Young People Living with Rare Neurological Disorders
December 1 @ 7:00 pm - 8:00 pm EST
Join us for TSF’s 10th and final U.S. webinar of 2026, a casual, candid conversation with young TSF ambassadors about what it’s really like to grow up with a rare neurological disorder. Beyond diagnoses and treatments, our panelists will share how their condition shows up in everyday life: navigating school, building a career, making and keeping friends, dating, and everything in between. Whether you’re a young person living with a rare disease, a parent, a caregiver, or a friend, you’ll come away with real stories, practical insight, and the reminder that you’re not alone.
Register HERE.
Tuesday, December 1, 2026
4:00 PM PT / 7:00 PM ET
Moderated by Taylor Macey
Made possible with support from Amgen and argenx.
