03/22/2026
I just attended the Patient Health Alliance event for the NMO community, where I had the chance to share my story again. Living with this rare condition, I’m grateful for the platform to speak out and encourage others to do the same. I remember how crucial community was for me after my diagnosis—I knew I needed support to get through it.
Huge thanks to Alexion and all the foundations that help us share our voices! Also, thank you Jesus Omar Gallegos for being my rock through this journey.
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