The Lennox-Gastaut Syndrome (LGS) Foundation is a Nonprofit Organization Dedicated To improving the lives of individuals impacted by LGS through Advancing Research, Awareness, Education, and Family Support.

At the LGS Foundation, every day we:

• Mobilize our resources to drive scientific breakthroughs for stabilizing treatments for LGS, and one day, develop preventive and reversative therapies for this devastating early-life epilepsy syndrome.
• Fight for a world where the best medical care is not based on luck and where navigating and quarterbacking the healthcare system does not fall heavily on the shoulders of overburdened caregivers and patient families.
• Build a strong, supportive, educated community.
• Offer timely, impactful support programs for patient families navigating the LGS journey.
• Build awareness within our own community and the larger epilepsy community.

Learn more about the LGS Foundation.