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
Thank You Dr. Ted Burns for Your Years of Dedication to the MG Community
Many colleagues and friends reflect on the life and contributions of
Dr. Ted Burns
MY MG Story: Felicia Jeffries
Felicia Jeffries is a strong voice for MG patients and their complex
journeys
MG Expert Series: Patient Reported Experiences as reported by an International MG Patient Council
New treatment discoveries based on BeatMG study helps researchers
learn valuable lessons about MG
Biking for MG Awareness: Lucero’s Brian Venable Takes on the Tour Divide
Lucero guitarist Brian Venerable honors his friend with MG with a
fundraising ride
MG Expert Series: Impact of COVID-19 on MG Patients and Safety of Vaccines
Data Supports Safety of COVID-19 Vaccines and Impact on MG
Patients
Coast to Coast Team Introductions
MG volunteers chair MGFA’s largest national fundraiser
– The Coast-to-Coast 2740 Challenge.
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.