Exploring the Social Impacts of a Summer Camp for Youth with Tourette Syndrome
Research in Outdoor Education
Cornell University Press
Although a wealth of research exists documenting the positive social outcomes promoted by summer camps, research specifically examining youths with Tourette Syndrome (TS) within the camp context is lacking. This study utilized a phenomenological approach to explore the social impacts of a weeklong camp specifically for youths with TS, involving focus groups with 18 campers aged 10–16, interviews with 10 staff members, and participant observations compiled by the researcher. Multiple themes and sub-themes concerning the social impacts of the camp experience were identified, including (a) relatedness (not alone and self-assurance); (b) social development (friendships, optimism, educational experience, and bullying); (c) programmatic outcomes (unique program opportunities and cabin bonding); and (d) various implications for professional practice and future research are discussed.
Griswold, M., Hegarty, C.B., Harrist, C., Trauntvein, N.E., & Griswold, D. (2014). Exploring the Social Impacts of a Summer Camp for Youth with Tourette Syndrome. Research in Outdoor Education, 12, 15-35.