Author Archive for: steshale
About Salom Teshale
Salom Teshale joined NASHP’s Behavioral Health, Aging, and Disability team in March 2020 and works on projects related to family caregiving and palliative care. Prior to joining NASHP, Salom was a postdoctoral fellow at the Administration for Community Living in the US Department of Health and Human Services and the University of Washington School of Medicine, where she conducted research on topics related to aging and well-being in adults aging with long-term disability. She holds a PhD from Brandeis University in social/developmental psychology, and a BA in psychology from the University of Chicago.
Entries by Salom Teshale
State Policies to Support Family Caregivers: Lessons Learned from Six States in the RAISE Act State Family Caregiving Institute
October 21, 2022 in Policy, The RAISE Act Family Caregiver Resource and Dissemination Center Connecticut, Delaware, Illinois, Maryland, New York, Utah Featured News Home, Reports State Resources, The RAISE Family Caregiver Resource and Dissemination Center /by Luke Pluta-Ehlers, Salom Teshale and Wendy Fox-GrageStates Use Appendix K and Emergency Waivers to Support Home- and Community-Based Services in Response to COVID-19
October 13, 2022 in COVID-19 State Action Center Charts, Featured News Home, Maps Care Coordination, Children/Youth with Special Health Care Needs, Chronic and Complex Populations, Chronic Disease Prevention and Management, COVID-19, Health Equity, Long-Term Care, Medicaid Managed Care, Physical and Behavioral Health Integration, Population Health, Social Determinants of Health /by Salom TeshaleHHS 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 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. 























































































































































