Aim: To describe perceptions about written and verbal information regarding diet and physical activity in women with breast cancer and to study possible differences between ages and perception. Method: A cross-sectional study was conducted and consisted of 57 women with breast cancer stages I-III who started adjuvant chemotherapy within a year (2007-2008). A questionnaire, regarding their perceptions about the written and verbal information they had received about diet and physical activity, was responded to three months following treatment completion. Between 67-93 % of the participants responded to the questions. The answers was analyzed with descriptive statistics and Mann Whitney U-test.

Background: Pressure ulcer is a complication that arises often due to a lowered general condition. Pressure ulcer arise because of long term compressive load application. That?s why it?s of utmost importance as a nurse to work in preventive ways, as the pressure ulcer lead to physical, psychological and social consequences for the patient. Purpose: The purpose was to describe the patients experiences of living with pressure ulcer.

Vård i livets slutskede är något som påverkar sjuksköterskor och vårdpersonal på olika sätt, exempelvis emotionellt. Vård i livets slutskede, även kallad palliativ vård, syftar till att lindra lidande för patienter i deras sista tid i livet. Litteraturstudiens syfte var att belysa upplevelserna av att vårda dessa patienter. Resultatet visade att upplevelserna påverkades av kulturen och de egna erfarenheterna. De teman som framkom var - omvårdnad av patienten, mötet med närstående, samarbete i teamet och existentiella upplevelser.

The aim of this study was to examine, in the work against bullying how collaboration between the school counselor and other professions is described by the different professions within the student health team as well as how they describe that the different competencies involved in such teams shapes problem definitions and solutions. The student health (swedish- elevhälsoteamet) team of which the study is based on consists of different professions such as school counselors, school nurses, special education teachers, school psychologists and school principles. We have interviewed representatives of all the above mentioned professions with the exception of school psychologists using a qualitative research design. In this study we have chosen to focus on two student health teams from two different primary schools located in a middle-sized municipality in southern Sweden. We have analysed the results using new institutional theory and the terms domain and power. The main conclusion of the study is that school counselors themselves feel they have a specific knowledge regarding bullying but have difficulties in capitalizing on it while collaborating with the other professions in the student health team.

Syfte: Att beskriva sjuksköterskors kunskap och attityder gentemot patienter som lever med HIV eller AIDS samt beskriva eventuella skillnader i kunskap och attityder mellan yngre och äldre sjuksköterskor. Metod: Föreliggande empiriska studie hade en kvantitativ ansats med en beskrivande jämförande design. Urvalsmetoden var ett bekvämlighetsurval där totalt 63 sjuksköterskor deltog och enkäter skickades ut till nio avdelningar på tre olika sjukhus. Resultat: Majoriteten av sjuksköterskorna hade god kunskap om HIV och AIDS, positiva attityder samt en vilja att vårda denna patientgrupp. En del av sjuksköterskorna uttryckte dock en rädsla för att smittas av HIV, ett behov av mer utbildning och negativa attityder gentemot vissa specifika grupper med sjukdomen.

Towards the end of the 1960s, the credit financed purchase was well established in Sweden. The Swedish households were able to purchase goods, which had been considered unnecessary, or even luxurious, in the past. On the other hand, effective means to handle the increasing amount of debt and potential debtors were introduced; credit rating was registered, trade with insecure claims increased and if debtors could not fulfil their obligations, the creditors often used harsh or undue methods. By introducing Inkassolagen (1974:182), the legislator hoped to regulate the debt recovery process and ensure the fair treatment of debtors. The legislator also introduced liability for damages caused by a creditor in the collection process.

                                  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.

?Sjuksköterskors kunskap inom hälsorådgivning kan alltid förbättras. En metod att bedriva hälsorådgivning kan vara det motiverande samtalet (MI). Syftet med denna litteraturstudie var att beskriva sjuksköterskors upplevelser av det motiverande samtalet vid patientrådgivning. 13 artiklar kvalitetsgranskades och användes i resultatet, där fyra kategorier bildades.

Background: In today's Swedish health care, it is required that the various professionals must work together in teams to safer care. Several professionals with various skills expected working together in the traumateam at the care of the traumapatient. At the same time, research shows that substandard teamwork leads to avoidable errors in care. One way to improve teamwork is to practice. Purpose: The purpose of this study is to shed light on the experiences of the traumateam exercises that exercise participants feel has been favorable for the patient at the initial care of trauma patients.

ABSTRACTBackground: People with colorectal cancer undergoing rectum amputation get a permanent colostomy, which affects the social life. It may be valuable for health care what these people experience living with colostomy in order to provide the greatest possible support. Objective: The aim of this study is to describe how people who received a colostomy experience their daily lives and the support they have received from the health services.Method: Qualitative interview study with six people, with a descriptive phenomenological approach.Results: The analysis of the interviews about how it's like to live with a colostomy resulted in three themes: 1) Living with a colostomy gives an uncertainty that affect the social life, 2) Physical and psychological impact of getting a colostomy and 3) Support for health care and relatives.Conclusion: Subjects had a positive attitude towards life, which contributed to that they could adjust to living with a colostomy and feel a meaningfulness of life. The study shows that all the interviewed people overall were satisfied with the information provided by the healthcare personnel. It was good with both oral and written information and very appreciated with repeated information. One aspect that could be improved was the information given aboute the closure of anus during surgery and the following complications.

The idea for this project was initiated together with one of the leaders in the forest, paper and packaging industry. To get through an A/R CDM process the company is exposed to the risk of failing the process or that the overall costs will exceed the benefits of the project. This would delete the incentives to invest in GHG removals compared to purchasing emission allowances on the carbon market. The questions that have been raised and needs clarification in the thesis are the following:? From a company perspective, what are the incentives for implementing Forest Clean Development Mechanism (CDM) projects?? What is a likely financial outcome of a reforestation CDM project on degraded land in the Guangxi province of the Peoples Republic of China?? When does an investment like this break even with the cost of buying market based carbon emission allowances? The objective of this master thesis is to carry out a research about the incentives for forest, paper and packaging companies to invest in reforestation through the clean development mechanism.

Bakgrund: Fenomenet självskadebeteende har blivit allt vanligare i vårt samhälle och väcker många reaktioner hos omgivningen. Sjuksköterskor möter patienter som skadar sig själva i flera olika miljöer. Det har dock visat sig att sjuksköterskor själva utrycker bristfällig kunskap då de upplever det svårt att bemöta patienter med självskadebeteende.Syfte: Syftet med litteraturstudien var att belysa faktorer som påverkar sjuksköterskors attityder till patienter med självskadebeteende, samt dess konsekvenser för omvårdnaden.Metod: En allmän litteraturstudie, där empiriska artiklar publicerade i vetenskapliga tidskrifter har analyserats. Fynd från artiklarna som svarade på syftet har identifierats och fyra kategorier skapades.Resultat: Resultatet presenteras utifrån fyra kategorier vilka är: Sjuksköterskors känslor och tankar, Sjuksköterskors erfarenhet och genus, Sjuksköterskors arbetsmiljö och Sjuksköterskors behov av utbildning. Detta är faktorer till sjuksköterskors attityder och påverkar den omvårdnad som patienterna får.Diskussion: Genom att påverka bakomliggande faktorer till sjuksköterskors attityder skulle de kunna förändras i en positiv riktning.

Bakgrund: Distriktssköterskearbetet är väldigt självständigt och mångsidigt. Distriktssköterskor möter patienter som lider av olika sjukdomar eller skador. De flesta kan inte klara de psykiska och fysiska påfrestningar och blir utbrända. Studier visar att med handledning kan tid för reflektion och bearbetning av bl. a stress möjliggöras vilket leder till mer trygghet och välbefinnande i yrkesrollen.Syfte: Syftet med denna studie är att undersöka om det finns behov av omvårdnads-handledning för distriktssköterskor för att minska stress i deras arbete.

Talking about sexuality -Medical staffs´ experiences of conversations about sexuality with patients at a cardiology unit The background of this essay is the taboo to talk about sexuality among people who suffer from some kind of illness. When a person gets ill and need medical attention, his or her life changes dramatically. The patients get treatment for their symptoms. The illness and treatment have often an influence on the patient?s sexuality.

ABSTRACTBackground: People with colorectal cancer undergoing rectum amputation get a permanent colostomy, which affects the social life. It may be valuable for health care what these people experience living with colostomy in order to provide the greatest possible support. Objective: The aim of this study is to describe how people who received a colostomy experience their daily lives and the support they have received from the health services.Method: Qualitative interview study with six people, with a descriptive phenomenological approach.Results: The analysis of the interviews about how it's like to live with a colostomy resulted in three themes: 1) Living with a colostomy gives an uncertainty that affect the social life, 2) Physical and psychological impact of getting a colostomy and 3) Support for health care and relatives.Conclusion: Subjects had a positive attitude towards life, which contributed to that they could adjust to living with a colostomy and feel a meaningfulness of life. The study shows that all the interviewed people overall were satisfied with the information provided by the healthcare personnel. It was good with both oral and written information and very appreciated with repeated information. One aspect that could be improved was the information given aboute the closure of anus during surgery and the following complications.