Pregnant after IF

Cystic Fibrosis gene carrier

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 

After 1.5 years TTC, IUI #2= BFP 12/2/12

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Re: Cystic Fibrosis gene carrier

  • Don't quote me, but I THINK I remember my OB saying if both MH and I were carriers there was ~25% chance the baby would have CF.
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  • imageKdgTeacher:
    Don't quote me, but I THINK I remember my OB saying if both MH and I were carriers there was ~25% chance the baby would have CF.

     

    Yes, I believe 25% chance baby has it, 25% chance baby doesn't have it, & 50% chance baby is a carrier. 

     

    My boss found out both him & his wife were carriers after she got pregnant & their baby is a carrier.


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  • Thanks for those stats, it puts things in perspective.  

    Does anyone know if I am correct in my thought that if my husband is not a carrier then we are most likely in the clear?

    After 1.5 years TTC, IUI #2= BFP 12/2/12

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  • Both KDG and Rachey have it right.

    as for your additional question, yes you would be OK. My RE had me tested before any treatments. Since DH has a history in his family, they started by testing me. Since my results were good, no further testing was done as it wasn't an issue.

    hope that makes sense. 


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  • Thanks for your feedback, everyone!
    After 1.5 years TTC, IUI #2= BFP 12/2/12

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  • My brother found out that he was a carrier when his baby was tested at birth and found to be a carrier. Because of this, I was tested in the initial round of bloodwork at my RE's office. I am also a carrier, but luckily, MH is not. There is still a crazy small chance that the baby could have it because they only test for the 20+ most common mutations of the gene. So, theoretically, MH could have a rare form, but that is unlikely.

    So, if YH is not a carrier, it is not 100% that baby can't get it because YH could have a rare form. That's very unlikely though. Good luck with YH's test! 

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