National Plan for Epilepsy Act passed the Senate 540 days after introduction and awaits a vote in the House
Written by the Congressional Research Service [2]. 134 words.
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.
- Committees
- Senate Health, Education, Labor, and Pensions Committee
- Policy area
- Health: 122 of 9,357 bills became law, 113th–118th (1.3%)
- Sponsor
- 1 of 78 bills enacted since 2013
- Text versions
- 3, from introduced in senate to engrossed in senate · 527 words
- Subjects
- Advisory bodiesCongressional oversightData collection, sharing, protectionHealth promotion and preventive careMedical researchNeurological disorders
- Latest action
- Aug 10, 2026: Held at the desk.
- Records
- Congress.gov · Bill text
Each bill appears once, under its strongest link. 1 in all.
Identical or companion · 1
- 119th H.R. 1189 National Plan for Epilepsy Act D · Introduced