T
tammykrumrey
Guest
Has your daughter had a sweat test done yet? And I do think that doing the more extensive panel for genetic testing is important. My husband carriers a mutation that does not pop up on the small panel of 24 or so. When my second daughter was born they ran the test prior to us leaving the hospital (at the request of our pediatrician) and two weeks later I was told that she was only a carrier. I felt in my heart that it was wrong and our CF clinic at SLCH told me to bring her down for a sweat test anyways. While getting the sweat test done, I asked to see my older daughters genetic test, and I found that my second daughter was not tested for one of the mutations and I knew then that my heart was correct. Of course the sweat test came back positive the following day and two weeks later it was confirmed with the more extensive panel. The mutation does show up in the most common 36 gene mutations in our case, just not the most common 24.
I am happy that our clinic didn't just stop with the first test done at birth. She could had went longer being undiagnosed, depending on when she would had started having problems. The sooner the better. Good luck with this. I am sure it is very frustrating for you.
I am happy that our clinic didn't just stop with the first test done at birth. She could had went longer being undiagnosed, depending on when she would had started having problems. The sooner the better. Good luck with this. I am sure it is very frustrating for you.