The LGS Foundation is honored to participate in the 2025 American Epilepsy Society (AES) Annual Meeting, the premier gathering for clinicians, researchers, and professionals dedicated to advancing epilepsy care and science. This year’s meeting is a vital opportunity to elevate...
Join us on Tuesday, December 16th at 8 pm ET. Topic: 2025, The Year That Was Let's look back on the past year. How has 2025 treated you and your family? Personally? Professionally? Come join our group as we reflect...
Únase a nosotros el jueves 18 de diciembre a las 8 pm ET Nadie debería caminar solo en este sendero El grupo de esperanza de LGS es un espacio seguro para reunirnos virtualmente y compartir nuestras historias. Únase a las...
New Family Orientation Meeting Date: Tuesday, January 6th, 2026Time: 7:00 – 8:30 PM ESTLocation: Virtual (Zoom) Are you new to the Lennox-Gastaut Syndrome (LGS) community? Whether you’ve just received a diagnosis or are new to the LGS Foundation, this meeting is designed...
Join us on Tuesday, January 13th at 8 pm ET. Topic: Setting Achievable Goals! It's all about finding BALANCE! As we look ahead to 2026, it’s a great time to reflect and set intentions. What is one personal goal you hope...
Únase a nosotros este mes para el Grupo de Esperanza de LGS, un espacio seguro y acogedor para reunirnos virtualmente, compartir nuestras historias y apoyarnos mutuamente. Este grupo mensual en español está facilitado por las cuidadoras Bertha Guillen, Michele Torres,...
Join us Tuesday, January 20th 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...
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....