Medical Stories - Neurofibromatosis Type 1: Aubrie's Story

Aubrie is a little girl who inherited a disfiguring medical condition known as neurofibromatosis type 1, or NF1. It's a rare autoimmune disorder that's unfortunately common in her family, including in her mother, Sarah, but Aubrie and her relatives manage to maintain a positive attitude despite their disease. This episode features in-depth commentary from renowned expert David Viskochil, MD, PhD, Professor of Pediatrics and Medical Geneticist, University of Utah. Please subscribe to our YouTube channel and look for Medical Stories on your Public Television station. Check your local PBS listings today! Or visit https://medicalstories.tv/ to learn more about this very popular documentary series. Follow us on Facebook:   / medicalstories.pubtv.pbs   Check us out on Instagram:   / medicalstories_pubtv_pbs   Subscribe to our YouTube Channel:    / @medicalstories   Look for us on TikTok:   / medicalstories.tv   #MedicalStories #MedStoriesTV #nf1 #neurofibromatosis Chapters: 0:00 Introduction 0:36 What is Neurofibromatosis Type 1 (NF1)? 1:20 Types of Neurofibromatosis 2:08 Family History & Inheritance 2:21 Early Symptoms Begin 2:36 Café-au-Lait Spots, Freckling, Skin Tumors, & Neurofibromas 3:00 Navigating Diagnosis 3:50 Learning & Development Challenges 4:13 Aubrie’s Tumor & First MRIs 4:50 Surgeries & Managing Tumor Growth 5:38 Living With Physical Challenges 5:57 Understanding NF1 Prognosis 6:36 Tumors, Pain, & Daily Symptoms 7:02 Cancer Risks in NF1 & Coping With Loss 7:39 Ongoing Surgeries & Tumor Growth 8:13 Emotional & Social Challenges 9:10 Learning Disabilities & ADHD 9:45 Finding Community & Support 10:36 Connecting With the NF Community 10:57 Hope, Strength, & Moving Forward