Disability studies

Online shopping is a common feature of modern adult life and is made easy with targeted advertisements, a large buy now button, and pre-entered credit card information. However, these features do not support making purchasing decisions based on what is best for the individual. Decision making about buying items requires an understanding of basic mathematics, one’s current finances and circumstances, and information about the product, then choosing whether to purchase the item. Adults with intellectual and developmental disabilities (IDD) need explicit instruction on how to make informed decisions regarding online purchases.
The current study sought to evaluate the effectiveness of an intervention package consisting of a mnemonic and behavior skills training (BST) delivered remotely to improve the decision making of three adults with IDD when shopping online through a multiple probe across participants design. Inter-observer agreement and procedural fidelity was assessed throughout each phase of the study and social validity interviews were conducted to measure perceptions of participants, parents, and professionals on the importance of the goals, procedures, and outcomes of the study.

The experiences of those with difficult to diagnose conditions, chronic illnesses, and disability lack intelligibility in an able-bodied world. Much of this originates in the disjuncture between first- and third- person experience as accounted for between patients and their doctors, caregivers, and the greater public. Utilizing the insights of feminist philosophy and disability studies, I will explore how these marginalized identities face consequences in the real world for their embodiment.
I propose that the best methodology to examine the experiences of chronically ill, hard to diagnose, and disabled individuals’ experiences is through the phenomenological perspective. Through utilizing case studies, I will demonstrate the importance of first- to third- person encounters in medicine and receiving adequate treatment. By examining such experiences, as well as my own, through such a perspective, I argue we can work towards creating a more equitable world for the chronically ill, hard to diagnose, and disabled.