Our Outcomes and Impact 2008 The LGS Foundation is founded by Christina SanInocencio, sister to Michael, an adult living with LGS. Team LGS Foundation attends the first National Walk for Epilepsy in Washington, DC. 2009 The LGS Foundation establishes its…
In everything we do, we believe every child and adult deserves a chance to live life to the fullest. Our Why The status quo is that young children with LGS and pre-LGS are having their lives robbed from them, and…
Our vision: To end the suffering and devastation caused by LGS. Our Mission: 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….
We are all in this together The LGS Foundation recognizes that by opening lines of communication, connecting patients, families, researchers, doctors, our fellow advocacy organizations, industry partners, regulators, policymakers, payors, and other community organizations, we can assure resources are leveraged,…