We Asked Aldelly 23 Questions: Introducing Our New Video Series
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're launching our new video series, "23 Questions."
A new video series
Getting to know Aldelly Vasquez
First up: our incredible patient leader Aldelly. She's a mom of two, a wife, a 30-something, and is "fabulously" living with NMO, despite the ups and downs. We asked her about her likes and dislikes, her life at home, and how things changed when she was diagnosed with NMO.
Let's ask Aldelly 23 questions
What didn't we ask Aldelly that you would love to know about her and her NMO journey? Put your questions in the comments!
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