Abstract
Purpose
To solicit breast cancer survivors’ perspectives on the variety of issues they face related to lymphedema self-care and identify support needs perceived as critical for managing their chronic medical condition.
Methods
Twenty-one breast cancer survivors with lymphedema participated in audio-recorded focus groups about barriers and facilitators of self-care. Transcripts were analyzed using ATLAS.ti software by two coders. Triangulation of findings provided for refinement and category confirmation.
Results
Themes identified included lack of social support, lack of resources for self-care activities, and self-advocacy by default. Lack of social support subthemes were feeling misunderstood, minimization of needs, and feeling criticized. Lack of resources for self-care activities subthemes were lack of both tangible self-care support and self-care supplies. Self-advocacy by default subthemes were the need to proactively manage lymphedema complications, the need to educate health-care workers, and feeling marginalized by the health-care system.
Conclusions
Lack of support and the failure of others to recognize lymphedema as a chronic condition set this patient population apart from other patients with chronic diseases and decreases the amount of help needed to manage the condition.
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Acknowledgments
Funding: Sheila H. Ridner, PhD, MSN, MSHSA, BSN, was supported by a Research Scholar Grant, RSG-13-022-01-CPPB, from the American Cancer Society.
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Ridner, S.H., Rhoten, B.A., Radina, M.E. et al. Breast cancer survivors’ perspectives of critical lymphedema self-care support needs. Support Care Cancer 24, 2743–2750 (2016). https://doi.org/10.1007/s00520-016-3089-2
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DOI: https://doi.org/10.1007/s00520-016-3089-2