Thank you.
My next question is for Dr. Dorian.
I think many of my colleagues have been questioning the whole issue of why the data isn't much more readily available. CIHI has that responsibility, in order, hopefully, to create some sort of national database that makes sense. You have referenced privacy concerns. I remember, when I was commissioner of health services and medical officer of health for York region, I was the health custodian for six different datasets, and according to our legal counsel, I couldn't talk to myself. In other words, I couldn't cross-reference patient X in one dataset with the same patient in another dataset.
To what extent have you talked to privacy commissioners to ensure that they understand that aggregating data analysis is just so vital for us to understand the science behind disease patterns, etc.? Have you as an association had those types of conversations?