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Latest Post

A New Era for the MG Patient Registry: Empowering Patients, Advancing Research

Kate Stober | October 28, 2025
MGFA is proud to announce the next stage in the evolution of the MG Patient Registry: the Vitaccess Real MG Registry.
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LATEST FROM THE MGFA INSIDER BLOG

The Snowflake Disease
Living with MG Stories

The Snowflake Disease

Greg Olsen | June 17, 2024
Just like a snowflake, myasthenia gravis symptoms can appear one minute and be gone the next.
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Our MG Story: Advice for Spouses and Caregivers
Living with MG Stories

Our MG Story: Advice for Spouses and Caregivers

Kate Stober | June 13, 2024
In this vlog, Cary asks her husband Zack some questions about his experience as an MG caregiver.
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Something to Chew On
Living with MG Stories

Something to Chew On

Aimee Sears | June 10, 2024
How is MG like a piece of chewing gum?
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Our MG Story: When Your Child Has Myasthenia Gravis
Living with MG Stories

Our MG Story: When Your Child Has Myasthenia Gravis

Motunrayo Ononuga | June 6, 2024
The Oronuga family’s life was turned upside down when Teniola was diagnosed with MG at age three. They share what it is like to battle this chronic autoimmune condition in Nigeria.
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Our MG Story: The Stehlik Sisters Give Back in Memory of Their Pops
Community Fundraising

Our MG Story: The Stehlik Sisters Give Back in Memory of Their Pops

Kate Stober | June 4, 2024
An MG diagnosis leads to a passion for raising awareness and giving back.
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Her Fight is My Fight
Community Fundraising

Her Fight is My Fight

Kate Stober | May 30, 2024
Raising awareness and racing for a cure with a one-of-a-kind fundraiser.
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Events

2025 MGFA National Patient Conference

Mike Antonellis | May 15, 2024
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Spotlight on the MG Community: Paul Strumph
MGFA News

Spotlight on the MG Community: Paul Strumph

Kate Stober | April 22, 2024
Learn more about a key member of our volunteer Board of Directors.
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Why the MG Walk Matters to Me
Community Fundraising

Why the MG Walk Matters to Me

Kate Stober | April 18, 2024
It's more important than ever to restart the MG Walk. We’re closer than ever to a world without MG. But to get there, we need you. 
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Running the Denver Colfax Marathon for a World Without Myasthenia Gravis
MG Articles

Running the Denver Colfax Marathon for a World Without Myasthenia Gravis

Kate Stober | April 10, 2024
“We want to find a way to give back to an organization that’s been tremendously helpful to us.” 
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