What is it about?

An interview study exploring how partners of people with Parkinson's experience dealing with health care professionals in relation to the care of their relative with Parkinson's.

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Why is it important?

Partners of people with Parkinson's play an essential role in the care in the community of individuals with PD, yet do not feel listened to. Taking account of their perspective may improve care for people with Parkinson's.

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This page is a summary of: I’m Losing the ‘Me’: Partners’ Experiences of Engagement with Parkinson's Health Professionals, Brain Impairment, September 2015, Cambridge University Press,
DOI: 10.1017/brimp.2015.19.
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