Citations (17)
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Leana Nichol, Sarah J. Wallace, Rachelle Pitt, Amy D. Rodriguez & Annie J. Hill. (2022) Communication partner perspectives of aphasia self-management and the role of technology: an in-depth qualitative exploration. Disability and Rehabilitation 44:23, pages 7199-7216.
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Katarina L. Haley, Adam Jacks, Blaise Morrison & Jessica D. Richardson. (2020) Balance and preference in activity participation for informal caregivers of people with aphasia: A questionnaire study. Aphasiology 34:9, pages 1182-1200.
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Michelle C. Attard, Yasmine Loupis, Leanne Togher & Miranda L. Rose. (2020) Experiences of people with severe aphasia and spouses attending an Interdisciplinary Community Aphasia Group. Disability and Rehabilitation 42:10, pages 1382-1396.
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Lauren K. Pettit, Kerstin M. Tönsing & Shakila Dada. (2017) The perspectives of adults with aphasia and their team members regarding the importance of nine life areas for rehabilitation: a pilot investigation. Topics in Stroke Rehabilitation 24:2, pages 99-106.
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Laura Fogg-Rogers, Stephen Buetow, Alison Talmage, Clare M. McCann, Sylvia H. S. Leão, Lynette Tippett, Joan Leung, Kathryn M. McPherson & Suzanne C. Purdy. (2016) Choral singing therapy following stroke or Parkinson’s disease: an exploration of participants’ experiences. Disability and Rehabilitation 38:10, pages 952-962.
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Monika Winkler, Victoria Bedford, Sarah Northcott & Katerina Hilari. (2014) Aphasia blog talk: How does stroke and aphasia affect the carer and their relationship with the person with aphasia?. Aphasiology 28:11, pages 1301-1319.
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Meghann Grawburg, Tami Howe, Linda Worrall & Nerina Scarinci. (2014) Describing the impact of aphasia on close family members using the ICF framework. Disability and Rehabilitation 36:14, pages 1184-1195.
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Meghann Grawburg, Tami Howe, Linda Worrall & Nerina Scarinci. (2013) Third-party disability in family members of people with aphasia: a systematic review. Disability and Rehabilitation 35:16, pages 1324-1341.
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Meghann Grawburg, Tami Howe, Linda Worrall & Nerina Scarinci. (2013) A qualitative investigation into third-party functioning and third-party disability in aphasia: Positive and negative experiences of family members of people with aphasia. Aphasiology 27:7, pages 828-848.
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Articles from other publishers (8)
Grace Lyon, Clare M. McCann, Suzanne C. Purdy & Celia Moore. (2022) “It’s improved the whole lifestyle”: Exploring the family perspective of participation in a Gavel Club for people with aphasia. Clinical Archives of Communication Disorders 7:2, pages 51-60.
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Eldre Wiida Beukes, Alyssa Jade Ulep, Gerhard Andersson & Vinaya Manchaiah. (2022) The Effects of Tinnitus on Significant Others. Journal of Clinical Medicine 11:5, pages 1393.
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Eldré W Beukes, David W Maidment, Gerhard Andersson, Marc A Fagleson, Eithne Heffernan & Vinaya Manchaiah. (2022) Development and psychometric validation of a questionnaire assessing the impact of tinnitus on significant others. Journal of Communication Disorders 95, pages 106159.
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Suzanne Beeke, Anna Volkmer & Claire Farrington-Douglas. (2021) TeleCPT: Delivery of a Better Conversations Approach to Communication Partner Training During a Global Pandemic and Beyond. Perspectives of the ASHA Special Interest Groups 6:6, pages 1776-1785.
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Helen Mach, Carolyn Baylor, Rebecca Hunting Pompon & Kathryn Yorkston. (2021) Beyond the Patient: A Mixed-Methods Inquiry Into Family Members' Involvement in the Treatment of Parkinson's Disease to Target Third-Party Disability. American Journal of Speech-Language Pathology 30:1, pages 169-185.
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Helen Mach, Carolyn Baylor, Rebecca Hunting Pompon & Kathryn Yorkston. (2019) Third-Party Disability in Family Members of People With Communication Disorders Associated With Parkinson's Disease. Topics in Language Disorders 39:1, pages 71-88.
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Darla Hagge. (2014) Alternative Service Delivery Model: A Group Communication Training Series for Partners of Persons with Aphasia. Perspectives on Neurophysiology and Neurogenic Speech and Language Disorders 24:3, pages 114-117.
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