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.

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.

Normal children acquire the necessary social habits without being consciously aware of this, they learn instinctively. (Author?s translation from Swedish to English) (Asperger & Frith, 1998, s. 21) This essay is about people who do not learn to socialize, the social habits, instinctively but through conscious learning. We have interviewed three adults with the diagnosis of Asperger syndrome with the aim to let them tell us about what it means to have a neuropsychiatric Disability.

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.

ABSTRAKTVäxjö universitetInstitutionen för pedagogikPedagogik med inriktning mot ungdoms -och missbrukarvård, Examensarbete 15hp Titel                                    HVB hemmens kompetens ? Funktionshindret ADHDEngelsk titel                       HVB home skills - Disability ADHDFörfattare                           Annette Dahlskog, Monika Eklund PerssonHandledare                        Marie Joelsdotter HallbäckDatum                                 Mars 2009Antal sidor                          18Nyckelord                          ADHD, HVB hem, funktionshinder Denna studie handlar om hur personalen på HVB-hem bemöter ungdomar som har funktionshindret ADHD. I studien undersöks personalens kompetens och bemötande och hur de arbetar med psykosociala och pedagogiska stödinsatser. Undersökningen baseras på en enkät undersökning med 40 utvalda HVB hem som tar emot ungdomar med funktionshindret ADHD. Resultatet av denna kvantitativa undersökning visar att kompetensen och bemötandet är gott och att psykosociala och behandlingspedagogiska stödinsatser används i stor utsträckning.

Introduction: Pain is a subjective experience. People subjected to pain often experience a reducedquality of life. Chronic pain is pain that has been going on for at least threemonths.Problem area: People with chronic pain are subjected to unnecessary suffering and Disability. Therefore it is crucial that the nursing staff takes their situation seriously.Purpose: The purpose of the study was to describe the patient's? experiences and apprehensionof living with chronic non-malignant pain, and how this affected their everydaylife.Method: Systematic analysis of 23 depicting articles.