Abstract
This article draws from an ethnographic study to examine the understanding of personhood that emerges as a Hispanic family from Southern Colorado responds to the diagnosis, illness, and loss of a child with a severe genetic disorder. The focus of this article is on the cultural/religious ethos that shaped this family's resistance to the ideologies and practices that threatened to define their son by his genetic disorder and to diminish his value as a person. The case study exemplifies, and is consistent with, other families in the larger study. The concept of personhood that emerges stands in sharp contrast to, and as a critique of, the ideologies and practices of “geneticization” that define and diminish the value of a person with a genetic disorder.
