National Plan for Epilepsy Act

senate

house

president

Legislation Details

Establishes a national plan to coordinate research on epilepsy.
Aims to prevent, diagnose, treat, and cure epilepsy.
Recognizes epilepsy as a significant health issue affecting millions in the U.S.
Highlights the need for improved understanding of epilepsy’s causes and types.
Addresses the high rates of uncontrolled seizures and associated risks, including early death and economic hardship.
Mandates the Secretary to create and maintain an integrated national plan for epilepsy.
Requires coordination of research and services across federal agencies.
Encourages development of effective treatments and strategies for individuals with epilepsy.
Calls for improved early diagnosis and care coordination for epilepsy patients.
Establishes an Advisory Council on Epilepsy Research, Care, and Services to provide guidance and recommendations.
Requires annual assessments of progress and reporting to Congress on federal efforts related to epilepsy.
Emphasizes the importance of public awareness and reducing stigma associated with epilepsy.
Mandates data sharing among relevant agencies to enhance research and reporting efforts.
Includes a sunset provision, ending the effectiveness of the section on December 31, 2035.

Establishes a national plan to coordinate research on epilepsy.
Aims to prevent, diagnose, treat, and cure epilepsy.
Recognizes epilepsy as a significant health issue affecting millions in the U.S.
Highlights the need for improved understanding of epilepsy’s causes and types.
Addresses the high rates of uncontrolled seizures and associated risks, including early death and economic hardship.
Mandates the Secretary to create and maintain an integrated national plan for epilepsy.
Requires coordination of research and services across federal agencies.
Encourages development of effective treatments and strategies for individuals with epilepsy.
Calls for improved early diagnosis and care coordination for epilepsy patients.
Establishes an Advisory Council on Epilepsy Research, Care, and Services to provide guidance and recommendations.
Requires annual assessments of progress and reporting to Congress on federal efforts related to epilepsy.
Emphasizes the importance of public awareness and reducing stigma associated with epilepsy.
Mandates data sharing among relevant agencies to enhance research and reporting efforts.
Includes a sunset provision, ending the effectiveness of the section on December 31, 2035.