Join us virtually as leading clinicians and researchers to share their work and connect with the experts in life with SCN8A: the families.
About this Event

2024 SCN8A Clinician, Researcher, and Family Gathering

Join us virtually for the . This event is a unique opportunity for clinicians, researchers, and families affected by SCN8A to come together and share knowledge, experiences, and support.

All ticket types include the Friday night livestream. Family tickets also include a livestream of Saturday's events.

Purchase a Gathering t-shirt!

Don't miss out on the chance to grab your official Gathering t-shirt and show your support! Not only is it a great way to commemorate the event, but all proceeds go directly to The Cute Syndrome Foundation, helping to fund critical research and provide resources for families affected by SCN8A. Wear your shirt with pride and join us in making a difference!