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A bill to establish a national plan to coordinate research on epilepsy, and for other purposes.
2/25/2025, 11:56 AM
Summary of Bill S 494
Epilepsy is a neurological disorder that affects the brain and causes seizures. It is estimated that around 3.4 million people in the United States have epilepsy, making it one of the most common neurological conditions in the country. Despite its prevalence, there is still much that is not known about epilepsy and how to effectively treat it.
The National Epilepsy Coordination and Research Act aims to address this issue by bringing together researchers, healthcare providers, and other stakeholders to develop a comprehensive plan for studying epilepsy. This plan will include strategies for improving the understanding of epilepsy, developing new treatments, and ultimately finding a cure for the condition. In addition to coordinating research efforts, the bill also includes provisions for increasing public awareness about epilepsy and improving access to care for individuals with the condition. It also calls for the establishment of a national database to track the prevalence of epilepsy and monitor trends in diagnosis and treatment. Overall, Bill 119 s 494 represents a significant step forward in the fight against epilepsy. By bringing together experts from various fields and creating a coordinated research plan, this legislation has the potential to improve the lives of millions of Americans living with epilepsy.
Congressional Summary of S 494
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.
Current Status of Bill S 494
Bipartisan Support of Bill S 494
Total Number of Sponsors
2Democrat Sponsors
0Republican Sponsors
2Unaffiliated Sponsors
0Total Number of Cosponsors
4Democrat Cosponsors
2Republican Cosponsors
2Unaffiliated Cosponsors
0Policy Area and Potential Impact of Bill S 494
Primary Policy Focus
Comments
River Kahn
10 months ago
This bill sounds important. Did you know it includes funding for new treatments?
