Lennox-Gastaut Syndrome (LGS) is a severe epilepsy syndrome that develops in young children and leads to a lifelong disability.
Join individuals with LGS, their families, and friends to raise funds and raise awareness of this rare and devastating syndrome. Learn more about the LGS Foundation and how they are driving the research to find the cures.
Enjoy food and family-friendly activities. Hear the stories of families and celebrate their loved ones with LGS.
Members of the public are invited to attend, donate, or volunteer.
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.