National Plan for Epilepsy Act
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Progress
Where this bill stands in the legislative process.
- Introduced
- Passed Senate
- Passed House
- To President
- Became Law
Overview
The National Plan for Epilepsy Act establishes a national program to coordinate efforts to prevent, diagnose, treat, and ultimately cure epilepsy. It mandates the Department of Health and Human Services to create a National Plan, establish an advisory council to provide guidance and recommendations, and submit annual reports to Congress outlining progress and priorities. The goal is to improve outcomes for individuals with epilepsy and their caregivers, addressing disparities and promoting research.
Key provisions
- Establishes a National Plan for Epilepsy led by the Department of Health and Human Services.
- Creates an Advisory Council on Epilepsy Research, Care, and Services comprised of federal and non-federal experts.
- Requires the Advisory Council to submit biennial reports to Congress with recommendations for improving epilepsy care and research.
- Mandates annual reports from the Secretary of HHS to Congress detailing progress on the National Plan.
- Directs the Department of Health and Human Services to coordinate research and services across all federal agencies.
- Requires the National Plan to address early diagnosis, care coordination, and the impact of epilepsy on health and well-being.
- Calls for public comments and consensus recommendations from the epilepsy community.
- Sets a sunset date of December 31, 2035, for the provisions of the Act.
Who is affected
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