The main purpose of this study was to examine how people who have felt mentally bad, describe their subjective experience of what leads to a mental well-being. The overall research questions were; how does the individual define mental well-being, how does the individual describe the turning-point during her tough period, and in what way does the individual consider that her own effort has influenced her well-being? In order to answer these questions, qualitative research interviews were conducted with persons who?ve felt mentally bad and who?ve got some kind of professional help, and who think that they have a mental well-being today. The empirical material was analyzed from a theoretical resilience perspective. The study?s result showed first of all, that there are different ways to define well-being.

A qualitative study about collaboration between librarians and nurses in the supplying of consumer health information (CHI) at The Hospital Library of The Mölndal Hospital in Mölndalnear Gothenburg, Sweden.The staff were interviewed about how their work is affected by the collaboration between thetwo occupational groups. The purpose of the study is to find out if there exists a strugglebetween the groups about the influence on and the control over the handling of this kind ofinformation. Despite some problems with the permission to do as many interviews as needed,the study shows some positive effects with the collaboration. The study gives a short backgroundto the development of CHI services in USA, the UK, Denmark and Sweden. Fourfurther CHI service centres in Sweden are shortly presented and one member of each staffwas interviewed by telephone..

The aim of this essay was to describe and interpret the managements and organizations impact regarding the caregivers working conditions. To examine this we used a qualitative method. We completed two group interviews and five individual interviews with a total of fifteen enrolled nurses that worked within elderly care. In our interviews we found that the enrolled nurses felt that the organizations economic interests collided with their personal values regarding good quality elderly care. We also found that the caregivers experienced that they had an impact on their working conditions and that their employer was the main reason for making it possible..

The aim of this undergraduate thesis was to study what the participation in the activities of the Fontain House in Stockholm means to its members. The research questions dealt with how the members describe their participation in the activities, whether they say that it has helped them, and, in that case, in which way. Furthermore, they dealt with how the members argue about their experiences of mental illness and of social help. The study was carried out within the framework of the narrative method. As tools for analyzing the narratives, parts of An-tonovsky?s theories as well as the theoretical concepts of inclusion and exclusion as described by Madsen, were used.

Aim Our aim is to highlight perceptions of fibromyalgia among health care personell.MethodsA systematic literature review conducted with a deductive approach.FindingsHealth care personell felt insecure because of a lack of understanding which lead to avoiding contact with these patients. Many felt that the fibromyalgia patient was categorised and that they would have been better served with another name of their disease. There was a great distrust against the diagnosis and its aetiology. The patient was perceived as troublesome, illness-fixated and draining the personell of energy. The paradox that the patient is looking so healthy but bearing so much pain was confusing for the health care personell.Conclusions Communication and an empathic encounter was identified as important elements for patient care.

Ungdomars hälsa påverkas av olika faktorer som den psykiska hälsan, övervikt, ätstörningar och självförtroende. Familjerelationer, kompisar och skolan är andra faktorer för att ungdomarna ska må psykiskt bra. För att kunna vägleda ungdomar på gymnasiet är det viktigt att skolsköterskor har kunskap om ungdomarnas egen syn på sin hälsa och vad de tycker är viktigt för att de ska må bra. Syftet med studien var att belysa gymnasieungdomars uppfattning om den egna hälsan. En systematisk litteraturstudie gjordes då den ger en bild av forskningsläget just nu.

Objective: To investigate the experiences of ambulance nurses when using Boussignac CPAPcompared to their previous model, and their suggestions for possible improvements in the use of CPAP in the care of patients with pulmonary oedema. Method: A qualitative study with a descriptive and exploratory approach. Data was collected through ten semi-structured interviews with ambulance nurses, seven men and three women. The analysis was conducted using Lundman and Graneheim?s content analysis.

The aim of this descriptive review was to elucidate how the literature describes how children of parents with mental illness experience and have knowledge about their parent?s illness. The aim was furthermore to describe how the children?s existence is affected, can be improved and why the children so often are invisible. Search through Medline (through PubMed) database and additional manual search was conducted.

                                  The study aimed to explore how patients with ICDs experience their quality of life with a focus on everyday life, electric shocks, and how support from the health service is perceived. The studydesign is descriptive with a qualitative approach. Semi-structured interviews were conducted with seven patients. Data collection lasted for three weeks and interviews were conducted in the participant´s homes, at the participants? workplaces or over the phone.The study shows that most participants have learned to live with the ICD.

The proponents for conscience wants to get a clause that will allow the health professionals to due. scruples waive certain duties. Swedens decision makers has despite pressure from the Christian De-mocrats and the Sweden Democrats decided not to implement freedom of conscience in health care. The purpose of this paper is to investigate whether Sweden has the obligation to provide for freedom of conscience in health care. Furthermore, it must be examined, whose rights according to the law will go first, health professionals right to freedom of conscience or the patient right to equal treat-ment.

Inledning: Psykisk ohälsa är ett växande problem som ses hos både individer och i samhället i stort, det medför stora kostnader och lidande för individer och anhöriga. Många av de med psykisk ohälsa söker hjälp i primärvården men primärvården är dåligt rustade för att hjälpa dessa personer. Distriktssköterskor träffar en stor del av befolkningen och därmed många människor med psykisk ohälsa. Med anledning av detta önskar uppsatsen beskriva distriktssköterskans arbete med patienter som upplever psykisk ohälsa. Syfte: Syftet med denna studie är att sammanställa och analysera forskning om distriktssköterskors omvårdnad riktad till patienter som upplever psykisk ohälsa, ur ett primärvårdsperspektiv.Metod: Forskningsplanen är utformad som en systematisk litteraturstudie med både kvalitativa och kvantitativa data, Mixed methods.

Syftet med föreliggande studie var att få fördjupad insikt i och att beskriva hur sjuksköterskor påverkas av, och förbereder sig inför, ett abstrakt hot såsom en förutspådd epidemi. Studien är empirisk med en enkätundersökning av kvalitativ karaktär. Inspiration till tolkning av data är hämtad från fenomenografin och resultatet belyses genom anknytning till KASAM. Studiens deltagare var 39 sjuksköterskor verksamma på en Akutklinik och en Infektionsklinik. Resultatet visade att sjuksköterskorna påverkas av hot om epidemier bland annat genom en rädsla att själva smittas.

Syftet med studien var att undersöka och beskriva attityder till psykisk ohälsa hos psykiatripersonal, samt att undersöka skillnader i attityd inom bakgrundsfaktorerna kön, ålder och utbildningsnivå. Studien har tagit del utav forskningsprojektet Psykisk ohälsa. En deskriptiv och komparativ design med kvantitativ ansats användes. Data insamlades från 216 returnerade enkäter från vårdpersonal inom psykiatrin. Frågeformuläret Nya CAMI-S med 29 påståenden användes.

ABSTRACTParental support is needed because it promotes a positive development in children, because parents ask for it and because it has positive effects on the public economy. Those responsible in Sweden for Child health care have shown an increased interest in supporting parenthood.Aim: The overall purpose of this study was to investigate what kind of support parents today desire from child health care. An additional purpose was to investigate if they feel their needs and wishes are met.Method: The study has a descriptive and qualitative design. The selection was eight parents of children under eighteen months of age: four mothers and four fathers. None of the participants were couples.

Syftet med studien var att se om det är möjligt att påverka resultatet på en kognitiv uppgift beroende på hur uppgiften presenteras. Är det möjligt att före ett test som kräver mental ansträngning genomföra en kort mental träning/förändring av inställning och på så sätt få ett bättre resultat på testet? Påverkar positiva eller negativa tankar prestationsförmågan? Undersökningen utfördes i två delmoment. Första delen av undersökningen var en enkät som användes för att undersöka studenternas attributioner inför ett prov. Andra delen av undersökningen var ett kvasiexperiment i form av ett minnestest uppdelat på två grupper vars uppdelning skedde med hjälp av enkätsvaren.