vidence-based health care is considered a gold standard for clinical practice, policy and planning, 1,2 but it is not yet an option for many Aboriginal communities in Canada. (Note that the term Aboriginal is used in this paper, rather than Indigenous, on the basis of guidance from the community-based Aboriginal Children's Health and Well-being Measure Advisory Committee. Aboriginal peoples include First Nations, Inuit and Métis.) First Nations health directors require local health data that extend beyond the biomedical. From their perspectives, the most meaningful data reflect First Nations models of health and are relevant to Aboriginal cultures and contexts. Decision-makers who are responsible for Aboriginal children's health are challenged when searching for relevant health statistics, because most available statistics are based on illness (e.g., rates of diabetes 3,4) rather than wellness. When health data are presented, the results are typically aggregated at the provincial or national level. 5 As a result, there is a critical absence of health data that are relevant at the local level. 6-8 While national and provincial data are helpful in identifying problems, this information is far less helpful in identifying solutions. Given that each Aboriginal population is distinct (culturally, politically and geographically), the assumption that decisions can be made on the basis of provincial or national estimates is inherently flawed. There have been several calls for solution-focused action to promote health among Aboriginal children in Canada. 9-12