Mandy Montgomery

Following an incredible Nevus Adults gathering in Milan, this special experience is coming to Orlando, July 23–26, 2026 ✨
Designed exclusively for adult nevus owners, this social long weekend is all about connection, laughter, and shared experiences—before the AMPLIFY Conference begins.
Come as you are. Stay as long as you’d like. 💙
Join your hosts Steven, Raissa, and Mandy and be part of a community that truly understands.
👉 Register your spot today at nevus.org/events

First gig of the year tonight. Come get down with us at tonight. 🤘💋

Today I am having my 64th surgery, and, tomorrow I am grateful to be turning thirty-two years old. I post in honor of the upcoming holiday, rare disease day. I live with Congenital Melanocytic Nevus. I spent this past weekend in Washington DC celebrating at the Rally for Rare. It is incredible seeing all of the gorgeous people living bold and owning their rare with my family. I am truly so grateful for all of the people I was able to connect with this weekend. After hiding my skin up until a few years ago I am so proud of being me. I love my resilient body, free spirit, and sexy skin. I am so thankful to be alive. Thank you to my friends, family, and extended support all over the globe that have truly transformed my life and how I love myself. For my birthday please consider donating to the lifesaving research and incredible organizations below. I am so happy to be able to advocate and bring awareness for and

Another super sick show in the books for ~~~We play next Saturday, September 21st at See you there 😘~~~