LGS Foundation funding has: Built a Community of Support with more than 6000 LGS patient family members. Funded 12 cutting-edge research grants to advance our understanding of LGS. Funded the first-ever animal model of LGS. Grown the LGS Family Conferences…
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 leveraging of resources,…