National Plan for Epilepsy Act
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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.
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
- Introduced in Senate Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). S. 494: National Plan for Epilepsy Act. 119th Congress. Open America. https://openamerica.io/bill/119-S-494/
"S. 494: National Plan for Epilepsy Act." 119th Congress, 2026, Open America, https://openamerica.io/bill/119-S-494/.
S. 494, 119th Cong. (2026), https://openamerica.io/bill/119-S-494/.
[S. 494: National Plan for Epilepsy Act](https://openamerica.io/bill/119-S-494/)