The use of art as a creative research method to understand psychosocial care needs for children with rare diseases

Author:

Buckle Niamh1ORCID,O’Neill Amy2,Sweeney Alison3,McNulty Sandra4,Bracken Shirley3ORCID,Awan Atif35,Sinnott Shannon36,Gibbs Lisa7,Larkin Philip8,Kroll Thilo1,Somanadhan Suja9

Affiliation:

1. UCD School of Nursing, Midwifery and Health Systems, University College Dublin, Belfield, Dublin, Ireland

2. School of Psychology, Trinity College Dublin, the University of Dublin College Green, Dublin, Ireland

3. Children’s Health Ireland at Temple Street, Dublin, Ireland

4. Childvision National Education Centre for Blind Children, Dublin, Ireland

5. RCSI University of Medicine and Health Sciences, Dublin, Ireland

6. Children’s Health Ireland at Crumlin, Dublin, Ireland

7. Melbourne School of Population and Global Health, University of Melbourne, Carlton, VIC, Australia

8. Lausanne University Hospital and University of Lausanne and Institute for Higher Education and Research in Healthcare (IUFRS), Switzerland

9. UCD School of Nursing, Midwifery and Health Systems, University College Dublin, Stillorgan Road, Belfield, Dublin D04 V1W8, Ireland

Abstract

Background: Even though a disease might be labelled as ‘rare’, it is estimated that 450 million people globally are affected by rare diseases, and 70% of these conditions are among children. All children have the right to good quality healthcare and to be heard despite the country or state they live in. While children’s drawings are increasingly used in qualitative research to understand children’s experiences and perceptions of illness, few studies in the rare disease field utilize this method. Objective: This study examined drawings of children with rare diseases to gain insight into their experience living with their condition. Design: A qualitative phenomenological research study was employed to explore and understand children’s and young people’s experiences and perceptions of living with rare diseases through research participants’ artistic expression in drawings and responses to semistructured interview questions. Methods: A purposively selected sample of children ( n = 7) attending tertiary paediatric healthcare was invited to participate in a once-off art session facilitated by an art therapist, followed by semi- structured interviews. A practical iterative framework for art-based data analysis was developed to incorporate art interpretations, semi-structured interviews and reflexive analysis. Results: As drawing is an open visual medium, a framework was developed to analyse the drawings thematically. The themes that emerged from the drawings were fitting in versus feeling different and supportive relationships. These themes highlight the contradictory experience of living with a rare disease and the role of family and friends in influencing the participants’ experiences. Conclusion: Developing an art analysis framework benefitted the thematic analysis of the participants’ drawings. This study concludes that art can help offer opportunities for children to express themselves and for health and social care professionals to understand the impact of rare diseases on their everyday lives.

Funder

Children’s Health Foundation

Publisher

SAGE Publications

Reference37 articles.

1. European Commission. Rare diseases, https://health.ec.europa.eu/non-communicable-diseases/expert-group-public-health/rare-diseases_en (n.d. accessed 28 February 2023).

2. Global Genes. Rare disease facts, https://globalgenes.org/learn/rare-disease-facts/ (n.d. accessed 29 February 2023).

3. A retrospective review of the contribution of rare diseases to paediatric mortality in Ireland

4. Healthcare access, satisfaction, and health-related quality of life among children and adults with rare diseases

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