Abstract
Children and adolescents with caring responsibilities are an uncontested reality in our society. Most are hidden from public view, and they perform a broad range of caring activities for chronically ill or disabled family members. The research literature has accumulated a comprehensive body of knowledge about young carers' personal needs. However, knowledge and understanding are limited regarding the needs of young carers' families. This knowledge can contribute to preventing children and adolescents from assuming inappropriate caring roles. A qualitative research approach was used to investigate the needs of young carers' families in terms of managing daily caring demands. Nine family interviews were conducted with 34 individuals including 15 young carers during spring/summer 2015 in eastern Austria. Open and axial coding procedures and constant comparison method were used to analyse the data. The findings revealed that young carers' families need to live in accordance with their inherent family logic. Family logic is generated and maintained via (i) family reciprocity that involves the natural help within the family, (ii) individual developmental space that allows family members to be perceived and act as individuals and (iii) network cooperation that offers formal and informal support and recognition from society in general. The findings contribute to understanding how families with caring children manage the caring demands of their everyday lives. The findings also indicate that formal support for families with young carers should consider the individuality of caring arrangements with respect to the holistic and personal needs and avoid stigmatising families that integrate children into caring.
Highlights
During the past two decades, children and adolescents have been recognised as central to the provision of care within the family. These children known as young carers are children and adolescents up to the age of 18 years who regularly provide a significant amount of care for a chronically ill or disabled family member (Becker & Becker, 2008)
Nine family interviews were conducted with 34 individuals, including 15 young carers
Data analysis shows that in order to manage caring demands, families with caring children want to live in accordance with their inherent logic
Summary
During the past two decades, children and adolescents have been recognised as central to the provision of care within the family These children known as young carers are children and adolescents up to the age of 18 years who regularly provide a significant amount of care for a chronically ill or disabled family member (Becker & Becker, 2008). An Austrian study suggests a rate of 3.5% young carers with an average age of 12.5 years and a majority of female young carers (Nagl-Cupal, Daniel, Koller, & Mayer, 2014) This national prevalence data support the notion that the prevalence of informal caring in the underage population is at minimum 2%–4% in all western countries (Becker, 2007)
Sign-in/Register to view highlights & summary Sign-in/Register to access full text options 
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
