The Lennox-Gastaut Syndrome (LGS) Foundation is dedicated to improving the lives of individuals impacted by LGS through advancing research, awareness, education, and family support. LGS is a rare, severe epilepsy syndrome that develops in young children and often leads to lifelong disability. Our Cure LGS 365 Grants Program funds scientists and physicians to advance research and clinical practice in ways that will impact those with LGS and their families. We seek review of our Research Agreement Contract. Further, we would like to modify the contract so that a fraction of any royalties resulting from LGSF-supported research will return to the Foundation.