I've just had the results back of a recent blood test and found out I'm a carrier for one of the common types of CF. Thankfully DP isn't a carrier of any of the common types but we want him to have a full screen to rule out the possibility of the baby having CF.
They were done at our local FMU. They rang me this afternoon with the results of our tests but said there was nothing further to be done at the moment and not to worry. We're seeing the consultant again mid January but I'll be 28 weeks by then so the element of choice won't be here anymore.
They did give me a number to call should I have any questions. I guess my first question will be can they please test DP for all CF mutations?!
Why wouldn't they offer me that as standard seeing as I'm a carrier?