About LGS
- Like many rare conditions, Lennox-Gastaut Syndrome can be a complete mystery when you first hear about it. Explore this section to get a thorough understanding of LGS—including its causes, symptoms, diagnosis and treatment.
New to LGS
- A diagnosis of LGS is deeply unsettling and can leave you at a loss as to where to turn for help and guidance. We’re here for you. In this section you will find information, resources, and communities of support for the challenging road ahead.
For Families
- If a loved one is living with LGS, the entire family shares in the difficult journey. How can you keep them safe? Find appropriate medical care? Get the support you need? This section gives answers to these and other critical questions.
About Research
- Even as our understanding of LGS grows, there is so much more to learn. From research grants to conferences, from publications to voice of the patient family, this section provides avenues for furthering your knowledge and impact.
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- Host a fundraiser. Volunteer at an event. Shop our LGS store. These are just some of the ways you can lend your personal support to our mission. Check out this section to get started.
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Home / Latest News / LGS Foundation at the AES Annual Meeting

LGS Foundation at the AES Annual Meeting

December 6 - 10, 2024

Thank you for joining us in Los Angeles for the 2024 American Epilepsy Society (AES) Annual Meeting.

Increased awareness and recognition positioned LGS as a mainstage topic at this years meeting where world-renowned experts in the field gathered to learn more about the latest in LGS research, support, and care.

(Learn More – Coming Soon)

Professional Resources

The LGS Foundation provides educational resources, support, and research funding opportunities for LGS professionals.

Click images below to learn more.

Updated 12/16/24 (KK)