B Ed (CQU), M HSc (CQU), PhD (La Trobe), RN, MRCN
Building 39, Room 219
(07) 4781 4474
(07) 4781 3183
Supervision for Honours and PhD students
Co-ordinate and teach postgraduate subjects in Health Professional Education and Qualitative research
Co-ordinator and teach MED3 subject: International Health
Teach a range of topics across MED 1 and 3 including, health behavioural change and motivational interviewing, professionalism, communication, ethics, dying and death.
Community health workshops on advanced care planning and motor neurone disease
Guest lecturer in Palliative Care for Allied Health
Curriculum review and development (social sciences)
Chair Student Selection Advisory Committee, School of Medicine and Dentistry
Supervised honours and masters students to completion.
Undertaken a range of teaching roles and curriculum development at undergraduate and postgraduate levels at three Universities in Medicine, Allied Health, Nursing, Health Promotion and Occupational Health
Provided community based support and education for people living with motor neurone disease
Provided short term teaching, consultation and support in Hong Kong and Bhutan
Conducted health promotion with National Heart Foundation across Central Queensland
Provided occupational health services for telecommunication workers in rural Victoria
Worked as a nurse/midwife in rural and regional areas in Victoria and Queensland
My research has two foci, selection and retention of rural workforce; and community palliative care with a particular focus on people living with motor neurone disease (MND), end of life and advance care planning, and social support in life-limiting illness. I use both qualitative methods and mixed methods approaches to investigate:
ways to promote quality of life, enhance social support and enable people to die well. I am also interested in improving access to services and appropriate care.
the connections between selection criteria, undergraduate medical training and rural intention.
My PhD research used ecomapping as a data gathering tool to capture the dynamic changes in support networks available to caregivers, challenging the government’s notion that support is readily available given the healthy nature of social capital in Australia. My work with caregivers of individuals living with MND has redefined emotional labour as it pertains to caregivers and developed the concept of socio-connective trust to describe the reflexive, shifting relationships between caregivers and the individual being cared for, caregivers and expert systems, and caregivers and social networks. My research is well received at local, interstate and international conferences.
Ray, R. A., & Kavanagh, A. (in press). Parkinson's disease, multiple sclerosis, motor neurone disease. In E. Chang & A. Johnson (Eds.), Chronic illness and disability. Marrickville: Elsevier Australia.
Ray, R. A., Brown, J., & Street, A. F. (2012). Dying with motor neurone disease, what can we learn from family caregivers? Health Expectations. doi: DOI: 10.1111/j.1369-7625.2012.00773.x
Ray, R. A., & Street, A. F. (2011). The dynamics of socio-connective trust within support networks accessed by informal caregivers. Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine.
Ray, R. A. (2009). Mapping relationships: a companion website to L. Richards (Ed.), Handling Qualitative Data (2nd ed.). London: Sage Publications available at http://www.uk.sagepub.com/richards/.
Ray, R. A., & McAnally, L. (2008). Parkinson's disease, multiple sclerosis, motor neurone disease. In E. Chang & A. Johnson (Eds.), Chronic illness and disability. Marrickville: Elsevier Australia.
Ray, R. A., & Street, A. F. (2007). Nonfinite loss and emotional labour: family caregivers' experiences of living with motor neurone disease. Journal of Clinical Nursing, 16(3a), 35-43.
Ray, R. A., & Street, A. F. (2006). Caregiver bodywork: family member's experiences of caring for someone living with motor neurone disease (MND). Journal of Advanced Nursing, 56(1), 35-43.
Ray, R. A. (2006). "It's all down hill from here," or is it? Living with loss and grief associated with motor neurone disease. Grief matters: The Australian Journal of Grief and Bereavement, 9(1), 8-11.
Ray, R. A., & Street, A. F. (2005). Engaging social support systems to improve quality of life for patients and carers. Amyotrophic Lateral Sclerosis and other motor neuron diseases, 6(Supp 1), 37-38.
Love, A., Street, A. F., Ray, R. A., Harris, R., & Lowe, R. (2005). Social aspects of caregiving for people living with motor neurone disease: Their relationships to carer wellbeing. Palliative and Supportive Care, 3, 33-38.
Ray, R. A., & Street, A. F. (2005). Who's there and who cares: age as an indicator of social support networks for caregivers among people living with motor neurone disease. Health and Social Care in the Community, 13(6), 542-552.
Ray, R. A., & Street, A. F. (2005). Ecomapping: an innovative research tool for nurses. Journal of Advanced Nursing, 50(5), 545-552.
Ray, R. (2001). Self-reported heart health behaviour patterns in a rural context. The Australian Journal of Rural Health, 9 (2) 59-63.
2011 International Allied Professionals ALS/MND Forum – Sydney, Using a circular model to build emotional readiness for conversations about advance care planning (ACP) in MND
International Society of Advanced Care Planning and End of Life Care Conference – London, Hear the right story and finish up in country: learning lessons from Aboriginal Australians implementing advance care planning
Palliative Care Australia Conference – Cairns, Building community capacity in palliative care – a north Queensland initiative.
2009 International Symposium on ALS/MND – Berlin, Germany Managing death in ALS/MND: identifying caregivers’ perspectives of the final days of life
2007 MND Australia Conference - Perth. Ambiguous loss and emotional labour: meeting family caregiver’s needs
2007 Clinical Education Conference – Melbourne. Living the connections between foundational learning and acute care practice: ongoing journey for clinical educators and students
2006 International Symposium on ALS/MND – Yokohama, Japan The impact of ambiguous loss and emotional labour on family caregivers
2006 International Allied Professionals ALS/MND Forum Yokohama Managing the degeneration of my loved one’s body: Family caregiver’s experiences of bodywork in ALS/MND
2006 Australian Palliative Care Nurses Conference. Melbourne Working with family caregivers to manage emotional labour in palliative care.
2006 MND Australia Conference invited speaker. Sydney Enhancing social support to improve quality of life for patients and caregivers.
2006 Ask the Experts Forum MND Association of Victoria. Melbourne Interventions that claim survival advantage, quality of life or treatment benefit for people living with ALS/MND
Full list of publications available at JCU Research Online