Som examensarbete valde jag att göra något så galet som att skriva en bok. Jag hade aldrig kunnat ana vad jag gav mig in i, och vilket oerhört lärorikt äventyr jag stod inför. Många gånger var jag nära att ge upp helt och tänkte att jag aldrig skulle kunna ro detta i land. Men den 1 maj 2012 skickades faktiskt boken till tryckeriet, en dag jag för evigt kommer att minnas med ett stort leende. Ingenting är omöjligt, så länge du är beredd att kämpa för det - och tro mig, det har jag verkligen gjort.Min bok heter We All Need Heroes.

People with Down syndrome are living longer lives today thanks to medical science. These people with their families are in need of assistance from goverments and professionals throughout their lives. It is therefore important to understand how familymembers affected by having a person with Down syndrome in the family. In this paper we focus on the siblings' experience. This study aims to examine four women's experiences of what it is like to have a sibling with Down syndrome and how the respondents have developed their role and identity as siblings, and what strategies they have developed for this role.

En hel del forskning finns inom området cancersjukdomar. Kunskap om personers upplevel-ser av att få återfall i cancer är otillräckliga vad gäller perspektiv på omvårdnad. Syftet med denna litteraturstudie var att studera personers upplevelse att få återfall i cancer. Sex interna-tionellt publicerade vetenskapliga artiklar analyserades enligt kvalitativ innehållsanalys. Ana-lysen resulterade i fem kategorier: att vinna kontroll över hälsan och lära sig att leva med sjukdomen, att inte bli hörsammad, att cancern aldrig försvinner och att man blir rädd att dö i förtid, att ha en Gudstro och att få stöd av någon som älskar en inger hopp och att sätta värde på livet och prioritera mer medvetet.

Many children in Sweden are exposed to maltreatment. Among the purposes of the Child health care (CHC) are to decrease mortality, infirmity and handicaps among mothers and their children, and to decrease hurtful strains for parents and their children. CHC-nurses get critizism for not reporting child maltreatment in high enough numbers to the Social service. The aim of this study was to chart how CHC-nurses finds their work with families suffering from maltreatment. Ten CHC-nurses were interviewed with semistructured interviews.

Background: Anorexia nervosa is a disease that often strikes teenager girls. The causes of the disease are not entirely known, but there are redeemed and maintenanced factors. The factors describes as biological, psychological and sociocultural. Aim: The aim of the study was to illuminate the nurses problem in caring of girls that developed anorexia nervosa. Method: The method of this essay is a literature study.

The aim with this project was to describe how nursing staff working in the home care environment perceive their level of knowledge regarding mental ill health and if this level of knowledge is sufficient / insufficient in their dealings with mentally ill patients. The study is empirical and a qualitative method has been used. Questionaires have been used and interviews have been carried out with nurses working in the home care system and data has also been collected from previous research in this area. Result The result show that home care nurses consider that they have inadequate knowledge of treating patients with mental ill health and they seek more training, guidance and collaboration with psychiatric nurses. Conclusion Increased knowledge of mental health care and continuous guidance would make home care nurses more confident in their dealings with patients suffering from mental ill health.

Background:Approximately 300 children get a malign cancer diagnosis every year in Sweden, 80 % of them survive. Parents of the children who have a cancer diagnosis experienced that they didn't have mental health, nurses care of parents are to keep a mental health so they can handle their parent role. Nurses should meet families through their life-world because caring should be done with dignity and integrity.Aim:The aim of this study was to describe how parents experience the daily life with a child who has a cancer diagnosis.Method:The method used in this study was a literature study based on autobiography, which means analysis of autobiographies. Four books were analyzed.Results:Four categories emerged from the analysis of the autobiographies, experience of powerless, desire of a regular, experience of anxiety and fear, to experience joy and have hope.Conclusion:This study shows how life changes when a child in the family gets a cancer diagnosis and how it affected the parents. The study points out the importants to create a great relationship between the nurses and the family so they can have a good care..

Syftet med denna uppsats har varit att beskriva vilka faktorer som är av betydelse i mötet med vårdaren enligt patienterna. Studien är en litteraturstudie, som utgått från en kvalitativ metodansats. Analysmetoden som använts har varit en latent innehållsanalys. Skillnaderna mellan "nursing" och "caring" som begerpp betonas ofta i litteraturen av olika forskare. Den empiriska forskningen visar emellertid att dessa begrepp är svåra att hålla åtskilda i verkligheten.

The aim of this study has been to create an understanding for the situation of an often forgotten group in foster care, the carers? own children. Our main focus has been the experience this group has of foster care, their experience of participation in caring for the foster children and their possible need of support and help. Our chosen method has been qualitative interviews with six adult children of foster carers, two men and four women. The theory used in this study has been Sense of Coherence.Our interviewees gave mainly a positive description of being part of a foster family even though they could give examples of difficult situation and of loss.

Syftet med denna uppsats har varit att beskriva vilka faktorer som är av betydelse i mötet med vårdaren enligt patienterna. Studien är en litteraturstudie, som utgått från en kvalitativ metodansats. Analysmetoden som använts har varit en latent innehållsanalys. Skillnaderna mellan "nursing" och "caring" som begerpp betonas ofta i litteraturen av olika forskare. Den empiriska forskningen visar emellertid att dessa begrepp är svåra att hålla åtskilda i verkligheten.

The family and relatives caring of older people in Sweden lies on an old tradition. By legislation the responsibility for the older people has gone through a development from the family to the society. According to the new social service law (2000) it is not that clear that the utmost responsibility lies on the society. According to the social service law ( 5th chapter, 10 §) the municipality should ease things up by giving support and relief for relatives taking care of older people, prolonged ill and function disabled people. The purpose with the study was to examine how the family care givers are finding their everyday work and their experience of the support that the society is giving.

Introduction:Violence towards women is an extensive and important problem in the society. Confronting women who are assulted by their male partner is a demanding task for the nurses.The aim of the study:The aim of this empirical study was to illustrate the experiences of nurses in the meeting with women exposed to violence by their male partner.Method:This is a qualitative interview study including nine female nurses. The material recieved from the interviews was analysed with help of content analysis. Categories were formed named Comunication, feelings, Ability to recognize the women, Lack of time, Need of support and further education. An application to the ethical council at the University of Kristianstad were remitted and approved.

Today patients are more aware of their rights regarding their own care. They are more informed, more engaged and have more and individual requirements, which leads to increased demands for information and participation increases. The Health Act sets out the patients´ right to participation. Participation increases patient satisfaction with care, promotes healing and increases adherence to health care advise. The patient doesn´t always experience participation in their own care to the extent they wish, which suggests that nurse?s does not always succeed in getting the patient involved.

Vid dysfagi är pneumoni en vanlig komplikation som ger ökade kostnader för vården, ett ökat lidande för patienter samt leder till fler dödsfall. Omvårdnadsåtgärder som minskar risken för pneumoni är därför av betydelse att identifiera. Syftet med denna litteraturstudie var att i vetenskapliga artiklar identifiera omvårdnadsåtgärder sjuksköterskan kan tillämpa som minskar risken för pneumoni vid dysfagi. I tio vetenskapliga artiklar utlästes sex kategorier via databearbetning. I resultatet identifierades att vinkeln på ryggen i sittande läge var viktigt att ta hänsyn till, användningen av vätskor med låg viskositet hade en förebyggande effekt och en intervention där hakan fälldes ner mot bröstet vid sväljning skyddade mot aspiration.

Omvårdnad av patienter med misstänkt hjärtinfarkt kräver dels ett etiskt förhållningssätt, en holistisk människosyn och vetenskapligt beprövade kunskaper inom områden såsom omvårdnad och medicin. Syftet med denna litteraturstudie var att beskriva sjuksköterskans akuta omvårdnad i mötet med en patient som söker sjukvård för en misstänkt hjärtinfarkt. Studien är litteraturbaserad och har en kvalitativ ansats. Litteraturstudien planerades och genomfördes enligt Polit och Hunglers (1999) arbetsgång. Sökningar efter artiklar gjordes i databaserna Pubmed, Cinahl samt via manuell sökning.