Help! I need to decide ASAP if we are going to do the NT scan or not. At first I wanted to do it and then changed my mind after talking with the OB and now I think that I want it again.
Basically I am concerned that the NT scan will make me worry (more than normal) throughout my pregnancy so I am trying to avoid that. However, I think that I need to know if something is going on with my babies, plus, selfishly I think I would like to try for guesses on the sexes. However, I doubt we would do amnios if it came down to it... I just don't know what the right decision is.
What did you guys decide and why? Does you mind change either way due to twins? Oh, other info, I am currently 33 but will turn 34 prior to the babies being born. Also, we didn't do the test for DS and I didn't regret it at all.
Re: NT scan, or not???
I did it and would do it again. Here are my thoughts (I was 36 for the NT scan, so that factored in) 1) I got to see a high resolution u/s of my baby 2) if something was wrong, I would want to know to either prepare myself mentally and have any other necessary precautions in place.
The NT scan was one of the best days of my life. It was the day it finally sank in that I was most likely going to have a baby. I was bawling on the table at the site of her. So, I'm pro-NT scan for sure.
I'm 33, and wasn't too concerned. We weren't going to terminate if anything was found wrong anyways, but I did it since it was covered. Plus I just wanted another U/S
)
IVF #1: ER 03/29/10; ET 04/01/10: transferred 2 embies; Beta #1 (9dp3dt)- 45; Beta #2 (11dp3dt)- 91= BFP
FET#1: ET 04/18/12: transferred 4 embies; Beta #1: >2 = BFN
IVF #2: ER 06/20/12; ET 6/25/12: transferred 2 embies; Beta #1 on 7/5/12= BFN
8/16: hysteroscopy for polyp removal
11/11: hysteroscopy #2 for yet another polyp removal
FET#2: ET 12/15/12: transferred 3 embies; Beta #1 (9dp5dt): 12/24/12: 426; Beta #2 (11dp5dt): 845= BFP
u/s 1/9= triplets!; miscarried all three on 1/10/13...
This is why we did not do it:
My OB stated that under 35, it is really more of a $$ maker for the Dr than anything. He offered me an extra ultrasound if that was why I would request one, but he did not see a reason to have one at my age, with our risk factors. It is an additional test, cost ect .
Because we're fancy like that.
I'm not sure we would've gotten it done had the midwife we had at first not assumed we were getting it done. BUT, it was the coolest thing ever. It's finally starting to sink in that we are having two babies. It was so awesome to see them kicking and moving around.
I, however, wouldn't do it just to see the genders because what we got today was just a guess and she wouldn't commit to anything when she told us. Good luck with your decision, I'm sure you'll make the right one!
Clomid M/C 8 weeks 2/08 *IVF #1-DD born 3/09
*Surprise BFP-T18 baby lost at 13w 1/10 *FET #1-DS born 2/11
Your hesitation sounds just like mine was, except we don't want to know genders. I am 36 but my donor was 30 so chances of any issues were quite small. Ultimately we decided to do it mostly so I could confirm all was ok and see the babies again (did not do the b/w part though). I also live in Canada so our health care system covered it.
and like pp said, it did make the babies seem more "real"!
Same here but I am 32. Good luck!
I always do every testing......I want to know everything-the good and the bad.
And, for us, if anything came back "abnormal," we would move forward with an amnio. So, I guess I'm not helping you with your decision!
If there is nothing else you would do with abnormal results, then I guess you could skip it.
But......here is a question to think about. If something is wrong, do you want to know during the pregnancy or at birth? If you can be 100% fine knowing at birth, then I guess you can skip the NT Scan.
GL with your decision!
Delurking and I am late on this, but wanted to share. We did the NT scan/quad screen and my bloodwork came back with an increased risk for Down Syndrome. My level two ultrasounds were normal. The doctor really pushed for an amnio, I went in for it and chickened out. My risk was about 1:180 which is high for my age (IVF was on my 34th birthday), that is still less than 1% chance . DD does not have DS and yes, I did worry until I saw her at birth. I was not consumed by it, because we were thrilled she was our little girl regardless of the diagnosis.
I would do the scan again, but I hope I can skip the blood work. If I had only had the scan I would not have been placed in an increased risk pool.
The maor benefit to me was that if they detect DS or a NTD, then you can plan to deliver at a hospital that can accomodate you. They can detect a lot of congenital abnormalities (heart/ skeletal, brain) at the 20 week scan.
Good luck on whatever you decide.
This was DH and I exactly. I'm someone who likes to be prepared. If the outcome would mean switching hospitals or a different pedi, then I wanted to know so I could be making arrangements. If I had it to do over, I'd totally do it again.
I did and am with this baby as well. Mainly because I wanted the extra ultrasound but I also wanted to be prepared if there were any problems.
Just FYI though - guesses that early could very well be wrong. Our girl at 12 weeks is definitely a boy!
BFP with no treatment!
It was recommended because of our age (36/37 at the time). So at 13w1d I went in for my scan. Pretty wild seeing how active ds was yet I couldn't feel a thing.
Because of my age and the fact that it was a MD recommended/ordered scan my insurance covered it 100% originally it was only going to be covered at 80%
Absolutely. They will be able to see way more at the anatomy scan.
I skipped the NT. I was 28 at the time and had a vanishing twin in there. I didn't want to see a false positive from the bloodwork due to the vanished twin and have to worry about that. I also knew that I would not have done a CVS or amnio if the NT came back positive. So I just waited until the anatomy scan to find out if there were any issues. I'm a huge worrywart though, so that was the best option for me.
FET #1 = BFP on 5/2011