
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.