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Titlebook: End of Life and People with Intellectual and Developmental Disability; Contemporary Issues, Roger J. Stancliffe,Michele Y. Wiese,Mary McCar

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樓主: 拿著錫
51#
發(fā)表于 2025-3-30 09:10:59 | 只看該作者
52#
發(fā)表于 2025-3-30 14:01:11 | 只看該作者
End-of-Life Issues and Support Needs of People with Profound Intellectual and Multiple Disability,ions, creating a need for decision-making about end-of-life care and support. Due to communication challenges, people with PIMD are likely to depend on others to articulate their will and preferences. To date, research focussed on end-of-life care and support needs for people with intellectual and d
53#
發(fā)表于 2025-3-30 17:39:40 | 只看該作者
54#
發(fā)表于 2025-3-30 23:35:07 | 只看該作者
Use of Do-Not-Resuscitate Orders, hospital-based chronic illness care. Such orders often reflect self-determination, avoidance of futile care and quality of dying principles. Reports during COVID-19 of physicians writing DNR/DNAR orders for people with intellectual disabilities at rates higher than the general population amplify pa
55#
發(fā)表于 2025-3-31 03:11:35 | 只看該作者
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發(fā)表于 2025-3-31 08:16:03 | 只看該作者
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發(fā)表于 2025-3-31 11:01:18 | 只看該作者
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58#
發(fā)表于 2025-3-31 14:22:16 | 只看該作者
https://doi.org/10.1007/978-3-030-98697-1Intellectual disability; Developmental disability; Autism; End of life; Death; Dying; palliative care; emer
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發(fā)表于 2025-3-31 18:24:34 | 只看該作者
60#
發(fā)表于 2025-3-31 23:46:20 | 只看該作者
Emilie Morwenna Whitaker,Paul Atkinsons, rather than the views of others such as caregivers and clinicians. Topics include their experiences when family or friends die, and engagement with their own dying and death. The extent to which people with intellectual disability actively participate in research about the end of life is critique
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