Latest Post
Laughing Despite (and, Sometimes, Because of!) Myasthenia Gravis: An Interview with Jane Marla Robbins
An actor and author living with MG shares how humor helps her cope
LATEST FROM THE MGFA INSIDER BLOG
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.
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