Abstract
Little is known about the experience of caring for a son with anorexia nervosa (AN). Prior research with parents of primarily daughters with AN indicate that they experience significant distress. Ten mothers participated in semi-structured interviews regarding their experiences taking care of a son (between the ages of 11 and 18) who had inpatient treatment for AN within 2 years of the interview and was residing at home. Consensual qualitative research methods were used to analyze the data. Mothers reported challenges accessing and navigating treatment, noting that front-line providers missed their sons’ AN because of their gender. Once their sons were diagnosed, mothers continued to experience distress and described negative changes in family relationships, including increased conflict with the diagnosed son, strained sibling relationships, and marital stress. The gender-atypical nature of AN negatively impacted perceived social support. Despite these negative findings, living with AN also offered an opportunity for growth, with some mothers reporting increased closeness with the diagnosed son, greater family unification, and strengthening of the marital bond. Based on these findings, it is recommended that treatment professionals provide greater psychological support and resources to mothers, who often assume primary caregiver responsibilities, and make treatment settings and approaches more gender inclusive.
Highlights
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Mothers experienced psychological distress, shame, guilt, isolation, self-doubt, and felt blamed by others.
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Obtaining an accurate diagnosis and appropriate treatment were perceived to be more difficult, due to their son’s gender.
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Mothers described receiving less social support, which they ascribed to their sons’ gender-atypical illness.
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Mothers reported challenges with healthcare professionals, including pediatricians, who minimized and dismissed their concerns.
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Validating mothers’ concerns and helping them find support may enhance their functioning as caregivers.
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This manuscript is based on an IRB-approved nonfunded qualitative study and presents no conflict of interest. This manuscript is based on the dissertation of the first author that was supervised by the second author as mentor and the third and fourth authors as readers. The fifth author was a member of the research team. All authors contributed to writing or editing of the manuscript.
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Appendix
Appendix
Interview Protocol
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What do you think is most important for me to know about your experience?
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What was it that first alerted you to the fact that your son was struggling with his eating, body image, and/or weight?
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When your son received a diagnosis of AN, could you describe how you felt?
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How, if at all, were your relationships affected during this time, including with your son?
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What did you do to cope throughout diagnosis and treatment?
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Please describe the process of accessing services and working with medical and mental health professionals.
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What challenges, if any, do you believe were exacerbated by the fact that you were dealing with a son, rather than a daughter, with AN?
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Overall, how would you say this experience has affected you?
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If you had to summarize the most stressful aspects (top 2–3) of this experience, what would they be?
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Overall, how was your marriage affected by your son’s AN?
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Overall, how, if at all, were the relationships among your family members affected?
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What do you believe were the contributing factors to your son’s illness?
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Is there anything we haven’t talked about that you think is important for me to know about your experience?
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Whitney, J.L., Keitel, M.A., Cummings, M.P. et al. Caring for Sons with Anorexia: The Perspective of Mothers. J Child Fam Stud 32, 2637–2651 (2023). https://doi.org/10.1007/s10826-022-02525-5
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DOI: https://doi.org/10.1007/s10826-022-02525-5