HI!
My husband was diagnosed with cf 1.5 years ago at 35. (I posted sometimes in this forum, but haven´t post for a long time). His health is very good and we are thinking of having children with ivf. In fact we are starting it this week!!!!!.
I have taken the full ambry test and I am negative for cf mutations.
The test sais that the risk I am a carrier would be 1/2500. So I guess that the risk of having a child with cf is very low, but I am still worried. I cannot help wondering is that risk stimate is accurate since we don´t know yet how many cf mutation exists.
Do you think I am "overworried"? Have any of you have a child with cf after having a negative full ambry test?.
The ginecologist said we could use a donor so we wouldn´t have any risk, but we would prefer to use his sperm if the risk is low.
Sorry this is so long <img src="i/expressions/face-icon-small-smile.gif" border="0">. I am so excited of starting IVF!!!!.
My husband was diagnosed with cf 1.5 years ago at 35. (I posted sometimes in this forum, but haven´t post for a long time). His health is very good and we are thinking of having children with ivf. In fact we are starting it this week!!!!!.
I have taken the full ambry test and I am negative for cf mutations.
The test sais that the risk I am a carrier would be 1/2500. So I guess that the risk of having a child with cf is very low, but I am still worried. I cannot help wondering is that risk stimate is accurate since we don´t know yet how many cf mutation exists.
Do you think I am "overworried"? Have any of you have a child with cf after having a negative full ambry test?.
The ginecologist said we could use a donor so we wouldn´t have any risk, but we would prefer to use his sperm if the risk is low.
Sorry this is so long <img src="i/expressions/face-icon-small-smile.gif" border="0">. I am so excited of starting IVF!!!!.