National Plan for Epilepsy Act

# National Plan for Epilepsy Act (HR 1189) Summary **What It Would Do** The National Plan for Epilepsy Act would direct the federal government to develop a comprehensive national strategy for addressing epilepsy in the United States. The bill would require the establishment of a coordinated plan to improve epilepsy prevention, detection, treatment, and support services. This includes promoting research into better treatments and cures, improving public awareness about the condition, and ensuring better access to care for people living with epilepsy. **Who It Affects and Key Provisions** The bill would primarily affect the roughly 3.4 million Americans living with epilepsy, as well as their families and caregivers.

It establishes oversight mechanisms and advisory bodies to coordinate epilepsy-related efforts across federal health agencies. The plan would focus on gaps in current services and research, encourage public education, and work to reduce stigma surrounding the neurological disorder. **Current Status** HR 1189 was introduced by Representative Jim Costa (D-CA) and is currently in committee, meaning it has not yet advanced to a full vote in the House. The bill remains in the early stages of the legislative process.