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"I'm not alone": a qualitative report of experiences among parents of children with eating disorders attending virtual parent-led peer support groups.
Grennan, Laura; Nicula, Maria; Pellegrini, Danielle; Giuliani, Kelly; Crews, Erica; Webb, Cheryl; Gouveia, Maria-Rosa; Loewen, Techiya; Couturier, Jennifer.
Afiliación
  • Grennan L; McMaster University, 1280 Main St W, Hamilton, ON, L8S 4L8, Canada.
  • Nicula M; McMaster University, 1280 Main St W, Hamilton, ON, L8S 4L8, Canada.
  • Pellegrini D; McMaster University, 1280 Main St W, Hamilton, ON, L8S 4L8, Canada.
  • Giuliani K; Reach Out Centre for Kids, 471 Pearl St, Burlington, ON, L7R 4M4, Canada.
  • Crews E; Reach Out Centre for Kids, 471 Pearl St, Burlington, ON, L7R 4M4, Canada.
  • Webb C; McMaster University, 1280 Main St W, Hamilton, ON, L8S 4L8, Canada.
  • Gouveia MR; McMaster Children's Hospital, 1200 Main St W, Hamilton, ON, L8N 3Z5, Canada.
  • Loewen T; Reach Out Centre for Kids, 471 Pearl St, Burlington, ON, L7R 4M4, Canada.
  • Couturier J; Phoenix Wings Eating Disorder Recovery Initiative, 872 Devonshire Ave, Woodstock, ON, N4S 5R8, Canada.
J Eat Disord ; 10(1): 195, 2022 Dec 15.
Article en En | MEDLINE | ID: mdl-36522772
The treatment of children who have eating disorders (EDs) requires extensive involvement from parents. Parents have voiced a need for greater support, and one way to meet this need is through peer support. Using end-of-study interviews, this study qualitatively described the experiences of parents of children who have EDs who participated in virtual parent-led peer support groups (vPLPSGs) for 6 months. Our findings suggest that vPLPSGs are beneficial for parents of children who have EDs. Participants had positive perceptions of the group organization and structure, the parent facilitators, and other parent attendees, and valued the support and educational resources received in the group. Parents noted it was particularly helpful to be able to speak with other parents who understood their experiences, which helped them feel less alone in their difficulties with their child. Parents also noted an improvement in their relationship with their child who has an ED, and believed that these groups should be readily available and accessible. Suggestions for improvement included dividing groups based on children's ED diagnosis, duration of illness, and geographical location. Further expansion and study of these groups is warranted, as they appear to be a valuable support for families affected by EDs.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Qualitative_research Idioma: En Revista: J Eat Disord Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Qualitative_research Idioma: En Revista: J Eat Disord Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido