Inherently, parents take care of their children until they become independent adults; similarly, children care for their progenitors in their old age. However, this socially normal order may be reversed when progenitors experience a chronic disease while their children are still young. This paper analyses the lived experiences of young caregivers (YCs) and how a family member’s illness affects them. The present study employs the intergenerational family solidarity (IFS) theory and draws on qualitative data gathered from in-depth, semi-structured interviews with YCs living in Spain (N = 8). The article reveals that the illness of a family member strengthens IFS and family unity, involves a learning process, causes psychological distress, and creates a need for emotional support. Additionally, the study identifies some minor differences based on the gender of YCs. The paper’s main contributions are twofold. Firstly, it contributes to the international literature on YCs using the theoretical perspective elaborated by Bengtson and Roberts in 1991, which is commonly applied to the relationship between adult children and elderly parents or grandparents and grandchildren. Secondly, the article provides new empirical considerations for the investigation and social recognition of YCs, particularly in Spain, where the family serves as a strong cornerstone of social protection, literature on this phenomenon is scarce, and social awareness is limited.
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Cavallotti et al. (2025) studied this question.
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