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Original Articles

The nature of benefit finding in multiple sclerosis (MS)

Pages 190-196 | Published online: 19 Feb 2007

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (14)

Emilie Wawrziczny, Aubane Corrairie & Pascal Antoine. (2021) Relapsing-remitting multiple sclerosis: an interpretative phenomenological analysis of dyadic dynamics. Disability and Rehabilitation 43:1, pages 76-84.
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Simon Langston, Mark S. Edwards & Michael Lyvers. (2018) Illness Perceptions, Coping, Benefit Finding, and Adjustment in Individuals with Hepatitis C. Australian Psychologist 53:1, pages 87-96.
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Kami A. Kosenko, Jacquelyn Harvey-Knowles & Elizabeth Craig. (2015) HPV infection as an occasion for personal and relational growth. Journal of Communication in Healthcare 8:3, pages 197-206.
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Vinayak Anand-Kumar, Mary Kung, Liz Painter & Elizabeth Broadbent. (2014) Impact of organ transplantation in heart, lung and liver recipients: Assessment of positive life changes. Psychology & Health 29:6, pages 687-697.
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Jessica M. Schultz, Elizabeth Altmaier, Saba Ali & Benjamin Tallman. (2014) A study of posttraumatic spiritual transformation and forgiveness among victims of significant interpersonal offences. Mental Health, Religion & Culture 17:2, pages 122-135.
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Rie Chiba, Yuki Miyamoto & Akiko Funakoshi. (2014) The concept of “benefit finding” for people at different stages of recovery from mental illness; a Japanese study. Journal of Mental Health 23:1, pages 20-24.
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Kathrin Boerner & StevenE. Mock. (2012) Impact of patient suffering on caregiver well-being: The case of amyotrophic lateral sclerosis patients and their caregivers. Psychology, Health & Medicine 17:4, pages 457-466.
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Louise Mozo-Dutton, Jane Simpson & Julia Boot. (2012) MS and me: exploring the impact of multiple sclerosis on perceptions of self. Disability and Rehabilitation 34:14, pages 1208-1217.
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Robert J. Buchanan & Chunfeng Huang. (2012) Caregiver perceptions of accomplishment from assisting people with multiple sclerosis. Disability and Rehabilitation 34:1, pages 53-61.
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Ross Wadey, Lynne Evans, Kieran Evans & Ian Mitchell. (2011) Perceived Benefits Following Sport Injury: A Qualitative Examination of their Antecedents and Underlying Mechanisms. Journal of Applied Sport Psychology 23:2, pages 142-158.
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Aviva Gaskill, Frederick W. Foley, Julie Kolzet & Mary Ann Picone. (2011) Suicidal thinking in multiple sclerosis. Disability and Rehabilitation 33:17-18, pages 1528-1536.
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Tatjana Barskova & Rainer Oesterreich. (2009) Post-traumatic growth in people living with a serious medical condition and its relations to physical and mental health: A systematic review. Disability and Rehabilitation 31:21, pages 1709-1733.
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Kenneth I. Pakenham. (2008) The nature of sense making in caregiving for persons with multiple sclerosis. Disability and Rehabilitation 30:17, pages 1263-1273.
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Articles from other publishers (42)

Helen M. Genova, Michelle H. Chen, Amanda Botticello, Gerald Voelbel, Grace Kim, Heba E. Elsayed, Zuzanna Myszko, John DeLuca, Robert E. McGrath, Peter Arnett & Yael Goverover. (2023) An Examination of Positive and Negative Outcomes During the COVID-19 Pandemic Among Persons With Multiple Sclerosis. The American Journal of Occupational Therapy 77:6.
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Hongli Yan, Jie Yang, Chenling Luo, Lei Zhang, Yihe Tian, Shasha Cui, Jing Wu & Jing Chu. (2023) Development and Psychometric Assessment of the Benefit Finding Scale for Chinese Older Adults With Chronic Diseases. Research in Gerontological Nursing 16:1, pages 44-52.
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Irene Gil-González, María Ángeles Pérez-San-Gregorio, Rupert Conrad & Agustín Martín-Rodríguez. (2022) Beyond the Boundaries of Disease—Significant Post-traumatic Growth in Multiple Sclerosis Patients and Caregivers. Frontiers in Psychology 13.
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Seada A Kassie, Jannat Alia & Lynda Hyland. (2021) Biopsychosocial implications of living with multiple sclerosis: a qualitative study using interpretative phenomenological analysis. BMJ Open 11:8, pages e049041.
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Amy Gorven & Larise du Plessis. (2018) Corporeal Posttraumatic Growth As a Result of Breast Cancer: An Interpretative Phenomenological Analysis. Journal of Humanistic Psychology 61:4, pages 561-590.
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Silvia Poli, Michela Rimondini, Alberto Gajofatto, Maria Angela Mazzi, Isolde Martina Busch, Francesca Gobbin, Federico Schena, Lidia Del Piccolo & Valeria Donisi. (2021) “If You Can’t Control the Wind, Adjust Your Sail”: Tips for Post-Pandemic Benefit Finding from Young Adults Living with Multiple Sclerosis. A Qualitative Study. International Journal of Environmental Research and Public Health 18:8, pages 4156.
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Rie Chiba, Akiko Funakoshi, Yoshihiko Yamazaki & Yuki Miyamoto. (2020) The Benefit Finding Questionnaire (BFQ): Scale Development, Validation, and Its Psychometric Properties Among People with Mental Illness. Healthcare 8:3, pages 303.
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Mahdi Moshki, Abdoljavad Khajavi, Shima Minaee, Farveh Vakilian & Haydeh Hashemizadeh. (2020) Perceived benefits of the disease: A qualitative study of patients' experiences of heart failure. Nursing & Health Sciences 22:2, pages 464-471.
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Maryam Sharifi, Hamid Taher Neshat Doost & Vahid Shayegannejad. (2020) ‘I want to be with you, but I have MS’: Challenges of interpersonal relationships from the MS patients’ point of view. Health & Social Care in the Community 28:3, pages 1030-1037.
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Caitlin M. O'Loughlin, David S. Bennett & C. Virginia O'Hayer. (2020) The nomological network of cognitive fusion among people living with HIV: Associations with rumination, shame, and depressive symptoms. Journal of Contextual Behavioral Science 15, pages 245-252.
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Sandra L. Neate, Keryn L. Taylor, George A. Jelinek, Alysha M. De Livera, Chelsea R. Brown & Tracey J. Weiland. (2019) Taking active steps: Changes made by partners of people with multiple sclerosis who undertake lifestyle modification. PLOS ONE 14:2, pages e0212422.
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Mahsa Salimi Kivi, Masomeh Jamei-Moghadam, Hekmat Khoshlahni, Mehdi Heidarzadeh, Aziz Kamran & Hosein Shahabi. (2019) Psychological Changes in Patients With Multiple Sclerosis. Journal of Holistic Nursing and Midwifery 29:1, pages 308-313.
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Mehdi Heidarzadeh, Maryam Rassouli, Jeannine M. Brant, Farahnaz Mohammadi-Shahbolaghi & Hamid Alavi-Majd. (2018) Dimensions of Posttraumatic Growth in Patients With Cancer. Cancer Nursing 41:6, pages 441-449.
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Kenneth Ian Pakenham & Stephen Cox. (2018) Effects of Benefit Finding, Social Support and Caregiving on Youth Adjustment in a Parental Illness Context. Journal of Child and Family Studies 27:8, pages 2491-2506.
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Antonella Delle Fave, Marta Bassi, Beatrice Allegri, Sabina Cilia, Monica Falautano, Benedetta Goretti, Monica Grobberio, Eleonora Minacapelli, Marianna Pattini, Erika Pietrolongo, Manuela Valsecchi, Maria Pia Amato, Alessandra Lugaresi & Francesco Patti. (2017) Beyond Disease: Happiness, Goals, and Meanings among Persons with Multiple Sclerosis and Their Caregivers. Frontiers in Psychology 8.
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Maciej Wilski & Tomasz Tasiemski. 2017. Multiple Sclerosis: Bench to Bedside. Multiple Sclerosis: Bench to Bedside 43 55 .
Virginie Voltzenlogel, Alexandra Ernst, Jérôme de Sèze, David Brassat, Liliann Manning & Fabrice Berna. (2016) Giving meaning to illness: An investigation of self-defining memories in patients with relapsing-remitting multiple sclerosis patients. Consciousness and Cognition 45, pages 200-209.
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Chiara Rollero. (2016) The Experience of Men Caring for a Partner With Multiple Sclerosis. Journal of Nursing Scholarship 48:5, pages 482-489.
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Melissa L Harris, Julie E Byles, Natalie Townsend & Deborah Loxton. (2016) Perceptions of coping with non-disease-related life stress for women with osteoarthritis: a qualitative analysis: Table 1. BMJ Open 6:5, pages e010630.
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Karen Strickland, Allison Worth & Catriona Kennedy. (2015) The experiences of support persons of people newly diagnosed with multiple sclerosis: an interpretative phenomenological study. Journal of Advanced Nursing 71:12, pages 2811-2821.
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Frederick W. Foley. 2015. Neuropsychiatric Symptoms of Inflammatory Demyelinating Diseases. Neuropsychiatric Symptoms of Inflammatory Demyelinating Diseases 107 119 .
Caroline Lafarge, Krishna Talsania, Julia M Townshend & Pauline Fox. (2014) Living with Charcot-Marie-Tooth Disease: a qualitative analysis. British Journal of Neuroscience Nursing 10:5, pages 226-235.
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Stig Wenneberg & Ann-Kristin Isaksson. (2014) Living with Multiple Sclerosis: The Impact of Chronic Illness. Nordic Journal of Nursing Research 34:3, pages 23-27.
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Takahiro Yamane. (2014) Stress-buffering effects of benefit finding on the psychological stress response in mothers of children with developmental disorders. The Japanese journal of psychology 85:4, pages 335-344.
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Hossein Karimi Moonaghi, Hossein Namdar Areshtanab & Leila Jouybari. (2014) The Efficacy of Optimism: Benefit Finding in the Treatment of Diabetes in Iranian Patients. ISRN Nursing 2014, pages 1-6.
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Tatjana Alexander & Rainer Oesterreich. (2013) Development and Evaluation of the Posttraumatic Growth Status Inventory. Psychology 04:11, pages 831-844.
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Diane M. Quinn & Valerie A. Earnshaw. (2013) Concealable Stigmatized Identities and Psychological Well‐Being. Social and Personality Psychology Compass 7:1, pages 40-51.
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David J. Rintell. 2012. Multiple Sclerosis. Multiple Sclerosis 263 282 .
Bronwyn A. Morris, Jane Shakespeare-Finch & Jennifer L. Scott. (2011) Posttraumatic growth after cancer: the importance of health-related benefits and newfound compassion for others. Supportive Care in Cancer 20:4, pages 749-756.
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MARK E. YOUNG & TRACY S. HUTCHINSON. (2012) The Rediscovery of Gratitude: Implications for Counseling Practice. The Journal of Humanistic Counseling 51:1, pages 99-113.
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Robert J. Buchanan & Chunfeng Huang. (2011) Informal Caregivers Assisting People with Multiple Sclerosis. International Journal of MS Care 13:4, pages 177-187.
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Michaela CoenenBirgit Basedow-Rajwich, Nicolaus König, Jürg Kesselring & Alarcos Cieza. (2011) Functioning and disability in multiple sclerosis from the patient perspective. Chronic Illness 7:4, pages 291-310.
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Diane M. Quinn & Valerie A. Earnshaw. (2011) Understanding Concealable Stigmatized Identities: The Role of Identity in Psychological, Physical, and Behavioral Outcomes. Social Issues and Policy Review 5:1, pages 160-190.
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Rie Chiba, Norito Kawakami & Yuki Miyamoto. (2011) Quantitative relationship between recovery and benefit-finding among persons with chronic mental illness in Japan. Nursing & Health Sciences 13:2, pages 126-132.
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Jane Shakespeare‐Finch & Bronwyn Morris. 2010. Posttraumatic Growth and Culturally Competent Practice. Posttraumatic Growth and Culturally Competent Practice 157 172 .
Rie Chiba, Yuki Miyamoto & Akiko Funakoshi. (2010) Characteristics of Benefit-finding in People with Mental Illness. Journal of Japan Academy of Nursing Science 30:3, pages 32-40.
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Steven Mock & Kathrin Boerner. (2010) Sense Making and Benefit Finding among Patients with Amyotrophic Lateral Sclerosis and Their Primary Caregivers. Journal of Health Psychology 15:1, pages 115-121.
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Efharis Panagopoulou, Areti Triantafyllou, Gesthimani Mitziori & Alexis Benos. (2009) Dyadic benefit finding after myocardial infarction: A qualitative investigation. Heart & Lung 38:4, pages 292-297.
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Kate Hefferon, Madeleine Grealy & Nanette Mutrie. (2009) Post-traumatic growth and life threatening physical illness: A systematic review of the qualitative literature. British Journal of Health Psychology 14:2, pages 343-378.
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Yuko HIRANO & Yoshihiko YAMAZAKI. (2009) Illness experiences of invasive mechanical ventilator-dependent amyotrophic lateral sclerosis patients in Japan : A study of trajectories and correlates of psychological well-being. Japanese Journal of Health and Human Ecology 75:3, pages 79-89.
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Kenneth I. Pakenham & Stephen Cox. (2008) Development of the benefit finding in multiple sclerosis (MS) caregiving scale: A longitudinal study of relations between benefit finding and adjustment. British Journal of Health Psychology 13:4, pages 583-602.
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Kenneth I. Pakenham. (2008) Making Sense of Illness or Disability. Journal of Health Psychology 13:1, pages 93-105.
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