Again, it goes to that jurisdictional quagmire. National health policies for indigenous people are set at the federal level. A lot of the data collection is happening in hospitals or at the provincial level. What is collected doesn't truly reflect what, maybe, the national data needs are.
I think we really need to push the provinces to ensure they're collecting the disaggregated data. Then, with public health at the local and regional levels, we need to be instilling how important this disaggregated data is. If we don't know who the people are who are being affected by this, I don't know how we even have a hope of addressing this at the community level.