A new year doesn’t mean starting over—it means continuing forward, together. Join parents and caregivers of adults with Lennox-Gastaut Syndrome for a supportive space to connect, share experiences, and feel understood. Caring for an adult with LGS brings evolving challenges,...
Join us on Tuesday, February 10th at 8 pm ET. Topic: How Do You Keep Track of EVERYTHING? Seizure Action Plan Awareness Week is every February. Join this month's support group and share how you track the seizures, behaviors, sleep...
Join us Tuesday, February 17th at 8 pm ET Hosted by dads, for dads. Join our exclusive support group for male caregivers and Dads as we talk, share, and offer encouragement to each other along this LGS journey. Bring your...
El Grupo de Esperanza de LGS es un espacio de apoyo, escucha y conexión para familias que viven con el síndrome de Lennox-Gastaut. Cada mes, las cuidadoras Bertha Guillen, Michele Torres, y Kelly Arrango nos guían en conversaciones significativas donde...
Connection matters—especially on the hardest days. This monthly support group brings together caregivers of adults with Lennox-Gastaut Syndrome for open conversation, shared insight, and encouragement. As caregiving needs change over time, this space offers reassurance that you are not alone....
Join us on Tuesday, March 10th at 8 pm ET. Topic: Community Connections Make Us Stronger Caregiving for someone with LGS can feel isolating, but we’re not meant to do this alone. Join us for this support group conversation as we explore simple, meaningful strategies to stay...
Join us Tuesday, March 17th at 8 pm ET Hosted by dads, for dads. Join our exclusive support group for male caregivers and Dads as we talk, share, and offer encouragement to each other along this LGS journey. Bring your...
Acompáñenos en marzo para el Grupo de Esperanza de LGS, un encuentro mensual en español creado para apoyar, animar y conectar a familias afectadas por el síndrome de Lennox-Gastaut. Facilitado por Bertha Guillen, Michele Torres, y Kelly Arrango, este grupo...
Caring for an adult with LGS is complex—but support makes it lighter. Join fellow parents and caregivers for a monthly, judgment-free space to share, listen, and connect. Whether you are navigating long-term caregiving or preparing for the transition to adulthood,...
Together for a Breakthrough April 2026 is Walk Month for Lennox-Gastaut Syndrome, a month-long movement that expands the Walk beyond just one day—giving families, advocates, and supporters everywhere more ways to walk, wheel, and make an impact. Walk your way....
Save the Date! | July 9–11, 2026 📍 Orlando, Florida Join us for the LGS Foundation’s 10th International Family & Professional Conference, a powerful three-day event that brings together hundreds of families, caregivers, and epilepsy professionals from around the globe. Held...