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The Sexual Lives of Women Living with Fibromyalgia: A Qualitative Study

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Abstract

This study examined women’s perceptions of the impact of FM on a broad range of aspects of their sexual well-being as well as on their romantic and sexual relationship. Participants were 16 women diagnosed with FM currently in a romantic relationship living in North America who participated in a semi-structured interview. Inductive thematic analysis identified four themes: (1) Do I want to have sex? That’s a complicated question; (2) The impact of FM on women’s sexual well-being is not uniform; (3) It’s about more than sex and more than just me; (4) Elements that ameliorate or exacerbate the effect of FM’s on SWB. Together, these results point to the variability and complexity of the effects of FM on women’s sexual well-being. The results are discussed in terms of the importance of assessing and addressing a wide range of aspects of the SWB of women with FM.

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Funding

This research was funded by a Banting Postdoctoral Fellowship [Canadian Institutes of Health Research] granted to Dr. Pablo Santos-Iglesias, and two University of New Brunswick Research Funds granted to Dr. Diane L. LaChapelle and Dr. E. Sandra Byers, respectively.

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Correspondence to Pablo Santos-Iglesias.

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The study was designed and performed in line with the ethical standards of the Canadian Psychological Association and was approved by the University of New Brunswick Research Ethics Board.

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Santos-Iglesias, P., Crump, L., Henry, J.L. et al. The Sexual Lives of Women Living with Fibromyalgia: A Qualitative Study. Sex Disabil 40, 669–685 (2022). https://doi.org/10.1007/s11195-022-09748-w

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