Join us at one of our many research conferences as we bring researchers and those living together to discuss how we can find the cures, together.
Every year, the LGS Foundation organizes the LGS Research Roundtable at the American Epilepsy Society (AES) annual meeting in an effort to #FreeTheData. Join us as we hear updates from our grant recipients and research collaborations. 2021 Roundtable Learn about the…
This two-day Virtual Conference brings together patients, families, doctors, researchers, industry partners, and advocacy organizations to discuss progress to date in understanding LGS and how we can find targeted treatments and cures for this horrible early-life epilepsy. Meeting of the…
Continue the conversation that started at our September 2021 Meeting of the Minds Conference. Join us! Developing Novel LGS Clinical Trails December 3rd, 2021 at AES Speakers Include: Dr. Dennis Dlugos – Moderator & Discussion Leader Dr. Sudha Kessler – How…
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. Over 100 people ranging from patients, caregivers, FDA representatives, pharmaceutical companies, device…
