National Epilepsy Plan: Better Care and Research Coordination
This act establishes a nationwide plan to combat epilepsy, aiming to improve diagnosis, treatment, and quality of life for those affected. Citizens can expect better coordination of research, access to information, and support for patients and caregivers. The act seeks to reduce the financial and health burden associated with epilepsy.
Key points
Establishment of a National Plan for Epilepsy to coordinate research and services for prevention, diagnosis, treatment, and cure.
Creation of an Advisory Council on Epilepsy Research, Care, and Services, including experts and patient representatives, to advise on epilepsy-related issues.
Requirement for annual assessments of progress in addressing epilepsy and regular reports to Congress, ensuring transparency and accountability.
Increased public awareness about epilepsy and reduction of stigma and discrimination.
Improved access to specialized care for people with epilepsy and reduction of disparities in access to treatment.
Introduced
Citizen Poll