Abstract
Alopecia Areata is an autoimmune disorder that impacts 6.2 million Americans and 142 million people worldwide. "The Lived Experience of Alopecia Areata" is a qualitative, phenomenological study that explored the essence of the experience of living without hair for the development of nursing therapeutics, support services, and sensitive provider resources.
Sigma Membership
Iota Epsilon
Type
Presentation
Format Type
Text-based Document
Study Design/Type
N/A
Research Approach
N/A
Keywords:
Alopecia Areata, Health Care Resources and Qualitative, Phenomenolgy Research
Recommended Citation
Caro, Sarah Ruth, "The Lived Experience of Alopecia Areata" (2019). Convention. 324.
https://www.sigmarepository.org/convention/2019/presentations_2019/324
Conference Name
45th Biennial Convention
Conference Host
Sigma Theta Tau International
Conference Location
Washington, DC, USA
Conference Year
2019
Rights Holder
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Acquisition
Proxy-submission
The Lived Experience of Alopecia Areata
Washington, DC, USA
Alopecia Areata is an autoimmune disorder that impacts 6.2 million Americans and 142 million people worldwide. "The Lived Experience of Alopecia Areata" is a qualitative, phenomenological study that explored the essence of the experience of living without hair for the development of nursing therapeutics, support services, and sensitive provider resources.
Description
45th Biennial Convention 2019 Theme: Connect. Collaborate. Catalyze.