Peer Support Experienced by Mothers of Children With Congenital Heart Defects in Sweden
Author:
Affiliation:
1. The Department of Women’s and Children’s Health, Uppsala University, Uppsala, Sweden
2. The Swedish Red Cross University College, Huddinge, Sweden
3. Ersta Sköndal Bräcke University College, Stockholm, Sweden
Abstract
Funder
Hjärtebarnsfonden
Publisher
SAGE Publications
Subject
Family Practice,Community and Home Care
Link
http://journals.sagepub.com/doi/pdf/10.1177/10748407211067788
Reference26 articles.
1. Bellander T., Nikolaidou Z. (2017). Building health knowledge online: Parents’ online information searching on congenital heart defects. Literacy and Numeracy Studies, 25(1), 4–19. https://doi.org/10.5130/Ins.v25i1.5358
2. Bernecker S. L., Williams J. J., Caporale-Berkowitz N. A., Wasil A. R., Constantino M. J. (2020). Nonprofessional peer support to improve mental health: Randomized trial of a scalable web-based peer counseling course. Journal of Medical Internet Research, 22(9), e17164. https://doi.org/10.2196/17164
3. Bratt E.L., Järvholm S., Ekman-Joelsson B.M., Johannsmeyer A., Carlsson S.Å., Mattsson L.Å., Mellander M. (2019). Parental reactions, distress, and sense of coherence after prenatal versus postnatal diagnosis of complex congenital heart disease. Cardiology in the Young, 29(11), 1328–1334. https://doi.org/10.1017/S1047951119001781
4. Bratt E.L., Järvholm S., Ekman-Joelsson B.M., Mattson L.Å., Mellander M. (2015). Parent’s experiences of counselling and their need for support following a prenatal diagnosis of congenital heart disease—A qualitative study in a Swedish context. BMC Pregnancy & Childbirth, 15, 171. https://doi.org/10.1186/s12884-015-0610-4
5. Bruce E., Lilja C., Sundin K. (2014). Mothers’ lived experiences of support when living with young children with congenital heart defects. Journal for Specialists in Pediatric Nursing, 19(1), 54–67. https://doi.org/10.1111/jspn.12049
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