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Latest Post

Webinar Recap: Financial Assistance Resources for the Myasthenia Gravis Community

Kate Stober | March 24, 2026
Affording care for myasthenia gravis remains a challenge for many patients. Find practical guidance on navigating patient financial support programs.
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LATEST FROM THE MGFA INSIDER BLOG

Only 6 More Days Until the MGFA National Conference – and I Can Hardly Wait!
Events

Only 6 More Days Until the MGFA National Conference – and I Can Hardly Wait!

Nancy Law | April 6, 2021
MGFA Board Chair Nancy Law Talks about her National Conference Memories and the Importance of this Annual Global Event.
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MGFA Partners with Rare Across America to Advocate for MG Patients
Our MG Voice Advocacy

MGFA Partners with Rare Across America to Advocate for MG Patients

Genna Mvalo | March 22, 2021
Volunteers Ensure Political Leaders Understand the Challenges of Rare Diseases like Myasthenia.
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CARE-MG Registry Will Help Us Understand How COVID-19 Affects MG Patients
MG Research

CARE-MG Registry Will Help Us Understand How COVID-19 Affects MG Patients

Srikanth Muppidi, MD | March 16, 2021
Dr. Srikanth Muppidi Using CARE-MG to Understand how COVID-19 Impacts the MG Community
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An Inspirational Myasthenia Hero for So Many in the MG Community
Our MG Voice Advocacy

An Inspirational Myasthenia Hero for So Many in the MG Community

Michelle Baumgartner | March 8, 2021
Lenora “Lynn” Waltz was an amazing advocate for the myasthenia community, with an inspiring story that touched so many people.
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Living with MG Stories

How to be Prepared for an MG Emergency

Rebecca Molitoris | February 26, 2021
An MG patient offers pragmatic and truly critical advice about preparing for an MG emergency BEFORE it happens.
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Two Myasthenia Patients Proudly Rolled Up Their Sleeves for COVID-19 Vaccination
Living with MG Stories

Two Myasthenia Patients Proudly Rolled Up Their Sleeves for COVID-19 Vaccination

Kate Stober | February 15, 2021
MG patients and nurses share unique experiences contracting COVID-19 and obtaining the vaccine.
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MG Superwoman, Taking It One Day at a Time
Community Fundraising

MG Superwoman, Taking It One Day at a Time

Kate Stober | February 5, 2021
MG “Superwoman” Paula McGinnis steps up to plan community events in Hawaii and Metropolis
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Golfing for Good
Community Fundraising

Golfing for Good

Kate Stober | January 19, 2021
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.
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Resiliency and Hope: My MG Story
Living with MG Stories

Resiliency and Hope: My MG Story

Kate Stober | December 23, 2020
Rosemarie D’Alessandro overcame her myasthenia to become an inspiring advocate for child safety after the murder of her daughter.
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MGFA Pilot Grant Awards Announced for 2020
MG Research

MGFA Pilot Grant Awards Announced for 2020

Genna Mvalo | December 15, 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.
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