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The National Plan for Epilepsy Act establishes a federal initiative to coordinate research, prevention, diagnosis, treatment, and care for epilepsy across federal agencies. The bill requires the Secretary of Health and Human Services to develop and maintain an integrated national plan, conduct annual assessments of progress, and establish an Advisory Council comprising federal representatives and epilepsy experts to provide recommendations. The Secretary must submit annual reports to Congress evaluating federally funded epilepsy efforts and recommending priority actions, with the program set to expire on December 31, 2035.
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