The experience of hope for adults with cystic fibrosis
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Dr. Janet P. Tracy, RN PhD
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Abstract
In this highly technical biomedical era, advances in diagnosis and aggressive treatments have altered the survival age for many chronically ill people. What is the meaning of hope to people who have lived beyond their expected life span? The purpose of this study was to describe and interpret the meaning of hope in people who have beaten the odds of statistics. A hermeutic-phenomenological design as informed by van Manen and influenced by Watson and Parse, guided and unfolded the meaning of hope for this population. Dialogical engagements (phenomenological interviews) were conducted with sixteen adults ages 23-48 years living with Cystic Fibrosis. Interviews elicited participants' experiences of living with CF and hoping for the future. Narrative stories of participants were presented illustrating lived experiences. Three themes unfolded from the phenomenological-hermeneutic analysis expressing the meaning of hope for the individual who lived beyond an expected life span: Fighting With Spirit and Energy, Connecting Through Self and Others, and Transcending Beyond the Statistical Odds to accept the gift of life.
Reflection with the literature on hope revealed the fighting and connecting themes have much in common with other researchers' findings. A contrasting finding for my participants was the lack of a trigger point or a specific threat needed for hope. The use of support groups and the Internet were two other findings not previously reported. The third theme--Transcending Beyond the Statistical Odds-- is the most unique finding of this study, expressing a focus on the meaning of life rather than the number of years lived. Participants contributed to the sense of greater community by volunteering for experimental drug protocols, lecturing to groups of patients, and lobbying for governmental assistance to the chronically ill.
Recommendations are made in the areas of nursing theory development, practice, and research. This study has relevance for other illnesses and conditions which extend the life span beyond the expected.
Description
This dissertation has also been disseminated through the ProQuest Dissertations and Theses database. Dissertation/thesis number: 9710315; ProQuest document ID: 304365042. The author still retains copyright.
Repository Posting Date
2020-06-19T19:34:09Z
Notes
This item has not gone through this repository's peer-review process, but has been accepted by the indicated university or college in partial fulfillment of the requirements for the specified degree.
Type Information
Type | Dissertation |
Acquisition | Proxy-submission |
Review Type | None: Degree-based Submission |
Format | Text-based Document |
Category Information
Evidence Level | Phenomenology |
Research Approach | Qualitative Research |
Keywords | Chronic Illness; Social Connection; Long-term Survival |
CINAHL Subject(s) | Cystic Fibrosis; Life Experiences; Hope; Survivors; Cystic Fibrosis--Psychosocial Factors; Life Experiences--Evaluation; Hope--Evaluation; Cystic Fibrosis--Psychosocial Factors--In Adulthood; Life Experiences--Evaluation--In Adulthood; Hope--Evaluation--In Adulthood |
Degree Information
Grantor | The University of Colorado Health Sciences Center |
Advisor | Magilvy, Joan K. |
Level | PhD |
Year | 1996 |
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