Lennox-Gastaut Syndrome (LGS) is a severe epilepsy syndrome that develops in very young children.
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
Tayla and Brian
Adopted mother to 16-year old Brian.
Swing “FORE” a Cure Golf Event for LGS
Event Date: July 23, 2022
Join us in Dublin, Ohio on Saturday, July 23, 2022 for an afternoon of fun as we Swing FORE A Cure for Lennox-Gastaut Syndrome (LGS).
2021 LGS Research Roundtable at AES
Every year, the LGS Foundation organizes the LGS Research Roundtable at the American Epilepsy Society (AES) annual meeting in an effort to advance research and #FreeTheData. Join us as we hear updates from our grant recipients and research collaborations.
“We are excited to gather the brightest minds tackling LGS across the globe,” said Dixon-Salazar. “And, we believe that now more than ever, our researchers are determined to solve the mystery of LGS.”
International LGS Awareness Day is Coming Soon!
November 1st: Help Us Raise Awareness about LGS