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HR 1189119th CongressIntroduced
National Plan for Epilepsy Act
Introduced: Oct 29, 2025
Civil Rights & JusticeHealthcareSocial Services
Standard Summary
Comprehensive overview in 1-2 paragraphs
The National Plan for Epilepsy Act establishes a coordinated federal strategy to prevent, diagnose, treat, and cure epilepsy through research integration, cross-agency collaboration, and improved care coordination, addressing the disease's significant health and socioeconomic impacts on millions of Americans.
Key Points
- 1The Secretary of Health and Human Services must create and maintain an integrated national plan for epilepsy research, treatment, and care coordination across all federal agencies including NIH, CDC, and FDA.
- 2An Advisory Council with diverse representation from patients, caregivers, healthcare providers, researchers, and nonprofits will provide recommendations and monitor progress through quarterly public meetings.
- 3Mandatory annual assessments and congressional reports will evaluate federally funded epilepsy efforts, recommend priority actions to reduce disparities, and address financial burdens on affected households.
Impact Areas
3 million Americans with epilepsy and their familiesFederal health agencies including NIH, CDC, and CMSHealthcare providers specializing in neurology and epilepsy careNonprofit organizations focused on epilepsy research and support
Generated by legislative-analyst-pro on Nov 3, 2025