New Jersey Parkinson's disease registry proposal
New Jersey's S2339 would establish a State Parkinson's disease registry and has moved from the Senate to Assembly committee review.
New Jersey · Active · Vote Jan 5, 2026
What it is
- What changed
- S2339 would establish a State Parkinson's disease registry; the official NJ Legislature page shows Senate passage on December 18, 2025 and Assembly committee movement on January 5, 2026.
- Why it matters
- Disease registries can improve service-planning visibility while raising plain-language questions for families about reporting, confidentiality, access to data, and whether registry participation changes care.
- Who it touches
- Family caregivers, Care providers and plans, People receiving care, Businesses and agencies that must complypeople with Parkinson's disease, Parkinson's caregivers, neurologists, public-health agencies
- What it does
- Plans, studies, registries or guidance
- Identifiers
- S 2339 (session 2024) · A 6094 (session 2024)
Sources
Last reviewed Jul 4, 2026. This is information, not legal advice; check the source for the current text.