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Journal of the Korean Child Neurology Society 2006;14(2):303-309.
Published online November 30, 2006.
The Experience of the 1st Daegu-Gyeongbuk Multicenter Epilepsy Camp for Children and their Parents to improve the understanding of Epilepsy.
Sung Min Cho, Soon Hak Kwon, Doo Kwun Kim, Jun Sik Kim, Jin Kyung Kim, Han Koo Moon, Woo Saeng Park, Ji Hyun Yeo, Hyun Hee Oh, Eun Ju Lee, Jun Hwa Lee, Bo Young Kim
1Department of Pediatrics, College of Medicine, Dongguk University Gyeongju, Korea. mhlee@smc.samsung.co.kr
2Department of Pediatrics, School of Medicine, Kyungpook National University, Daegu, Korea.
3Department of Pediatrics, School of Medicine, Keimyung University, Daegu, Korea.
4Department of Pediatrics, College of Medicine, Catholic University of Daegu, Daegu, Korea.
5Deptment of Pediatrics, College of Medicine, Yeungnam University, Daegu, Korea.
6Department of Pediatrics, College of Medicine, University of Ulsan, Ulsan, Korea.
7Department of Pediatrics, Daegu Fatima Hospital, Daegu, Korea.
8Department of Pediatrics, Masan Samsung Hospital, College of Medicine, Sungkyunkwan, University, Masan, Korea.
9Graduate School of Social Welfare, Ewha Womans University, Seoul, Korea.
Abstract
PURPOSE
This study was undertaken to announce our experience of the 1st Daegu- Gyeongbuk Multicenter Epilepsy Camp for children and their parents to improve the understanding of epilepsy. METHODS:We held the camp on February 25th to 26th, 2006 at Gyeongju. 33 families with epileptic childlend joined the camp. At the end of the camp, we performed a survey with 37 questionnaires to obtain data concerning the parents' understanding of epilepsy and the satisfaction with the camp. Data was analyzed with SPSS 10.0 program using frequency analysis. RESULTS:Parents knew about epilepsy but for some degrel still wanted to get more information about epilepsy. Parents were satisfied with the educational programs but not with the recreation programs. CONCLUSION:This study suggests that more social approaches such as an epilepsy camp is needed to provide the families with more information fot the understanding about epilepsy.
Key Words: Epilepsy, Epilepsy camp, Stigma
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