Citations (37)
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Elly Quinlan, Frank Deane & Trevor Crowe. (2018) Interpersonal problems amongst mental health carers: a qualitative study. Social Work in Mental Health 16:5, pages 518-539.
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Andrea Petriwskyj, Barbara Adkins & Jill Franz. (2017) Parent, carer, person: future plans and the identities of parent carers for people with disabilities. Disability & Society 32:1, pages 93-109.
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Elise K. Eifert, Rebecca Adams, William Dudley & Michael Perko. (2015) Family Caregiver Identity: A Literature Review. American Journal of Health Education 46:6, pages 357-367.
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Catherine Ward-Griffin. (2012) Supportive Care to Family Caregivers is Not Supportive Enough: Moving Towards an Equitable Approach to Dementia Home Care. Neurodegenerative Disease Management 2:2, pages 173-181.
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Articles from other publishers (32)
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Joanna Fox. (2022) Experiences of Being Cared-For: The Perspective of an Expert-by-Experience in Mental Health. Frontiers in Psychiatry 13.
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Hannah M. K. McGillivray, Elisabetta E. L. Piccolo & Richard J. Wassersug. (2021) “Partner”, “Caregiver”, or “Co-Survivor”—Might the Label We Give the Partners of Cancer Patients Affect the Health Outcome of the Patients and Their Partners?. Current Oncology 29:1, pages 122-129.
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Darryl Maybery, Irene Casey Jaffe, Rose Cuff, Zoe Duncan, Anne Grant, Melissa Kennelly, Torleif Ruud, Bjorg Eva Skogoy, Bente Weimand & Andrea Reupert. (2021) Mental health service engagement with family and carers: what practices are fundamental?. BMC Health Services Research 21:1.
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Zoë V. R. Boden‐Stuart, Michael Larkin & Chris Harrop. (2021) Young adults’ dynamic relationships with their families in early psychosis: Identifying relational strengths and supporting relational agency. Psychology and Psychotherapy: Theory, Research and Practice 94:3, pages 646-666.
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Kimberley Bassett, Judith Gullifer & Ramon L. Varcoe. (2018) Accepting, active and in control: older women's experiences of ageing with peripheral arterial disease. Ageing and Society 39:12, pages 2605-2630.
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Sahar Suleiman AlMakhamreh. (2017) Exploring experiences of informal carers of mental health: Developing community intervention in social work in Jordan. International Social Work 61:6, pages 1042-1053.
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Elly Quinlan, Frank P. Deane & Trevor Crowe. (2018) Pilot of an acceptance and commitment therapy and schema group intervention for mental health carer's interpersonal problems. Journal of Contextual Behavioral Science 9, pages 53-62.
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Sarah Knowles, Ryan Combs, Sue Kirk, May Griffiths, Neesha Patel & Caroline Sanders. (2015) Hidden caring, hidden carers? Exploring the experience of carers for people with long‐term conditions. Health & Social Care in the Community 24:2, pages 203-213.
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Fiona E. Glenn, Kenneth M. McFadyen & Zounish Rafique. (2013) Adopting New Identities When a Partner has Depression: An Interpretative Phenomenological Analysis. Interpersona: An International Journal on Personal Relationships 7:2, pages 282-298.
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Mary V Seeman. (2012) Bad, burdened or ill? Characterizing the spouses of women with schizophrenia. International Journal of Social Psychiatry 59:8, pages 805-810.
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Nic Hughes, Louise Locock & Sue Ziebland. (2013) Personal identity and the role of ‘carer’ among relatives and friends of people with multiple sclerosis. Social Science & Medicine 96, pages 78-85.
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VALERIE EGDELL. (2012) Who cares? Managing obligation and responsibility across the changing landscapes of informal dementia care. Ageing and Society 33:5, pages 888-907.
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Valerie Egdell. (2012) Development of Support Networks in Informal Dementia Care: Guided, Organic, and Chance Routes through Support. Canadian Journal on Aging / La Revue canadienne du vieillissement 31:4, pages 445-455.
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Terry Carney. (2012) Australian mental health tribunals—‘Space’ for rights, protection, treatment and governance?. International Journal of Law and Psychiatry 35:1, pages 1-10.
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Hadass Goldblatt, Orit Karnieli-Miller & Melanie Neumann. (2011) Sharing qualitative research findings with participants: Study experiences of methodological and ethical dilemmas. Patient Education and Counseling 82:3, pages 389-395.
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ANNE CORDEN & MICHAEL HIRST. (2010) Partner care at the end-of-life: identity, language and characteristics. Ageing and Society 31:2, pages 217-242.
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Julie Ridley, Susan Hunter & Ann Rosengard. (2010) Partners in care?: views and experiences of carers from a cohort study of the early implementation of the Mental Health (Care & Treatment) (Scotland) Act 2003. Health & Social Care in the Community 18:5, pages 474-482.
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soonmi lee & Hyekyung KIM. (2009) Elerly hubands' caregiving for their sick wives: narratives of husbands and wives. Family and Culture 21:4, pages 63-94.
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Phyllis Montgomery, Pat Bailey, Sheri Johnson Purdon, Susan J Snelling & Carol Kauppi. (2009) Women with postpartum depression: "my husband" stories. BMC Nursing 8:1.
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Cait Fraser & Deborah J. Warr. (2008) Challenging Roles: Insights Into Issues for Men Caring for Family Members With Mental Illness. American Journal of Men's Health 3:1, pages 36-49.
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J. Rapaport & J. Manthorpe. (2008) Family Matters: Developments Concerning the Role of the Nearest Relative and Social Worker under Mental Health Law in England and Wales. British Journal of Social Work 38:6, pages 1115-1131.
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Deborah L. O'Connor. (2007) Self-identifying as a caregiver: Exploring the positioning process. Journal of Aging Studies 21:2, pages 165-174.
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Liz Forbat & Jeanette Henderson. (2016) “Stuck in the Middle with You”: The Ethics and Process of Qualitative Research th Two People in an Intimate Relationship. Qualitative Health Research 13:10, pages 1453-1462.
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