This Act directs the Secretary of Health and Human Services to review and update existing federal programs, activities, and strategic plans related to epilepsy research, prevention, early identification, diagnosis, and treatment. The review will encompass evidence-based research on epilepsy, federal programs related to epilepsy, opportunities for coordination among programs and global efforts, collaboration between federal agencies and stakeholders, and public health strategies. The Secretary will also solicit input from federal agencies and relevant stakeholders and submit a report with findings and recommendations to Congress. The goal is to identify and address knowledge gaps and improve health outcomes related to epilepsy.
National Plan for Epilepsy Act
This bill requires the Department of Health and Human Services (HHS) to establish a national plan, form an advisory council, and take other actions to address epilepsy. The requirements sunset on December 31, 2035.
Specifically, the bill requires HHS to carry out a National Plan for Epilepsy to prevent, diagnose, treat, and cure epilepsy. In carrying out the plan, HHS must implement activities such as coordinating research and services across all federal agencies and soliciting public comments.
Also, HHS must establish an Advisory Council on Epilepsy Research, Care, and Services. The advisory council must report to HHS and Congress every two years with an evaluation of federally funded efforts.
Additionally, HHS must annually report to Congress with recommended actions based on its assessments of the nation’s progress on epilepsy.
