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Research Article

Describing the impact of aphasia on close family members using the ICF framework

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Pages 1184-1195 | Received 14 Jan 2013, Accepted 12 Aug 2013, Published online: 24 Sep 2013

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Edna M. Babbitt, Linda Worrall & Leora R. Cherney. (2022) “It’s like a lifeboat”: stakeholder perspectives of an intensive comprehensive aphasia program (ICAP)”. Aphasiology 36:3, pages 268-290.
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Jamileh Azizbeigi-Boukani, Ahmad Reza Khatoonabadi, Saman Maroufizadeh & Siamak Abdi. (2021) Validity and reliability of the Persian version of the Stroke and Aphasia Quality of Life Scale-39 (SAQOL-39). Aphasiology 35:6, pages 859-873.
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Tanya A. Rose, Sarah J. Wallace & Sibin Leow. (2019) Family members’ experiences and preferences for receiving aphasia information during early phases in the continuum of care. International Journal of Speech-Language Pathology 21:5, pages 470-482.
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Sarah J. Wallace, Caroline Baker, Caitlin Brandenburg, Lucy Bryant, Guylaine Le Dorze, Emma Power, Madeleine Pritchard, Miranda L. Rose, Tanya Rose, Brooke Ryan, Kirstine Shrubsole, Nina Simmons-Mackie, Leanne Togher & Megan Trebilcock. (2019) A how-to guide to aphasia services: celebrating Professor Linda Worrall’s contribution to the field. Aphasiology 33:7, pages 888-902.
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Venusia Covelli, Alberto Raggi, Chiara Paganelli & Matilde Leonardi. (2018) Family members and health professionals’ perspectives on future life planning of ageing people with Down syndrome: a qualitative study. Disability and Rehabilitation 40:24, pages 2867-2874.
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Michelle C. Attard, Yasmine Loupis, Leanne Togher & Miranda L. Rose. (2018) The efficacy of an inter-disciplinary community aphasia group for living well with aphasia. Aphasiology 32:2, pages 105-138.
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Sarah J. Wallace, Linda Worrall, Tanya Rose, Guylaine Le Dorze, Madeline Cruice, Jytte Isaksen, Anthony Pak Hin Kong, Nina Simmons-Mackie, Nerina Scarinci & Christine Alary Gauvreau. (2017) Which outcomes are most important to people with aphasia and their families? an international nominal group technique study framed within the ICF. Disability and Rehabilitation 39:14, pages 1364-1379.
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Tamilyn Bakas, Nenette M. Jessup, Susan M. McLennon, Barbara Habermann, Michael T. Weaver & Gwendolyn Morrison. (2016) Tracking patterns of needs during a telephone follow-up programme for family caregivers of persons with stroke. Disability and Rehabilitation 38:18, pages 1780-1790.
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Rebecca L. Nund, Nerina A. Scarinci, Bena Cartmill, Elizabeth C. Ward, Pim Kuipers & Sandro V. Porceddu. (2016) Third-party disability in carers of people with dysphagia following non-surgical management for head and neck cancer. Disability and Rehabilitation 38:5, pages 462-471.
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Michelle C. Attard, Lucette Lanyon, Leanne Togher & Miranda L. Rose. (2015) Consumer perspectives on community aphasia groups: a narrative literature review in the context of psychological well-being. Aphasiology 29:8, pages 983-1019.
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Miranda l. Rose & Michelle C. Attard. (2015) Practices and challenges in community aphasia groups in Australia: Results of a national survey. International Journal of Speech-Language Pathology 17:3, pages 241-251.
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Katie Monnelly, Jane Marshall, Lucy Dipper & Madeline Cruice. A systematic review of Intensive Comprehensive Aphasia Programmes – who takes part, what is measured, what are the outcomes?. Disability and Rehabilitation 0:0, pages 1-15.
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Ellayne S. Ganzfried. (2018) Living With Aphasia: Realities, Challenges, and Opportunities. Perspectives of the ASHA Special Interest Groups 3:2, pages 68-79.
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