Do you all go through a CF center for care? My daughter is 10 months old and we don't go to a "center" but we are at Mayo which used to be accredited (?) but I'm just wondering what your opinions are on this? She's been healthy thus far (diagnosed via newborn screen and subsequent sweat tests and DNA testing at 6 wk) so I'm not worried about anything major at this time and don't know that I necessarily would be, I feel very comfortable with her DR (we are most likely moving up north and I would like to keep Mayo as her CF care clinic, am skeptical of U of M) I just read a lot of your questions/answers and see that many of you do a lot more therapy than we do with my daughter (CPT 2x/day)...wondering if the common treatment is to do more than what we're doing?...thoughts greatly appreciated!!