With a maximum of 20 members, who have recent experience of being a patient or carer, the panel meet monthly to provide a patient’s perspective on Trust services and developments.
Individual members also sit on a large number of committees such as Corporate Governance, Equality and Diversity, Research and Development and Patient Records.
The aim of the group is to build a strong partnership between the Trust, patients and the public and ensure that everyone’s ’voice’ is heard. The panel also advise on Trust policies, as they develop and change.
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