I am getting it done. My midwife made it seem like it was fairly routine, but other people have told me that it has a high rate of false negatives and their doctors suggested that they not add to their worry. It is still three weeks away, so I will definitely be reading more about it between now and then. One thing I do know is that it involves a really good ultrasound and after my last fuzzy one I am ready to see my baby again!
I got mine done the other day - loved see everything and making sure everything was on track and baby had all its parts lol. It's a nice relief too. I understand the undue stress that comes from false positives (or false risk calculations I should say)but I think it's also important to be prepared if anything is wrong and to be proactive in working with specialists, etc.
Feb '16 Siggy Challenge: Favorite Thing About Fall: Haunted Houses and Scary Movies!
Yep, I got a referral to get it done - so probably doing that in 3 weeks after I come back from vacation. It was either that or the genetic testing. Besides, it's an extra ultrasound to see the LO!
I was going to but it would have costed us $600 out of pocket since it's not covered by insurance and we haven't reached our deductible yet.. Oh well. Stupid money!!
Our insurance covers it so we're doing it. I'd prefer to know of any underlying issues prior as would my H.
Also, a big fear of mine becoming pregnant again was not being able to build as strong of a bond with this baby. With my twins, I got to see them on the ultrasound once a week so I felt like I "knew" then exceptionally well before they were even earthbound. If I have a free opportunity to see the baby, I'm gonna take it (despite that not being what this is for)
Mine's next week. I had it done with my son too. No risk that I know of since it's a simple ultrasound and it's covered by my insurance. I just see it as another opportunity to see the little bean, since I had the blood test which should rule out most of the things the NT scan looks for.
We decided not to, even though I do understand why people do want it. I just can't imagine getting a false negative and dealing w/ it until baby was born or whenever they rule out anything actually being wrong. Too stressful for me to handle. We didn't have it w/ our other 2 either. I think if we had family history or other indicators, we may have.
I'm having my NT ultrasound in a week. I had it done with my son in 2012 and am ok with any noninvasive tests. It's just a screening though, so no proof that anything is wrong. However it will help us decide if we want to pursue any other testing.
I'm having mine in a week... It's comforting just to get the next ultrasound!! If anything should be wrong with baby or detected, I would just want to prepare myself as much as possible rather than be surprised later.
My Dr.'s office pairs the NT scan with the blood work that screens for chromosomal abnormalities. I'm doing both, which due to my age and history are fortunately covered by my insurance. When my daughter had issues I felt like we had too little information way too late, so I'm trying to avoid that this time.
It's really comforting to know I'm not the only one! I feel like I really want to be as prepared as possible if there is something wrong but it threw me off that I didn't know anyone else doing the screening. I have no reason to think there will be a problem, I'm mostly just excited to get another look at my baby!
I had planned to get it done, but my insurance won't give a straight answer on whether or not it will be covered since it is paired with the blood test and they only cover genetic screening if THEY, not my doctor, deems it necessary. BCBS of FL are TWs.
F16 Sep Siggy Challange - Fav Thing About Fall (even though "fall" won't be here until at least Dec)
My drs office is finding a place for me in another city that will take my insurance, and see what's covered for me. How nice of them. They said they will call me with my appt date and everything
I had planned to get it done, but my insurance won't give a straight answer on whether or not it will be covered since it is paired with the blood test and they only cover genetic screening if THEY, not my doctor, deems it necessary. BCBS of FL are TWs.
Grr! Doesn't that drive you crazy when insurance companies think they know better than your own doctor?!!
I'm going in for this test today... It will be my first U.S. since 6 weeks, so I hope all is fine. I'm also doing the blood screening for Down syndrome at the same time, so I'm worried, but somewhat excited to see it again:)
I have a call into my dr to clarify, but what is the 12 week test called that's a blood test for Down syndrome? I thought I was doing the NT test via blood this week, but it sounds like it's more of an ultrasound, and now I'm confused. (And i know it's not the harmony % test)
I have a call into my dr to clarify, but what is the 12 week test called that's a blood test for Down syndrome? I thought I was doing the NT test via blood this week, but it sounds like it's more of an ultrasound, and now I'm confused. (And i know it's not the harmony % test)
I think we're talking about the same thing. At least at my doctor, I'll have an ultrasound and then a blood test and they'll combine those results to get the likelihood the baby will have Down syndrome or one of the other trisomy
There's a blood test that's been around for quite a while called a quad screen that I think looks for hormones that can indicate chromosomal abnormalities. . The NT is a nuchal translucency (sp?) scan that uses ultrasound to measure behind baby's neck. If it's over a certain length it can be a marker for chromosomal abnormalities. The newer blood test which looks at baby's DNA that's floating around in Mom's bloodstream is called several different things including Materniti21 and Harmony.
Had my NT scan yesterday and it came back "slightly abnormal" at 3.2. Trying not to freak out while I wait 2 weeks for blood test results. If the risk comes back high I'll probably do amnio diagnostic test.
I had mine yesterday 12+1 and the NT was 1.6mm I don't know what that means the sonographers barely explain anything... She said the baby looked really good though so I'm guessing it was normal.
Did it today. My OB office does it routinely; they don't even ask if you want it. I didn't realize it was something so many people opted out of. I liked seeing our little sweetie waving and jumping!
I had mine yesterday 12+1 and the NT was 1.6mm I don't know what that means the sonographers barely explain anything... She said the baby looked really good though so I'm guessing it was normal.
Mine was 1.5mm and dr. said you can't get a better result so be happy- all is normal. They'll also do blood work in second tri and take both tests into account to give final result, but as of now, all is good.
Feb '16 Siggy Challenge: Favorite Thing About Fall: Haunted Houses and Scary Movies!
Did it today. My OB office does it routinely; they don't even ask if you want it. I didn't realize it was something so many people opted out of. I liked seeing our little sweetie waving and jumping!
So funny how different OB offices are. We were asked if we wanted it and even had to sign extra paperwork because we did.
This is exactly what's happening for me in a few days. I get a blood draw w/NT screen (u/s) but it's not for the cell free tests like Harmony or MaterniTi.
I have a call into my dr to clarify, but what is the 12 week test called that's a blood test for Down syndrome? I thought I was doing the NT test via blood this week, but it sounds like it's more of an ultrasound, and now I'm confused. (And i know it's not the harmony % test)
I think we're talking about the same thing. At least at my doctor, I'll have an ultrasound and then a blood test and they'll combine those results to get the likelihood the baby will have Down syndrome or one of the other trisomy
Did it today. My OB office does it routinely; they don't even ask if you want it. I didn't realize it was something so many people opted out of. I liked seeing our little sweetie waving and jumping!
So funny how different OB offices are. We were asked if we wanted it and even had to sign extra paperwork because we did.
Yea I had no clue people opted out either. My doctor just said to schedule it with the hospital kind of matter of factly ... But I'm glad I did it for some peace of mind.
Feb '16 Siggy Challenge: Favorite Thing About Fall: Haunted Houses and Scary Movies!
I had my NT ultrasound and first blood test at 11 weeks and 2 days. The results give you an indicator (percentage) of abnormality. You can choose to do further testing of the indication is high.
My doctor presented it as, "It's optional, but mostly everyone does it because it's noninvasive and provides helpful information." As first time parents, we want this information and it's a huge bonus to get to see our munchkin on the ultrasound again.
The way she explained it to me was similar to what some others are saying: that they combine the info they get from the measurements via ultrasound with the blood work (mine is "Sequential 1") to give you a predictor. For us, it wouldn't cause us to make any decisions other than to do our research and prepare IF there was a high probability that our baby would need extra or special care after birth.
I was recommended to do the test because of my age (34). The u/s people told me a scan at 13weeks and the blood at 10. These two combined give you a risk category... Won't find out til 2nd week of August!
Re: Nuchal Translucency Screening
It's a nice relief too. I understand the undue stress that comes from false positives (or false risk calculations I should say)but I think it's also important to be prepared if anything is wrong and to be proactive in working with specialists, etc.
Also, a big fear of mine becoming pregnant again was not being able to build as strong of a bond with this baby. With my twins, I got to see them on the ultrasound once a week so I felt like I "knew" then exceptionally well before they were even earthbound. If I have a free opportunity to see the baby, I'm gonna take it (despite that not being what this is for)
Spontaneous pregnancy #1
DD1 July 31, 2011
Trying for #2 since Oct 11
Spontaneous pregnancy #2= Ectopic #2= lost left tube
Spontaneous pregnancy #3= DD2 January 29, 2016
Spontaneous pregnancy #4= Ectopic #3
Spontaneous pregnancy #5= Baby #3 is a BOY!!!
Child #1 June 2012
Child #2 Feb 2014
Child #3 Feb 16
BFP 3/9/17
Me: 32 Hubby: 31
Married 12/29/12
Started TTC July 2014
Miscarriage August 2014
Emmett born February 2016
Expecting Baby #2 in August 2017
http://www.fertilityfriend.com/home/544e80
guessing it was normal.
Mine was 1.5mm and dr. said you can't get a better result so be happy- all is normal. They'll also do blood work in second tri and take both tests into account to give final result, but as of now, all is good.
Yea I had no clue people opted out either. My doctor just said to schedule it with the hospital kind of matter of factly ... But I'm glad I did it for some peace of mind.