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Original Research

Communication change in ALS: engaging people living with ALS and their partners in future research

ORCID Icon, ORCID Icon & ORCID Icon
Pages 675-681 | Received 29 Mar 2018, Accepted 06 Jul 2018, Published online: 04 Oct 2018

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Read on this site (1)

Dominika Lisiecka, Helen Kelly & Jeanne Jackson. (2021) How do people with Motor Neurone Disease experience dysphagia? A qualitative investigation of personal experiences. Disability and Rehabilitation 43:4, pages 479-488.
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Articles from other publishers (3)

Anna Huynh, Kerry Adams, Carolina Barnett-Tapia, Sanjay Kalra, Lorne Zinman & Yana Yunusova. (2023) Accessing and Receiving Speech-Language Pathology Services at the Multidisciplinary Amyotrophic Lateral Sclerosis Clinic: An Exploratory Qualitative Study of Patient Experiences and Needs. Journal of Speech, Language, and Hearing Research, pages 1-13.
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Camille Paynter, Susan Mathers, Heidi Gregory, Adam P. Vogel & Madeline Cruice. (2022) The impact of communication on healthcare involvement for people living with motor neurone disease and their carers: A longitudinal qualitative study. International Journal of Language & Communication Disorders 57:6, pages 1318-1333.
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Anne Hogden, Camille Paynter & Karen Hutchinson. (2020) How can we improve patient-centered care of motor neuron disease?. Neurodegenerative Disease Management 10:2, pages 91-97.
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