TTC since Sept 2012 M/C on 5/01/13 at 8 wks
AF finally appeared 11 wks later per Provera
Diagnosed with PCOS on 7/29/13
Three Failed Medicated Cycles, NTNP Indefinitely BFP #2 9/14/14, EDD 5/23/14...MMC discovered @ 9w2d; D&C 10/23/14
Yay! Congrats on the girl and the great test results. I just had my blood drawn yesterday for the same test. Can't wait to get the results. How long did it take you to get your results?
@mrshall1027 I'm a FTM as well. As my Ob explained to me it's where they take blood from the mother and run these tests. They look for, I believe, three different chromosomal abnormalities. I suppose it gives parents the option to terminate or on the other hand, gives parents the time to get appropriate medical assistance for after baby is born.
For example, my initial opinion was that I wouldn't terminate so why get the test and just worry for the rest of the pregnancy. But after talking it through with DH, he said he may feel paralyzed if given bad news at delivery and so he would like to get past that moment before baby arrives so we could plan whatever assistance we need to bring baby home and have the same happy birth moments because we prepared. That's just us, everyone is different and that's ok.
The bonus of the test, is that they can tell the sex of the baby because they're looking at the chromosomes.
My dr said it's only a $25 fee for the test and another $25 for the other common test...uhh I'm blanking on what that is right now, spina bifida?
Edit to add: I'm only 27, not high risk, so I'm not sure why my dr said our fee was $25. But she did say it was to the doctors office, so maybe it's based on insurance or maybe it can be based on your doctors office. I'm not sure, but after reading some women say they only were offered if AMA I thought I would share that I am not AMA, and was still offered, at what I would say is an inexpensive fee.
This test is a bit more in depth than the Quad test, right?
Yes. It is not the same thing as the Quad or Sequential screening. Those tests only screen and give you a statistical risk.
The MaterniT21 and Harmony actually analyze fetal DNA through the mother's blood. Typically, it is offered and covered through insurance if you are AMA or are considered high risk. You can cash pay if you are not, but it's not cheap.
Thanks so much ladies! Sorry for the post and run--had to take a fellow candidate to lunch.
So the MaterniT21 tests for trisomies 21, 13 and 18 (I believe) and what it does is check the mom's blood for circulating fetal blood and looks for extra chromosomal material. If they note any extra chromosomes, including extra sex chromosomes, then the screen is positive for that particular abnormality. It's not diagnostic, but is 99% accurate. When testing the sex chromosomes--extra Xs or Ys can mean things like Turner syndrome or Kleinfelter's syndrome--they can also determine the sex of the baby. You can opt out of that, but we did not want to.
So yeah that's it! I don't know about cost--my insurance covers if because I'm 35 and it covers 35+. We were thrilled with the outcome and I'm way excited to have a girl! It's kinda what I was hoping for, but of course I'm happy either way that so far things look healthy. We will have an ultrasound next week at 12 weeks--no NT scan needed since we did this test.
This is so cool!! I was just reading about all the tests. DH and I are going to talk about it tonight. But I didn't realize finding out sex was an option until now!! Did they give you a % chance it was right/wrong?
"The best and most beautiful things in the worldcannot be seen or even touched, they must be felt with the heart." ~ Helen Keller MAY '15 DEC. SIGGY CHALLENGE- FAV. CHRISTMAS MOVIE
Dating- 3/1/1999 ~ Married- 10/10/2004 DD#1- Sweet Pea ~ Born on her Due Date 3/1/2007 DD#2- Pumpkin ~ Due 9/29/2010 Arrived 10/1/2010 ~ BFP: 6/12/2013 EDD: 2/21/2014 NT Scan: 8/5/2013 (11w3d) MMC D&C: 8/8/2013 ~
~BFP: 3/15/2014 EDD: 11/24/2014 CP 4 weeks 4 days ~
This is so cool!! I was just reading about all the tests. DH and I are going to talk about it tonight. But I didn't realize finding out sex was an option until now!! Did they give you a % chance it was right/wrong?
Keep in mind, these are not done to find out the sex for funsies. It's done to test for trisomy diagnosis, some of which are not compatible with life. Since they are analyzing the DNA, it's either an X or a Y. It's not like an ultrasound where it can be wrong.
This is so cool!! I was just reading about all the tests. DH and I are going to talk about it tonight. But I didn't realize finding out sex was an option until now!! Did they give you a % chance it was right/wrong?
Keep in mind, these are not done to find out the sex for funsies. It's done to test for trisomy diagnosis, some of which are not compatible with life. Since they are analyzing the DNA, it's either an X or a Y. It's not like an ultrasound where it can be wrong.
What she said. It's just as accurate as the rest of the test. The sex determination was optional, as was sex chromosome abnormality testing. If we just stuck with the trisomies, they wouldn't have run sex chromosomes
This is so cool!! I was just reading about all the tests. DH and I are going to talk about it tonight. But I didn't realize finding out sex was an option until now!! Did they give you a % chance it was right/wrong?
Keep in mind, these are not done to find out the sex for funsies. It's done to test for trisomy diagnosis, some of which are not compatible with life. Since they are analyzing the DNA, it's either an X or a Y. It's not like an ultrasound where it can be wrong.
What she said. It's just as accurate as the rest of the test. The sex determination was optional, as was sex chromosome abnormality testing. If we just stuck with the trisomies, they wouldn't have run sex chromosomes
Yeah I totally understand the purpose of the tests. I was flooded with brochures yesterday about it at my first appt. I know it's looking for markers, was just curious about the sex discovery side.
I've read instances today of it being incorrect, I am wondering if they told you, for instance it's a 99% chance of being a girl. But I can't remember if it was the harmony or Maternit21
Re: AW: Chromosome test back and we're having...
My BFP Chart
TTC since Sept 2012
M/C on 5/01/13 at 8 wks
AF finally appeared 11 wks later per Provera
Diagnosed with PCOS on 7/29/13
Three Failed Medicated Cycles, NTNP Indefinitely
BFP #2 9/14/14, EDD 5/23/14...MMC discovered @ 9w2d; D&C 10/23/14
My Chart
***** All ALers welcome *****
I'm curious how long you had to wait also. We did ours a week & a half ago and haven't gotten the results yet. The suspense is killing me!
BFP #2: 7/24/13, MC: 8/28/13 @8weeks, 3days
Siggy challenge:
@mrshall1027 I'm a FTM as well. As my Ob explained to me it's where they take blood from the mother and run these tests. They look for, I believe, three different chromosomal abnormalities. I suppose it gives parents the option to terminate or on the other hand, gives parents the time to get appropriate medical assistance for after baby is born.
For example, my initial opinion was that I wouldn't terminate so why get the test and just worry for the rest of the pregnancy. But after talking it through with DH, he said he may feel paralyzed if given bad news at delivery and so he would like to get past that moment before baby arrives so we could plan whatever assistance we need to bring baby home and have the same happy birth moments because we prepared. That's just us, everyone is different and that's ok.
The bonus of the test, is that they can tell the sex of the baby because they're looking at the chromosomes.
My dr said it's only a $25 fee for the test and another $25 for the other common test...uhh I'm blanking on what that is right now, spina bifida?
Edit to add: I'm only 27, not high risk, so I'm not sure why my dr said our fee was $25. But she did say it was to the doctors office, so maybe it's based on insurance or maybe it can be based on your doctors office. I'm not sure, but after reading some women say they only were offered if AMA I thought I would share that I am not AMA, and was still offered, at what I would say is an inexpensive fee.
TTC #2 since 8/2012
IUI #1 April 2014: BFN
IUI #2 July 2014: BFN
IUI #3 August 2014: BFN
BFP: September 15, due May 22nd 2015
The MaterniT21 and Harmony actually analyze fetal DNA through the mother's blood. Typically, it is offered and covered through insurance if you are AMA or are considered high risk. You can cash pay if you are not, but it's not cheap.
So the MaterniT21 tests for trisomies 21, 13 and 18 (I believe) and what it does is check the mom's blood for circulating fetal blood and looks for extra chromosomal material. If they note any extra chromosomes, including extra sex chromosomes, then the screen is positive for that particular abnormality. It's not diagnostic, but is 99% accurate. When testing the sex chromosomes--extra Xs or Ys can mean things like Turner syndrome or Kleinfelter's syndrome--they can also determine the sex of the baby. You can opt out of that, but we did not want to.
So yeah that's it! I don't know about cost--my insurance covers if because I'm 35 and it covers 35+. We were thrilled with the outcome and I'm way excited to have a girl! It's kinda what I was hoping for, but of course I'm happy either way that so far things look healthy. We will have an ultrasound next week at 12 weeks--no NT scan needed since we did this test.
Thanks again! I love-tit all of you.
M/C 5w6d 6.25.14
Hoping for a rainbow!
M/C 5w6d 6.25.14
Hoping for a rainbow!
Me 33, DH 37 -- TTC since Jan'12 -- Low AMH (0.78) & endo, SA w/ low motility
IUI's 1-3 = BFN, IVF converted to IUI 4/13 = BFN
IVF 1.2: 8R 6M 4F -- 2 blastocysts frozen, FET 8/15 = BFP!!
Beta #s = 445;1,098; 9,545 -- EDD 5/2 -- Team Pink!
Yay for Baby girl!!
MAY '15 DEC. SIGGY CHALLENGE- FAV. CHRISTMAS MOVIE
Dating- 3/1/1999 ~ Married- 10/10/2004
DD#1- Sweet Pea ~ Born on her Due Date 3/1/2007
DD#2- Pumpkin ~ Due 9/29/2010 Arrived 10/1/2010
~ BFP: 6/12/2013 EDD: 2/21/2014 NT Scan: 8/5/2013 (11w3d) MMC D&C: 8/8/2013 ~
~BFP: 3/15/2014 EDD: 11/24/2014 CP 4 weeks 4 days ~
~BFP: 7/2/2014 EDD: 3/15/2015 CP 4 weeks ~
~BFP: 8/31/2014 EDD: 5/10/2015
*All are Welcome*
M/C 5w6d 6.25.14
Hoping for a rainbow!
Yeah I totally understand the purpose of the tests. I was flooded with brochures yesterday about it at my first appt. I know it's looking for markers, was just curious about the sex discovery side.
I've read instances today of it being incorrect, I am wondering if they told you, for instance it's a 99% chance of being a girl. But I can't remember if it was the harmony or Maternit21
DS2 born 2/22/13
MMC 5/16/14@8w2d
DD due 5/9/15 Please be our RAINBOW