228 research outputs found

    Engendering homelessness: an ethnographic study of homeless practices in a post-industrial city

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    The aim of this thesis is to examine the extent to which homelessness is a gendered phenomenon. In the homelessness literature direct comparisons between men and women are rare, and the ability to compare is complicated by the tendency for research to be either on 'single homelessness' or 'family homelessness'. This thesis addresses this gap and systemically explores the ways in which homelessness is a gendered phenomenon. The research for this thesis focused on homelessness practices in a specific British city. The approach was an ethnographic one and included interviews with homeless people, homeless service providers, statutory housing officers and an observational element in specialist homeless person's assessment centres. The research found that the services provided to homeless people are not neutral in respect to gender. There were found to be differences in the treatment of men and women while homeless and in the options available to them. There were gender differences in the staff and client approaches at the homeless person's assessment centres. The use of discretion in the provision of help and support for homeless people led to different treatment for women and men. Housing officers generally viewed homeless women as more vulnerable than men, and felt that reduced options for women in terms of service provision and accommodation meant that they deserved more favourable treatment as a result. There were also found to be gendered assumptions built into homelessness legislation. Although homeless women are often seen as more vulnerable than men this was not found to translate into better service provision or options for women. In general there was less emergency and supported accommodation for women although that which was available was smaller and often better quality than men's. There were some clear gaps in provision for homeless people, especially for people with children. The uptake of resettlement services was affected by staff perceptions that women were more able and willing to move into independent accommodation than men

    Interview with Helen Norman

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    An interview with Helen Norman regarding her experiences in a one-room school house.https://scholars.fhsu.edu/ors/1174/thumbnail.jp

    Shared decision making in consultations for hypertension:Qualitative study in general practice

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    Abstract Background Hypertension is mainly managed in primary care. Shared decision making is widely recommended as an approach to treatment decision making. However, no studies have investigated; in detail, what happens during primary care consultations for hypertension. Aim To understand patients’ and clinicians’ experience of shared decision making for hypertension in primary care, in order to propose how it might be better supported. Design Longitudinal qualitative study. Setting Five general practices in south‐west England. Method Interviews with a purposive sample of patients with hypertension, and with the health‐care practitioners they consulted, along with observations of clinical consultations, for up to 6 appointments. Interviews and consultations were audio‐recorded and observational field notes taken. Data were analysed thematically. Results Forty‐six interviews and 18 consultations were observed, with 11 patients and nine health‐care practitioners (five GPs, one pharmacist and three nurses). Little shared decision making was described by participants or observed. Often patients’ understanding of their hypertension was limited, and they were not aware there were treatment choices. Consultations provided few opportunities for patients and clinicians to reach a shared understanding of their treatment choices. Opportunities for patients to engage in choices were limited by structured consultations and the distribution of decisions across consultations. Conclusion For shared decision making to be better supported, consultations need to provide opportunities for patients to learn about their condition, to understand that there are treatment choices, and to discuss these choices with clinicians. Patient or Public Contribution A patient group contributed to the design of this study
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