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The consequence of “doing nothing”: Family caregiving for Alzheimer's disease as non-action in the US
Journal article   Peer reviewed

The consequence of “doing nothing”: Family caregiving for Alzheimer's disease as non-action in the US

Aaron T Seaman
Social science & medicine (1982), Vol.197, pp.63-70
01/2018
DOI: 10.1016/j.socscimed.2017.12.001
PMID: 29222996

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Abstract

Ethnography Family caregiving Relationality Medicalization United States Alzheimer's disease

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