Background:Alzheimer's disease is a disease that primarily affects the elderly but also younger people. Alzheimer's disease is a type of dementia which means that you get changes in the cerebral cortex and cells gradually die. The disease causes memory loss and things that were obvious before will be difficult for the sufferer. Alzheimer's disease also affects next of kin to a large degree; they will have to take a great responsibility. The next of kin are entitled to support from healthcare.Aim:The aim was to highlight next of kin' experiences of healthcare to their family members with Alzheimer's disease.Method: The study was based on narratives, which in this case means analysis of autobiographies.

The purpose of this study was to examine and describe how politicians and directors of care define and experience quality in aged care facilities. Further on we wanted to compare on which fundamental principles the participants base their opinion about quality and how they work with quality. To reach our aim we conducted five interviews with politicians and directors of care. The results show that it is hard to determine quality in an unambiguous and objective way. Quality in aged care appears to be about relations and encounters amongst people.

Den här uppsatsen har för avsikt att undersöka och förstå hur det är att vara förälder till ett barn som är trans. Studien är kvalitativ och semistrukturerade intervjuer har använts. Genom de fem intervjuerna som jag har genomfört med föräldrar till transpersoner har jag undersökt föräldrarnas upplevelser och erfarenheter samt förhoppningar och önskningar i relation till att deras barn är transpersoner. Resultatet pekar i två riktningar där den ena handlar om föräldrarnas tankar och känslor och det andra om deras behov och förhoppningar. Det föräldrarna tog upp i den första riktningen av resultatet handlade om sorg, tvivel, oro men även att det har varit berikande.

Background:Alzheimer's disease is a disease that primarily affects the elderly but also younger people. Alzheimer's disease is a type of dementia which means that you get changes in the cerebral cortex and cells gradually die. The disease causes memory loss and things that were obvious before will be difficult for the sufferer. Alzheimer's disease also affects next of kin to a large degree; they will have to take a great responsibility. The next of kin are entitled to support from healthcare.Aim:The aim was to highlight next of kin' experiences of healthcare to their family members with Alzheimer's disease.Method: The study was based on narratives, which in this case means analysis of autobiographies.

När en patient drabbas av en total hjärninfarkt och blir aktuell för organdonation ställs det höga krav på intensivvårdssjuksköterskan. Tidigare studier visar att intensivvårdssjuksköterskor oroas av att vårda blivande organdonatorer och samtidigt stödja dennes närstående. Syftet var att belysa intensivvårdssjuksköterskors upplevelse av att stödja närstående till patienter med total hjärninfarkt i samband med organdonation. En kvalitativ metod med innehållsanalys av en fokusgruppsintervju genomfördes.Det framkom två huvudkategorier, Närståendes behov och Intensivvårdssjuksköterskans förmåga att ge stöd. Intensivvårdssjuksköterskans upplevelse påverkades i hög grad av hur närstående reagerade på situationen gällande organdonationsprocessen.

During the past decade, consumer health information-centers have been developed at the hospital libraries in Sweden in order to meet the increasing demand from patients and their relatives concerning consumer health information. In 1993, the hospital libraries in Falun, Västervik and Karlstad launched a consumer health information database called PION. The aim of this Master's thesis is two-fold. My first aim is to describe and discuss the principles of user-oriented evaluation. In my attempt to convey the theoretical discussion into the everyday life of librarianship, my second and most important aim is to conduct a user-oriented evaluation of the database PION.

Bakgrund: En av sjuksköterskans uppgifter är att visa de efterlevande hänsyn och omtanke när någon avlider. Vårdutbildningar är till stor del somatiskt inriktade och ute i den kliniska verksamheten ges mycket knapphändig information kring hur dödsbesked ska levereras. Ett bristfälligt bemötande från sjuksköterskans sida kan leda till att närståendes sorgearbete kompliceras. Syfte: Syftet var att undersöka närståendes situation i samband med ett plötsligt dödsfall samt beskriva relevanta omvårdnadsåtgärder i detta skede. Metod: En litteraturstudie som bygger på fem kvalitativa och fem kvantitativa vetenskapliga artiklar.

This study aims to find out what students think about bilingualism as well as whether there are advantages and disadvantages of it, based on the children's perspective. All children in this class are bilingual, is thus a mother tongue other than Swedish. All were born in Sweden but has parents who are originally from / born in other countries in addition to having mom who was born in Sweden but originally from another country. In my study I have chosen to use qualitative methods in which I used semi-structured interviews and non participant observations. In the study, I have come to interview the children think that being bilingual is good, they mean that there are some drawbacks to this except that it can sometimes be a bit hard when someone does not understand.

The object of this two years master's thesis has been to study a specific genre of personal archives by examiningthe archives of nine parents who have lost one or several infants. Using internet-based methods, (e-mail, Skypeand digital photographs), I have conducted qualitative research using a general interview guide technique. Usingresearch from archival theory as well as other fields, my material has been arranged and analysed according tothemes and recurring thoughts picked up from my informants during the interviews.My main theoretical aid has been that the role of parent who has lost a child is the starting point for the creationof the personal archives. Another important theory is my definition of the term ?document? as not dependent onmedium and format, but on usage: if an object has been used as a part of an archive, it is a document.

BACKGROUND: Chronic Obstructive Pulmonary Disease (COPD) is a slow progressive disease affecting the family caregivers by limiting their lifestyle. Subsequently the situation can be experienced as stressful for both the afflicted and the relatives. To easier understand the needs of the caregivers of family members suffering from COPD have, it is important to get an insight into their experience of every-day life, so that medical staff can help, support and promote their health according to their needs. AIM: To illustrate caregivers? experiences of living with a family member suffering from Chronic Obstructive Pulmonary Disease.

Multiprofessional teams is a common way of organizing the work in rehabilitationmedicine clinics. Team members are usually physicians, physiotherapists, occupationaltherapists, counselors and nurses where the counselor is the only one from the psycho-social discipline. Team care interventions are provided from a holistic perspective inwhich the patient's physical, psychological and social rehabilitation is taken intoconsideration. The meetings between the professional team and patient have the mainpurpose to increase patient participation. The aim of the study is to observe and analyzecommunication between the professionals, the patient and their relatives during teammeetings.

The purpose of this thesis is to study the personal problems that can occur when defecting from a destructive cult, and what kind of support you may need from social authorities. The aim is to develop guidelines for social workers who are in contact with sect defectors. It?s a qualitative study based on interviews with six defectors from Jehovah?s witnesses. The results shows that all the defectors that have been interviewed have had anxiety problems, lost contact with friends and relatives, low level of education, and low self esteem when defecting or after.

The purpose of the study was to investigate how young female Kurd immigrants experienced their existence between two different cultures, namely Swedish compared to the immigrants parents culture. How their experience behavioural conduct between the opposite sex before marriage and if the young female Kurds thought the mass media picture of them was thought of as a correct image of their lives in general or whether they experienced it as a generalisation only. We chose qualitative methods for our study and used suitable literature based on the theories of this subject to be able to understand the problem. To go deeper whit the study five young female Kurds aged between eighteen and twenty years were asked if they would participate in an interview on the subject. These participants proved that they had no problem at all being multicultural.

Background:Alzheimer's disease is a disease that primarily affects the elderly but also younger people. Alzheimer's disease is a type of dementia which means that you get changes in the cerebral cortex and cells gradually die. The disease causes memory loss and things that were obvious before will be difficult for the sufferer. Alzheimer's disease also affects next of kin to a large degree; they will have to take a great responsibility. The next of kin are entitled to support from healthcare.Aim:The aim was to highlight next of kin' experiences of healthcare to their family members with Alzheimer's disease.Method: The study was based on narratives, which in this case means analysis of autobiographies.

Syftet med studien var att beskriva sjuksköterskans upplevelser av plötslig oväntad död relaterat till sig själv och mötet med anhöriga.Metoden var en beskrivande litteraturstudie baserad på elva vetenskapliga artiklar utifrån databaserna Cinahl och PubMed. En metodologisk granskning genomfördes också av artiklarnas urvalsmetod.Resultatet visade att sjuksköterskorna upplevde att de saknade utbildning och kunskap i att ta hand om anhöriga vid plötslig oväntad död. De anser att det är deras arbetsuppgift att ta hand om anhöriga till patienter som hastigt avlidit och de beskriver att de upplever detta som tungt och ledsamt på ett personligt plan. För att bearbeta dessa känslor anser sjuksköterskorna att de finner det bästa stödet i att prata med kollegor inom personalgruppen.Slutsatsen är att en kunskapslucka finns hos sjuksköterskan gällande oväntad död och omhändertagande av anhöriga till patienter som plötsligt avlidit. Adekvat utbildning inom området skulle leda till ökat självförtroende och kompetens i att hantera svåra situationer och därmed ge ett bättre omhändertagande till anhöriga..