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Journal of Mental Health Volume 11, 2002 - Issue 4
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Research Article

The service and illness experiences described by users of the Mood Swings Network

John A. Baker High Dependency Unit, Department of Psychiatry, Tameside General Hospital, Ashtonunder- Lyne, Lancashire, UK
Pages 453-463 | Published online: 06 Jul 2009

Citations (18)

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Read on this site (3)

Marie Rusner, Gunilla Carlsson, David Arthur Brunt & Maria Nyström. (2012) The Paradox of Being Both Needed and Rejected: The Existential Meaning of Being Closely Related to a Person with Bipolar Disorder. Issues in Mental Health Nursing 33:4, pages 200-208.
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Marie Rusner, Gunilla Carlsson, David Brunt & Maria Nyström. (2010) A dependence that empowers—the meaning of the conditions that enable a good life with bipolar disorder. International Journal of Qualitative Studies on Health and Well-being 5:1.
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Marie Rusner, Gunilla Carlsson, David Brunt & Maria Nyström. (2009) Extra dimensions in all aspects of life—the meaning of life with bipolar disorder. International Journal of Qualitative Studies on Health and Well-being 4:3, pages 159-169.
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Articles from other publishers (15)

Kelly Davenport, Gillian Hardy, Sara Tai & Warren Mansell. (2018) Individual experiences of psychological‐based interventions for bipolar disorder: A systematic review and thematic synthesis. Psychology and Psychotherapy: Theory, Research and Practice 92:4, pages 499-522.
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Rosemary C Stenhouse. (2013) ‘Safe enough in here?’: patients' expectations and experiences of feeling safe in an acute psychiatric inpatient ward. Journal of Clinical Nursing 22:21-22, pages 3109-3119.
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Linda C. Orr, Rosaline S. Barbour & Lawrie Elliott. (2012) Carer involvement with drug services: a qualitative study. Health Expectations 16:3.
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Marie Rusner, Gunilla Carlsson, David Brunt & Maria Nyström. (2012) Towards a more liveable life for close relatives of individuals diagnosed with bipolar disorder. International Journal of Mental Health Nursing 22:2, pages 162-169.
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Josephine E. Ocloo & Naomi J. Fulop. (2011) Developing a ‘critical’ approach to patient and public involvement in patient safety in the NHS: learning lessons from other parts of the public sector?. Health Expectations 15:4, pages 424-432.
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Daryl G. Kroner. (2012) Service user involvement in risk assessment and management: The Transition Inventory. Criminal Behaviour and Mental Health 22:2, pages 136-147.
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Lisa Wood, Pramila Lala, Naomi Fearns & Andrew Higginbotham. (2012) Coming together: Evaluating the efficacy of group psychoeducation for people diagnosed with bipolar disorder. Clinical Psychology Forum 1:229, pages 47-51.
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Caroline Vandekinderen, Griet Roets, Rudi Roose & Geert Van Hove. (2012) Rediscovering Recovery: Reconceptualizing Underlying Assumptions of Citizenship and Interrelated Notions of Care and Support. The Scientific World Journal 2012, pages 1-7.
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R. C. STENHOUSE. (2011) ‘They all said you could come and speak to us’: patients' expectations and experiences of help on an acute psychiatric inpatient ward. Journal of Psychiatric and Mental Health Nursing 18:1, pages 74-80.
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Deirdre Heenan. (2009) Mental Health Policy in Northern Ireland: The Nature and of Extent of User Involvement. Social Policy and Society 8:4, pages 451-462.
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Terence V. McCann, Eileen Clark, John Baird & Sai Lu. (2008) Mental health clinicians' attitudes about consumer and consumer consultant participation in Australia: A cross-sectional survey design. Nursing & Health Sciences 10:2, pages 78-84.
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Penny Bee, John Playle, Karina Lovell, Pamela Barnes, Richard Gray & Philip Keeley. (2008) Service user views and expectations of UK-registered mental health nurses: A systematic review of empirical research. International Journal of Nursing Studies 45:3, pages 442-457.
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Richard Laugharne & Stefan Priebe. (2006) Trust, choice and power in mental health. Social Psychiatry and Psychiatric Epidemiology 41:11, pages 843-852.
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Jenny Weinstein. (2006) Involving mental health service users in quality assurance. Health Expectations 9:2, pages 98-109.
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Elizabeth Anderson, Michael Shepherd & Chris Salisbury. (2006) 'Taking off the suit': engaging the community in primary health care decision-making. Health Expectations 9:1, pages 70-80.
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