Premium
Religious coping and the use of prayer in children with sickle cell disease
Author(s) -
Cotton Sian,
Grossoehme Daniel,
McGrady Meghan E.
Publication year - 2012
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.23038
Subject(s) - prayer , coping (psychology) , medicine , qualitative research , disease , clinical psychology , psychiatry , pathology , theology , social science , philosophy , sociology
Abstract Background While adolescents and adults with sickle cell disease (SCD) have reported using religion to cope with SCD, there is no data examining religious coping in young children with SCD. The purpose of this qualitative study was to: (1) describe the types of religious coping used by children with SCD; (2) describe the content and frequency of prayer used in relation to SCD; and (3) examine how children viewed God/Higher Power in relation to their SCD. Procedure Children with SCD participated in a semi‐structured interview and an art drawing exercise focused on the use of general coping and religious coping. Interviews were coded, organized, and analyzed using a template organizational style of interpretation and NVivo 8.0 qualitative software. Results Of the 19 participants, the average age was 8.05 years (SD ±1.81); 11 were female (58%); all (100%) were African‐American and 9 (47%) were Protestant. Children used religion to gain control, make meaning, and find comfort. Most children reported praying to get well, to keep from getting sick, and to get out of the hospital. Children described a functional God who made them take their medicine or took them to the hospital and an emotional God who made them happy and comforted them when they were sad or scared. Conclusions These children with SCD reported using religion to help cope with the illness. Providers should be aware of the importance of religion to many of these children and integrate religion, as appropriate, into discussions about coping with SCD. Pediatr Blood Cancer 2012; 58: 244–249. © 2011 Wiley Periodicals, Inc.