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From Diagnosis to Remission: My MG Story
I woke up on my birthday – it was January 1993 – and I was seeing double.
LATEST FROM THE MGFA INSIDER BLOG
Myasthenia Gravis Can Be a Tough Act to Swallow
Eating can be hard work for MG patients but KJ Fallon provides some
good tips.
Hungarian MG Patients Use Social Media to Connect Across the Miles
Andrea Ujj is connecting Hungarian MG patients as part
of our global MG community.
Thymectomy and MG
Dr. Kevin O’Connor discusses Thymectomy and why
symptoms persist after the procedure.
Only 6 More Days Until the MGFA National Conference – and I Can Hardly Wait!
MGFA Board Chair Nancy Law Talks about her National Conference
Memories and the Importance of this Annual Global Event.
MGFA Partners with Rare Across America to Advocate for MG Patients
Volunteers Ensure Political Leaders Understand the Challenges of
Rare Diseases like Myasthenia.
CARE-MG Registry Will Help Us Understand How COVID-19 Affects MG Patients
Dr. Srikanth Muppidi Using CARE-MG to Understand how COVID-19
Impacts the MG Community
An Inspirational Myasthenia Hero for So Many in the MG Community
Lenora “Lynn” Waltz was an
amazing advocate for the myasthenia community, with an inspiring story that touched so many
people.
How to be Prepared for an MG Emergency
An MG patient offers pragmatic and truly critical advice about
preparing for an MG emergency BEFORE it happens.
Two Myasthenia Patients Proudly Rolled Up Their Sleeves for COVID-19 Vaccination
MG patients and nurses share unique experiences contracting COVID-19
and obtaining the vaccine.
MG Superwoman, Taking It One Day at a Time
MG “Superwoman” Paula McGinnis steps up
to plan community events in Hawaii and Metropolis