This report details the main findings of research conducted through a survey of people affected by Parkinson’s looking at health and social care costs incurred during the past 12-month period. The data is enriched by five in-depth interviews with people with Parkinson’s and their caregivers who responded to the survey, providing a longitudinal view of their lived experience of the condition from the time around diagnosis up till the time of interview.

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Final Report (PDF, 3 MB) (PDF, 2.7MB)
Executive Summary (PDF, 680 KB) (PDF, 676.2KB)