RAISE Act State Policy Roadmap for Family Caregivers
In September 2022, the RAISE Act Family Caregiving Advisory Council and the Advisory Council to Support Grandparents Raising Children, with input from family caregivers and the people they support, released the 2022 National Strategy to Support Family Caregivers. The Strategy includes actions to ensure that family caregivers have the resources they need to maintain their own health, well-being, and financial security while providing crucial support for others.
The federal government alone cannot implement the recommendations set forth by the National Strategy; it will need to work in partnership with state and local governments and the private sector. The goal of this publication is to provide a roadmap for state officials to better understand the state policy landscape for supporting family caregivers of older adults and to identify opportunities for innovation in their own states.
This roadmap was made possible by support from The John A. Hartford Foundation and the RRF Foundation for Aging.
Explore each section of the roadmap using the links on this page, or get an overview of the policy strategies and promising practices highlighted in this roadmap.









For individuals living with complex, often chronic conditions, and their families, palliative care can provide relief from symptoms, improve satisfaction and outcomes, and help address critical mental and spiritual needs during difficult times. Now more than ever, there is growing recognition of the importance of palliative care services for individuals with serious illness, such as advance care planning, pain and symptom management, care coordination, and team-based, multi-disciplinary support. These services can help patients and families cope with the symptoms and stressors of disease, better anticipate and avoid crises, and reduce unnecessary and/or unwanted care. While this model is grounded in evidence that demonstrates improved quality of life, better outcomes, and reduced cost for patients, only a fraction of individuals who could benefit from palliative care receive it. 























































































































































