National Plan for Epilepsy Act

HR 10210 establishes a National Plan for Epilepsy to coordinate federal efforts in preventing, diagnosing, treating, and curing epilepsy. It requires the Secretary to create an Advisory Council with patient representatives, caregivers, medical experts, and researchers, and mandates annual assessments and reports to Congress on progress and recommendations. The law directly affects millions of people with epilepsy in the U.S. (nearly 3 million adults and 456,000 children) and directs federal agencies like NIH and CDC to share data and improve services. Annual reports will track progress toward reducing uncontrolled seizures, improving care access, and addressing disparities in epilepsy care.