The aim of this study was to explore perceptions of people with Parkinson’s disease and family carers about the use and impact of health and social care services, community and voluntary sector resources for the management of Parkinson’s disease. Resources from outside the formal health care system and collaborations between different levels and sectors could address the unmet needs of people with Parkinson’s disease and their family carers and improve the management of Parkinson’s disease in the community setting. An integrated and person-and-community-centred approach, which includes the participation of the health, social, voluntary and community sectors, is desired by people with Parkinson’s disease and their family carers to improve the management of Parkinson’s in the community setting.