The LGS Foundation's mission is to improve the lives of individuals affected by Lennox-Gastaut Syndrome (LGS) through research, family support programs, and education. The LGS Foundation promises to be unrelenting in its search for better research and therapies for its community, and is building a network of researchers, clinicians, and patients to develop shared research priorities and co-develop new therapies.
For more information, visit: https://www.lgsfoundation.org.
