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Invisible No More
Three musicians living with myasthenia gravis come together on the song "Invisible People" for MG Awareness Month
LATEST FROM THE MGFA INSIDER BLOG
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.
MGFA Pilot Grant Awards Announced for 2020
MGFA is pleased to award research grants each year to help advance
the understanding of myasthenia gravis. Congratulations to the amazingly creative medical
professionals and researchers who earned the 2020 funding grants.