Individuals and families face challenges at the end of life that can vary significantly depending on social and cultural contexts. More than ever, knowledge about the needs that cut across the great diversity of experiences in the face of dying and death is essential. Perspectives on Palliative and End-of-Life Care: Disease, Social and Cultural Contexts explores how behavioural interventions and clinical approaches can be used to address a range of issues for those in need of end of life care.
Key Features
- Comprehensive Insights: Perspectives from experienced clinicians, providers, and caregivers worldwide.
- Evidence-Based Practice: A strong foundation in contemporary evidence-based practices alongside seasoned practice insights.
- Diverse Interventions: Explores interventions for varied needs, including HIV caregivers in Africa and individuals dying with dementia.
- Policy Impact: Discusses the impact of policy regulations on the availability and access to palliative care.
- Caregiver Comparison: Compares the different issues experienced by family caregivers and formal caregivers.
Additional Information
This book serves as a companion volume to Perspectives on Behavioural Interventions in Palliative and End-of-Life Care. It will be of interest to a wide variety of individuals, including academics, researchers, and postgraduates in mental health, medicine, psychology, and social work. It is also essential reading for healthcare providers and trainees from psychosocial and palliative medicine, social work, and nursing.
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