I'd like to come back to the question of the testing, because I think it's so critical. You said a number of times that it's hard to make a diagnosis, but I kind of wonder about that. It could be partly, as you say, lack of awareness on the part of medical practitioners, but there is a test available. We heard Mr. Young's story about its availability in very few places. It seems to me that's more the issue. Unfortunately, this is quite a familiar story that we hear.
There are incredible technologies available in Canada for health care, but it's accessibility, so I think it's linked very much to the need for national guidelines and a national treatment program. It seems so inequitable that in some places you might be able to get the test, if you know where to look, and in other places you don't have a hope in Hell, because the right one doesn't exist.
I'll put this question as well to the foundation. I think they're here on Tuesday. But I wonder if you have more information about that. It's not that the diagnosis is hard, it's that people don't have access to the testing and they're not being referred to it. Is that a more accurate description?