Abstract

This personal essay uses the first-person voice to describe the author's experience as a dependent adult growing up in America after the Americans with Disabilities Act of 1990. The author's personal story is contextualized as a reality specific to her race, gender, class, and degenerative physical disability. Descriptions of the author's need for significant assistance serve as anchors for the essay's more open-ended questions concerning care on a massive scale for multiple generations of people. Such questions seek new social imaginaries that challenge Western social values of independence, individuated desires and activities, and an autonomous private life.

pdf

Share