OUR MISSION:

The LGS Foundation's mission is to improve the lives of individuals affected by Lennox-Gastaut Syndrome (LGS) through research, family support programs, and education. 

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Elevate Patient Assistance

Program.

News & Updates:

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Seizure Action Plan

Awareness Week 

Seizure Action Plan Awareness Week is held annually, starting on the second Monday in February in acknowledgment of International Epilepsy Awareness Day.

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6th Annual Walk 'n' Wheel for LGS

The LGSF is excited to host the 6th Annual Walk n' Wheel for Lennox-Gastaut Syndrome on Saturday, June 5th, 2021. 

LGSF Announces New Executive Director

The Lennox-Gastaut Syndrome (LGS) Foundation is pleased to announce that Dr. Tracy Dixon-Salazar is now the new Executive Director of the LGS Foundation. 

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