Hi I was starting this thread for everyone who has NIPT testing done. We got our results back today. Everything is low risk. Thank god. I've been so stressed this entire week. we also found out........ We are having a little girl!!!! I can't believe it. We are both over the moon!!
Me: 29DH: 30
Happily Ever After: 05-15-2015
TTC since June 2015
BFP 3/21! - E.D.D. 11/28/16!

September Football Siggy
Re: NIPT TESTING RESULTS
Make a pregnancy ticker
I'm getting mine drawn next week too...can't wait!
TTC Since: November 2015
BFP: March 31, 2016
DS: November 21, 2016
HSG - All clear, ectopic kidney didn't affect uterus (yay!)
CT Adrenal Scan - no tumors!
SA - sperm count excellent, 2% Morphology
March/April IUI scheduled - surprise BFP w/ help of Progesterone - 3/18/2016
Beta #1 @ 11dpo - 45.7 #2 @ 14dpo - 163 #3 @ 18dpo - 997 #4 @ 21dpo - 3799
EDD 12/1 based on O, 11/28 per Ob/Gyn (but he's wrong lol).
*TEAM BLUE!*
TTC since June 2015
September Football Siggy
HSG - All clear, ectopic kidney didn't affect uterus (yay!)
CT Adrenal Scan - no tumors!
SA - sperm count excellent, 2% Morphology
March/April IUI scheduled - surprise BFP w/ help of Progesterone - 3/18/2016
Beta #1 @ 11dpo - 45.7 #2 @ 14dpo - 163 #3 @ 18dpo - 997 #4 @ 21dpo - 3799
EDD 12/1 based on O, 11/28 per Ob/Gyn (but he's wrong lol).
*TEAM BLUE!*
Congrats on the good results and on the girl!!!
Bet you can't stop thinking about names now.
I am 8w5d today and will get the blood work done at 10w.
Me: 40 | DH: 45 | together 14 years
TTC since 9/2015
We trust and pray that God will continue to bless us with a full-term, smooth pregnancy and the delivery of a healthy baby.
BFP1 04/24/2015 EDD Dec 2015 MMC 10W5d;
BFP 2 09/25/2015 EDD June 2016 MMC 9wks;
BFP 3 03/22/2016 EDD Dec 6th 2016
TTC #2 starting 9/2019
BFP 7/13/2020!
Due 3/18/2021
TTC #1 since 2/2015
Diagnosis: Unexplained Infertility 9/2015
Moving to IVF with ICSI and PGS 5/2016-6/2016 Just kidding, BFP 4/4/2016!
Spencer Elliott born 12/7/2016
We have our NT scan on Monday and (I believe) will have the option of cell free DNA or the standard first tri genetic screening blood tests but it's definitely possible/likely that we will have to pay out of pocket for the cell free DNA. I was also told that, for women who are paying out of pocket, they use some company that only screens for T21 and T18, not T13 or any sex aneuploidys. So I'm not sure.... I think the standard first tri genetic screening is less sensitive but also screens for T13.... FTM here so happy to hear thoughts/experiences.
BFP1 04/24/2015 EDD Dec 2015 MMC 10W5d;
BFP 2 09/25/2015 EDD June 2016 MMC 9wks;
BFP 3 03/22/2016 EDD Dec 6th 2016
TTC since June 2015
September Football Siggy
My Wedding Bio!
TTC since June 2015
September Football Siggy
I went to my a early risk assessment appointment today and am happy to share what they told me for those who might find it helpful. FWIW, I am not AMA and I have no known risk factors, previous history of genetic abnormalities in my family, etc.
The office I go to has everyone get the NT scan. The ultrasound measures the width of the quantity of fluid at the nape of the neck and also looks for nasal bones. Apparently, if there is too much fluid at the nape of the neck and/or the nasal bones aren't formed by 12 weeks then that can indicate a greater likelihood of Down's syndrome.
They then offered the standard blood work or the cell free DNA. They use MaterniT21 for the cell free DNA, which looks for trisomies 21, 18 and 13. This specific test does not screen for other genetic abnormalities other than those 3, and she said it's much better at detecting T21 and 18 than T13 but it is not as accurate at detecting abnormalities in women under 35 as it is at detecting abnormalities in women over 35 and the positive predictive value of the test is lower (meaning that if it comes back negative it's unlikely that there's a problem but if it comes back positive it still has a fair chance of being wrong). This would likely not be covered by my insurance because I am not high risk and she didn't estimate the cost but I have heard MaterniT21 is one of the more expensive testing options (compared to Harmony and Panorama) - but who knows if that's true.
The standard blood work (which is covered by most insurance companies) looks at 3 different markers in the blood. They then combine those results with the results of the NT scan and information about other risk factors and give you a risk ratio of how likely the baby has a genetic abnormality on a scale from 1:5 - 1:10,0000. This blood work can detect T21, T18, T13, and she said it can also detect other genetic abnormalities. So she said if we weren't specifically concerned about T21, she would recommend this test as a better overall screening test. She also said that because we will likely have to pay out of pocket for MaterniT21, that we could get it at any time (like, we could get the standard one now because it has to be done between certain ages, but get the MaterniT21 later if we still wanted it). If the standard screening comes back abnormal, then we could get MaterniT 21 or an amniocentesis. If the MaterniT21 comes back abnormal then the next step is also amio.
We ended up getting the standard screening blood work and NT scan bc it's free and then if it comes back abnormal we can decide what to do then. Our NT scan was normal and we'll have to wait a week or so to find out the results of the bloodwork.
Again in this is only the advice and options that my doctors office recommends so other people might hear something different but I hope it's helpful.
This is helpful information, and obviously I will double check with my dr when we see them, but I am mainly concerned about being out of the window for the Materni21 or Verify etc.
I have thus far had 2 babies who had soft markers for trisomy 18 at their anatomy scan and both time we went through weeks of hell while waiting for more in depth ultrasounds etc. I know that at one point I was even told I was too late for the free cell DNA tests.
This time I was leaning towards a free cell DNA test, but it is not covered by insurance at this point - it would be really nice to know if the free cell is an option at 18-20 weeks if we were to find soft markers again.
Married to DH 10.29.11
DD born 1.26.13
DS born 6.12.14
#3 due 12.6.16
HSG - All clear, ectopic kidney didn't affect uterus (yay!)
CT Adrenal Scan - no tumors!
SA - sperm count excellent, 2% Morphology
March/April IUI scheduled - surprise BFP w/ help of Progesterone - 3/18/2016
Beta #1 @ 11dpo - 45.7 #2 @ 14dpo - 163 #3 @ 18dpo - 997 #4 @ 21dpo - 3799
EDD 12/1 based on O, 11/28 per Ob/Gyn (but he's wrong lol).
*TEAM BLUE!*
BFP1 04/24/2015 EDD Dec 2015 MMC 10W5d;
BFP 2 09/25/2015 EDD June 2016 MMC 9wks;
BFP 3 03/22/2016 EDD Dec 6th 2016
We had our NT scan yesterday and from what I researched online the measurement is within normal limits so that is good
BFP#1 & MC:August 2015 BFP: #2 10/01/2015 MC: 10/09/2015 BFP #3: 12/22/2015 @ 5 weeks MC/CP: 12-23-2015
Fertility Appointment: Feb 23/16, Hysteroscopy 03/02/2016,
BFP #4: 03/31/16 EDD 12/01/2016
G born 10/25/12 | H born 3/25/14
TTC#3 since 7/2015
Early loss 12/2015 most likely due to low progesterone
Began medicated cycles (Femara/Ovidrel/Endometrin) with TI 1/2016
BFP 3/22, EDD 12/4/16 ~ It's a GIRL!
HSG - All clear, ectopic kidney didn't affect uterus (yay!)
CT Adrenal Scan - no tumors!
SA - sperm count excellent, 2% Morphology
March/April IUI scheduled - surprise BFP w/ help of Progesterone - 3/18/2016
Beta #1 @ 11dpo - 45.7 #2 @ 14dpo - 163 #3 @ 18dpo - 997 #4 @ 21dpo - 3799
EDD 12/1 based on O, 11/28 per Ob/Gyn (but he's wrong lol).
*TEAM BLUE!*
TTC since June 2015
September Football Siggy
Are you hoping more for either sex? We really want a boy but I would be happy with a mini-me
HSG - All clear, ectopic kidney didn't affect uterus (yay!)
CT Adrenal Scan - no tumors!
SA - sperm count excellent, 2% Morphology
March/April IUI scheduled - surprise BFP w/ help of Progesterone - 3/18/2016
Beta #1 @ 11dpo - 45.7 #2 @ 14dpo - 163 #3 @ 18dpo - 997 #4 @ 21dpo - 3799
EDD 12/1 based on O, 11/28 per Ob/Gyn (but he's wrong lol).
*TEAM BLUE!*
oooh I'm an Ontarioan too lol (southwestern) good to know, I'll have to check with my doctor when I see her next!!!
BFP#1 & MC:August 2015 BFP: #2 10/01/2015 MC: 10/09/2015 BFP #3: 12/22/2015 @ 5 weeks MC/CP: 12-23-2015
Fertility Appointment: Feb 23/16, Hysteroscopy 03/02/2016,
BFP #4: 03/31/16 EDD 12/01/2016