Author Archive for: Kimberly Hodges
About Kimberly Hodges
Kimberly Hodges joined NASHP in November 2021 as a policy associate on the Behavioral Health, Aging, and Disability team. Her work focuses on long-term services and supports, specifically the respite and family caregiving service models. Prior to her tenure at NASHP, she served as a New York State Excelsior Service Policy Fellow for the NYS Office for People With Developmental Disabilities, where she assisted NYS with Medicaid policy for individuals with intellectual and developmental disabilities live in home and community-based settings.
Kimberly is passionate about the ways in which both research and dialogue play in promoting best practices within state health policy. Kimberly holds a BA from the State University of New York College at Fredonia and a MA from the Maxwell School of Citizenship and Public Affairs at Syracuse University.
Entries by Kimberly Hodges
HHS Releases Family Caregiving National Strategy and Asks for Public Comment: Joint Council Meeting Summary
October 11, 2022 in The RAISE Act Family Caregiver Resource and Dissemination Center Blogs, Featured News Home Council Meeting Materials and Resources, The RAISE Family Caregiver Resource and Dissemination Center /by Salom Teshale and Kimberly HodgesStates Cover Respite Care and Adult Day Services in Medicaid Managed Long-Term Services and Supports (MLTSS)
August 26, 2022 in The RAISE Act Family Caregiver Resource and Dissemination Center Featured News Home, Maps State Resources, The RAISE Family Caregiver Resource and Dissemination Center Respite Care /by Kimberly HodgesSign Up for Our Weekly Newsletter
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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. 























































































































































