Understanding the Mundane Nature of Self-care: Ethnographic Accounts of People Living with ...
summary
Ethnographic work based on repeated in‑depth interviews and analysis of over 5,000 online posts finds self‑care for Parkinson’s is routine, negotiated, and often invisible rather than clinical. Concrete findings: complex multi‑dose medication schedules, pills placed around the house as cues, deliberate delay medication strategies to time “on” periods, and informal exercise like broom‑stick routines or doing dishes as therapy. Recommendation: design tools that count informal activity, support flexible replanning, and surface the work of everyday care.
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