Sponsors (4)
This resolution promotes better palliative and hospice practices and patient-centered end-of-life care through training and awareness, but because it is nonbinding and provides no funding, its practical impact on access and provider burden will be limited without follow-up resources or mandates.
Patients with serious illness and their families would receive greater emphasis on symptom control, pain management, and emotional supports, improving quality of life near the end of life.
Health care workers would have increased interdisciplinary palliative/hospice training opportunities, helping improve the quality and consistency of end-of-life care.
Encouraging patients to learn about and share their care preferences could increase patient-centered decisionmaking and better align delivered care with patient wishes.
The resolution's findings are nonbinding and do not provide funding or mandate service expansion, so access gaps and uneven availability of palliative/hospice care are likely to persist.
Emphasis on increased training could translate into new expectations or requirements that impose costs on hospitals, health systems, and hospice providers if no funding accompanies those expectations.
Encouraging patients to document and share care preferences may create additional administrative burdens for clinicians and health systems to document, honor, and track those preferences without added resources.
Based on analysis of 2 sections of legislative text.
Recognizes the importance of palliative care and hospice services and encourages broader access, training, and awareness so people of all ages and backgrounds can get high-quality, team-based support for serious illness and end-of-life needs. Highlights hospice priorities like pain and symptom management, caregiver assistance, emotional and spiritual support, volunteer roles, and grief/bereavement services, and urges patients to learn and share their care preferences.
Introduced December 16, 2025 by Jacklyn Sheryl Rosen · Last progress December 16, 2025