Help Raise LGS Awareness This November!
November 1st International LGS Awareness Day Each year, the LGS Foundation organizes a social media campaign and in-person events worldwide in recognition of International LGS Awareness Day. Our goal is to raise awareness of LGS and bring LGS families together….
Every two years, the LGS Foundation organizes a comprehensive multi-day educational meeting. The conference brings together more than 350 LGS family members and epilepsy professionals from around the world to better understand the causes, treatments, and how to live with…
Every year, the LGS Foundation organizes the LGS Research Roundtable at the annual American Epilepsy Society (AES) meeting in an effort to advance LGS research and #FreeTheData. Join us as we hear updates about LGS research and discuss future advances. 2021…
Externally-Led PFDD Meeting on the Developmental and Epileptic encephalopathies (DEEs), including LGS On November 1, 2019, the LGS Foundation convened the first patient-focused drug development meeting (PFDD) for the DEEs (developmental and epileptic encephalopathies) including Lennox-Gastaut Syndrome in College Park….
