Citations (18)
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Anne Marit Mengshoel. (2022) A long, winding trajectory of suffering with no definite start and uncertain future prospects – narratives of individuals recently diagnosed with fibromyalgia. International Journal of Qualitative Studies on Health and Well-being 17:1.
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Lucia Polakovská & Tomáš Řiháček. (2022) What is it like to live with medically unexplained physical symptoms? A qualitative meta-summary. Psychology & Health 37:5, pages 580-596.
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Victoria Mailen Arfuch, AQ Gonçalves, Rosa Caballol Angelats, Carina Aguilar Martín, Noèlia Carrasco-Querol, Maria Cinta Sancho Sol, Gemma González Serra, Immaculada Fusté Anguera & Anna Berenguera. (2021) Patients’ appraisals about a multicomponent intervention for fibromyalgia syndrome in primary care: a focus group study. International Journal of Qualitative Studies on Health and Well-being 16:1.
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Merja Sallinen & Anne Marit Mengshoel. (2019) “I just want my life back!” - Men’s narratives about living with fibromyalgia. Disability and Rehabilitation 41:4, pages 422-429.
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Merja Sallinen, Anne Marit Mengshoel & Kari Nyheim Solbrække. (2019) “I can’t have it; I am a man. A young man!” – men, fibromyalgia and masculinity in a Nordic context. International Journal of Qualitative Studies on Health and Well-being 14:1.
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Sandra VanderKaay, Sandra E. Moll, Rebecca E. Gewurtz, Pranay Jindal, Adalberto Loyola-Sanchez, Tara L. Packham & Chun Y. Lim. (2018) Qualitative research in rehabilitation science: opportunities, challenges, and future directions. Disability and Rehabilitation 40:6, pages 705-713.
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Nicole Brown. (2018) Exploring the lived experience of fibromyalgia using creative data collection methods. Cogent Social Sciences 4:1.
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Mieko Homma, Yoshihiko Yamazaki, Hirono Ishikawa & Takahiro Kiuchi. (2016) ‘This really explains my case!’: biographical reconstruction of Japanese people with fibromyalgia meeting peers. Health Sociology Review 25:1, pages 62-77.
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Articles from other publishers (10)
Melinda Nicola, Helen Correia, Graeme Ditchburn & Peter D. Drummond. (2022) Defining pain-validation: The importance of validation in reducing the stresses of chronic pain. Frontiers in Pain Research 3.
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Victoria Mailen Arfuch, Rosa Caballol Angelats, Carina Aguilar Martín, Noèlia Carrasco-Querol, Maria Cinta Sancho Sol, Gemma González Serra, Immaculada Fusté Anguera, Alessandra Queiroga Gonçalves & Anna Berenguera. (2020) Assessing the benefits on quality of life of a multicomponent intervention for fibromyalgia syndrome in primary care: patients’ and health professionals’ appraisals: a qualitative study protocol. BMJ Open 10:11, pages e039873.
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Soly Inga-Maj Erlandsson, Linda Lundin & Nicolas Dauman. (2020) The Experience of Tinnitus and Its Interaction With Unique Life Histories—Life Events, Trauma and Inner Resources Narrated by Patients With Tinnitus. Frontiers in Psychiatry 11.
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Grethe Eilertsen, Heidi Ormstad, Marit Kirkevold, Anne M Mengshoel, Siv Söderberg & Malin Olsson. (2015) Similarities and differences in the experience of fatigue among people living with fibromyalgia, multiple sclerosis, ankylosing spondylitis and stroke. Journal of Clinical Nursing 24:13-14, pages 2023-2034.
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Joeri Calsius, Imke Courtois, Jolien Stiers & Jozef De Bie. (2015) How Do Fibromyalgia Patients With Alexithymia Experience Their Body? A Qualitative Approach. SAGE Open 5:1, pages 215824401557463.
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Young Uk Ryu. (2014) Online Discourse on Fibromyalgia: Text-Mining to Identify Clinical Distinction and Patient Concerns. Medical Science Monitor 20, pages 1858-1864.
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Robert Ferrari & Anthony Science Russell. (2014) Pain Mystery Score Beliefs: A Comparison of Fibromyalgia and Rheumatoid Arthritis. International Journal of Rheumatology 2014, pages 1-5.
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Ohad Oren & Jacob Ablin. (2013) Precision medicine: the emerging approach to the chronic pain patient. International Journal of Clinical Rheumatology 8:4, pages 491-499.
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Jacob N. Ablin & Dan Buskila. (2012) Personalized Treatment of Pain. Current Rheumatology Reports 15:1.
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