Join us at one of our many research conferences as we bring researchers and those living with LGS together to discuss how we can find the cures, together.
-Save the Date- 2023 LGS Meeting of the Minds: Advancing Clinical Research September 13-15, 2023: Researcher Meeting Days September 16, 2023: Family Science Day The LGS Foundation is hosting its second Meeting of the Minds to discuss how we can…
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. Thank you for joining us at…
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…
Finding Disease-Modifying Therapies in LGS Research Conference Outcomes: In September 2021, over 250 researchers and family members from 7 different countries joined the LGS Foundation for a 2-day discussion focused on finding LGS Disease-Modifying Therapies. “This meeting was critical! It…
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…
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….
