I think that the costs of having people being misdiagnosed are actually pretty slight because most of the people who are getting the so-called false positive result get the treatment and then they get better.
One other thing, if I could.... Why aren't the patients represented? Because there's this kind of misunderstanding. In CanLyme, we have a lot of people who are doctors, research scientists, geologists. We have a lot of people and a lot of expertise. They would love to help, but they're being blocked. They're not being taken seriously. That's my real question. Why are patient advocates blocked from being in the room, asking the difficult questions?