Check out the latest LGS Research News.
Our 2nd Biennial LGS Research Meeting of the Minds was an Overwhelming Success! Watch the short recap video from our Executive Director, Tracy Dixon-Salazar, PhD Over 150 people attended this two-and-a-half-day hybrid research meeting in Baltimore, MD to discuss…
Over the past five years, LGS research has experienced significant advancements, providing hope for individuals and families affected by this complex disorder. At the LGS Foundation, we know that patient-driven research plays a vital role in driving research on topics…
Sept. 14-16, 2023 at Hilton Baltimore Inner Harbor
Thank you for helping us create a vision to advance clinical research in LGS! The LGS Foundation hosted its second Meeting of the Minds, Sept. 14-16, 2023, to discuss how we can Advance Clinical Research in LGS. This hybrid conference…
Join the LGS Foundation in Orlando, FL December 1 – 5, 2023 Are you attending the American Epilepsy Society Annual Meeting in Orlando, Florida, in December? Visit us in the Epilepsy Resource Area of the Exhibit Hall (booth N844). Here, our…
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…
meet the amazing doctors and scientists that make up our medical Science Advisory Council (MSAC) This amazing group of individuals is taking a stand against Lennox-Gastaut Syndrome by helping our team in the Foundation’s mission to accelerate LGS research. The…
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…
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…
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 can…
