The purpose of this study was to examine the construction of "mild" motor disabilities from the viewpoint of life-span
development. The criteria for "mild" disability were that: 1) the individual acknowledged his/her disability as "mild",
2) he/she held an officially registered concession, and that 3) the individual was able to maintain an independence in
his/her activities of daily living. The author conducted individual, semi-structured interviews with three subjects who
had cerebral palsy or birth palsy. The collected data were analyzed qualitatively, focusing on how the subjects
reconstructed their lives. The results suggested that the subjects had coped with devaluation of their experiences, and
situated their disabilities at the core of the self. They also started to recognize other disabled peers. Moreover, this
study indicated that these subjects were frequently unable to obtain support in social environments ruled by the ablebodied,
and their disabilities could not be easily understood by others. Hence, they fell into the dilemma of careseeking,
when support was needed.
View full abstract