HI HB952

Establishes a Parkinson's Disease Research Collection Database within the State Health Planning and Development Agency to collect data on incidence, prevalence, diagnosis, and treatment of Parkinson's disease and related Parkinsonisms in Hawaii

Requires hospitals, physicians, and healthcare providers to report Parkinson's disease and Parkinsonism cases to the agency; patients may opt-out of data collection in writing but basic incidence data is still required

Creates a Parkinson's Disease Research Collection Database Advisory Committee with at least 9 members, including neurologists, movement disorder specialists, primary care physicians, patients, and researchers, serving 3-year terms

Requires the agency to create a public webpage by January 1, 2026 and submit annual reports to the legislature on disease incidence by county and demographic information by age, gender, and race

Appropriates unspecified general fund amounts for fiscal years 2025-2026 and 2026-2027 to establish and administer the database, with an effective date of July 1, 3000 (placeholder date)