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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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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DOI: https://doi.org/10.1007/s11195-022-09748-w