What it is
- What changed
- New York signed Chapter 479 of 2025 establishing an FTD registry and directing DOH to publish registry information and family resources through a public webpage.
- Why it matters
- FTD is often misdiagnosed and heavily caregiver-intensive; the row connects neurodegenerative disease policy to diagnosis delay, family resource navigation, and public data.
- Who it touches
- Family caregivers, Care providers and plans, People receiving carepeople with FTD, dementia caregivers, families seeking diagnosis, clinicians
- What it does
- Plans, studies, registries or guidance
- Identifiers
- S 598 (session 2025)
Sources
Last reviewed Jun 18, 2026. This is information, not legal advice; check the source for the current text.