Abstract

AbstractObjective: Medical advances have transformed the rare disease cystinosis from fatal in childhood to chronic and manageable well into adulthood, creating new challenges for patients, families, and providers. In response, families are adapting strategies to meet the demands of the illness and its treatments during a developmentally dense stage of life. Method: The study uses a classic grounded theory approach to understand the experience of adults and emerging adults living with cystinosis. Data were collected through focus groups and/or semi-structured interviews with 46 individuals (22 patients and 24 parents) recruited through national cystinosis advocacy/support organizations. Constant comparative analysis guided data collection and analysis. Results: In the context of much uncertainty, these patients and families described interconnected strategies to negotiate childhood and adolescence, enter into adulthood with self-care skills, and integrate normative developmental tasks with adequate manage...

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