The Psychosocial Impact of Post-Stroke Dysphagia on the Familial Dyad

dc.contributor.advisorShune, Dr. Samantha
dc.contributor.advisorGallagher, Dr. Daphne
dc.contributor.advisorBayne, David
dc.contributor.authorJones, Lija
dc.date.accessioned2022-07-12T20:26:01Z
dc.date.available2022-07-12T20:26:01Z
dc.date.issued2022
dc.description.abstractApproximately 39 to 81% of stroke survivors experience dysphagia or swallowing difficulties (Khedr et al., 2021). Post-stroke dysphagia can have a lasting effect on the quality of life of both the stroke survivor and their informal caregiver. The purpose of the current study was to investigate the psychosocial impact of post-stroke dysphagia on the family dyad. Individual and dyadic semi-structured interviews were conducted. Throughout the data collection and transcription processes, the research team engaged in memo writing. The memos and transcripts were analyzed as primary sources of data in the qualitative study. Results revealed a perceived loss of autonomy and independence, the presence of family and friend support systems, a lack of support from healthcare professionals, and the toll of post-stroke dysphagia and the stroke recovery process on the dyad’s mental health. These findings suggest the importance of providing individualized medical and psychological support for both members of the dyad, including the uncompensated family caregiver who has now altered their lived experiences to better support the survivor.en_US
dc.identifier.orcid0000-0001-7590-3886
dc.identifier.urihttps://hdl.handle.net/1794/27342
dc.language.isoen_US
dc.publisherUniversity of Oregon
dc.rightsCC BY-NC-ND 4.0
dc.subjectDysphagiaen_US
dc.subjectCaregiver Burdenen_US
dc.subjectDyaden_US
dc.subjectCommunication Disordersen_US
dc.subjectSwallowing Difficultiesen_US
dc.titleThe Psychosocial Impact of Post-Stroke Dysphagia on the Familial Dyad
dc.typeThesis/Dissertation

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