Hi Jeff.
Ditto to what most people here have said. Even though we all would rather not have to be here, this is a great way to find support and answers to questions that you might have. Welcome.
Many people have said to write down some questions that you have for when you go to the CF Center. Also, you might want to make sure to bring a paper and pen so that you can write down more questions as you have them and any info that you find important.
Some questions you might want to ask are:
Will she need enzymes?
What is the best thing I can do right now to help her health in the future?
How do I do CPT?
What kind of approach do you (as a clinic/doctor) use with CF? Is it more of a "wait and see" or more of a pro-active approach.
I'm sure that you will have many more questions than this, but these are a few that we remember having.
As Liza said, remember that she is still your little girl. If she is your first baby, treat her with all the love that you would had she not had CF. Yes, she has CF, but first and foremost, she is your child.