2nd Trimester

Baby with a Congential Heart Defect

I am pregnant with my second child and my first child was born with 3 heart defects that required surgery when she was 4 days old. Layla is now almost 4 and has done remarkably well. We have our fetal echo on February 26th and the last couple of weeks I have been nervous that this baby may have heart problems as well.

Has anyone had a child that had a CHD and then the next child didn't?

Re: Baby with a Congential Heart Defect

  • One of my best friends is one of four kids, and she is the only one with a CHD.  I know she has at least one little brother.
    DS born 12/2012
    Little Squeaker due 6/2015
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  • I have done some research and from what I can tell that it is rare to have more than one child with a CHD, I have just been having these dreams lately that have me paranoid, I am sure for no reason. Thank you for your inputs!

  • Yes.  My first had a severe complex cardiac defect and sadly did not survive.  My second was a perfectly healthy boy.  We had prenatal echo at 22 weeks and repeat echo when he was about 3 months old.  

    Best wishes to you!
    TTC #1 12/2009
    BFP #1 1/2010, M/C 6 weeks
    BFP #2 6/2010, DD lost to
    congenital heart diseasewe are heartbroken.

    TTC #2 4/2011, diagnosed MTHFR, FVL
    Four natural cycles BFN; Clomid IUI BFN; Follistim IUI BFN;
    1/2012 IVF #1 BFN
    4/2012 FET BFP #3
    5/2012 7w1d u/s: anembryonic demise; M/C @ 8w.
    6/2012 found Stage II/III endo on laparoscopy, removed w/ laser.
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    Vacation, break, second opinions, on to new RE.
    1/2013 Surprise chemical pregnancy BFP #4 (break cycle), IVF #3 postponed.
    2/2013 TI w/ hormonal support, prednisone, aspirin, Lovenox, acupuncture gave us a miracle BFP #5!
    Heartbeat on U/S at 6w1d!
    Baby,please stay!!
    Our miracle baby boy arrived 10/2013!  We are so in love!!

    10/2014 Surprise BFP #6
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  • My first had a heart defect and my second had no sign of any defects whatsoever. The chances of another child having a defect are so slim. Hoping the best for you. I know how stressful it is!
  • My first had a CHD that was corrected at 5 months old.  He is a happy, energetic 2 year old now.

    We just had our Echo for the pregnancy.  Everything checked out perfect.  

    I was told by the cardiologist that two siblings with heart defects is very, very rare.  It's hard to find a lot of literature about it...it just doesn't happen.

    I will add that I was incredibly nervous and scared going to our appointment last week.  I cried every day for a week.  There was nothing I could do about it, but I was still so scared of something being wrong.  Once you have that bad experience (a negative anatomy scan), it is hard to forget it.  

    It is okay to be emotional - just try to stay positive.  It also helped to keep my mind off of it.  It should be exciting - but for Mom's like us, it is terrifying.

    ME: 31 PCOS - DH: 32 Perfect. 
    TTC #1 started 8.2010. 
    BFP #1 3.2.11Blighted ovum, missed m/c, 4.3.11-6.22.11 Provera

    BFP #2 Aug 2011 Clomid 50mg+Met missed m/c found 9w5d | cytotec 10.26.11 
    BFP #3 - CD36 - Jan. 2012 - 100mg Clomid + 2000met-  Baby Boy born 10.06.12 with 1 in a billion CHD. Perfect otherwise. 

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    Open Heart Surgery @ 5 months old.Happy, healthy, and as normal as could be!  We thank God every day.EP/BF for 12.5 months

    TTC#2 - November 2012

    BFP #4:  O'd on CD25 (Aug. 2014).  DD May 6, 2015. RCS planned.
    Beta@14dpo: 184, 17dpo: 520.  44 hr. doubling time.  p4: 54U/S 8 weeks 1 day, 161 bpm
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  • My older sister was born with 3 congenital heart defects in 1986. She didn't survive. I was born with a murmur that went away on its own as I grew. My brother was born with a very small VSD that also healed on its own. Our issues were so minor compared to our sister.

    I am 18 weeks into my first pregnancy. My anatomy scan is in 2 weeks and I will also have a fetal echo at the end of January. I was told by my OB that the heart defects are not genetic. They are doing the echo as a precaution based on the family history.

    I am so happy to hear your daughter is well and I hope everything goes well with your echo. I would try not to worry too much.
  • This is a huge fear of mine. I had a congenial defect that when undignosed until I was almost 30. Open heart surgery is not a walk in the park. I don't want my child to have to go through this. I do think that typically defects are not to be genetic. I think that sometimes genetics do play a roll.

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