Latest Post Walking for MG Awareness in Halifax Kate Stober | June 12, 2025 Struggling with MG symptoms but determined to make a difference, Nadine steps out of the shadows. Read More
Our MG Voice Advocacy When Rare Disease Advocacy Is Personal Kate Stober | April 11, 2022 For Brenda Colmenares, an MG diagnosis set her on a path of rare disease advocacy and awareness. Read More
Living with MG Stories A Patient’s Perspective on Muscle Cramping Rebecca Molitoris | March 17, 2022 Advice on dealing with muscle cramps when you live with myasthenia gravis. Read More
Living with MG Stories Water Skiing into the New Year Jane Marla Robbins | February 15, 2022 My doctor says “always try to get the patient back to water skiing.” Read More
Community Fundraising MG Walk’s “Rookie of the Year” Finds Power in Sharing Her Story Kate Stober | January 21, 2022 “Rookie of the Year” Priscilla Forrester finds power in sharing her story Read More
Living with MG Stories My MG Story: Diagnosed as a Teen, Emily’s MG is in Remission Thanks to Thymectomy Kate Stober | December 2, 2021 Boyle Family Realizes the Powerful Benefits of Thymectomy. Read More
MG Research New Book by a Leading Doctor Will Help You Cope with Myasthenia Dr. Aziz Shaibani, M.D. | November 3, 2021 All proceeds from Coping with Myasthania Gravis book will benefit MGFA Read More
Living with MG Stories Newly diagnosed? Here’s What You Need to Know. Rebecca Molitoris | October 12, 2021 Newly-Diagnosed with MG? Here are Some First Steps to Take Read More
Living with MG Stories Evan Greene Reaches New Peaks in Spite of His MG Evan Greene | October 4, 2021 Evan Greene’s Climbs Mount Whitney – MG Cannot Take His Spirit and Sense of Life Read More
Living with MG Stories From MG to MD: a story of hope and persistence Kate Stober | September 27, 2021 MG patient is inspired by his disease to enter healthcare and become an MD. Read More
Our MG Voice Advocacy MG Patient Advocates Make Their Voices Heard During Rare Disease Week 2021 Genna Mvalo | August 24, 2021 MG Advocates Describe Their Experiences During Rare Disease Week Read More