Abstract

Food allergy (FA) may be disproportionately prevalent and burdensome among populations of non-White race/ethnicity and/or populations with lower socioeconomic status in the US. To ameliorate health disparities in FA, data are needed regarding barriers to successful management—particularly among patients who are at-risk. Specifically, this study aims to better understand relationships between FA-related psychosocial burden, disease management, and food insecurity (FI).

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