Latest Post
Walking for MG Awareness in Halifax
Struggling with MG symptoms but determined to make a difference, Nadine steps out of the shadows.
LATEST FROM THE MGFA INSIDER BLOG
When Rare Disease Advocacy Is Personal
For Brenda Colmenares, an MG diagnosis set her on a path of rare
disease advocacy and awareness.
A Patient’s Perspective on Muscle Cramping
Advice on dealing with muscle cramps when you live with myasthenia gravis.
Water Skiing into the New Year
My doctor says “always try to get the patient back to
water skiing.”
MG Walk’s “Rookie of the Year” Finds Power in Sharing Her Story
“Rookie of the Year” Priscilla Forrester
finds power in sharing her story
My MG Story: Diagnosed as a Teen, Emily’s MG is in Remission Thanks to Thymectomy
Boyle Family Realizes the Powerful Benefits of
Thymectomy.
New Book by a Leading Doctor Will Help You Cope with Myasthenia
All proceeds from Coping with Myasthania
Gravis book will benefit MGFA
Newly diagnosed? Here’s What You Need to Know.
Newly-Diagnosed with MG? Here are Some First Steps to
Take
Evan Greene Reaches New Peaks in Spite of His MG
Evan Greene’s Climbs Mount Whitney – MG
Cannot Take His Spirit and Sense of Life
From MG to MD: a story of hope and persistence
MG patient is inspired by his disease to enter healthcare and become
an MD.
MG Patient Advocates Make Their Voices Heard During Rare Disease Week 2021
MG Advocates Describe Their Experiences During Rare Disease
Week