Syftet med detta examensarbete var att utifrån forskning på området göra en kunskapsöversikt gällande kvinnor med funktionsnedsättning och riskfaktorer för att utsättas för övergrepp. Våra teman var funktionsnedsättning, övergrepp och riskfaktorer. Vi har tolkat resultaten med hjälp av rutinaktivitetsteori. Vi har utifrån forskningen identifierat olika faktorer som kan vara förknippade med ökad risk för att utsättas för övergrepp. Att vara kvinna, beroende av andra och isolering är exempel på riskfaktorer.

The development of five individual pupils? writing abilities, as reported by six of their teachers, is analysed. The thoughts and reflexions inspired by the everyday interaction between the teacher and the pupil suffering from some kind of reading and writing disability are presented. The purpose is to capture what was unique and characteristic in the measures that triggered a positive response in the pupils. Some of the questions answered in this study are: How does the phenomenon of reading and writing disabilities manifest itself in the classroom, and what are the consequences for the individual pupil of the various pedagogical measures available?One conclusion that may be drawn from this study is that there is no cut-and dried method for working with pupils suffering from reading and writing disabilities.

The purpose with this study was to investigate how parents experience their situation in life, having personal assistance at home to support their small children with disabilities. Different areas were investigated. What made them apply for personal assistance? How does the support affect the family and their parenthood? What would it mean if their children would not have personal assistance? The study was made using a qualitative method and the material was gathered through interviews. A combination of symbolic interactionism and system theory were used as theoretical perspectives.

The aim of our study has been to investigate what kind of space there is to exert influence for adult persons with mild intellectual disabilities who live on group housing. We wanted to investigate what kind of hindrance and possibilities there were to exert influence for people on group housing. Our study has been built on qualitative group discussions with 9 persons with mild intellectual disabilities and 6 care-keepers. We have analysed our discussions on the basis of the theory of empowerment. Our result indicates that there is different kind of factors that affect the possibilities for people with mild intellectual disabilities to increase their influence, and it does not always have to do with the disability how the persons can make their voices heard.

The purpose of the study isto,based on network theory, systems theory and development ecological systems theory,understand parent?sexperiences of having children with autismspectrum, as well as understand the importance of social networksfor the parents. All of the intervieweeswere mothers. The results showed that it is important to parentsto have contact with other parents who are in the same situation as them. Many of the interviewees had a small social network.

Vårt syfte är att undersöka motivet till att en socialarbetare väljer att ta med hästen som del i sitt arbete. Detta försökte vi finna svar på genom intervjuer med sex stycken utövare av hästunderstött socialt arbete (HUSA). Vår tanke var att försöka förstå varför man väljer att tillföra hästen i ett redan komplext område. Det vi ville få reda på var vilka faktorer som är avgörande för valet att arbeta med häst? Vilka kunskaper ligger till grund för valet att arbeta med HUSA? Och Påverkar tidigare erfarenheter valet att börja arbeta med HUSA? Vårt datamaterial vi fått ut av de semi-strukturerade intervjuerna har vi sedan tolkat utifrån den tidigare forskningen men också genom perspektiv som beskriver komplexiteten i socialt arbete, kunskap och kunskapsformer men också evidensbaserad praktik.

The purpose of the study was to examine how exercise of authority social worker´s view and work with normality has changed. Together with the role of changes in society, as LSS (Act concerning Support and Service for Disabled), user influence and the principle of normalization had in this context. The material has been collected through a qualitative method with semi-structured interviews which were held with eight social workers. Three of them had not been active within the field of this study for more than ten years and five of them are currently working. The collected material was analyzed through the theoretical perspective social constructivism and the theoretical concept case management.

Uppsatsens syfte var att få kunskap och förståelse för vilka attityder högskolestudenter kan ha till psykisk sjukdom och personer med psykiska funktionshinder. De forskningsfrågor som besvarades var: Hur resonerar studenter om psykisk sjukdom och personer med psykiska funktionshinder? Hur i det vardagliga talet reproduceras studenternas attityder till psykisk sjukdom och personer med psykiska funktionshinder? För att besvara forskningsfrågorna genomfördes samtal i fokusgrupper med högskolestudenter från olika utbildningsprogram. Resultatet visade att studenterna hade ambivalenta attityder och att attityderna var situationsbundna. Studenterna associerade psykisk sjukdom som något negativt vilket de relaterade till medias påverkan.

Stroke are a common disease and it comes with big chances of disability after rehabilitation. Life after stroke can bring a different lifestyle and lots of feelings around this situation. Purpose: The purpose of this study was to analyze how people feel after being injured with stroke. Method: We have assumed that studying qualitative research articles according to Evans description of content analysis. Information has been sought in the databases Cinahl, PubMed and Discovery Results: The study results in four themes; Loneliness, trust, Despair and obstacles to health.

The purpose of this essay is to study how parents of children with disabilities young people make their choice of support and service LSS. The study takes its lead from questions designed to determine which interventions parents use for their children. What parents think about today's choice and if satisfactory, or if they have other wishes. It is also about how parents experience the freedom of choice and participation in the selection of interventions. Furthermore how the parent discuss the topic of choice from childhood and parental perspective.

This paper explores the accessibility for patrons with different physical disabilities in regards to materials, service, the library building and its website at two typical, medium-sized public libraries in Sweden.The case study is based on interviews, observations, and document and literature studies. As a theoretical framework for this study, Buckland?s model of information barriers is used to describe, discuss and evaluate how the two libraries work with accessibility. In addition, international and national guidelines are used to measure whether additional actions are required of the libraries to improve the accessibility.The results show that both libraries are well suited in various respects to provide for the different needs and the requirements of patrons with physical disabilities. Some obstacles still exist in both libraries, especially in the lack of literature in accessible formats in different languages.

Det finns mycket forskning kring hur individer med Parkinson har möjlighet att förbättra sina fysiologiska funktioner genom träning. Det finns dock få studier som beskriver upplevelser av träningen. Syftet med denna studie var att beskriva upplevelser av sjukgymnastledd gruppträning hos individer med Parkinson och undersöka hur resultatet överensstämde med domänerna i Internationella klassifikationen av funktionstillstånd, funktionshinder och hälsa (ICF). En kvalitativ deskriptiv innehållsanalys tillämpades. Fem deltagare medverkade i studien.

Aim: The aim was to describe adult patients quality of life after cardiac arrest and resuscitation with CPR. Method: A literature overview based on eight scientific articles and one master thesis. Results: The result is presented in three categories, physical, psychological and social quality of life. Sleeping disorders, fatigue and low energy level affected the physical quality of life in a negative way. The psychological quality of life was often impaired the first time after the cardiac arrest, to be improved over time.

Kronisk smärta är vanligt förekommande bland befolkningen och kan ge stor påverkan på det dagliga livet. Personer med kronisk smärta blir ofta överkänsliga i det centrala nervsystemet (central sensitisering). Läkemedlet capsaicin är potent för att lindra smärta och lugna ett överretat nervsystem. Syfte: Att utvärdera effekten av capsaicinkräm på självskattad smärta och aktivitetsnivå hos patienter med långvarig, benign smärta från rörelseapparaten. Metod: Av 40 tillfrågade personer valde 13 att delta.

This essay aims to examine the meaning work at daily activity centers gives people with intellectual disabilities and the questions these people consider necessary to ask in quality surveys. This has been done by interviews with twelve respondents in various daily activitiy centers within a private care company in the Stockholm area. The theories that has been used to analyze the empirical data is SOC - sence of coherence, stigma and empowerment. The result shows that the meaning of daily activity is to create and maintain social contacts, feeling important and needed by others and an opportunity to feel ?normal? and like everybody else.