The LGS Foundation's mission is to improve the lives of individuals impacted by Lennox-Gastaut Syndrome (LGS) through research, family support programs, and education.
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News & Updates:
Do you care about others? Are you creative and compassionate? Do you often find yourself helping those around you? The LGSF is looking for people like you to serve the members of our community with a helping hand.
Two-day Virtual Conference, we will bring together patients, families, doctors, researchers, industry partners, and others to review progress to date in understanding LGS and how we can find targeted treatments and cures for this horrible early life epilepsy.
Thanks to continued collaboration with Zogenix and more than 10 rare epilepsy advocacy groups, we are now able to provide important new resources to support siblings and their families.