Mason Archival Repository Service

One in a Million: Navigating Health Information and Advocacy in Rare Disease Diagnosis and Treatment

Show simple item record

dc.contributor.advisor Kreps, Gary L.
dc.contributor.author Hughes, Lindsay en_US
dc.creator Hughes, Lindsay en_US
dc.date.accessioned 2013-08-09T15:38:04Z
dc.date.available 2013-08-09T15:38:04Z
dc.date.issued 2013 en_US
dc.identifier.uri http://hdl.handle.net/1920/8219
dc.description.abstract Background: Rare diseases represent an important public health issue; prevalence is an estimated 30 million patients in the United States. Efforts from advocacy organizations and governmental outreach based on assumptions derived from mainstream diseases fail to address the unique challenges rare diseases present, resulting in alienation, isolation, stigmatization, and poor health outcomes. Methods: Current ehealth practices were compared with needs reported by patients and HSOs with a selected rare disease via 1. content analysis of threads (n=852) from a pre-eminent online advocacy community; 2. content analysis of advocacy, government, and non-scientific resources 3. Cross-sectional surveys (n=57); 4. In-depth interviews (n=28); 5. Focus Group Discussions (n=12). Findings: Analyzed qualitatively and quantitatively using a priori codes to evaluate Weick's model of organizing and Uncertainty Management Theory as well as codes emerging via Grounded Theory, the exemplar rare disease community fails to meet the needs described by patients and HSOs. Interactions were low (mean = 1.81 responses, median and mode = 0) using the mainstream mechanism. Conversely, patients informally organizing reported a reduction in isolation and equivocality and were more equipped with strategies to manage their health. However, they lacked ability to advocate on a large scale and questioned information credibility. Conclusions: Rare disease patients rely on peers for social support and information. Leveraging the resources of well-known advocacy groups with a patient-centered model will enable peer-to-peer support and information sharing, leading toward the understanding of the pathogenesis and side effects associated with rare diseases. en_US
dc.format.extent 216 pages en_US
dc.language.iso en en_US
dc.rights Copyright 2013 Lindsay Hughes en_US
dc.subject Public health en_US
dc.subject Behavioral sciences en_US
dc.subject Organizational behavior en_US
dc.subject ehealth communication en_US
dc.subject grassroots community mobilization en_US
dc.subject online health communities en_US
dc.subject rare disease communication en_US
dc.subject uncertainty management theory en_US
dc.subject Weick en_US
dc.title One in a Million: Navigating Health Information and Advocacy in Rare Disease Diagnosis and Treatment en_US
dc.type Dissertation en
thesis.degree.level Doctoral en
thesis.degree.discipline Communication en
thesis.degree.grantor George Mason University en


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search MARS


Browse

My Account

Statistics