390
Views
5
CrossRef citations to date
0
Altmetric
Articles

Symptoms without disease: Exploring experiences of non-Western immigrant women living with chronic pain

&
Pages 322-342 | Received 03 Apr 2017, Accepted 18 Aug 2017, Published online: 16 Oct 2017

References

  • Blom, S. (2008). Innvandreres helse 2005/2006 [Immigrants health] (No. 35) (p. 62). Oslo–Kongsvinger: Statistisk sentralbyrå Statistics Norway. Retrieved from http://www.ssb.no/emner/00/02/rapp_200805/
  • Côté, D. (2013). Intercultural communication in health care: Challenges and solutions in work rehabilitation practices and training: A comprehensive review. Disability and Rehabilitation, 35(2), 153–163.
  • Dansie, E. J., & Turk, D. C. (2013). Assessment of patients with chronic pain. British Journal of Anaesthesia, 111(1), 19–25.
  • Degni, F., Pöntinen, S., & Mölsä, M. (2006). Somali parents' experiences of bringing up children in Finland: Exploring social-cultural change within migrant households. Forum Qualitative Sozialforschung / Forum: Qualitative Social Research, 7(3). Retrieved from http://www.qualitative-research.net/index.php/fqs/article/view/139
  • Finnström, B., & Söderhamn, O. (2006). Conceptions of pain among Somali women. Journal of Advanced Nursing, 54(4), 418–425.
  • Hellström, O., Bullington, J., Karlsson, G., Lindqvist, P., & Mattsson, B. (1999). A phenomenological study of fibromyalgia. Patient perspectives. Scandinavian Journal of Primary Health Care, 17(1), 11–16.
  • Helman, C. (2007). Culture, Health and Illness (5th ed.). London: Hodder Arnold.
  • Hjörleifsdottir Steiner, K., Johansson, S.-E., Sundquist, J., & Wändell, P. E. (2007). Self-reported anxiety, sleeping problems and pain among turkish-born immigrants in Sweden. Ethnicity & Health, 12(4), 363–379.
  • Ingstad, B. (2007). Medisinsk antropologi. En innføring [Medical anthropology. An introduction]. Bergen: Fagbokforlaget.
  • International Association for the Study of Pain. (2017). IASP Taxonomy – IASP. Retrieved from http://www.iasp-pain.org/Taxonomy#Pain
  • Jovchelovitch, S., & Bauer, M. W. (2000). Narrative interviewing. In M. W. Bauer & G. Gaskell (Eds.), Qualitative researching with text, image and sound: A practical handbook. (pp. 57–74). London, UK: SAGE.
  • Kleinman, A., Eisenberg, L., & Good, B. (1978). Culture, illness, and careclinical lessons from anthropologic and cross-cultural research. Annals of Internal Medicine, 88(2), 251–258.
  • Kornelsen, J., Atkins, C., Brownell, K., & Woollard, R. (2016). The meaning of patient experiences of medically unexplained physical symptoms. Qualitative Health Research, 26(3), 367–376.
  • Kristiansen, M., Mygind, A., & Krasnik, A. (2007). Health effects of migration. Danish Medical Bulletin, 54(1), 46–47.
  • Kumar, B. N. (2008). The Oslo Immigrant Health Profile (No. 7) (p. 59). Oslo: Folkehelseinstituttet. Retrieved from http://www.fhi.no/dav/920ab22ad5.pdf
  • Kurita, G. P., Sjøgren, P., Juel, K., Højsted, J., & Ekholm, O. (2012). The burden of chronic pain: A cross-sectional survey focussing on diseases, immigration, and opioid use. PAIN, 153(12), 2332–2338.
  • Kvale, S., & Brinkmann, S. (2015). InterViews: Learning the craft of qualitative research interviewing (3rd ed.). Los Angeles: Sage Publications, Inc.
  • Löfvander, M. B., & Engström, A. W. (2007). The immigrant patient having widespread pain. Clinical findings by physicians in Swedish primary care. Disability and Rehabilitation, 29(5), 381–388.
  • Malterud, K. (2012). Systematic text condensation: A strategy for qualitative analysis. Scandinavian Journal of Public Health, 40(8), 795–805.
  • Malterud, K., & Solvang, P. (2005). Vulnerability as a strength: Why, when, and how? Scandinavian Journal of Public Health, 33(66 suppl.), S3–S6.
  • Michaëlis, C., Kristiansen, M., & Norredam, M. (2015). Quality of life and coping strategies among immigrant women living with pain in Denmark: A qualitative study. BMJ Open, 5(7)
  • Monsivais, D. B., & Engebretson, J. C. (2012). ‘I'm just not that sick’: Pain medication and identity in Mexican American women with chronic pain. Journal of Holistic Nursing, 30(3), 188–194.
  • Morris, D. B. (1993). The culture of pain. Berkely, CA: University of California Press.
  • Morris, D. B. (2012). Narrative and pain: Towards an integrative model. In R. J. Moore (Ed.), Handbook of pain and palliative Care (pp. 733–751). New York, NY: Springer New York.
  • Müllersdorf, M., Zander, V., & Eriksson, H. (2011). The magnitude of reciprocity in chronic pain management: Experiences of dispersed ethnic populations of Muslim women. Scandinavian Journal of Caring Sciences, 25(4), 637–645.
  • Nortvedt, L., Hansen, H. P., Kumar, B. N., & Lohne, V. (2015). Caught in suffering bodies: A qualitative study of immigrant women on long-term sick leave in Norway. Journal of Clinical Nursing, 24(21–22), 3266–3275.
  • Norwegian Directorate of Health. (2009). Norway and Health. An introduction (No. IS-1730E). Retrieved from. https://helsedirektoratet.no/Lists/Publikasjoner/Attachments/302/Norway-and-health-an-introduction-IS-1730E.pdf
  • Norwegian Ministry of Health and Care services. (2007). Report No. 20 (2006–2007) to the Storting: National strategy to reduce social inequalities in health, Oslo: Deparmentenes servicesenter. (English version available at https://www.regjeringen.no/contentassets/bc70b9942ea241cd90029989bff72d3c/en-gb/pdfs/stm200620070020000en_pdfs.pdf)
  • Pearlin, L. I., Schieman, S., Fazio, E. M., & Meersman, S. C. (2005). Stress, health, and the life course: Some conceptual perspective.. Journal of Health and Social Behavior, 46(2), 205–19.
  • Råheim, M., & Håland, W. (2006). Lived experience of chronic pain and fibromyalgia: Women's stories from daily life. Qualitative Health Research, 16(6), 741–761.
  • Robinson, K., Kennedy, N., & Harmon, D. (2013). Constructing the experience of chronic pain through discourse. Scandinavian Journal of Occupational Therapy, 20(2), 93–100.
  • Saadati, M., & Hanssen, I. (2015). “Disse smertene plager min sjel”: En kvalitativ intervjustudie av iranske kvinner i Norge: “This pain torments my soul”: A qualitative interview study of Iranian women in Norway. Nordic Journal of Nursing Research, 35(1), 38–44.
  • Schouten, B. C., & Meeuwesen, L. (2006). Cultural differences in medical communication: A review of the literature. Patient Education and Counseling, 64(1–3), 21–34.
  • Småland Goth, U. G., & Berg, J. E. (2011). Migrant participation in Norwegian health care. A qualitative study using key informants. European Journal of General Practice, 17(1), 28–33.
  • Snelgrove, S., & Liossi, C. (2009). An interpretative phenomenological analysis of living with chronic low back pain. British Journal of Health Psychology, 14(4), 735–749.
  • Statistics Norway (2017). Immigration and immigrants. Retrieved from http://www.ssb.no/en/innvandring-og-innvandrere/nokkeltall/immigration-and-immigrants
  • Steihaug, S., Ahlsen, B., & Malterud, K. (2002). “I am allowed to be myself”: Women with chronic muscular pain being recognized. Scandinavian Journal of Public Health, 30(4), 281–287.
  • Stone, L. (2014). Managing the consultation with patients with medically unexplained symptoms: A grounded theory study of supervisors and registrars in general practice. BMC Family Practice, 15(1), 192.
  • Svenaeus, F. (2005). Sykdommens mening; og møtet med det syke mennesket [The meaning of illness; and the meeting with the sick individual]. Oslo: Gyldendal Akademisk.
  • Tavafian, S. S., Gregory, D., & Montazeri, A. (2008). The experience of low back pain in Iranian women: A focus group study. Health Care for Women International, 29(4), 339–348.
  • Thapa, S. B., Dalgard, O. S., Claussen, B., & Sandvik, L. (2007). Psychological distress among immigrants from high- and low-income countries: Findings from the Oslo health study. Nordic Journal of Psychiatry, 61(6), 459–465.
  • Thesen, J. (2005). From oppression towards empowerment in clinical practice–offering doctors a model for reflection1. Scandinavian Journal of Public Health. Supplement, 66, 47–52.
  • Tiilikainen, M. (2003). Somali women and daily Islam in the Diaspora. Social Compass, 50(1), 59–69.
  • Toye, F., & Barker, K. (2010). ‘Could I be imagining this?’ – the dialectic struggles of people with persistent unexplained back pain. Disability and Rehabilitation, 32(21), 1722–1732.
  • Umberson, D., & Montez, J. K. (2010). Social relationships and health a flashpoint for health policy. Journal of Health and Social Behavior, 51(1 suppl), S54–S66.
  • van Manen, M. (1997). Researching lived experience: Human science for an action sensitive pedagogy (2nd ed.). London, ON, Canada: Althouse Press.
  • van Ravenzwaaij, J., olde Hartman, T., van Ravesteijn, H., Eveleigh, R., van Rijswijk, E., & Lucassen, P. (2010). Explanatory models of medically unexplained symptoms: A qualitative analysis of the literature. Mental Health in Family Medicine, 7(4), 223–231.
  • Wahl, A. K., Rustøen, T., Rokne, B., Lerdal, A., Knudsen, Ø., Miaskowski, C., & Moum, T. (2009). The complexity of the relationship between chronic pain and quality of life: A study of the general Norwegian population. Quality of Life Research, 18(8), 971–980.
  • Werner, A., Isaksen, L. W., & Malterud, K. (2004). “I am not the kind of woman who complains of everything”: Illness stories on self and shame in women with chronic pain. Social Science & Medicine (1982), 59(5), 1035–1045.
  • Werner, A., & Malterud, K. (2003). It is hard work behaving as a credible patient: Encounters between women with chronic pain and their doctors. Social Science & Medicine (1982), 57(8), 1409–1419.
  • Wiking, E., Saleh-Stattin, N., Johansson, S.-E., & Sundquist, J. (2009). A description of some aspects of the triangular meeting between immigrant patients, their interpreters and GPs in primary health care in Stockholm, Sweden. Family Practice, 26(5), 377–383.
  • Wilkinson, R., & Marmot, M. (Eds.). (2003). Social determinants of health. The solid facts. WHO: Europe. Retrieved from http://www.euro.who.int/en/what-we-publish/abstracts/social-determinants-of-health.-the-solid-facts
  • Wuytack, F., & Miller, P. (2011). The lived experience of fibromyalgia in female patients, a phenomenological study. Chiropractic & Manual Therapies, 19, 22.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.