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Dan and Aidan share stories about getting through airport security as young men with visible signs of a disorder that not many people have heard of, neurofibromatosis type 1. Click the CC button to enable Closed Captions. Click here to subscribe the Children’s Tumor Foundation YouTube channel, and click the bell so that you receive alerts when new videos are posted: https://www.youtube.com/user/ctforg?s... What is the Children's Tumor Foundation? Children’s Tumor Foundation (CTF) began as the first grassroots organization solely dedicated to finding treatments for NF. Today, CTF is a highly recognized global nonprofit foundation, the leading force in the fight to end NF, and a model for other innovative research endeavors. Visit our website at https://www.ctf.org/ Donate today at https://www.ctf.org/ways-to-give/ Follow us on our social media platforms: Facebook - / childrenstumor Instagram - / childrenstumor Twitter - / childrenstumor LinkedIn - / children's-tumor-foundation #endnf #nf1 #nf2 #nf2swn #swn #childrenstumor #neurofibromatosis #schwannomatosis #nervetumor #tumor