Smith et al., 2021 - Google Patents
Family imaginaries in the disclosure of a blood‐borne virusSmith et al., 2021
View PDF- Document ID
- 10255823391568602905
- Author
- Smith A
- Persson A
- Drysdale K
- Bryant J
- Valentine K
- Wallace J
- Hamilton M
- Gray R
- Newman C
- Publication year
- Publication venue
- Sociology of Health & Illness
External Links
Snippet
Contemporary sociological work has emphasised that family is not static, but actively shaped by ideas of who and what makes family. Disclosure of an illness, including diagnosis of stigmatised infections such as HIV, hepatitis B virus and hepatitis C virus, can change the …
- 241000700605 Viruses 0 title abstract description 13
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Ekman | Practising the ethics of person‐centred care balancing ethical conviction and moral obligations | |
| Bergenholtz et al. | Talking about end of life in general palliative care–what’s going on? A qualitative study on end-of-life conversations in an acute care hospital in Denmark | |
| Faulkner | Survivor research and Mad Studies: the role and value of experiential knowledge in mental health research | |
| Greenhalgh et al. | Communicative and strategic action in interpreted consultations in primary health care: a Habermasian perspective | |
| Brown et al. | The perspectives of stakeholders of intellectual disability liaison nurses: a model of compassionate, person‐centred care | |
| Stoklosa et al. | A review of US health care institution protocols for the identification and treatment of victims of human trafficking | |
| Kim et al. | Engineering care in pandemic technogovernance: The politics of care in China and South Korea’s COVID-19 tracking apps | |
| Watermeyer | ‘Are we allowed to disclose?’: A healthcare team's experiences of talking with children and adolescents about their HIV status | |
| Smith et al. | Family imaginaries in the disclosure of a blood‐borne virus | |
| Maquibar et al. | Primary healthcare nurses' experiences of addressing intimate partner violence in supportive legal and health system contexts | |
| Brown et al. | Trust as a means of bridging the management of risk and the meeting of need: a case study in mental health service provision | |
| Fry et al. | The tasks of self-managing hepatitis C: The significance of disclosure | |
| Kaplan et al. | A culture of understanding: reflections and suggestions from a genomics research community board | |
| Bartholomew | Madness (Eemwengu) and its sources: Conceptualizing mental illness in Namibian Ovambo culture | |
| DeJong | Blogs and tweets, texting and friending: Social media and online professionalism in health care | |
| Curtin et al. | “She was more than a friend”: Clinical intervention strategies for effectively addressing disenfranchised grief issues for same-sex couples | |
| FRIMPONG‐MANSOH | Culture and voluntary informed consent in African health care systems | |
| Sinclair et al. | Peer work in Australian mental health policy: What ‘problems’ are we solving and to what effect (s)? | |
| Mulipola et al. | Using fa'afaletui to explore samoan consumers' experience and interpretation of mental health person‐centred care in aotearoa, new zealand | |
| O’Dowd et al. | A qualitative exploration of service users’ experiences of violence risk assessment and management in forensic mental health settings: An interpretative phenomenological analysis | |
| Capurro | Witnessing the ward: On the emotional labor of doing hospital ethnography | |
| Rashid et al. | Muslim faith healers' views on substance misuse and psychosis | |
| Foreman et al. | Not just another long term chronic illness—social work and HIV in Ireland | |
| Bernthal et al. | Mothers’ decision-making during times of stress as a lone parent: a qualitative study | |
| Graham et al. | More than medication: evaluating the role of the pharmacist independent prescriber in a community team for learning disabilities and behaviours deemed to be challenging |