Latest Post
From Diagnosis to Remission: My MG Story
I woke up on my birthday – it was January 1993 – and I was seeing double.
LATEST FROM THE MGFA INSIDER BLOG
Beating the Heat During Summer Months
Many people with myasthenia gravis will tell you symptoms flare up during the summer months. Here are a few tips to help you manage MG in hot weather.
The Snowflake Disease
Just like a snowflake, myasthenia gravis symptoms can appear one
minute and be gone the next.
Our MG Story: Advice for Spouses and Caregivers
In this vlog, Cary asks her husband Zack some questions about his
experience as an MG caregiver.
Our MG Story: When Your Child Has Myasthenia Gravis
The Oronuga family’s life was turned upside down when
Teniola was diagnosed with MG at age three. They share what it is like to battle this
chronic autoimmune condition in Nigeria.
Our MG Story: The Stehlik Sisters Give Back in Memory of Their Pops
An MG diagnosis leads to a passion for raising awareness and giving
back.
Her Fight is My Fight
Raising awareness and racing for a cure with a one-of-a-kind
fundraiser.
Spotlight on the MG Community: Paul Strumph
Learn more about a key member of our volunteer Board of
Directors.
Why the MG Walk Matters to Me
It's more important than ever to restart the MG Walk.
We’re closer than ever to a world without MG. But to get there, we need
you.