Dr. Emmanuel Bilirakis and Honorable Jennifer Wexton National Plan to End Parkinson’s Act

This bill (HR 2365, Public Law 118-66) directs the U.S. Department of Health and Human Services (HHS) to establish the National Parkinson’s Project. It requires HHS to create and update a coordinated national plan for preventing, diagnosing, treating, and researching Parkinson’s disease and related disorders (including multiple system atrophy and progressive supranuclear palsy), while coordinating federal research and care efforts across agencies like the NIH, CDC, and VA. The law mandates annual progress assessments, an advisory council with patient advocates and diverse experts, and annual reports to Congress on federal Parkinson’s programs and recommendations for improvement. It affects federal agencies managing Parkinson’s-related programs and aims to improve care coordination and research efficiency for patients and caregivers, with the law sunsetting in 2035.