At the LGS Foundation, every day we build a strong, supportive, educated community. We offer timely, impactful support programs for patient families navigating the LGS journey. Building awareness within our own community and the larger epilepsy community around the devastation and suffering caused by LGS. We believe no one in our community should walk this path alone.
Our Vision: To End The Suffering And Devastation Caused By LGS.
Our Mission: 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.
