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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

This Isn’t My Story, But It Is My Life: My Father Has MG
Living with MG Stories

This Isn’t My Story, But It Is My Life: My Father Has MG

Lizeth V. | September 4, 2023
I was five years old, and I didn't understand what was going on. All I knew was that I was scared.
Read More
A Tribute to Stan Way: A dedicated Volunteer Leader in the MG Community
MG History

A Tribute to Stan Way: A dedicated Volunteer Leader in the MG Community

Kate Stober | August 23, 2023
Remembering a visionary educator, community builder, and champion of the internet’s power to create connections.
Read More
Myasthenia Gravis Considerations in Dentistry
Living with MG Stories

Myasthenia Gravis Considerations in Dentistry

Kate Stober | August 22, 2023
On August 17, dentist and MG patient Dr. Gene Cassagrande led a Wellness Webinar focused on having a successful dentist visit when you have myasthenia gravis. Dr. Cassagrande practiced dentistry for 30 years before transitioning into a role as a medical device salesperson. With his deep knowledge of dentistry and his lived experience with MG, […]
Read More
Targeting B cells may help people with MuSK Myasthenia Gravis
MG Research

Targeting B cells may help people with MuSK Myasthenia Gravis

Kate Stober | August 7, 2023
“For me, precision medicine has always been the holy grail of what we’re trying to achieve.” 
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Finding a Place to Stay When You Travel for Medical Care
Living with MG Stories

Finding a Place to Stay When You Travel for Medical Care

Jim Sliney | July 27, 2023
Options for discounted lodging for patients and their families.
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What is it like to have a loved one with myasthenia gravis?
Living with MG Stories

What is it like to have a loved one with myasthenia gravis?

Kate Stober | July 13, 2023
Bru Ajueyitsi shares his perspective on his mother’s MG journey and the ripple effects of the disease.
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Researcher Investigates MG Mechanisms of Disease Thanks to Donor and MGFA Support
MG Research

Researcher Investigates MG Mechanisms of Disease Thanks to Donor and MGFA Support

Kate Stober | July 6, 2023
As a child in Iran, Dr. Fatemeh Khani Habibabadi was always interested in the world around her. Now her research in autoimmune neurological disorders is making a difference for people with MG.
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My MG Story – I Persevere Because There’s Hope
Living with MG Stories

My MG Story – I Persevere Because There’s Hope

Meena Outlaw | June 29, 2023
What I want others to know after nearly a decade with MG.
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My MG Story: Balancing MG with Life, Work, and Friends
Living with MG Stories

My MG Story: Balancing MG with Life, Work, and Friends

Sam Lam | June 22, 2023
I hope my story can help folks, especially younger patients, feel that they are not alone.
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Better Together: We Share a Myasthenia Gravis Diagnosis
Living with MG Stories

Better Together: We Share a Myasthenia Gravis Diagnosis

Mike Antonellis | June 15, 2023
How two people living with myasthenia gravis found each other.
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