Resources for caregivers and families of patients with L ennox‐ G astaut syndrome

Abstract

Resources Lennox-Gastaut syndrome (LGS) has an ongoing high burden of care. Like epilepsy in general, the impact on the child and family depends on several factors, includ-ing the level of social support and extent of the resources available to deal with the condition. Health care provid-ers should recommend these resources to patients with LGS and their families. National support, education, and advocacy groups that serve families with LGS include the following.