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Tag: Living with MG Stories

Nicole’s MG Story: A Working Mom’s Journey with MG
Living with MG Stories

Nicole’s MG Story: A Working Mom’s Journey with MG

Kate Stober | June 19, 2025
Out of nowhere, blurry and double vision struck. It was myasthenia gravis.
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Invisible No More
Living with MG Stories Our MG Voice Advocacy

Invisible No More

Kate Stober | June 13, 2025
Three musicians living with myasthenia gravis come together on the song "Invisible People" for MG Awareness Month
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Walking for MG Awareness in Halifax
Community Fundraising Living with MG Stories

Walking for MG Awareness in Halifax

Kate Stober | June 12, 2025
Struggling with MG symptoms but determined to make a difference, Nadine steps out of the shadows.
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“Swimming Was Scary” – How Myasthenia Gravis Nearly Ended Everything for a Star Student-Athlete
Living with MG Stories

“Swimming Was Scary” – How Myasthenia Gravis Nearly Ended Everything for a Star Student-Athlete

Tia Chakrapani | May 31, 2025
High school swimmer Tia Chakrapani shares her myasthenia gravis story to help others understand: MG may be an invisible illness, but it is still very real.
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Laughing Despite (and, Sometimes, Because of!) Myasthenia Gravis: An Interview with Jane Marla Robbins
Living with MG Stories

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
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My MG Story: Danielle’s Journey with Seronegative Myasthenia Gravis
Living with MG Stories

My MG Story: Danielle’s Journey with Seronegative Myasthenia Gravis

Kate Stober | February 27, 2025
Danielle wants to share her treatment journey to help others understand the challenges of finding the right approach.
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Running for a World Without MG: Kristy’s Story
Living with MG Stories

Running for a World Without MG: Kristy’s Story

Kristy Edmonds | February 12, 2025
Kristy shares her MG story and why helping others living with the disease is important to her.
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We somehow always find a way to get back up: My MG story
Living with MG Stories

We somehow always find a way to get back up: My MG story

Rose Diop | January 3, 2025
Rose was diagnosed with myasthenia gravis in the summer of 2022. Born in Senegal, she has lived in Canada for 20 years. She works as a project manager and a content creator in the personal beauty industry. She first noticed MG symptoms while applying her makeup one day. She started seeing double and noticed her […]
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Pediatric MG: Listen to This Podcast Episode
MG Research

Pediatric MG: Listen to This Podcast Episode

Kate Stober | April 4, 2023
MGFA’s Meridith O’Connor talks with Dr. Jonathan Strober, director of the Neuromuscular Clinic at Benioff Children’s Hospital.
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