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SUMMARY:Young People Living with Rare Neurological Disorders
DESCRIPTION: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. \nRegister HERE. \nTuesday\, December 1\, 2026 \n4:00 PM PT / 7:00 PM ET \nModerated by Taylor Macey \nMade possible with support from Amgen and argenx.
URL:https://www.sumairafoundation.org/event/young-people-living-with-rare-neurological-disorders/
CATEGORIES:From The Experts,TSF Programming,TSF Webinar
ATTACH;FMTTYPE=image/png:https://www.sumairafoundation.org/wp-content/uploads/2026/11/TSF-Youth-3.png
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