National Plan for Epilepsy Act

# National Plan for Epilepsy Act - Summary **What the Bill Does** The National Plan for Epilepsy Act would direct the U.S. Department of Health and Human Services (HHS) to create a comprehensive national strategy focused on preventing, diagnosing, treating, and curing epilepsy. To implement this plan, HHS would coordinate research and services across federal agencies, gather input from the public, and establish an Advisory Council on Epilepsy Research, Care, and Services. The council would evaluate federally funded epilepsy efforts and report findings to HHS and Congress every two years, while HHS would also submit annual progress reports to Congress with recommendations for next steps. **Who It Affects and Current Status** This bill would primarily benefit people with epilepsy and their families by potentially improving research funding, care coordination, and treatment options.

It would also affect HHS and other federal health agencies tasked with implementing the national plan. The requirements would expire on December 31, 2035. As of now, the bill (S 494) is in committee and has not yet been voted on by the full Senate. It was introduced by Senator Eric Schmitt (R-MO).