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Latest Post

Laughing Despite (and, Sometimes, Because of!) Myasthenia Gravis: An Interview with Jane Marla Robbins

Kate Stober | April 25, 2025
An actor and author living with MG shares how humor helps her cope
Read More

LATEST FROM THE MGFA INSIDER BLOG

What’s Your Antibody?
MGFA Programs

What’s Your Antibody?

Kate Stober | December 14, 2023
Knowing your antibody status helps you manage your myasthenia gravis.
Read More
You’ve Got a Friend in Me
Living with MG Stories

You’ve Got a Friend in Me

Kate Stober | November 21, 2023
How the MG Friends program makes a difference – for patients and volunteers.
Read More
How to Keep Physical Fitness in Your Life, Despite the Challenges MG Brings
Living with MG Stories

How to Keep Physical Fitness in Your Life, Despite the Challenges MG Brings

Kate Stober | November 9, 2023
When bodybuilder Barry Stalker found out he had myasthenia gravis, his life did a 180. “I went from being able to squat 400 pounds to my wife having to help me off the sofa.” 
Read More
Mistakes Caregivers Make and How to Avoid Them
Living with MG Stories

Mistakes Caregivers Make and How to Avoid Them

Toni Claire Gitles | November 2, 2023
Get started transforming the mistakes into your success strategies.
Read More
MGFA Invited to Participate in the INSPIRE Advisory Board and MSMilan Patient Community
        Day Conference
MGFA News

MGFA Invited to Participate in the INSPIRE Advisory Board and MSMilan Patient Community Day Conference

Mike Antonellis | October 30, 2023
Collaborating with others to drive increased awareness about rare disease around the world
Read More
Corticosteroids: A Love/Hate Relationship
Living with MG Stories

Corticosteroids: A Love/Hate Relationship

Krystel El Koussa | October 26, 2023
You are not your weight.
Read More
Learn about Medical Financial Assistance from the PAN Foundation
MGFA Programs

Learn about Medical Financial Assistance from the PAN Foundation

Kate Stober | October 19, 2023
Amy Niles of the PAN Foundation shares how the organization can help MG patients pay for out-of-pocket prescription medicine costs.
Read More
Running the NYC Marathon for a World without Myasthenia Gravis
Community Fundraising

Running the NYC Marathon for a World without Myasthenia Gravis

Kate Stober | October 17, 2023
MGFA sat down with MG patient Julie and her boyfriend, Zack, who is running the marathon for MG awareness, to talk about why supporting the MGFA matters to them both.
Read More
My MG Story: Getting My Smile Back
Living with MG Stories

My MG Story: Getting My Smile Back

Hannah Ensor | October 10, 2023
As a new mom, Hannah Ensor faced challenging and confusing medical symptoms.
Read More
Requesting Accommodations for Myasthenia Gravis at Work
Living with MG Stories

Requesting Accommodations for Myasthenia Gravis at Work

Kate Stober | September 29, 2023
Tips for ensuring you are seen, heard, and accommodated.
Read More

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