Objective: To determine the experience of sick individuals with sickle cell anemia and their self-care strategies. Methods: This was a qualitative study of 17 individuals with sickle cell anemia. Data collection and analysis occurred simultaneously by open codification and categorization, according to steps in the theory based on data. This procedure led to the development of categories related to the experience of individuals who have sickle cell anemia and their self-care. Results: Experiences of patients who became chronically ill enabled the construction of strategies to better determine the disease, changes in daily life, and the manner in which it affects how patients observe and experience time. Also identified were specific skills for self-care that were developed from lessons learned and mistakes made. Conclusion: We found that individuals with sickle cell anemia had several favorable approaches for adapting to having become sick during adulthood.
CITATION STYLE
Cordeiro, R. C., Ferreira, S. L., & Da Cruz Santos, A. C. (2014). Experiências do adoecimento de pessoas com anemia falciforme e estratégias de autocuidado. ACTA Paulista de Enfermagem, 27(6), 499–504. https://doi.org/10.1590/1982-0194201400082
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