Celebrating Impact: Our 2024 Achievements

Together, we are improving the lives of individuals impacted by Lennox-Gastaut Syndrome (LGS).

The LGS Foundation is a nonprofit organization that acts as a convener of the LGS community. Since our inception in 2008, we have engaged and educated all of our community stakeholders – patient families, clinicians, researchers, industry partners, and others – to advance better treatments, and one day find the cures, for LGS.

Click on the images below to learn more about our impact and how you can get involved.

Our Plan of Action

The purpose of this 4-year strategic plan is to articulate the long‐range direction and priorities for the LGS Foundation. We derived the content for our strategic plan by examining the LGS landscape. We gathered input from key community stakeholders on current priorities, emerging needs, and organizational strengths and vulnerabilities.

2024 Event Outcomes

Walk ‘n’ Wheel for LGS Research

International Family & Professional Conference

International LGS Awareness Day

(Coming Soon)

2024 Highlights

2023 Annual Report

Join Us – Help end the devastation & suffering caused by LGS

Together, we are transforming lives. We couldn’t do it without you!

Within our prospectus, there are various sponsorship opportunities available, including virtual and in-person meetings, international events, and family events. Most sponsorships also provide you with the opportunity to connect with patients, families, and other stakeholders in the LGS Community.

Updated 12/03/24 (KK)