LGS Virtual Valentine’s Dance Party

Join the LGS Foundation and DJ's Kara & Tayla for an LGS Virtual Valentine's Dance Party!  Meet up with friends virtually for dancing and socializing! You might even make some new friends! Have some snacks and drinks ready. Dress Up...

Dad to Dad Support Group

Dad’s and our Male caregivers are the centers of the LGS Family. 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 favorite beverage and...

Caregiver of Adults with LGS Support Group

Living with LGS is a marathon, not a sprint. Caring for an adult with LGS can be every bit as demanding as caring for a child with LGS, and the need for support is great.  Not only do the needs...

Behind the Mystery of LGS on Lifetime TV

“Rare Disease doesn’t come with a manual, it comes with a mother who never gives up!” Tune In – February 20 & 28, 2023 For A Special Segment Of Behind The Mystery Featuring LGS Foundation Executive Director, Tracy Dixon-Salazar, PhD  ...

2023 Walk ‘n’ Wheel for Lennox-Gastaut Syndrome Research in Florida

All People’s Community Park & Life Center 6105 E. Sligh Ave., Tampa, FL

Join us in Tampa, FL at our 8th Annual Walk 'n' Wheel for LGS Every year hundreds of community members come together in person and virtually to raise awareness and funds for the LGS Foundation's "Finding the Cures, Together" Research...

LGS Meeting of the Minds

-Save The Date- 2023 LGS Meeting Of The Minds: Advancing Clinical Research September  13-15, 2023: Researcher Meeting Days September 16, 2023: Family Science Day The LGS Foundation is hosting its second Meeting of the Minds to discuss how we can...