Cystic fibrosis in newborns? Do you have a child with CF?
My daughter will be two weeks old tomorrow. We got a call from the pediatrician today that her newborn screening tests came back and she needs to go having further screening to test for cystic fibrosis. Did anyone have to do this and have the tests come back negative that they don’t have it? Neither me or my husband have a family history of CF, so this was a surprise. I’m very worried and hoping it’s a false alarm.

Does anyone have a child with CF? What symptoms did they have as a newborn?

I did read about CF online, but am curious about what other people have experienced with their babies.

Thanks for any information you have.

I’m pregnant with my first baby and I got some tests done and the doctors informed me that my daughter will have Cystic Fibrosis. My mother had a brother and sister who died from the disease when they were quite young. Anyway, I’m wondering what is the current life expectancy for children/people with Cystic Fibrosis and how can you best take care of them to maximize their life?

I found out that my twin daughters have cystic fibrosis, what is the average current life-expectancy for people with this disease and how can the you maximize their life expectancy?