Abstract
With the advent of the modern hospice movement in mid-twentieth century, longer life expectancy reflective of medical advances, growing attention to ethical issues, and development of palliative medicine, increased attention has been paid to palliative and end-of-life care in general. Similarly, interest in issues pertaining to end-of-life care for people with intellectual and developmental disabilities (IDD) also has gained more attention in the professional and lay media. Despite these developments, there continues to be many misconceptions issues specific to people with IDD at end of life. Current medical, social, ethical, and practical issues, as well as challenges faced by children and adults with IDD, reflect the gains that have been made and the ongoing need for further refinement of systems and supports.
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Friedman, S.L., Helm, D.T. (2016). End-of-Life Care. In: Rubin, I.L., Merrick, J., Greydanus, D.E., Patel, D.R. (eds) Health Care for People with Intellectual and Developmental Disabilities across the Lifespan. Springer, Cham. https://doi.org/10.1007/978-3-319-18096-0_145
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DOI: https://doi.org/10.1007/978-3-319-18096-0_145
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