Hi Ladies,
I just got some b/w results back, and apparently I am a carrier for a cystic fibrosis gene mutation (??). DH now needs to get tested to see if he is also a carrier. Unfortunately the nurse I spoke to could not give me a whole lot of info because in her words she "is not a genetic specialist", so I was left to my own devices and googled. It seems the only risk for baby is if we are both carriers, which seems fairly unlikely. Still, I am nervous, and wondering if anyone has experienced anything similar?
TIA...
ETA- Spelling