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Running for Those Who Can’t
Why I Run: Living With NMO
Time until race starts
Outrun the Odds
This fall, I’ll be lacing up for the 2025 Berlin Marathon, a dream for any runner, but for me, it’s something much deeper. Every mile is a step toward visibility, community, and action for those living with rare neurological diseases like Neuromyelitis Optica (NMO).
My Story
In 2020, I was diagnosed with NMO. Weeks later, a life-altering relapse left me partially paralyzed. I had to learn to walk again, and then I ran. Every stride became an act of resistance. Every run, a declaration that this disease would not define me.
Running became my voice. My movement. My purpose.
Why I Run
I run to:
Raise awareness for NMO and other rare neurological diseases
Advance advocacy for earlier diagnosis and equitable treatment
Build a vibrant, inclusive community of hope and support
I’m not running toward a finish line.
I’m running to change the narrative.
Join Me
If my story moves you, I invite you to stand with me:
Donate to help fund awareness and advocacy efforts
Share this page to spread the word
Support the movement so that no one faces a rare disease alone
With heartfelt gratitude,
Marion Jones
The Rare Marathoner | NMO Patient Advocate