At one point I was going every 6 months (probably grade school), then it went to every 3 months (high school maybe), and then I actually got to where I was going every two weeks right before the transplants. During the times that I was not going very often, if I was sick, it was more often than the every three months. Now that I have had the transplants, I still see my CF doc, but it's only every 6 months again. He just checks on me to keep track of the diabetes (from the transplants) and my GI problems. I go to the Cleveland Clinic for my lung problems now since that is where I had the transplants.