Every year on International SCN8A Awareness Day, February 9th, we host a live event to celebrate where we’ve been over the previous year and where we’re headed in the year(s) to come. With lots of mini-chats, we will discuss the State of SCN8A. Join us to hear from a lineup of doctors, researchers, caregivers, and […]

Join us for a special gathering exclusively for grandparents of children with SCN8A. This is a warm and welcoming space to share your unique experiences, exchange support, and connect with others who understand your journey. Whether you’re seeking advice, offering encouragement, or simply looking to connect, this meetup is here for you. Together, we’ll celebrate

A dedicated space for parents and caregivers, including those newly navigating an SCN8A diagnosis, to find answers, practical advice, and connection. Learn what SCN8A means for your child, how to manage symptoms, and what treatment options are available. Gain insights into the latest research, hear from other families, and connect directly with Dr. Hammer, an

A dedicated space for parents and caregivers, including those newly navigating an SCN8A diagnosis, to find answers, practical advice, and connection. Learn what SCN8A means for your child, how to manage symptoms, and what treatment options are available. Gain insights into the latest research, hear from other families, and connect directly with Dr. Hammer, an

A dedicated space for parents and caregivers, including those newly navigating an SCN8A diagnosis, to find answers, practical advice, and connection. Learn what SCN8A means for your child, how to manage symptoms, and what treatment options are available. Gain insights into the latest research, hear from other families, and connect directly with Dr. Hammer, an