The purpose of this research was to learn about the needs of young adults living with newly diagnosed cancer and undergoing chemotherapy and/or radiation treatment in order to enhance oncology care providers’ understanding of these needs. This was a qualitative investigation of the perspectives of young adults with cancer using interpretation description methodology (Thorne, 2008). Semi-structured interviews were conducted with seven individuals to gain a deeper insight into the subjective experience of being a young adult with cancer with consideration of quality of life issues. Eight interpretive themes were revealed from the data: It Is Hard Being a Parent with Cancer, Symptom Management Is a Challenge, Social Support is Imperative, Information Access is Essential, Fear of Recurrence and Mortality, Trusting Relationships with Health Care Professionals Make a Difference, Financial Worries, and Follow Up Care. These concepts represent a critical analysis which can serve to guide oncology care and oncology nursing practice.
| Identifer | oai:union.ndltd.org:uvic.ca/oai:dspace.library.uvic.ca:1828/1313 |
| Date | 30 December 2008 |
| Creators | Parkins, Jennifer |
| Contributors | Hayes, Virginia |
| Source Sets | University of Victoria |
| Language | English, English |
| Detected Language | English |
| Type | Thesis |
| Rights | Available to the World Wide Web |
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