Just to be clear, I think the doctor respectfully referred to them as 2006 guidelines, as though they were significantly outdated, but I think it's important to note that they were extensively reviewed again in 2016.
One way to resolve these kinds of debates is to ensure, as we go forward, that besides the scientists, the doctors, and the others whom PHAC would be engaging, there's also the community of caregivers, such as our doctors here, and some of the patients' or advocacy groups that have formed around people with Lyme disease.
Do you see a way of engaging those voices in reviewing guidelines, in ensuring that we're staying current, and that alternative guidelines are being considered through the engagement of patients and—