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Träfflista för sökning "WFRF:(Thorén Jönsson Anna Lisa 1946) "

Sökning: WFRF:(Thorén Jönsson Anna Lisa 1946)

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1.
  • Olsson, Anna-Karin, 1966, et al. (författare)
  • Occupational Therapists' Experience Concerning Occupational Performance in Adults With Asperger Syndrome
  • 2013
  • Ingår i: Occupational Therapy in Mental Health. - 0164-212X .- 1541-3101. ; 29:1, s. 42-59
  • Tidskriftsartikel (refereegranskat)abstract
    • Persons with Asperger Syndrome often seem to have difficulty performing everyday occupations. This study aimed to describe occupational therapists’ experience concerning abilities to occupational performance among adults with Asperger Syndrome. Data were collected in interviews with eight occupational therapists and analyzed using a qualitative method. Results showed that clients with Asperger Syndrome often possess abilities but seem to have difficulties knowing when, where, and how they should use them. The ability to adapt behavior in accordance with cues from the environment was identified as the core category. Environment plays a major role in how these persons interact in different situations.
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2.
  • Thorén-Jönsson, Anna-Lisa, 1946, et al. (författare)
  • Changes in ability, perceived difficulty and use of assistive devices in everyday life: a 4-year follow-up study in people with late effects of polio.
  • 2009
  • Ingår i: Acta neurologica Scandinavica. - : Hindawi Limited. - 1600-0404 .- 0001-6314. ; 120:5, s. 324-330
  • Tidskriftsartikel (refereegranskat)abstract
    • Background - There are numbers of persons living in the community with late effects of polio, of which many develop new symptoms, but the course of progression is unclear. Objectives - To assess changes after 4 years in ability and perceived difficulty in persons with late effects of polio. Material and methods - Community dwelling persons from a polio clinic. Information was gathered by questionnaire and interview on demographics, age at polio onset, affected body parts, health problems, the use of assistive devices, housing condition and activities of daily living (ADL) function as well as perceived difficulties. Results - There were no significant increase in frequency of ADL dependency but perceived difficulties increased significantly and more used mobility devices. Conclusions - Over 4 years, more persons perceived difficulties and the use of assistive devices increased. This is might reflect adaptation and acknowledgement of problems previously ignored. Time is a factor in integrating knowledge and adaptation.
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3.
  • Cederlund, Ragnhild, et al. (författare)
  • Coping strategies in daily occupations three months after a severe or major hand injury
  • 2010
  • Ingår i: Occupational Therapy International. - : Wiley. - 1557-0703 .- 0966-7903. ; 17:1, s. 1-9
  • Tidskriftsartikel (refereegranskat)abstract
    • Coping strategies used in performing daily occupations 3 months after a severe or major hand injury were explored. A semi-structured interview was performed with 13 participants with hand injuries based on Hand Injury Severity Scoring System and analysed using content analysis. Six groups of strategies were identified: ‘Changing performance of daily occupations’, ‘Actively processing trauma experience’, ‘Changing occupational patterns’, ‘Receiving assistance’, ‘Using emotional strategies’ and ‘Keeping up a social network’. The problem- and emotional-solving strategies identified in this study can be used to support other patients early in rehabilitation. Patients with few coping strategies should be recognized. Information and practical handouts to patients, therapists and relatives should stimulate and help patients with hand problems enabling in meaningful occupations and preventing unnecessary stress. Furthermore, social support should be encouraged and family should be actively involved in rehabilitation. To insure trustworthiness, member checks were used on four randomly selected participants, but could possibly be used with all participants. Further research is needed in a longitudinal study to explore which coping strategies or adaptation patients use to perform daily occupations at a later stage.
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4.
  • Kenne Sarenmalm, Elisabeth, 1956, et al. (författare)
  • Making Sense of Living Under the Shadow of Death: Adjusting to a Recurrent Breast Cancer Illness
  • 2009
  • Ingår i: QUALITATIVE HEALTH RESEARCH. - : SAGE Publications. - 1049-7323 .- 1552-7557. ; 19:8, s. 1116-1130
  • Tidskriftsartikel (refereegranskat)abstract
    • Women with recurrent breast cancer face many difficulties and challenges, from clinical symptoms of disease progression and treatment to a range of emotional responses. Guided by grounded theory methodology, we explored the main concerns of women with recurrent breast cancer, and how they were dealing with their situations. Data were collected from 40 in-depth interviews with 20 women diagnosed with recurrent breast cancer. The core category illustrated the process of “making sense of living under the shadow of death,” and was based on the women's experiences of adjusting to living with a persistent life-threatening illness. Confronting a recurrence of breast cancer was a life-altering event. Moving through a difficult and challenging time, women eased their distress by letting go of losses and reassessing important values. Through a personal transition women transcended living with a life-threatening illness. These findings emphasize the importance of recognizing existential distress in clinical practice.
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5.
  • Larsson, Inger, et al. (författare)
  • The Swedish Speech Interpretation Service: an exploratory study of a new communication support provided to people with aphasia.
  • 2007
  • Ingår i: Augmentative and alternative communication (Baltimore, Md. : 1985). - : Informa UK Limited. - 1477-3848 .- 0743-4618. ; 23:4, s. 312-22
  • Tidskriftsartikel (refereegranskat)abstract
    • Until recently, people with complex communication needs have had no access to professional interpreters. The Swedish Speech Interpretation Service (SSIS) is attempting to address this problem. This qualitative study reports on how 12 persons with aphasia experienced the services of a professional interpreter from the SSIS. The results are presented in two themes: (a) The purpose of using an interpreter, which addresses issues relating to autonomy, privacy, and burden on family members; and (b) perceptions of quality of service, which addresses issues relating to the skills and professionalism of and accessibility to interpreters. Results highlight the ongoing need for the SSIS and its importance to the participants. The professional interpreter as an augmentative and alternative communication (AAC) "tool" that could be used to enhance the participation of people with aphasia in the community-at-large, is also discussed; as is whether relatives and other non-professionals or professional interpreters should interpret for people with aphasia.
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6.
  • Santos Tavares, Iolanda, et al. (författare)
  • Confidence in the future and hopelessness: Experiences in daily occupations of immigrants with late effects of polio
  • 2013
  • Ingår i: Scandinavian Journal of Occupational Therapy. - : Informa UK Limited. - 1103-8128 .- 1651-2014. ; 20:1, s. 9-20
  • Tidskriftsartikel (refereegranskat)abstract
    • Sweden today may be described as multicultural. Those who are immigrants and have a disability are described as doubly vulnerable. Aims: To explore and describe how immigrants with late effects of polio experience their daily occupations. Method: The experiences were explored by interviews with 12 immigrants with late effects of polio, from Eastern Africa. Data analysis was carried out according to grounded theory. Results: Experiences in daily occupations affected the participants' view of the future, which in turn was influenced by the participants' conception of occupational self. This was dependent on their participation in daily occupations. Five categories influenced their experiences: rootedness in society, estimation of others, treatment by others, belonging to social networks, and the process of change in life. The social environment played an important role in determining how the participants experienced their daily occupations. Conclusions: The participants' experiences could not be seen in isolation; consequences of their disability and migration interact. The study showed that the complexity of daily life among immigrants with disability requires individual treatment and points to a need for consideration of differences in cultural background, including the therapist's own cultural lens.
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7.
  • Santos Tavares Silva, Iolanda, et al. (författare)
  • Processes influencing participation in the daily lives of immigrants living with polio in Sweden: A secondary analysis.
  • 2017
  • Ingår i: Journal of Occupational Science. - : Informa UK Limited. - 1442-7591 .- 2158-1576. ; 24:2, s. 203-215
  • Tidskriftsartikel (refereegranskat)abstract
    • This paper explores and describes conditions influencing participation in daily occupations and how these interact with each other, in the daily lives of immigrants with late effects of polio. A secondary analysis of interviews with 12 immigrants from Eastern Africa now residing in Sweden was performed, using a grounded theory approach to probe deeper into the complexity of the concept of participation. This study highlighted that participation occurs through a participation process, which was identified as the core category. It emerged that participation took place through a complex dynamic interaction of subprocesses that contributed to value and identity development. The five subprocesses influencing participation in daily life were based on participants striving to achieve mastery of daily occupations, meaning in daily life, connection to places and people, belonging to groups, and trust of others. The findings indicate the need for awareness of the complexity, when conditions for participation are in question. With a deep understanding of participation as an interactional process with socioemotional meaning, both the individual and sociopolitical aspects of participation became evident. The intersection of disability and migration could lead to disadvantages and social exclusion within this population. These factors warrant consideration on an individual, a political and a social level. Politically, structures preventing and enabling participation must be considered. Similarly, attention must be paid to the social, and underlying conditions must be created in everyday meetings.
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8.
  • Santos Tavares Silva, Iolanda, et al. (författare)
  • Struggling to be part of Swedish society: Strategies used by immigrants with late effects of polio
  • 2015
  • Ingår i: Scandinavian Journal of Occupational Therapy. - : Informa UK Limited. - 1103-8128 .- 1651-2014. ; 22:6, s. 450-461
  • Tidskriftsartikel (refereegranskat)abstract
    • Objective: To explore and describe strategies in daily occupations among immigrants with late effects of polio. Method. The strategies were explored by interviews with 12 immigrants from Eastern Africa with late effects of polio. Sampling and data analysis was carried out according to grounded theory. Results: The participants struggled for occupational participation and normality in an effort to participate in, and be part of, society. The study identified 14 strategies used by the immigrants in their daily occupations. The strategies can be presented in the following four categories: managing physical capacity; promoting occupational performance; strategies for gaining respect; and preparing the ground for one's existence. The participants struggled to find a balance between physical capacity and meaningful occupations, conception of their own and others' norms and values, and living conditions in Swedish society. The strategies were related to the participants' will to manage daily occupations, maintain social relationships, and be part of society. Conclusions: The strategies revealed that the participants strive to participate in occupations and society. This study reinforces the importance of occupation for immigrants with disability. The results highlight the need for adequate health care and rehabilitation but should also alert other social institutions.
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