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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...

So I think I'm finally coming out of my "denial" about my 9 month old daughter having CF...so I thought I would introduce myself and my situation. We found out she had CF after a newborn screen showed one mutation, then went through 2 sweat tests and genetic testing to determine the other...