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Hello! I am new to the group. I have two children my son will be 3

in two weeks, w/o CF and my daughter who is 5 months w/ CF. I am

having a hard time knowing what to do with all the emotions that this

diagnosis brings and would like some advise from those who have been

through it. Our daughter was diagnosed at 1 week of age and has been

on Creon since 3 weeks. She is very healthy for which we are very

thankful, but I feel like I am waiting for the ball to drop and just

woudl like to know what to expect. Any advise on how to focus on the

positive instead of the negative aspects of this disease would also be

appreciated.

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