This article describes a qualitative focus group research study designed to evaluate the role of an advocacy organization in assisting individuals with spinal cord injury to meet their goals in the community. The importance of basing health services and policy decisions on rigorous research that involves the intended service recipients will be discussed. The findings reinforce the importance of environmental factors, support from family and peers, adequate financial support and access to resources, living life with purpose, and social involvement in contributing to community participation and reintegration. Recommendations are made for ongoing program and service planning.

community programs, program evaluation, qualitative research, rehabilitation, spinal cord injury
This content is only available as a PDF.