GPs were thought to be reactive rather than proactive which discouraged carers from asking for help. 3) There was ambiguity about the legitimacy of carer needs and about the role of the primary health care team in supporting carers, from both the perspective of the carers and the health professionals. 2) As the cared-for person’s condition deteriorated, the caring role often became all-encompassing so that carers were managing competing demands, and felt unable to look after their own needs as well as those of the cared-for person. Often it was health and social care professionals who encouraged carers to consider themselves as an unpaid carer. 1) Taking on the care of another person is often a gradual process, carers did not immediately identify with being a ‘carer’ – preferring to think of themselves in relational terms to the patient e.g. We integrated findings from three data sources – a review of the caregiving literature a workshop with researchers who have undertaken research with those caring at the end of life, and focus groups with carers and health professionals. This study set out to explore the barriers to, and consider strategies for, identifying carers in primary care.
Neither are carers self-identifying and requesting support. Despite initiatives for general practices to identify carers and their needs, many remain unidentified.
Carers can experience poor physical and psychosocial wellbeing, yet they remain largely unsupported by health and social care services. Many of these carers make a significant contribution to supporting patients at the end of life. Approximately 10% of the UK population have an unpaid caring role for a family member or friend.