We Asked Mo 23 Questions
Last updated: September 2022
Getting to know each other a bit better
As we know, NMO is an exceedingly rare disease. When you meet someone who also lives with NMO, it's only natural to want to know everything about them and how their life has changed since their diagnosis. It's because of this desire to learn more about each other that we launched our new video series, "23 Questions."
More about the video series
Have you ever seen one of Vogue's "73 Questions" videos? This series will be something like that, except the videos will be a bit shorter, and we probably won't be interviewing Taylor Swift.
Getting to know Mo Jones
Let's get to know our all-star advocate and patient leader Mo. She is a wife and mom of three, completed her Associate's Degree in Small Business Management & Entrepreneurship, and runs 3 businesses; one of which she started after her vision loss and during a global pandemic. Having been a diabetic for over a decade Mo was used to hitting bumps in the road, but it was the NMO diagnosis that knocked her off her feet. We asked Mo about her likes and dislikes, her life at home, and how things changed when she was diagnosed with NMO.
How does social media affect your life with NMO?
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