The challenges are tough. So are we.
While there is no cure for LGS, there is a hopeful path forward. On this site, you will find useful information and resources – and most importantly, a community of support.Find Support What is LGS?
LGS is a severe epilepsy syndrome that develops in children and leads to lifelong disability.
More Facts About LGS
Our little unicorn
Every mother will say their child is special. But my sweet Josie truly is. She is the definition of a warrior.
Fighting for a Cure for LGS
Savannah (age 28) & Tracy's Story
The Lennox-Gastaut Syndrome (LGS) Foundation is a nonprofit organization dedicated to improving the lives of individuals impacted by LGS through advancing research, awareness, education, and family support.
Walk ‘n’ Wheel for LGS Research
Stepping Towards a Cure, Together!
May 6, 2023
The LGS Foundation is excited to host the 8th Annual Walk ‘n’ Wheel for Lennox-Gastaut Syndrome on Saturday, May 6, 2023.