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National Epilepsy Plan: Better Diagnosis, Treatment, and Support

This act establishes a nationwide plan to combat epilepsy, aiming to improve diagnosis, treatment, and care for individuals affected by the condition. Citizens can expect better coordinated research, faster diagnosis, and increased access to specialized care, leading to improved quality of life and reduced financial burdens associated with the disease.
Key points
Establishment of a National Plan for Epilepsy to coordinate federal efforts in preventing, diagnosing, treating, and curing epilepsy.
Creation of an Advisory Council on Epilepsy Research, Care, and Services, composed of experts and patient representatives, to advise on epilepsy-related issues.
Implementation of annual assessments of progress in combating epilepsy and regular reports to Congress, ensuring transparency and effectiveness of actions.
Increased public awareness about epilepsy, reduction of stigma and discrimination, and improved access to expert and specialized care for people with epilepsy.
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Status:
Introduced
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Additional Information
National Plan for Epilepsy Act
Print number: S 494
Sponsor: Sen. Schmitt, Eric [R-MO]
Process start date: 2025-02-10