Found out at my 12 week appt that my insurance won’t cover NIPT, so I now have to decide if the 300 dollars is worth the testing. I have my NT scan on Wednesday, so perhaps those results will help me make the decision. I certainly don’t feel the need to test for gender at this point, but it’s more about the trisomy testing...
I am going through the same dilemma. $300 isn't going to break the bank, but I think I'm leaning toward not doing it and just doing the NT. Although I don't remember my Dr. even giving me the option of the NT, so I need to call and figure out what is happening.
Insurance companies are such pain in the butts! I’m looking into the whole thing, as we will likely meet our deductible with the birth, so it may make sense to just pay towards it now. I have to make sure my mind has that right, tho! Either way we will do the tests because of our loss history, but I totally agree that they aren’t completely necessary and people could take it or leave it!
I’m likely having the Progenity blood draw done on Tues after my next appt. I’ve never done an NT scan before with my other pregnancies, but my next appt is with my new OB so we’ll see what she recommends. I’ll definitely be paying out the ass for the birth ($4K out of pocket max) so it’s all going toward that anyway.
*TW*
Me: 32 │ DH: 35 Married 8/16/13 BFP#1 DS 11/13/16 BFP# 2 MMC dx @ 13w 10/30/18 BFP# 3 Preemie DD born at 38w (IUGR) on 8/28/19 weighing 5.5lbs. Our little miracle
TBH, I have no clue how much it's gonna cost but I will be meeting my deductible and OOP this year for sure so it’s not gonna be a huge deal for us if we pay now or later, LOL.
I have only lived in CA for it, so I don’t know how other states do it. CA has a 1st tri screening (1 vial of blood), then the NT US, then the 2nd tri screening (also known as quad screen - 1 vial of blood). Does other states do this also? Or do you just have the panorama test?
We were given the option to do the panorama test, but declined because we don’t really care about finding baby’s sex early and we thought the CA tests covered our bases well.
@lillywonderland I have to call and see if they’d allow it towards my deductable, but because of my RE appts in the beginning of the year, I’ve almost met it for the whole year. It could help tho push me over the edge
@chichiphin insurance is beyond annoying. If you think it’s worth it for you, I think you can call the company directly and negotiate a price. I found out accidentally when I got a bill from Natera for 8k last time and called (after losing my mind). They basically asked me how much I could pay and said that they want to make this test accessible etc. they had great customer service. They put it through insurance and all was well but it taught me that it’s alwsys worth a call (again, if you want to do it).
I did the panorama (from Natera) which is what I did last time as well. I gave the sample at 9+4 and got a fetal fraction of 15.2% (I think that’s the cell free fetal dna percentage). Low risk and we are having a girl. I am 36 and dh 41 - we aren’t old by any stretch of the imagination but we like to do the genetic testing to have all the info we can. We will be doing the NT scan in 2 weeks.
@rms924 if I were 35 or older, it would be paid for! it’s so frustrating how much disparity there is between insurance coverage in the states. I plan on calling them and asking a few more questions before writing it off. Tbh I get so stubborn with things like this I almost go 100% the other way, meaning now I don’t even want to find out the gender! I’m so exhausted from all the run around! hahaha
@rms924 if I were 35 or older, it would be paid for! it’s so frustrating how much disparity there is between insurance coverage in the states. I plan on calling them and asking a few more questions before writing it off. Tbh I get so stubborn with things like this I almost go 100% the other way, meaning now I don’t even want to find out the gender! I’m so exhausted from all the run around! hahaha
@chichiphin I totally get you (I’m like that too!). Age is def the primary consideration for us. The gender- we find out regardless in 10 w. Personally, from my research **TW loss mom TW**, the anatomy scan gives a ton of info about the health of the fetus. So I am still anxious waiting on the AS. Between the NT and AS (I think) you get a good amount of reassurance. This was a level one, ok, I can breathe and wait until Mar 7.
I think insurance in general is ridiculous. The whole thing is a farce. The recent acog recommendations actually state that the tri 1 genetic testing should be up to mom and provider discretion. As usual, insurance companies haven’t (or won’t) catch up.
@chichiphin How much is your OOP max? Honestly, if it’s only a few k more you’ll prolly hit it this year so maybe take that into account. Just the fee from my OB alone for his part in the delivery (and prenatal care) is exceeding my deductible, and we know from experience that the L&D stay at the hospital is going to put us way over (with DS it was like $8k at my hospital). The NT US is great, but that in combination with the NIPT gives you a more accurate picture. KWIM? Of course, it’s totally up to you...i just want you to know that there’s a chance you might max out this year so the NIPT might be “free”.
I am doing the Maternity Genome, it's more extensive then the Maternit21 and recommended by my Dr if I choose not to do an amino which is his #1 recommendation for me. I'm 38 and Dh is 50 is we have increase for a lot of issues. I have to reach my deductible first before it's covered by the lab has a special pricing so people don't have to pay thousands of dollars.
I think last time it costs me under $100. I'd like to do it again this time if just for seeing the baby. I'll ask about it at my 10w appointment today and schedule.
We did the progenity test, and will have the scan at 12 weeks. For the progenity, we have Aetna insurance. My doctor told me that they are notorious for not covering it and people have gotten astronomical bills (even though I am over 35, I guess Progenity tests for more genetic abnormalities than other tests do so they don't feel it is necessary?) so what they told me to do was to have my blood draw taken at my OB's office & they would send it to a lab that partners with Progenity and I likely wouldn't get any type of bill at all as Progenity wants the test to be accessible to all. I've gotten my results back, but I haven't seen any type of bill yet, so I'll update if I do receive one!
I've decided to suck it up and pay the 299. I was assured that the maternT21 "questionnaire" you fill out to get the discount would NOT be tied to my results. I will be double-checking that though.
My insurance never covers the NIPT test. I’m considering going to a boutique that does the blood test near me for $150, better than $300-$400. Deciding if I want to do it or not. This is my last one so I don’t want to wait until the anatomy scan.
I had my blood drawn for the Innatal test yesterday at 10w2d. They promised me that I will get a heart-attack inducing EOB from insurance but that they will work with me so I can pay a reasonable amount. This science is so amazing - def wasn’t around when I was pregnant with DS 10+ years ago!
Figure I better update on here. Possible **TW** ahead.
Our NT scan showed a cystic hygroma at 7mm from the neck to the top of the skull, essentially fluid under the skin. We immediately met with a MFM in perinatal who explained our outcomes are not in our favor. Essentially 50% likelihood of a major chromosomal issue, 47-49% likelihood of another “abnormality”, and 1-3% likelihood of a normal outcome. The likelihood of miscarriage regardless of Dx is also very high. They took bloodwork for materniT21 yesterday morning and we have a genetic counseling appt on Monday and a repeat U/S on the 13th. We are in shock and aren’t sure what the future holds, except that we have to make some massive, heart wrenching decisions in the near future.
@chichiphin, I am so sorry you are going through this. I have not been through exactly what you are going through, but (in our first pregnancy a few years ago) I received totally unexpected NIPT results - never even considered that I'd be that small fraction of a percent - that were later confirmed through a CVS, so I know some of the emotions you and your husband are probably feeling. I'm so sorry; it's so hard to have your life (and expectations) rocked in this way (and especially while you wait for certainty and imagine all the unknowns). So many hugs. I will be thinking of you while you wait for more information.
@chichiphin Sending you some more love and strength for the tough days ahead. I wish we lived closer so I could give you the biggest hug IRL. Remember that whatever decision you and YH make together, it is the right one for your family. Don’t let anyone make you believe otherwise. Love you so much, friend. ❤️
@chichiphin so sorry for this heartbreaking news. Lots of internet hugs to you and YH!
*TW* History
TTC #1 since 7.2017 Dx: low morph (1%), ANA positive, low decidualization score, high TSH and testosterone, histone antibodies
IUI #1-3| all BFN IVF #1 | 6.11.19 | 24R, 17M, 15F, 6B, PGT-A tested - 5 normal, 3 girls & 2 boys FET #1 | 9.10.19 | BFN "I know you, but we've never met. I'm with you, but I don't know your name" RPL, Receptiva, & ERA testing | all normal/negative, recommended going on gluten and dairy free diet for next FET FET #2 | 3.31.20 | Opted to cancelled due to pandemic, continued diet and tried naturally over the summer 2nd Opinion with another RE | 8.20.20 | Not immune to measles (received 1 dose); SA results similar to 2 years ago; decided to move forward with FET #2 redo at start of next cycle Surprise natural BFP! | 9.22.20 | MC 10.23.20 at 8 weeks TTCAL naturally | starting 11.22.20 Initial consultation with Reproductive Immunologist | 9.14.21 Decidualization score biopsy | 10.1.21 | abnormal - low score of 1; endometrial scratch recommended and progesterone supplementation Saline sono | 10.15.21 | normal Bloodwork | 10.21.21 | high TSH, high testosterone, positive for anti-nuclear antibodies and histone antibodies, high protein S, multiple genetic mutations BFP! | 11.3.21 | EDD 7.14.22 | biopsy provided same effect as endometrial scratch; added supplemental progesterone and estrogen, prednisone, levothyroxine, and MTX Support to maintain pregnancy DS born 7.19.22 after induction
TTC #2 begins 6.2023 Consultation with RI | 6.6.23 Saline sono, endometritis biopsy, skin & eye check | all normal Labs | high TSH, Factor XIII mutation, high %CD56 Follow up | 8.8.23 | prescribed metformin, prednisone, plaquenil, and levothyroxine Repeat labs after 3 weeks on meds Follow up | 11.9.23 | Green light!, increase in prednisone, added lovenox Repeat labs in 8 weeks Follow up | 1.16.24 | Green light continues TTC ended due to filing divorce **New relationship starting May 2024** Surprise BFP!! | 9.7.25 | EDD 5.11.26
*lurking @chichiphin Sorry to hear this news. My thoughts are with you and YH. Sending you so much strength to get through these next difficult days
Me: 35 DH: 35 TTC since 9/2018
Dx: MFI 10/19- First RE visit 2/20- DH had surgery for bilateral varicoceles 7/20- IUI with 5 mg letrozole- BFN 9/20- IVF. 9 eggs retrieved, 9 mature, 8 fertilized with ICSI, 7 blasts, 4 PGT-A normal 11/20- Mock transfer/ERA 12/20- FET #1- transferred one 4AB- BFN 3/21- FET #2- transferred one 3AB- BFP! Due Dec 2021 12/21- Baby girl born!
Re: NT/NIPT Discussion Thread
married 11.1.14
ttc #1 since 5.18
bfp 12.22.18 letrozole + progesterone
d&e due to trisomy 13/hydrops at 15wks
bfp 7.21.19 letrozole + IUI
little girl A born 3.26.20
Married 8/16/13
BFP#1 DS 11/13/16
BFP# 2 MMC dx @ 13w 10/30/18
BFP# 3 Preemie DD born at 38w (IUGR) on 8/28/19 weighing 5.5lbs. Our little miracle
I have only lived in CA for it, so I don’t know how other states do it. CA has a 1st tri screening (1 vial of blood), then the NT US, then the 2nd tri screening (also known as quad screen - 1 vial of blood). Does other states do this also? Or do you just have the panorama test?
We were given the option to do the panorama test, but declined because we don’t really care about finding baby’s sex early and we thought the CA tests covered our bases well.
married 11.1.14
ttc #1 since 5.18
bfp 12.22.18 letrozole + progesterone
d&e due to trisomy 13/hydrops at 15wks
bfp 7.21.19 letrozole + IUI
little girl A born 3.26.20
married 11.1.14
ttc #1 since 5.18
bfp 12.22.18 letrozole + progesterone
d&e due to trisomy 13/hydrops at 15wks
bfp 7.21.19 letrozole + IUI
little girl A born 3.26.20
I did the panorama (from Natera) which is what I did last time as well. I gave the sample at 9+4 and got a fetal fraction of 15.2% (I think that’s the cell free fetal dna percentage). Low risk and we are having a girl. I am 36 and dh 41 - we aren’t old by any stretch of the imagination but we like to do the genetic testing to have all the info we can. We will be doing the NT scan in 2 weeks.
DS: 18 months
Dx DOR AMH .2
<a href="http://www.thebump.com/?utm_source=ticker&utm_medium=HTML&utm_campaign=tickers" title="Pregnancy"><img
married 11.1.14
ttc #1 since 5.18
bfp 12.22.18 letrozole + progesterone
d&e due to trisomy 13/hydrops at 15wks
bfp 7.21.19 letrozole + IUI
little girl A born 3.26.20
I think insurance in general is ridiculous. The whole thing is a farce. The recent acog recommendations actually state that the tri 1 genetic testing should be up to mom and provider discretion. As usual, insurance companies haven’t (or won’t) catch up.
DS: 18 months
Dx DOR AMH .2
<a href="http://www.thebump.com/?utm_source=ticker&utm_medium=HTML&utm_campaign=tickers" title="Pregnancy"><img
1st Baby 5/12/17, Henry
married 11.1.14
ttc #1 since 5.18
bfp 12.22.18 letrozole + progesterone
d&e due to trisomy 13/hydrops at 15wks
bfp 7.21.19 letrozole + IUI
little girl A born 3.26.20
Our NT scan showed a cystic hygroma at 7mm from the neck to the top of the skull, essentially fluid under the skin. We immediately met with a MFM in perinatal who explained our outcomes are not in our favor. Essentially 50% likelihood of a major chromosomal issue, 47-49% likelihood of another “abnormality”, and 1-3% likelihood of a normal outcome. The likelihood of miscarriage regardless of Dx is also very high. They took bloodwork for materniT21 yesterday morning and we have a genetic counseling appt on Monday and a repeat U/S on the 13th. We are in shock and aren’t sure what the future holds, except that we have to make some massive, heart wrenching decisions in the near future.
married 11.1.14
ttc #1 since 5.18
bfp 12.22.18 letrozole + progesterone
d&e due to trisomy 13/hydrops at 15wks
bfp 7.21.19 letrozole + IUI
little girl A born 3.26.20
@chichiphin, I'm so very sorry for this heartbreaking news. Thinking of you ❤❤❤
Married 8/16/13
BFP#1 DS 11/13/16
BFP# 2 MMC dx @ 13w 10/30/18
BFP# 3 Preemie DD born at 38w (IUGR) on 8/28/19 weighing 5.5lbs. Our little miracle
@chichiphin
I am so sorry for you and your husband. Sending all the love and thoughts to you both. ❤️
@chichiphin I’m so sorry you are having to deal with this. Sending all the strength and love to you and your husband ❤️
@chichiphin I am so sorry for what you and your H are going through. Sending you love, and hugs. You will be in my thoughts. 💜
married 11.1.14
ttc #1 since 5.18
bfp 12.22.18 letrozole + progesterone
d&e due to trisomy 13/hydrops at 15wks
bfp 7.21.19 letrozole + IUI
little girl A born 3.26.20
@chichiphin So sorry you and YH are going through this. Sending all the love, strength, and prayers your way! ❤️❤️❤️
Diagnosed with PCOS & Hashimoto's
@chichiphin - My heart dropped when I read your post. I'm so so sorry that you and YH are going through this. My prayers are with you.
@chichiphin so sorry for this heartbreaking news. Lots of internet hugs to you and YH!
Dx: low morph (1%), ANA positive, low decidualization score, high TSH and testosterone, histone antibodies
IUI #1-3 | all BFN
IVF #1 | 6.11.19 | 24R, 17M, 15F, 6B, PGT-A tested - 5 normal, 3 girls & 2 boys
FET #1 | 9.10.19 | BFN "I know you, but we've never met. I'm with you, but I don't know your name"
RPL, Receptiva, & ERA testing | all normal/negative, recommended going on gluten and dairy free diet for next FET
FET #2 | 3.31.20 | Opted to cancelled due to pandemic, continued diet and tried naturally over the summer
2nd Opinion with another RE | 8.20.20 | Not immune to measles (received 1 dose); SA results similar to 2 years ago; decided to move forward with FET #2 redo at start of next cycle
Surprise natural BFP! | 9.22.20 | MC 10.23.20 at 8 weeks
TTCAL naturally | starting 11.22.20
Initial consultation with Reproductive Immunologist | 9.14.21
Decidualization score biopsy | 10.1.21 | abnormal - low score of 1; endometrial scratch recommended and progesterone supplementation
Saline sono | 10.15.21 | normal
Bloodwork | 10.21.21 | high TSH, high testosterone, positive for anti-nuclear antibodies and histone antibodies, high protein S, multiple genetic mutations
BFP! | 11.3.21 | EDD 7.14.22
DS born 7.19.22 after induction
TTC #2 begins 6.2023
Consultation with RI | 6.6.23
Saline sono, endometritis biopsy, skin & eye check | all normal
Labs | high TSH, Factor XIII mutation, high %CD56
Follow up | 8.8.23 | prescribed metformin, prednisone, plaquenil, and levothyroxine
Repeat labs after 3 weeks on meds
Follow up | 11.9.23 | Green light!, increase in prednisone, added lovenox
Repeat labs in 8 weeks
Follow up | 1.16.24 | Green light continues
TTC ended due to filing divorce
**New relationship starting May 2024**
Surprise BFP!! | 9.7.25 | EDD 5.11.26
TTC since 9/2018
10/19- First RE visit
2/20- DH had surgery for bilateral varicoceles
7/20- IUI with 5 mg letrozole- BFN
9/20- IVF. 9 eggs retrieved, 9 mature, 8 fertilized with ICSI, 7 blasts, 4 PGT-A normal
11/20- Mock transfer/ERA
12/20- FET #1- transferred one 4AB- BFN
3/21- FET #2- transferred one 3AB- BFP! Due Dec 2021
12/21- Baby girl born!