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Patient Advisory Panel

The Patient Advisory Panel provides a source of composite advice and patient perspective to the Lymphoedema Wales Clinical Network National Team.  The Panel reviews the progress of the LWCN Programme and agrees any necessary action.  Members of the Patient Advisory Panel (PAP) may also be invited to become members of or attend other LWCN governance boards.

The Panel meets quarterly for approximately 1.5hours with its membership reflecting the current patient profile and is representative of all seven Health Boards.