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 / Donation Matching Program

Donation Matching Program

Thanks to the generosity of our supporters, the LGS Foundation is able to fund cutting-edge research that brings hope for better treatments and one day a cure for Lennox-Gastaut Syndrome (LGS) and associated developmental and epileptic encephalopathies.

Many corporations match donations made by employees to nonprofits, to support employee charitable giving and to extend corporate philanthropy. Often this may double or even triple your donation. Use the tool below to help determine if your employer has a donation matching program.

The LGS Foundation is registered as a tax-exempt public charity by the Internal Revenue Service under Section 501(c)(3). Our tax identification number is 26-2051377. If you have any questions, please email info@lgsfoundation.org.

Thank you for supporting the LGS Foundation and the LGS community.