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.
Get Involved
- 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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LGS Foundation @ AES

December 6 - December 10

Join us at AES in Los Angeles, California

Are you attending the American Epilepsy Society Annual Meeting in December?

We invite you to stop by Booth N2148 in the Epilepsy Resource Area of the Exhibit Hall. Our team will be available from December 7 – 9, 2024 to support and assist with inquires.

To learn more about the LGS Foundation’s Research Programs, visit our Finding the Cures, Together page.

Details

Start:: December 6
End:: December 10

Venue

: THE LOS ANGELES CONVENTION CENTER
: South Figueroa Street
Los Angeles, CA 90015 United States