My doctor said it was optional and was basically saying that unless you are going to terminate the pregnancy if there is a problem, then there is really no need to do it. DH and I talked and if there is something wrong, we still would not terminate, so we opted out. Any one else?
Re: Anyone not getting the NT scan?
this, even more so w/ my DH, he wants as much info as is available.
We would not terminate the pregnancy if something were to be found either -- but we still decided to do the NT scan. It was recomended to me and I get to see LO again - so I figured why not. I am also low risk so I was not really concerned about it or anything. It just gives you your odds - it's not a positive/ negative - pass/ fail type of test.
~Still rooting for my TTC buddy ShanRich0810~
~ DD 5/15/00 ~ DS 2/27/03 ~ DD 9/29/04 ~ DS 7/3/07 ~
Daughter #1 - February 12, 2010
natural m/c March 11, 2011 at 8 1/2 weeks
Daughter #2 - January 11, 2012
Ectopic pregnancy discovered November 6, 2012 at 6 weeks
Daughter #3 - January 19, 2014
Started our exploration into the world of international adoption June 2012. We have no idea what this is going to look like but we are excited to find out!
We are not.
Brayden (5 1/2) born 12.28.06
Hailey (4 1/2) born 2.25.08
Taylor (8 Months) born 12.26.11
First off, I've been reading (on here) about the NT scan and everyone is talking 12 weeks - my doctor doesn't do any testing for it until between 15-17 weeks. Secondly, my doctor's office orders blood work and unless the blood work is questionable, he doesn't do the NT scan. My husband and I would not terminate but we're not worried because there is absolutely no history of anything like that in our families.
Good luck!!!!
I have a friend who found out at the NT scan that her baby had a terminal condition. The baby would probably never make it to full term and would die in utero. Or if the baby did make it would die during or shortly after. She terminated because she didn't want to make her child suffer. If she hadn't done the NT she would not have known about this until her 20 week u/s and it would have been a MUCH more heartbreaking decision to be halfway through the pregnancy.
I'm getting it. Not trying to scare anyone, but just letting you know that there are more things that it looks for than Downs and spina bifida,conditions that could be lived with.
Oh my ob would have a field day chewing your doctor out! When we talked about the NT scan last year, I told her I wouldn't terminate and she got pissed and said "the purpose of the test is not to have you terminate the pregnancy if something is wrong, it is to prepare us for the future". She went on to talk about how if you have a high risk for a downs baby that downs babies carry risks of heart problems and they need to be born at a hospital with a higher level NICU and to have specialists on board at the birth to make sure the baby is taken care of correctly.
Yes, if you deliver at a regular hospital and find these things out at the birth they can transfer your baby to high level NICU hospital and get the specialists in but then you would be in a different hospital than your baby. There is the chance that they may have problems where time is of the essence and if you are having to transfer them to another hospital, who knows what may happen.
After hearing her views of things, I decided it is best to do the optional non-invasive testing.
The test is non-invasive and I see it as a means to prepare myself. I wish that I would have known about DS's condition before he was born (even though we had a NT scan, it could have never predicted it).
Additionally, in response to a PP, just because there is no history of genetic disorders in your family doesn't mean that it can't happen. We have no genetic disorders in our family.
Make a pregnancy ticker
I agree. Well said. We don't know what we'd do - most likely never terminate - but there are far worse conditions that won't make it past second tri or be stillbirth, so I never say never. We are doing the NT scan so that we can be prepared for a special needs child, if need be. Last pregnancy I found out at our NT scan that I'd had a missed miscarriage that week due to Trisomy 18. We wouldn't have known for a while, had we not had that scan. I am therefore scared as hell to have this (simple, non-invasive) procedure again, but I want all the information I can get.
To each their own, I guess, right?
BFP#1 - 8/27/10 - D&C 10/27/10 @ 13 weeks to Trisomy 18
Missing our Angel Baby Gabriel
BFP#2 - 3/18/11 - CP 3/19/11 BFP#3 - 4/27/11 - Due 1/9/12
From what I understand from talking with my OB, scans for genetic disorders have a high screen positive rate, but about 98% of those with positive results go on to have healthy babies. We ruled out the genetic disorders we are high risk for (ex: Cystic Fibrosis) before TTC, and we wouldn't terminate if LO did have a problem, so we're skipping the early scans. We'll see him/her in 2nd tri. But that's just us...we're young, healthy people with no past history of any problems. To each their own.
We are doing it because it is rec'd because I am of AMA. We have no plans to terminate the pregnancy but my OB says it is always best to prepare with as much info and early detection if there is a problem.
If the scan/bloodwork comes back in favor of downs we will opt out of the amnio. We wouldn't want to risk miscarriage with getting the amnio done.
Married 1/2/99.
TTC since 4/09.
Diagnosed PCOS. Diagnosed Hypothryoid 11/09.
SHG & SA normal. PCOS Research study started 5/10.
Clomid/Femara cycle #1 - 6/10 = BFN
Clomid/Femara cycle #2 - 7/10 = BFP #1 - Missed miscarriage 9/2/10
11/12 - BFP #2 - 11/22 - m/c
5/1/11 - BFP #3 - Pre-eclampsia, IUGR & bed rest from 32w. DD born via induction 1/4/12.
Ok, this is just wrong. Sorry. The NT scan does NOT test for genetic disorders. It tests for 3 trimsomies: Down Syndrome, Trisomy 13 and Trisomy 18. These are NOT genetic. These don't run in the family; if someone in the family had one of these, it does NOT mean you have an increased risk of your baby having it. Conversely, if no one in either family has these, it DOESN'T mean that your baby isn't at risk.
Also, there aren't "false positives". The results are given to you in a ratio: 1:2000; 1:10,000 etc. If you come back "at risk", say 1:25, it's NOT a confirmation that the baby has one of these. Only an amnio can confirm.
But as to whether you get the scan, that's up to the individual couple. I wanted to be prepared, but that's just me. It was non-invasive and gave me real piece of mind.
I don't know where you're getting your info from, but having a family Hx of Down's does indeed put you at a higher risk for having a baby with Downs, and more OB's will strongly recommend the testing if you do have a family Hx. Maybe it gave you peace of mind, but like I mentioned in my earlier post, it also gives some people undue stress and anxiety.