Research Blog

Lennox-Gastaut Syndrome Research Update

The Latest in LGS Research - July 2024

While there are no cures for LGS, current LGS Foundation-funded researchers are focused on two areas where their efforts can lead to improved lives for those with LGS and their families.  One of these areas is seizure control and another…

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3 Takeaways from the Recent AES Annual Meeting

The recent AES Annual Meeting brought together more than 6,000 healthcare providers, scientists, patient advocates, industry partners, and other professionals dedicated to better outcomes for people with epilepsy. It was really energizing to attend this meeting and hear about all…

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The Meeting of the Minds Blew Our Minds

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…

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Discovering Breakthroughs and Innovations in LGS Research

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…

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