The 'place' of data.

Health disparities research has been at the forefront for many researchers, organizations, and funding agencies. Collecting, interpreting, and disseminating data on particular disparate populations are at the core of this research process, data which have been interpreted to be meaningful to the benefit of and use by communities. The purpose of this paper is to explore the question, "How is data used?" with an appreciation for indigenous beliefs and community based research.