Abstract Background and Objectives Only a fraction of the 53 million caregivers in the United
States use available formal community services. This scoping review synthesized the …

Context There is growing recognition of the value to patients, families, society, and health
systems in providing healthcare, including end-of-life care, that is consistent with both …

Background Informal caregivers represent the foundation of the palliative care workforce
and are the main providers of end of life care. Financial pressures are among the most …

Purpose The needs and experiences of palliative home care for patients with advanced
cancer have received little research attention. We aimed to explore the needs and …

Objective End‐of‐life caregiving is associated with poorer mental health compared with
other caregiving. The objective of this study was to examine the association between …

Background: Family caregivers provide the majority of palliative care. The impact of family
caregiving on employment and finances has received little research attention in the field of …

Background: For informal carers of people with life-limiting illness, social welfare policy
related to income support and housing has been associated with varied psychosocial …

Objective: Informal caregivers (ICs) providing care for those at the end-of-life face physical,
psycho-social, emotional, and/or financial challenges. However, there is a paucity of …

Background: Caring at end-of-life is associated with financial burden, economic
disadvantage, and psychosocial sequelae. Health and social welfare systems play a …

The Saskatchewan Caregiver Experience Study sought to map the experiences of family
and friend caregivers of older adults in the Canadian province of Saskatchewan. This study …