This bill aims to address the impact of epilepsy by establishing the "National Plan for Epilepsy." The plan includes activities such as coordinating research and services related to epilepsy, improving early diagnosis, and enhancing treatment and care coordination for individuals with epilepsy. It also includes the establishment of an Advisory Council to evaluate federally funded efforts in epilepsy research and provide recommendations for priority actions, and mandates annual reports on the progress made in carrying out the National Plan. This plan will impact epilepsy prevention, diagnosis, treatment, and support services for individuals and families affected by epilepsy through collaborative efforts and data-driven initiatives.
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.