Access. Improving access to quality care; and supporting public health programs like Medicaid and those at the CDC that improve the lives of people with epilepsy.
Research. Advocating for federal funding for research at NIH, CDC, and other agencies to discover new treatments, find a cure, and expand our understanding of epilepsy, seizures, mortality in epilepsy and SUDEP (Sudden Unexpected Death in Epilepsy).
Innovation. Bringing the epilepsy community’s voice to the discovery, development, approval, and delivery of new treatments by strengthening engagement at FDA, CMS, and PCORI.