Jour

Focuses on a research on older people who combine the caring role with paid employment. Stages of data collection used in the study; Findings of the research concerning employment policies; Reasons behind the decrease in the number of informal carers.

Despite calls for health and social services to respond to the needs of informal carers, there is little evidence to guide practioners in the best way to provide support and/or information in situations of complex need such as brain injury. This study addressed such an intervention in a prospective descriptive study, using both qualitative and quantitative methodology. Eighty-nine patients who had been admitted to a regional neurorehabilitation unit for management of traumatic or haemorrhagic brain injuries were consecutively discharged to the community over a period of 12 months.

Objectives: This study examines the relationship between caring for older parents and the financial well-being of caregivers by investigating whether a reciprocal association, or vicious cycle, exists between female caregiver’s lower household incomes and caring for elderly parents.

Method: Data for women aged 51 or older with at least 1 living parent or parent-in-law were drawn from the Health and Retirement Survey 2006, 2008, and 2010 (N = 2,093). A cross-lagged panel design was applied with structural equation modeling.

Informal care of older people, including a summary of research on the attitudes towards willingness to care for an elderly person among members of the general public aged 20-39 years and 40-59 years. Nurses' attitudes towards elderly care nursing are also discussed. It is suggested that nurses can influence attitudes to the elderly and engage with informal carers. [(BNI unique abstract)] 11 references

Objectives: Identify factors of informal caregivers, caregiving, and people with multiple sclerosis (MS) receiving assistance that are associated with perceptions of caregiver accomplishment. Methods: National data were collected in a telephone interview survey of 530 informal caregivers and analyzed using an ordered logistic regression model to identify factors associated with perceptions of caregiver accomplishment among 442 of these informal caregivers (caregivers providing all data in their survey responses needed for the regression model). Results: We found t

Aim.  To throw light on the lived experiences of female partners of patients with Parkinson disease living at home.

Background.  It is known that daily life with a partner with Parkinson’s disease entails radical upheaval in the family, in particular for the female partner.

Methodology.  A phenomenological hermeneutic approach was used. Interviews with female partners (N = 10) of patients with Parkinson disease who were living at home were conducted in Denmark in 2008. The French philosopher Ricoeur’s theory of interpretation guided the data analysis.

Long-term care in the UK relies heavily on informal and unpaid carers. Statistical data regarding the number of carers in the 2001 Census compared with the 2011 Census identify an increase of around 600 000 carers. It is also significant that many of these carers are themselves in their late middle age. The reasons for taking on the caring role are varied, but there are significant potential physical, mental and financial issues associated with taking on the caring role. Positive benefits in terms of support provision for the carer do exist, but support services across the UK are variable.

Increasingly there is greater emphasis on user/carer involvement in the delivery of mental health care. There are five levels of participation from none at all to partnership and optimal involvement. A two-year pilot steering group was established by a health authority in December 2000 and criteria for independent evaluation agreed. These included the context, data collection, analysis and report, and recommendations based on the findings to increase user/carer involvement in all aspects of mental health service delivery.

This article suggests that relational approaches and carer-centred practice in mental health and other services might alleviate some of the burden on the health – both physical and mental – experienced by informal carers. Unhelpful staff attitudes and poor communication are barriers to effective engagement between professionals and carers.