I'm sure there are a few of us in J17 doing or considering doing NIPT. At my 8 week appointment today the nurse gave me some information on Harmony, but I know there are also a few others (Maternit21, Panorama, etc.). Has anyone done these before with previous pregnancies that want to share any info? Or anyone considering doing the testing with this pregnancy that wants to discuss?
Re: NIPT (Noninvasive Prenatal Testing)
I want to ask if i can do it anyway because the results of the NIPT come back faster. The full NT/quad screen results weren't in for me until 18 weeks. I don't want to wait that long.
I would do it if my insurance covered it - I just like to have as much information as possible - but I've heard that it can cost many hundreds of dollars out of pocket, and that it's only covered by insurance if you are considered high risk. If my doctor is going to consider me AMA I might do it, but I'm on the fence (my due date should be like 3 days before my 35th birthday).
I will say that I think it's a great option for people who are high risk or who have genetic disorders running in their families to make sure that the baby is healthy. But I do a massive side-eye on people that are all OMG I WANT TO KNOW THE SEX OF THE BABY 8 WEEKS EARLIER THAN THE ANATOMY SCAN SO I'LL DO THIS. It can take 2 weeks to get results because the labs are so backed up, I absolutely side-eye people that are just doing it for funzies, as that delays the response time for people that have actual genetic concerns that they are testing for (that opinion may be better served as a FFFC, but whatever).
Insurance did cover my NT scan and quad screen, so I did that. Not as accurate, but it was something. It came back with as close to a zero percent chance of issues as possible, so no further testing was necessary. but then our first pediatrician was a complete idiot, and told us at DD's 2 month appointment that she thought she might have Down Syndrome (based, apparently, on her almond shaped eyes (which look just like mine) and the fact that she didn't resemble DH or I strongly) and it was a whole thing where we freaked out for two weeks waiting to see a specialist who looked at DD for about 3 minutes and said "there is no way on earth this baby has Down Syndrome." Long story short, we have a new pediatrician now, and that whole experience made me really want the NIPT if my insurance would cover it or it would be affordable, so that I don't have to go through that again. I have heard that some doctors offices have deals with the labs that do the testing where if your insurance doesn't cover it, they just charge you a flat fee of like $95 or $200 or something like that...I'm going to ask my doctor about that and if I can make it work I will.
In the meantime I need to research the actual OOP cost. I know these companies usually offer discount vouchers. If it's doable I think that'll be my preference.
ETA: that's the cost quoted for the Harmony
MaterniT21 $200
Harmony $130
Verifi $226 (They sometimes offer a "Peace of Mind" discount you may qualify for, dropping the price to $99.)
Panorama $795-$995
Keep in mind, I am in no way affiliated with any of these companies. These prices may not be set in stone, but these were the answers I got when I called. I thought all of the prices were very reasonable with the exception of Panorama.
Does anyone know if one test is necessarily better or more accurate than the others? It seems like they all test for the same things.
Me: 25 | DH: 29
MC: March 2016
BFP #2: October 2016
Our fur-baby is a black Labrador Retriever.
https://www.fertilityfriend.com/home/5a8aa2/
@mirdamae03 and @mrlight that is awesome info on the costs, thanks! I'm definitely planning to ask my doctor about it. Though it would be kind of a bummer to miss the NT scan because I do really like to see the baby! I assume it's just one or the other and not both.
And I agree with @motherofdragons it does take a while to get full quad screen results. The NT scan and first round of blood work I did at 12 weeks last time, but there was one other thing they couldn't test until 16 weeks, I forget what it was. I got the 12 week results in about 4 days, released to me online, and that included the odds on Down Syndrome and Trisomy 13 and 18. I totally forget what the 16 week blood draw was for, but again that took an additional 3-4 days to get released to me. I want to say that one was spina bifida? but I can't remember. At any rate, I felt comfortable enough once I got the 12 week results to tell people about my pregnancy.
When is the NIPT done? Is that like 10 weeks, and you have results around 12 weeks? I have two friends that did it because they were AMA so it was covered by insurance, and another friend that was high risk due to type 1 diabetes, so her insurance covered it as well.
I dont know if theres there's value in doing the NT scan to assess risk of non-chromosomal abnormalities in addition to doing the cell-free DNA test. I'll plan to ask my MW about that.
This time I would really like to get NIPT right off the bat to avoid that potential scare scenario again, but it will depend on cost.
anyhow. In hte past we never did hte early screenings, mainly for me because I've known so many people who had things flag as a possible issue and then got pushed into high risk categories, with fear looming over hte pregnancy and a lot of interventions. We also were always team Green. This time, after 3 boys, we both very much want a girl and Aden absolutely fin ding out.
This time dh is a little freaked about my being older and since it is a surprise too, he's just more concerned. I'm not particularly concerned for hte testing, but I'm fine doing it since we will find out hte sex early. Flame worthy on my end, yes absolutely, but half the equations wants the testing.
11/18/16 missed m/c 9w1
08/03/17 no hb 8w
TTC #1 since 9/2015
BFP #1 1/14/16, MC 3/23/16
BFP #2 9/21/2016, EDD 5/30/2017
Thanks for this post, btw. I was so emotional when we discussed this with the doctor and it kind of ruined my appointment and day. My husband put it in good perspective, he said if we can afford to do it, just add it to the list of tests they already do, assume you'll get good results like everything else, and put it out of your head. Which is exactly what I'm doing.
We are team green, and were previously as well. You can't put a notation in your paperwork so when they send the results you don't find out the sex of the baby.
We became pregnant February of this year with a very much wanted pregnancy. Due to my age (37 at the time), the testing was offered to me and we decided to do it. You just get your blood drawn and they send it off to the lab for testing. The test itself is much more accurate than the NT as it tests the baby's DNA which is in your bloodstream. My OB wanted it done at 10 weeks exactly. A week a half later I received a voicemail and knew it was bad news when it was my OB herself calling me. We were the .5% and the results came back that my son had Trisomy 21. She said the test was over 99.8% accurate but it was still a screen and not an actual diagnostic. So my dh and I decided we wanted to have CVS done to verify the diagnosis before we made any decisions. In the meantime, we had a Disney cruise that had been planned for over a year so we went and gave my son the time of his life. In hindsight, it was nice to have that last bit of time with my baby. Every night I would sit out on the balcony and talk to him and sing and just spend time with him. When we got back home we went in to speak with a genetic counselor and then went in for the CVS. During the u/s we discovered he had already passed away. He was measuring 13w6d and it had just happened. We went ahead with testing after his passing which confirmed the T-21 diagnosis.
Sorry for the book, but I'm here if anybody has any questions about the test and what happens. Needless to say, I'm sitting here in blind terror until we can have the NPT done and confirm this little one is healthy. The chance of a repeat diagnosis is only 1%, but odds don't mean anything once it's happened to you. That said, I'm grateful for the test and the opportunity for an early diagnosis. I can't imagine not finding out until later. 10 weeks gives you enough time to get all the facts and make an informed decision about how to proceed. I'm hoping and praying that every single one of us gets good news this time around.
Gavin - 8/27/10
*TW*
Gabriel - 2nd tri loss 5/17/16 Trisomy 18 & 21
Hope - 2nd tri loss 12/7/16 complications from pneumonia
Me: 25 | DH: 29
MC: March 2016
BFP #2: October 2016
Our fur-baby is a black Labrador Retriever.
https://www.fertilityfriend.com/home/5a8aa2/
@mrlight at my appt today the dr said Panorama will negotiate down to $100-$200 for people who do not have coverage for it. We currently have BCBS which is not covered.
I had Materniti21 with my son and an NT scan/quad blood work. I'm assuming that I will have the same this time.
With that said - my NT scan failed us with our third. We had zero soft or hard markers and I was 1 in 1000. We ended up w a birth diagnosis. It was traumatic to say the least. He is now almost 15 months though and an absolute joy! Its DS awareness month and I've been sharing little nuggets of info over on Instagram if anyone would like to follow.
I am a nervous wreck. The NIPT's are simply screenings, not diagnostic. A part of me thinks we should also do CVS for peace of mind, but I hate the risks. We wouldn't terminate a pregnancy, but I couldn't handle another surprise like we had a year ago! This pregnancy alone has been surprise enough to last me the next 8 months haha! I was on the mini pill and got pregnant soooooo....maybe we should buy a lotto ticket since we seem to be the "small chance" in two different scenarios haha!
and this is a mini pill pregnancy here too
11/18/16 missed m/c 9w1
08/03/17 no hb 8w
@LilLee11 I would love to follow your instagram if you want to DM me. I can't imagine a birth diagnosis, especially with all of the emotions and craziness of dealing with birth and pp. I'm very much a planner by nature and I think that's why the NIPT would definitely help give me peace of mind and I'd at least feel like I could get somewhat prepared if something raised a flag on the test.
@LilLee11 - you sound like an awesome mama / lady
BFP #1 6/13 DD 3/14
Mirena 10/14-5/16
BFP #2 9/2/16, CP confirmed 9/8/16
BFP #3 10/10/16 EDD 6/22/17
My insurance does not cover it, but said they would this time since I've had so many losses. We did not do it with DD's pregnancy because they did not cover it and it costs $900. So we decided not to do it again this time even though they will cover it.
Our thoughts are that it wouldn't change anything about our decision of what to do with our child, so even though it would be nice to know a bit earlier than the 20 week ultrasound, I'll probably stress less if I find out something is wrong at 20 weeks instead of 12 weeks.
17 months TTC and 1miscarriage, 1 chemical pregnancy, rainbow baby born 2/16/15
TTC 2.0
16 months TTC, 2 chemical pregnancies, EDD 6/3/17
The insta is psashleybbutler Its public since Ive been sharing our journey, so I dont mind sharing here.
@AshcicleGAH! I knew I'd be calling myself out if I replied to this thread. ha! Im not ready to announce to the group yet...probably wait until we do genetic testing around 11 weeks. This wasnt planned aaaaaat all. For a couple like us that plan every single thing in our life, Cameron and this pregnancy have been crazy! Remember when my doctor found that cyst? I went in a week later because I felt so awful and wanted to check the cyst. Well, found out I was pregnant...whoa! Im super early, 6 weeks, so this is going to be my longest pregnancy yet
Awe thank you!! Thank goodness for good beach lighting that made me look waaaay better than in reality