Check out the latest LGS Research News.
Epilepsy Awareness Month Focuses on Solving the Mystery of LGS and Other Rare Epilepsies
Donate now International LGS Awareness Day brought together thousands of people around the world to show that the challenges associated with LGS are tough, but so are those affected by this rare disease. This also kicked off Epilepsy Awareness Month…
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…
Upcoming Webinars: September 22, 2021 Following our recent LGS Research Meeting of the Minds (MoM) conference, the LGS Foundation’s Executive Director, Dr. Tracy Dixon-Salazar, will answer any questions the community may have about LGS Research, LGS Foundation Funded Grants, and…
