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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Home / LGS Foundation Anniversary Dinner

LGS Foundation Anniversary Dinner

You’re Invited!

Join us as we celebrate our 15th Anniversary of service to the LGS Community! For 15 years, with your help, we have improved the lives of those impacted by LGS through advancing research, awareness, education, and family support.

Get Your Tickets Now

Want to Give Hope for the Future? Consider Sponsoring the Event or Donate to the Silent Auction.

Please email us at Giving@LGSFoundation.org.

Individuals and families impacted by LGS can email Amber@LGSFoundation.org to request the Family Discount Code prior to purchasing tickets.

Click here to learn more about our regional sponsorship opportunities.

Thank You to Our International LGS Awareness Day Partners

Updated 09/20/2023