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Journal of Mental Health Volume 14, 2005 - Issue 1
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Original Article

Economic deprivation and its effects on subjective wellbeing in families of people with multiple sclerosis

Margaret A De Judicibus School of Psychology, Deakin University, Victoria, AustraliaCorrespondence[email protected]
&
Marita P McCabe School of Psychology, Deakin University, Victoria, Australia
Pages 49-59 | Published online: 06 Jul 2009

Citations (18)

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Read on this site (2)

Daniel Ståhl, Ylva Bjereld & Anna Dunér. (2022) Disabled in Society - A Scoping Review on Persons Living with Multiple Sclerosis and Disability. Journal of Multidisciplinary Healthcare 15, pages 375-390.
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Paul McCrone. (2018) 'Money doesn’t talk, it swears'. Journal of Mental Health 27:6, pages 485-486.
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Articles from other publishers (16)

Vladimira Timkova, Pavol Mikula, Miriam Fedicova, Jarmila Szilasiova & Iveta Nagyova. (2021) Psychological well-being in people with multiple sclerosis and its association with illness perception and self-esteem. Multiple Sclerosis and Related Disorders 54, pages 103114.
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Gabriela Topa, Marco Depolo & Carlos-Maria Alcover. (2018) Early Retirement: A Meta-Analysis of Its Antecedent and Subsequent Correlates. Frontiers in Psychology 8.
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Michael Wiberg, Emilie Friberg, Magnus Stenbeck, Kristina Alexanderson, Anders Norlund, Jan Hillert & Petter Tinghög. (2015) Sources and level of income among individuals with multiple sclerosis compared to the general population: A nationwide population-based study. Multiple Sclerosis Journal 21:13, pages 1730-1741.
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Marita McCabe, Katherine J. Ebacioni, Rex Simmons, Elizabeth McDonald & Lisa Melton. (2015) Satisfaction with service needs among people living with multiple sclerosis. NeuroRehabilitation 36:2, pages 167-173.
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Janine Feicke, Ulrike Spörhase, Jürgen Köhler, Claudia Busch & Markus Wirtz. (2014) A multicenter, prospective, quasi-experimental evaluation study of a patient education program to foster multiple sclerosis self-management competencies. Patient Education and Counseling 97:3, pages 361-369.
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Shaloo Gupta, Amir Goren, Amy L. Phillips & Michelle Stewart. (2012) Self-Reported Burden Among Caregivers of Patients with Multiple Sclerosis. International Journal of MS Care 14:4, pages 179-187.
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Margaret H Vickers. (2015) Financial turning points and transitions for people with multiple sclerosis: Towards sustainable employment outcomes. Journal of Management & Organization 18:3, pages 346-362.
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Margaret H Vickers. (2015) Financial turning points and transitions for people with multiple sclerosis: Towards sustainable employment outcomes. Journal of Management & Organization 18:3, pages 346-362.
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Margaret H. VickersPhDPhD. (2012) Financial Turning Points and Transitions for People with Multiple Sclerosis (MS): Towards Sustainable Employment Outcomes. Journal of Management & Organization, pages 362-401.
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Gabriela Topa, Juan A. Moriano, Marco Depolo, Carlos-María Alcover & Ana Moreno. (2011) Retirement and Wealth Relationships. Research on Aging 33:5, pages 501-528.
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Samar AounRuth McConigleyAmy AbernethyDavid C. Currow. (2010) Caregivers of People with Neurodegenerative Diseases: Profile and Unmet Needs from a Population-Based Survey in South Australia. Journal of Palliative Medicine 13:6, pages 653-661.
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Julie Barlow, Andy Turner, Rhiannon Edwards & Mollie Gilchrist. (2009) A randomised controlled trial of lay-led self-management for people with multiple sclerosis. Patient Education and Counseling 77:1, pages 81-89.
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Marita P. McCabeElodie J. O'Connor. (2009) A longitudinal study of economic pressure among people living with a progressive neurological illness. Chronic Illness 5:3, pages 177-183.
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Margarita Corry & Alison While. (2009) The needs of carers of people with multiple sclerosis: a literature review. Scandinavian Journal of Caring Sciences 23:3, pages 569-588.
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Mieke Rijken & Peter P. Groenewegen. (2007) Money does not bring well‐being, but it does help! The relationship between financial resources and life satisfaction of the chronically ill mediated by social deprivation and loneliness. Journal of Community & Applied Social Psychology 18:1, pages 39-53.
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Lori Perez, Jennifer Huang, Liz Jansky, Cindy Nowinski, David Victorson, Amy Peterman & David Cella. (2007) Using Focus Groups To Inform the Neuro-QOL Measurement Tool: Exploring Patient-Centered, Health-Related Quality of Life Concepts Across Neurological Conditions. Journal of Neuroscience Nursing 39:6, pages 342-353.
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