{"id":{"repo_id":"soton","oai_identifier":"oai:eprints.soton.ac.uk:162159"},"canonical_url":"https://search.dev.ndltd.org/etd/soton/oai:eprints.soton.ac.uk:162159","repository":{"repo_id":"soton","name":"University of Southampton","base_url":"https://eprints.soton.ac.uk/cgi/oai2"},"display":{"title":"An exploration of the effect of a life-limiting diagnosis on an individual’s relationship with their body: a qualitative study","abstract":"To date there has been limited research into the lived experiences of individuals with a life-limiting diagnosis, particularly with regard to the ways in which they make sense of, and ascribe meaning to, their experiences.<br/><br/>The first part of this thesis contains a review that evaluates the present literature on the lived experiences of individuals with a life limiting diagnosis. The review explores the types of narrative-based ‘meaning making’ processes that are generated by individuals experiencing life-limiting disease. The discussion is extended to specifically consider the ways in which disease related changes to the body impact upon narrative processes. The<br/>relationship between bodily experience and narrative identity is explored. It is identified that there is minimal empirical research investigating these experiences.<br/><br/>The second part of this thesis contains a qualitative research study, which aims to provide a rich account of 11 participants’ relationship with their body in the light of their lifelimiting diagnosis. Participants were interviewed about their relationship with their body<br/>and Interpretive Phenomenological Analysis was applied to the interview transcripts. The analysis yielded eight over-arching themes and 24 higher-order themes.<br/><br/>Themes that emerged from the data included: the experience of the changed body, fear of the body’s future, threats to the individual’s sense of ownership of the body within the<br/>context of the medical encounter, and adaptivity to disease. Discussion of these constructs focussed on the experience of embodiment that can be seen to underlie participants lived experience of disease.","abstract_html":"To date there has been limited research into the lived experiences of individuals with a life-limiting diagnosis, particularly with regard to the ways in which they make sense of, and ascribe meaning to, their experiences.&lt;br/&gt;&lt;br/&gt;The first part of this thesis contains a review that evaluates the present literature on the lived experiences of individuals with a life limiting diagnosis. The review explores the types of narrative-based ‘meaning making’ processes that are generated by individuals experiencing life-limiting disease. The discussion is extended to specifically consider the ways in which disease related changes to the body impact upon narrative processes. The&lt;br/&gt;relationship between bodily experience and narrative identity is explored. It is identified that there is minimal empirical research investigating these experiences.&lt;br/&gt;&lt;br/&gt;The second part of this thesis contains a qualitative research study, which aims to provide a rich account of 11 participants’ relationship with their body in the light of their lifelimiting diagnosis. Participants were interviewed about their relationship with their body&lt;br/&gt;and Interpretive Phenomenological Analysis was applied to the interview transcripts. The analysis yielded eight over-arching themes and 24 higher-order themes.&lt;br/&gt;&lt;br/&gt;Themes that emerged from the data included: the experience of the changed body, fear of the body’s future, threats to the individual’s sense of ownership of the body within the&lt;br/&gt;context of the medical encounter, and adaptivity to disease. Discussion of these constructs focussed on the experience of embodiment that can be seen to underlie participants lived experience of disease.","abstract_has_math":false,"creators":["Beadon, Paul"],"institution":"University of Southampton","degree_name":"Ph.D.","degree_level":"doctoral","degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Coleman, Peter G.","Kalus, Christine"],"committee_chairs":[],"committee_members":[],"year":2009,"date_issued":"2009-06","date_published":"2009-06","updated_at":"2026-07-24T04:36:17Z","subjects":[],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":null,"outbound_label":null,"outbound_source":null},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Coleman, Peter G.","Kalus, Christine"]},{"key":"dc:creator","label":"Author","values":["Beadon, Paul"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2009-06"]},{"key":"dc:date.issued","label":"Date","values":["2009-06"]},{"key":"dc:publisher.department","label":"Dc Publisher Department","values":["Psychology (pre 2011 reorg)","School of Psychology"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["University of Southampton"]},{"key":"dc:relation.isreferencedby","label":"Dc Relation Isreferencedby","values":["https://eprints.soton.ac.uk/162159/"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["doctoral"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["Ph.D."]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://eprints.soton.ac.uk/162159/1/Thesis_-_Paul_Beadon.pdf"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["To date there has been limited research into the lived experiences of individuals with a life-limiting diagnosis, particularly with regard to the ways in which they make sense of, and ascribe meaning to, their experiences.<br/><br/>The first part of this thesis contains a review that evaluates the present literature on the lived experiences of individuals with a life limiting diagnosis. The review explores the types of narrative-based ‘meaning making’ processes that are generated by individuals experiencing life-limiting disease. The discussion is extended to specifically consider the ways in which disease related changes to the body impact upon narrative processes. The<br/>relationship between bodily experience and narrative identity is explored. It is identified that there is minimal empirical research investigating these experiences.<br/><br/>The second part of this thesis contains a qualitative research study, which aims to provide a rich account of 11 participants’ relationship with their body in the light of their lifelimiting diagnosis. Participants were interviewed about their relationship with their body<br/>and Interpretive Phenomenological Analysis was applied to the interview transcripts. The analysis yielded eight over-arching themes and 24 higher-order themes.<br/><br/>Themes that emerged from the data included: the experience of the changed body, fear of the body’s future, threats to the individual’s sense of ownership of the body within the<br/>context of the medical encounter, and adaptivity to disease. Discussion of these constructs focussed on the experience of embodiment that can be seen to underlie participants lived experience of disease."]},{"key":"dc:format","label":"Dc Format","values":["text"]},{"key":"dc:title","label":"Title","values":["An exploration of the effect of a life-limiting diagnosis on an individual’s relationship with their body: a qualitative study"]}]}],"canonical_facts":{"dc:contributor.advisor":["Coleman, Peter G.","Kalus, Christine"],"dc:creator":["Beadon, Paul"],"dc:date":["2009-06"],"dc:date.issued":["2009-06"],"dc:description.abstract":["To date there has been limited research into the lived experiences of individuals with a life-limiting diagnosis, particularly with regard to the ways in which they make sense of, and ascribe meaning to, their experiences.<br/><br/>The first part of this thesis contains a review that evaluates the present literature on the lived experiences of individuals with a life limiting diagnosis. The review explores the types of narrative-based ‘meaning making’ processes that are generated by individuals experiencing life-limiting disease. The discussion is extended to specifically consider the ways in which disease related changes to the body impact upon narrative processes. The<br/>relationship between bodily experience and narrative identity is explored. It is identified that there is minimal empirical research investigating these experiences.<br/><br/>The second part of this thesis contains a qualitative research study, which aims to provide a rich account of 11 participants’ relationship with their body in the light of their lifelimiting diagnosis. Participants were interviewed about their relationship with their body<br/>and Interpretive Phenomenological Analysis was applied to the interview transcripts. The analysis yielded eight over-arching themes and 24 higher-order themes.<br/><br/>Themes that emerged from the data included: the experience of the changed body, fear of the body’s future, threats to the individual’s sense of ownership of the body within the<br/>context of the medical encounter, and adaptivity to disease. Discussion of these constructs focussed on the experience of embodiment that can be seen to underlie participants lived experience of disease."],"dc:format":["text"],"dc:identifier.uri":["https://eprints.soton.ac.uk/162159/1/Thesis_-_Paul_Beadon.pdf"],"dc:publisher.department":["Psychology (pre 2011 reorg)","School of Psychology"],"dc:publisher.institution":["University of Southampton"],"dc:relation.isreferencedby":["https://eprints.soton.ac.uk/162159/"],"dc:title":["An exploration of the effect of a life-limiting diagnosis on an individual’s relationship with their body: a qualitative study"],"dc:type":["Thesis"],"dc:type.qualificationlevel":["doctoral"],"dc:type.qualificationname":["Ph.D."]},"updated_at":"2026-07-24T04:36:17Z"}