Latest Post
Webinar Recap: Financial Assistance Resources for the Myasthenia Gravis Community
Affording care for myasthenia gravis remains a challenge for many patients. Find practical guidance on navigating patient financial support programs.
LATEST FROM THE MGFA INSIDER BLOG
MGFA Partnership with argenx Helps Bring New Treatment Option to MG Patients
The story of argenx and MGFA’s collaboration to bring
about a new MG treatment.
Janet Myder Was the Epitome of Dedication to MG Advocacy
Janet Myder was a Dedicated MG
Volunteer.
Identifying MG Weakness – A Patient Perspective
Coming to grips with MG-induced
muscle weakness takes time but is essential to your
wellness.
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