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So my hubby and I were talking today and I feel SOOO regretful for getting that amnio. I feel like we were completely railroaded into it and Im actually kind of pissed now! We didnt stick to our original plans of no invasive treatments unless absolutely necessary. Well, figuring out if its one of 2 easily dealt with syndromes is NOT necessary! (to me)
It seemed to me that the genetics counselor played on our emotions when she told us that we could mentally prepare for whats going to happen, that we could go on community boards and meet people in Sacramento with the same thing and while that sounded reassuring at the time, I have my family and close friends for support if or when that time comes. SHe also said that my pregnancy would be different with an abnormality, the baby will be very small and fragile but birth would be the same. Well, Im halfway done and Im fine and the baby is the perfect weight and height so SOMETHING is working right! AND when I asked her if we could take the day and think it over because both David and I were VERY overwhelmed with all the info, she said "Well today is really the only chance you have, we have time, the doc is here and our appointments fill up fast you wouldnt be able to get one" so we had to do it 15 minutes after we had the u/s.
The last thing Im realizing is that on the first u/s they DEFINITELY saw all these problems, the level 2, they didnt see ANY of the big ones seen in the first but "think" they saw a heart defect and the nuchal fold is "barely noticeably thick" I asked her how thick it was and she said" not much, but I did notice it".
So, finally after all this bi*ching I just did, our decision is to NOT get the results of the amnio and stay in this peaceful bliss
: that we are experiencing over being blessed with another daughter. And also to wait until the baby is bigger (farther along) to go to the cardioligist. Her tiny heart is SO small, (but its obviously working because shes right on track), that I think that waiting till its bigger would be beneficial because they could get better pics and wouldnt have to guess.
So I need your honest advice, does anybody think I should see the cardiologist now? (Ill call my mw tomorrow) Would there be anything seen on an echo now that cant wait a couple months?
It seemed to me that the genetics counselor played on our emotions when she told us that we could mentally prepare for whats going to happen, that we could go on community boards and meet people in Sacramento with the same thing and while that sounded reassuring at the time, I have my family and close friends for support if or when that time comes. SHe also said that my pregnancy would be different with an abnormality, the baby will be very small and fragile but birth would be the same. Well, Im halfway done and Im fine and the baby is the perfect weight and height so SOMETHING is working right! AND when I asked her if we could take the day and think it over because both David and I were VERY overwhelmed with all the info, she said "Well today is really the only chance you have, we have time, the doc is here and our appointments fill up fast you wouldnt be able to get one" so we had to do it 15 minutes after we had the u/s.
The last thing Im realizing is that on the first u/s they DEFINITELY saw all these problems, the level 2, they didnt see ANY of the big ones seen in the first but "think" they saw a heart defect and the nuchal fold is "barely noticeably thick" I asked her how thick it was and she said" not much, but I did notice it".
So, finally after all this bi*ching I just did, our decision is to NOT get the results of the amnio and stay in this peaceful bliss

So I need your honest advice, does anybody think I should see the cardiologist now? (Ill call my mw tomorrow) Would there be anything seen on an echo now that cant wait a couple months?
