The purpose of my research is to examine how copreneurial couples make sense of their lived experience of working in a copreneurial business and shape their mutual identity. The research context is copreneurs operating micro-businesses in the Greek leisure and tourism industry. Given the size of the tourism industry worldwide and the fact that many businesses within this sector are family-owned, this is an important area of inquiry. The aim is twofold: 1. To build theory in the field of entrepreneurship by focusing specifically on the undertheorized topic of how copreneurs understand and shape their identity and responsibilities within copreneurial businesses 2. To bring an under-utilized methodology to entrepreneurship studies, that of interpretive phenomenological analysis (IPA), as a means of enhancing the understanding of the lived experience of copreneurs. Drawing on phenomenological philosophy, IPA foregrounds the meanings research participants give to their experience and therefore offers rich interpretations from copreneurial couples While taking an idiographic approach, which focuses on the first-person experience of copreneurs in a particular context, the findings will resonate with other copreneurs. The contribution of this research therefore lies in advancing our understanding of copreneurship and familial entrepreneurship by elucidating the interrelationship between personal and business partnerships. The study makes visible the often invisible recursive links between paid work and family life for men and women

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No description available.

Bakgrund: Diabetes typ 1 är en kronisk autoimmun sjukdom som orsakar att personen behöver regelbunden behandling. Det påverkar deras vardag och kan orsaka både kort- och långsiktiga komplikationer. Livet som ung vuxen kan vara utmanande och att samtidigt leva med kronisk sjukdom kan skapa svårigheter, i en redan komplex period i livet. Utökad kunskap om detta är därför viktigt för hälso- och sjukvårdspersonal. Syfte: Att beskriva unga vuxnas upplevelser av att leva med diabetes typ 1. Metod: Litteraturstudien baseras på kvalitativa studier och analyserades med kvalitativ manifest innehållsanalys med induktiv ansats. Resultat: Data resulterade i 7 slutkategorier: Stöttande omgivning är betydelsefullt och ger trygghet, Svårighet att hitta balans mellan diabeteshanteringen och livet, Det ökade ansvaret är betungande men leder även till personlig utveckling, Önskan att passa in och inte stigmatiseras, Behov av frihet och kontroll kan påverka diabeteshanteringen, Att det finns barriärer inom hälso- och sjukvården, Rädsla över komplikationer och graviditet. Slutsatser: Upplevelser av att leva med diabetes typ 1 varierade mellan de unga vuxna. Det fanns en gemensam önskan över ökad kunskap och förståelse i samhället och hos hälso- och sjukvårdspersonal för att de ska kunna tillgodose individuella behov och en personcentrerad vård.

This thesis explores the lived experiences of individuals living with HIV in Tarrant County through an ethnographic research design. This study highlights four emergent themes: the beginning of one's healthcare journey, stigma within a medical care setting, the lasting provider-patient relationships that can form, and shifting relationship dynamics. Participants' experiences reveal their challenges, from discomfort in a healthcare setting to disclosing their status to their support system. Insights from these individuals informed feasible strategies to combat HIV-related stigma.

Western psychology has in its current position and definition laid claim to the “psychology” landscape, despite being the construction of one epistemology. This imposition allows western psychology to dominate and control the “psychology” landscape, to the detriment of other equally valid and “scientific” “psychologies”. We argue for redefinition of western psychology in terms of lived experience or soul, so that it can co-exist with other “psychologies”. This should co-facilitate the process of repositioning western psychology into a dialogically equal relationship with indigenous african psychology. Redefinition of western psychology is dependant on psychologist’s appreciation of the relativity of epistemological frameworks and ability to challenge their own subjectivities. This in turn requires epistemological curiosity. This study adopts a conceptual, autoethnographic approach and methodology. Our aim is not to provide answers, but rather create a context for dialogue. / Psychology / M.A. (Psychology)

The purpose of this hermeneutic phenomenology study was to explore and describe the meaning employees attribute to the lived experiences of returning to work after cancer treatment. Semi-structured interviews were held with eight participants and a thematic data analysis method was used. The results indicate that cancer survivors experience various challenges that make it difficult to function as they did before the diagnosis when they return to work. A critical hermeneutical reflection against the literature followed the structural analysis and resulted in a contextual framework that incorporated the individual and organisational perspective on the various influences involved in supporting cancer survivors to maintain their wellbeing when they return to work. Four phases, repression, comprehension, activation and reintegration, were identified when they tried to cope/adjust on their return to work. The corresponding forms of organisational support they expected through these phases were labelled motivation, information, navigation and stabilisation. / Industrial and Organisational Psychology / M. Com.

Depuis plusieurs années, la définition des soins palliatifs a été élargie pour inclure toutes les maladies ayant un pronostic réservé. Le Québec s’est doté d’une politique de soins palliatifs dont l’un des principes directeurs est de maintenir les patients dans leur milieu de vie naturel. Alors que présentement environ 10 % de la population nécessitant des soins palliatifs en reçoit, on peut s’attendre à une augmentation des demandes de soins palliatifs à domicile dans les CSSS du Québec. La présente étude a pour but de décrire et comprendre l’expérience de dispenser des soins palliatifs à domicile pour des infirmières travaillant dans un contexte non spécialisé. Une étude qualitative ayant comme perspective disciplinaire la théorie de l’humain-en-devenir de Parse a été réalisée. Des entrevues ont été effectuées auprès de huit infirmières travaillant au maintien à domicile d’un CSSS de la région de Montréal qui font des soins palliatifs dans un contexte non spécialisé. L’analyse des données a été effectuée selon la méthode d’analyse phénoménologique de Giorgi (1997). Les résultats s’articulent autour de trois thèmes qui décrivent l’expérience de dispenser des soins palliatifs à domicile pour des infirmières qui travaillent dans un contexte non spécialisé. Elles accompagnent les patients et leur famille, en s’engageant à donner des soins humains, et développant une relation d’accompagnement avec le patient et ses proches. Elles doivent composer avec les réactions du patient et de sa famille et doivent parfois informer le patient de la progression de son état de santé. De plus, elles se préoccupent de donner des soins de qualité en composant avec la complexité des soins palliatifs à domicile tout en s’assurant de soulager les symptômes des patients et de tenter de développer leur expertise. Finalement, le fait d’être confrontée à la mort permet de cheminer. Ainsi, les infirmières vivent des émotions, reçoivent du soutien, sont touchées personnellement par la mort, éprouvent de la satisfaction envers les soins qu’elles donnent et apprennent personnellement de leur expérience. L’essence du phénomène à l’étude est que lorsque les infirmières font un véritable accompagnement du patient et de sa famille en s’efforçant de donner des soins de qualité, cela crée des conditions permettant qu’un cheminement personnel et professionnel sur la vie et la mort soit effectué par les infirmières. / In the past few years, the definition of palliative care was extended to include all diseases with a poor prognosis. The province of Quebec modified the health care system to focus more on ambulatory care and created a palliative care policy with one of its principal directives being to maintain patients in their own milieu. As only 10% of patients requiring palliative care presently receive it, we can expect an increase in demands for palliative home care in the CSSS’s of Quebec. The goal of the present study is to describe and understand the lived experiences of the nurses of a CSSS of the Montreal sector who deliver palliative home care in a nonspecialized context. A qualitative phenomenological research was developed with the Human Becoming Theory of R.R. Parse as a theoretical framework. Eight semi-directed interviews were done with nurses working in home care of a CSSS of the Montreal region. These nurses do palliative care in a non-specialized context. Giorgi’s (1997) phenomenological method was used for data analysis. Three themes describing the experiences of home care nurses providing palliative care in a non specialized context emerged from the analysis. Nurses accompany patients and their families, by committing themselves to providing humane care and by developing an accompaniment relationship with the patient and his/her loved ones. Nurses must cope with the patient’s and family’s reactions and often need to inform the patient of the progression of his/her disease. Secondly, nurses are dedicated to provide quality care by dealing with the complexity of providing palliative care at home, while doing symptoms management and attempting to develop their expertise. Finally, the theme which has the most interesting results is that being confronted by death allows nurses to grow. Nurses personally go through emotions, received support, are personally touched by death, experience satisfaction by the care they give and personally learn by their experience. The essence of the phenomenon is that when nurses providing palliative home care in a non specialized context accompany truly patients and their family, while giving quality care, it creates conditions for the nurses to grow personally and professionally on their views of life and death.

À ce jour, peu d’études ont été conduites pour mieux comprendre le phénomène de la demande d’aide auprès d’hommes dans le contexte du cancer. Les études consultées suscitaient de nombreuses questions et hypothèses sur la signification que pouvaient accorder ces hommes à la demande d’aide. C’est pourquoi l’étudiante chercheuse a réalisé cette étude phénoménologique auprès d’hommes atteints d’un cancer de la sphère otorhinolaryngologique, afin de mieux comprendre ce phénomène. Huit hommes ont accepté de participer à l’étude. Suite aux entrevues semi-structurées, l’analyse des données, assistée par la méthode proposée par Giorgi (1997), a fait ressortir les thèmes centraux suivants : 1) Se sentir capables de faire face seuls aux diverses adversités; 2) Bénéficier du soutien des proches et de l’équipe de soins; et 3) Utiliser des stratégies cognitives. Les résultats ont révélé que la signification accordée à la demande d’aide est intimement liée à la construction sociale du genre, c’est-à-dire aux normes d’identité masculine acquises culturellement. Les valeurs accordées à l’autonomie, à l’estime de soi et à « l’égo masculin » expliqueraient en partie pourquoi les hommes interviewés demandent peu d’aide. Par ailleurs, la présence constante de la conjointe et le soutien de l’équipe professionnelle de santé semblent avoir grandement modulé les comportements de demande d’aide des participants en anticipant leurs besoins avant même qu’ils puissent les exprimer; ce qui invite à une réflexion sur l’empowerment, stratégie d’intervention fondée sur la responsabilisation individuelle. Des recommandations pour la pratique et la recherche infirmières sont formulées afin d’optimiser le soin et le développement du savoir infirmier dans ce domaine d’intérêt. / To date, few studies have been conducted to better understand the phenomenon of help seeking of men in the context of cancer. The reviewed studies elicited many questions and hypotheses about men’s understanding of help seeking in the context of cancer. Therefore, the research student has conducted a phenomenological study to describe this phenomenon in men with otorhinolaryngological cancer. Eight men have agreed to participate in the study. Following semi-structured interviews, the data analysis, assisted by the method proposed by Giorgi (1997), highlighted the following key themes: 1) Feeling able to cope alone with the various adversities, 2) Having the support of the family and the care team, and 3) Using cognitive strategies. The results showed that the lived experience of help seeking is closely linked to the social construction of gender, that is to say to the culturally acquired male norms. Values of autonomy, self-esteem and “male ego” explain in part why most of the participants did not ask for help. Moreover, the constant presence of the spouse and the support of the professional health care team appear to have greatly modulated participants’ help seeking behaviors by anticipating their needs, before they could even express them; this issue invites us to a reflection on the phenomenon of empowerment, intervention strategy based on the individual responsabilisation. Recommendations for practice and nursing research are formulated to optimize nursing care and to insure the pursuit of the development of nursing knowledge in this area of interest.

Mémoire numérisé par la Division de la gestion de documents et des archives de l'Université de Montréal.