BACKGROUND: Previous research shows that many nurses feel that patients with borderlinepersonality disorder (BPD) are more difficult to provide care to than patients with otherdiagnoses. Experiences of these meetings with BPD patients are often negative. With thisbackground, a literature study was made in order to elucidate the patients' perspective. AIM:Compiling knowledge of how patients diagnosed with BPD experience their treatment and themeeting with health care professionals. METHOD: Through the databases PsycINFO andPubMed, twelve qualitative articles were selected and summarized in a literature study.

The purpose of this study was to examine health promotion and ill-health prevention in the workplaces of the City District Committees in the City of Malmö. More specifically, we wanted to find what types of health problems there were and what kinds of strategies were applied to prevent them. Furthermore, the aim was to examine whether the leaders of the City of Malmö saw any effects of the strategies in use and if so, which. Finally, the intention was to compare our empirical results to previous research in the field of health promotion and ill-health prevention in workplaces. We conducted a qualitative study consisting of semi-structured interviews with five leaders in different levels, two personnel secretaries, two employees assigned to improve the health of the personnel in the City Districts, and one safety representative.

Aim: The aim was to investigate and describe, how students on high school level in Kronoberg county self rated their health with relation to irritation, nervousness/anxiety insomnia and gender. An additional aim was to investigate if there are differences between students born in Sweden by Swedish parents, students born in Sweden by foreign-born parents and foreign-born students. Methods: A quantitative method was used to analyse data gathered from students (n=1936) on high school level in 2006. All statistical analyses were made with help of SPSS V-12. Finding: The findings showed that most of the students self rated their health as ?good?, however migrant students self rated their health as ?not so good? and they had more problems with insomnia. The overall findings showed gender differences. Particularly, foreign-born girls self rated their health as ?not so good? and reported more problems with insomnia. There was no divergence between the groups regarding irritation, nervousness/anxiety. Conclusion: School nurses and health workers must have deep knowledge about differences in gender, self- rated health and insomnia when they work with public health.

Idag lever ett stort antal människor med Multipel Skleros (MS) av varierande grad i Sverige. MS påverkar livskvaliteten negativt genom att personen kan få koordinationsstörningar, känselnedsättning, miktionsbesvär samt problem med gångfunktionen och den sexuella funktionen. Det finns många studier gjorda på livskvalitet hos personer med MS men dock ingen gemensam litteraturöversikt och sammanställning av dess resultat. Syftet med studien var att analysera den hälsorelaterade livskvaliteten hos personer med MS utifrån granskning och sammanställning av studier där mätinstrumentet MSQOL-54 använts. En litteraturöversikt med fem studier har genomförts där det kvantitativa mätinstrumentet MSQOL-54 använts.

Body esteem is the affective aspect of body image, which is shaped by social experience. Compared with men, women have a more negative body image, which is more frequently correlated with depression and dysfunctional thoughts, especially in the case of eating disorders. The purpose of the present study was to examine gender differences in body esteem and its subcategories, and to find out whether there exists a stronger link between negative body esteem and higher levels of dysfunctional thoughts in women. The relationship between body esteem, dysfunctional thoughts and mental illness was examined. Participants were 73 college students doing social sciences and sports training educations.

Aim: The aim of this study is to examine roma women´s experiences of health professionals? attitudes towards them in Swedish health care. Method: Exploratory qualitative study with individual interviews was used. Semi-structured interviews were conducted with eight women of Roma origin. Data were analyzed using a qualitative content analysis.

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.

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.

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 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.

Background: The need for structured practice has in recent years appeared in connection with the request for a more evidence-based nursing. In psychiatric care with its complex disabilities, it is important to have methods to identify these. Research has demonstrated the importance of patient participation in nursing that has been shown to affect their Mental health. It is essential to get to know how patients with mental illness are capable of involvement in their life situation. The ICF emerged as a useful theoretical framework for development of questionnaires of patient participation.Aim: The aim of the present pilotstudy was to develop and test a questionnaire for participation, based on ICF.

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.