top of page

LGS Foundation

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:


Disclaimer: The information contained in this page is provided by the partnering patient organization for informational purposes only.  The 40 Percent Inc. does not warrant its completeness or accuracy, and it should not be construed as an endorsement by The 40 Percent Inc. or relied upon as a basis for your support for the partnering patient organization.  The information is subject to change without notice.

bottom of page