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Nicole’s MG Story: A Working Mom’s Journey with MG
Out of nowhere, blurry and double vision struck. It was myasthenia gravis.
LATEST FROM THE MGFA INSIDER BLOG
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.
Spreading MG Awareness, One Step at a Time By Advocating
Drea Carbone began her MG advocacy almost as soon as she was
diagnosed and she hasn’t slowed down since.
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
Golfing for Good
Jeff Abramson’s wife Patti had myasthenia, and when
she left this world, Jeff planned a golf event in her honor. Little did he know how much he
would impact the MG Community.
Resiliency and Hope: My MG Story
Rosemarie D’Alessandro overcame her myasthenia to
become an inspiring advocate for child safety after the murder of her
daughter.