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.
Sue and Tony McCain
Parents to 23-year old Matthew, diagnosed with LGS at age seven.
Tayla and Brian
Adopted mother to 16-year old Brian.
International LGS Awareness Day
Each year, the LGS Foundation organizes in-person events worldwide and a social media campaign to recognize International LGS Awareness Day. In addition, more than 50 locations will Illuminate for LGS by lighting up in purple and green to raise awareness for Lennox-Gastaut Syndrome.