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Bill

S 2339

Establishes State Parkinson's disease registry.

2024-2025 Regular Session Introduced by Patrick Diegnan and 2 co-sponsors

New Jersey bill establishes a state Parkinson's disease registry to collect patient data for public health monitoring and disease research tracking.

Reported out of Senate Committee, 2nd Reading
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Bill Summary · S 2339

Legislative bill overview

S 2339 establishes a state registry to collect and maintain data on Parkinson's disease cases in New Jersey. The registry would compile information about patients diagnosed with the condition, enabling public health monitoring and research tracking at the state level.

Why is this important

A Parkinson's registry creates epidemiological data that helps state health officials understand disease prevalence, demographics, and trends within the population. This information supports public health planning, identifies potential environmental or occupational risk factors, and facilitates research partnerships that could advance treatment understanding.

Potential points of contention

  • Privacy concerns: Collecting patient medical data requires robust safeguards; questions may arise about who accesses the information and how it's protected from misuse or breaches
  • Implementation costs: Establishing and maintaining a registry requires funding for staff, technology infrastructure, and ongoing database management—budget uncertainty remains given the bill's committee trajectory
  • Participation rates: Registry effectiveness depends on voluntary or mandatory reporting from healthcare providers; unclear requirements could affect data completeness and usefulness

Compiled from official sources — confirm details with the bill’s official record.

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