Experiences of Tourette Syndrome Caregivers With Supportive Communication
The experiences of Tourette syndrome (TS) caregivers with supportive communication are examined in this qualitative investigation. TS is a childhood-onset neurodevelopmental disorder marked by a combination of involuntary verbal and motor tics lasting for more than 1 year. Although individuals are i...
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Veröffentlicht in: | Qualitative health research 2020-08, Vol.30 (10), p.1480-1490 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The experiences of Tourette syndrome (TS) caregivers with supportive communication are examined in this qualitative investigation. TS is a childhood-onset neurodevelopmental disorder marked by a combination of involuntary verbal and motor tics lasting for more than 1 year. Although individuals are impacted the most by TS, the stress for caring for a child with TS takes an emotional and physical toll on the caregiver. Eleven participants shared their experiences with receiving supportive communication by taking part in semi-structured interviews. Data analysis yielded three themes: (a) TS caregivers describe their experiences as a struggle; (b) they seek out specific social support from friends and families; and (c) they frequently receive social support that increases instead of reducing stress. |
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ISSN: | 1049-7323 1552-7557 |
DOI: | 10.1177/1049732320915444 |