145 results on '"Lewis, Sophie"'
Search Results
2. Towards enhancing animal welfare standards in UK media: Part 1; insights from public opinion and attitudes
3. Complexities in supportive care for people with metastatic breast cancer: a qualitative study
4. Finding my tribe: a qualitative interview study of how people living with metastatic breast cancer perceive support groups
5. Attitudes to End-of-Life Care and Voluntary Assisted Dying Amongst Members of the Australian Jewish community
6. Friendship, connectedness and (in)authenticity for those with chronic illness: Trading in one social gain for another
7. Professionally led support groups for people living with advanced or metastatic cancer: a systematic scoping review of effectiveness and factors critical to implementation success within real-world healthcare and community settings
8. Making the unbearable, bearable: Qualitative examination of patient, family and nurses’ perspectives on the role and value of specialist metastatic breast care nurses
9. Healthcare workers’ perceptions of strategies supportive of their mental health
10. There but not really involved: The meanings of loneliness for people with chronic illness
11. International tax update for the banking sector
12. International tax update for the banking sector
13. Chronic condition self-management is a social practice
14. A Woman is a Woman? : Lillian Faderman's selective histories
15. Targeting 1.5 degrees with the global carbon footprint of the Australian Capital Territory
16. The Impact of Voluntary Assisted Dying on Grief and Bereavement for Family Members and Carers in the Australian State of Victoria: A Qualitative Study
17. Finding my tribe: a qualitative interview study of how people living with metastatic breast cancer perceive metastatic breast cancer support groups
18. A time for self-care? Frontline health workers’ strategies for managing mental health during the COVID-19 pandemic
19. Potential inequities in availability of care from breast care nurses: a qualitative study reporting the experiences and perspectives of women with metastatic breast cancer in Australia
20. Coping with COVID-19: The sociomaterial dimensions of living with pre-existing mental illness during the early stages of the coronavirus crisis
21. Multi-channel dilution analysis.
22. Sociomaterialities of health, risk and care during COVID-19: Experiences of Australians living with a medical condition
23. Hopeful dying? The meanings and practice of hope in palliative care family meetings
24. The hidden costs of the intercollegiate membership of the Royal College of surgeons examinations: Can trainees afford it?
25. The impossible juggle of work and care
26. Feeling valued and appreciated
27. Overwork, burnout, and resignation
28. Introduction
29. Supporting emotional wellbeing
30. Self-care struggles and strategies
31. Not able to hug a dying patient
32. Showing up all the cracks
33. Pervasive, precarious, and perilous
34. Dispensable and disillusioned
35. Looking back, looking forwards
36. Postscript
37. A roller-coaster of mood and meaning
38. Purpose, compassion, and gratitude
39. Leadership and teams
40. Communication and understanding
41. Missing the human connection
42. Are we informing our patients correctly? Evaluation of perioperative counselling for paediatric intestinal stoma formation: a national study.
43. “I was told I either came back or I lost my job”: a qualitative study of the experiences of Australian women navigating the return-to-work following early pregnancy loss.
44. Learning about COVID-19: a qualitative interview study of Australians’ use of information sources
45. Choreographing a good death: Carers’ experiences and practices of enacting assisted dying.
46. The incurable self: Negotiating social bonds and dis/connection with metastatic breast cancer.
47. The incurable self: Negotiating social bonds and dis/connection with metastatic breast cancer
48. Massachusetts to provide grant funding for immigration legal services for migrants
49. Should voluntary assisted dying in Victoria be extended to encompass people with dementia?
50. Friendship, connectedness and (in)authenticity for those with chronic illness: Trading in one social gain for another
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