The LGS Foundation Research Award  provides funding for young and established investigators, physician residents, and clinicians who seek to advance our understanding of Lennox-Gastaut Syndrome (LGS). Grants may be one-year or two-years and support research projects that answer questions related to the underlying biology, clinical aspects, therapies, and/or causes of LGS. Grant recipients are asked to give a presentation at the LGS Foundation's annual research meeting at the American Epilepsy Society the following year to discuss their work. The LGS Foundation does not require an LOI, however, we will evaluate LOI's from investigators prior to submission of a full application

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Questions? Contact Tracy Dixon-Salazar at