No one is born with LGS, instead, it develops over time from childhood seizures.
Brittany and Amaree
Single mother to Amaree (age 11), diagnosed with LGS at age three.
Tayla and Brian
Adopted mother to 16-year old Brian.
Sue and Tony McCain
Parents to 23-year old Matthew, diagnosed with LGS at age seven.
Walk ‘n’ Wheel for LGS Research
Stepping Towards a Cure, Together!
March 26, 2022
The LGS Foundation is excited to host the 7th annual Walk ‘n’ Wheel for Lennox-Gastaut Syndrome on Saturday, March 26th, 2022.