Help Us Stand with Families Living with LGS Lennox-Gastaut Syndrome (LGS) is not just epilepsy. It is daily seizures. It is emergency medications. It is hospital stays. It is sleepless nights. It is therapies, specialists, adaptive equipment, and constant uncertainty. For families living with LGS, life changes overnight, and it never slows down. Many of these families are balancing: • Costly medical treatments not fully covered by insurance • Specialized equipment and mobility needs • Travel to out-of-state specialists • Lost income due to full-time caregiving • Emotional and physical exhaustion And yet, they show up every single day with strength and love. Your donation makes a real difference. It helps fund critical research to find better treatments. It supports family resources and education. It eases financial burdens for those navigating constant medical care. It gives hope to families who desperately need it. When you donate, you are not just giving money. You are giving relief. You are giving support. You are giving families the reminder that they are not alone. Every dollar matters. Every share matters. Every act of kindness matters. Please consider donating today and standing beside LGS families as they fight battles most people never see. Together, we can bring awareness. Together, we can bring support. Together, we can bring hope.

In April 2026, families, advocates, and partners around the world will step forward together—walking, wheeling, and showing up in their own communities—to raise awareness, strengthen connection, and advance progress for Lennox-Gastaut Syndrome. If you would like to join us for the walk here in Colorado, it will be held at Clement Park in Littleton on April 25th. Learn more at www.lgsfoundation.org/walk.