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.
Newly Diagnosed
- 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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Media

Contact

Media members and anyone seeking more information about LGS or the LGS Foundation by direct inquiries to:

Tracy@lgsfoundation.org

News Release Archive

September 8, 2021
First-ever LGS Research Meeting of the Minds Scheduled for September 13-14 with a Family Research Day on September 18.

May 31, 2021
Sixth Annual LGS Walk Scheduled for June 5 Raising Critical Funds for Research

February 1, 2021
Seizure Action Plan Awareness Week Scheduled for February 8-14

December 3, 2020
LGS Foundation Announces New Executive Director

November 1, 2020
New Coalition Launches to Promote Importance of Seizure Emergency Plans

October 29, 2020
LGS Awareness Day to Kick Off Epilepsy Awareness Month