Pregnant after IF

Genetic test was wrong! I'm having a boy!

So my instincts, the OB, and MFM were all right in their guesses back at 14 weeks! This is the first time they've seen this happen! I always knew I was having a boy even when I got the results of the ultrascreen genetic test! I called the number 5 times and listened to the recording, "congratulations, you are having a girl!"

Re: Genetic test was wrong! I'm having a boy!

  • edited November 2013
    What genetic test did you take that was wrong? Wait I'm confused is it a boy or a girl? Sorry if I'm a little slow lol

    Eta: spelling
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  • That's so weird!  Congrats though!  :-)
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  • Did they give you a possible reason for the confusion/mix-up? If you had the genetic test done early is there anyway it was baby b they "picked up"? I hope that isn't an insensitive question! I'm genuinely curious as to how that happens.

    ***************************************Child mentioned********************************************

    Me 28 DH 32

    TTC naturally 05/2011-10/2012= All BFNs

    Nov 2012 Jan 2013 Clomid= BFN

    IVF #1 scheduled for April 2013 Stims started 04/09 ER 04/19/2013- 26 Retrieved and 24 Fertilized 3 day Fert Report- 10 are 8 cell ET cancelled-all embryos arrested at day 3

    IVF #2 scheduled for June 2013 -Transferred 1 day 5 Blast

    07/04/2013 HPT- BFP! Beta 10dp5dt-35Beta 12dp5dt-82 Ultrasound 6 weeks 4 days- Heart rate 123bpm!!

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    Team Green turned Team BLUE!!!

    Baby M born premature at 33 weeks 5 days, he spent 22 days in the NICU before coming home!

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  • What!!!! Oh my gosh! Yay for a baby girl, but how can a genetic test be wrong?
    Shock of a lifetime! Crazy!!
    Me:35,  DH: 39   
    TTC since March 2011. All bloodword, SA & HSG are normal.  
    8/12: Clomid & TI - BFN 
    10/12: Colmid & TI - BFN 
    3/13:  Clomid, Trigger & IUI - BFN 
    4/13: Gonal F, Trigger & IUI: BFN  
    6/13: IVF #1 (1AA blast & 1BB blast) = BFN 
    8/13: FET #1= BFN
    10/13: FET #2= BFP!!!

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  • Omg- that is crazy!!!
    Me 36/DH 46 Me: Low AMH (.21) DOR, mild endo; Started seeing RE 11/12
    Jan-March '13 3 IUIs Clomid + Trigger = BFN
    April '13 IVF 1 MDLF converted to 4th IUI due to 3 runaway follicles! BFN
    July/Aug '13 IVF 1.2 Long Lupron = 7R, 6F, 2T= BFP!!!
    Beta 1=512, Beta 2=1,368 Beta 3= 4,128
    It's a boy!!!!
    SUA, GD
    EDD 4/26/14

    He's Here! Arrived 4/15/14!!!!

    September 2015 - FET with remaining embryos
    Twins! EDD: 6/14/15

    PAIF/SAIF Everyone welcome!
  • I have to wonder if they gave me someone else's results by mistake or if the twin we lost was a girl and it skewed the results somehow?
  • Insane! So exciting!!
    Me:35,  DH: 39   
    TTC since March 2011. All bloodword, SA & HSG are normal.  
    8/12: Clomid & TI - BFN 
    10/12: Colmid & TI - BFN 
    3/13:  Clomid, Trigger & IUI - BFN 
    4/13: Gonal F, Trigger & IUI: BFN  
    6/13: IVF #1 (1AA blast & 1BB blast) = BFN 
    8/13: FET #1= BFN
    10/13: FET #2= BFP!!!

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  • Wow that's crazy!  Congrats on your baby boy!

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    TTC #1 since August 2011

    My Blog

    September 2012: Start IF testing

    DH (32): SA is ok, slightly low morph, normal SCSA  Me (32): Slightly low progesterone, hostile CM, carrier for CF, Moderately high NKC, High TNFa, heterozyogous mutated Factor XIII, and +APA

    October 2012-May 2014: 4 failed IUIs, 3 failed IVFs, and 1 failed FETw/donor embryos

    November 2014: IVF w/ICSI #4 Agonist/Antagonist with EPP and Prednisone, Baby Aspirin, Lovenox, and IVIG for immune issues.  Converted to freeze all due to lining issues.  2 blasts frozen on day 6!

    January 2015: FET #2 Cancelled due to lining issues

    April 2015: FET #2.1


    PAIF/SAIF Welcome!

  • wow!!! i'll have to change the 2nd tri list now! :)  

    congrats! 
    Me (37) DH (39); PCOS changed to Unexplained, changed to DOR in 2012 (finally a correct diagnosis!); 
    Started TTC 2009 with RE after 6 months.  
    Clomid + Trigger x2; 
    IUI + Femara x1,
    IUI + Follistim x2;
    IVF #1 (MDL) February 2013- BFN.
    IVF #2 (antagonist) May 2013, First BFP of my life. 
    Identical twin miracle BOYS (!!) headed our way- due date is technically 2/4/14 but c section is scheduled for 1/7! 


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  • Genetic testing is based on DNA, so it is 99.9 percent correct. I am not sure what they got wrong. I am confused. But either way you get to find out soon enough! 
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  • Welcome to team blue!! That is crazy, but it just goes to show you to trust your instincts! :)
    *** Trigger Warnings ***

    TTC #1 since March 2011
    Dx = Unexplained IF
    1 medicated TI cycle & 4 clomid IUIs = all BFNs
    June 2013 IVF #1 = 6 frosties + BFP!
    DS1 born 2/14

    TTC #2 since December 2014
    May 2015 unassisted BFP ended in m/c at 7wks
    April 2016 FET #1 = BFN
    June 2016 FET #2 = c/p
    August 2016 FET #3 = BFP!
    DS2 born 4/17
  • Was this just a test of your blood? Or did they do an amnio? If the former, it can be wrong because they are just looking for the presence of male dna. If they don't find it, they call female. So, my guess is that the sample was too small or they just didn't detect the male dna.
    IF DX: DOR & Fragile X pre-mutation carrier
    2011: FSH 13.3 & E 99; AMH 0.54 2nd FSH 6.2 E 40's AFC: 8
    BFP from Clomid/IUI ~ Pre-e and IUGR during pregnancy ~ DS born 9/4/12
    Feb./March 2013: AMH less than 0.16 (undectable) and AFC = 4;
    BFP from supps ~ DS#2 due May 2014

    May 2014 January Siggy Challenge:
    image
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  • IBackBevo said:

    Was this just a test of your blood? Or did they do an amnio? If the former, it can be wrong because they are just looking for the presence of male dna. If they don't find it, they call female. So, my guess is that the sample was too small or they just didn't detect the male dna.

    This. How many weeks did you do the bloodiest? Which one was it? The earlier you do the test the more likely this can happen. It will not pick up the y chromosome dna and call it female. For this reason, it could be wrong with saying it's a female but I don't think it would be wrong if it said male.

    <Image and video hosting by TinyPic
    Married June 2011 Dx: anovulatory due to prolactinoma (1.5cmx 1.5cm in 2006)
    April 2012: MRI- questionable cyst 8mg by 12mm in pituitary ; referred to RE by Ob-gyn after amenorrhea x 4+ months, provera ineffective, low estrogen level
    cycle 1: May 2012, clomid 50mg; cycle cancelled, thin lining, no response
    cycle 2: June 2012, femara 5mg; cycle cancelled, no response
    cycle 3: July 2012, femara 7.5mg; cycle cancelled (largest folli on Cd12 & cd 16: 11, lining 4)
    Repeat MRI July 25,2012- Cyst unchanged, likely old infarction.
    Aug. 8: met with RE, move to injectables if HSG and SA normal
    Aug. 23: HSG all clear; DH- perfect
    Switched to a new RE in early Sept. IVF here we come
    Genetic testing reveals: Fragile X- Intermediate risk/grey zone.
    IVF#1: ER 11/30: 14 retrieved, 10 mature, 7 fertilized. E2 prior to trigger 5200. Decision made to freeze 6 embryos and transfer later due to OHSS.
    IVF#1.2/FET #1: estrogen injects start 1/18, FET delayed to try to thicken lining. lining 5.4mm. FET- 2/18- transferred one 3AA expanded blast. BFP 5dp5dt. Beta #1- 2/27 9dp5dt- 102.27 beta #2 3/1: 147 :(, beta #3 3/4: 268 told to stop meds and let nature take its course. requested 4th beta (3/6); Beta hell for 2 months.

    FET # 2: endometrial scratch 5/6, added estrace vaginally and ASA to delestrogen and PIO. June 10- transferred one 4AA hatched embryo, BFP 4dp6dt, Beta 1 (9dp6dt) 187, Beta 2 (11dp6dt): 412; Beta 3 (15dp6dt ): 4452. U/S #1- one beautiful embryo with a heartbeat of 133 at 7 weeks.  8 weeks: heartbeat 156. EDD 2/26/2014: born 2-3-14 induced due to Pre-E and HELLP at 36w5d.

    12/1: met with RE to discuss trying for #2


  • RoeniRoeni member
    edited November 2013
    I got the test at 14 weeks...it was not early and two doctors could already see boy parts. The ultrascreen is just like panorama or materni21
  • :) how exciting!!! congratulations!

    TTC#2
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    Our little IVF miracle born 5/7/2014
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  • I am nearly positive that the ultrascreen is the same test I had with DS (and will have with this LO) where they tell you the sex, too.  My guess is that the sample they got from you was not large enough and there just happened to not be any male dna in the sample.  My understanding is that they only look for the presence of male dna--i.e. y chromosomes. They probably did not see any and so called "girl."  I think it is easier to have a false "girl" reading than a false boy reading because of this reason.  I have also read where the results are about only 99%...so, really, 1 out of every 100 times it is going to be wrong. 

    IF DX: DOR & Fragile X pre-mutation carrier
    2011: FSH 13.3 & E 99; AMH 0.54 2nd FSH 6.2 E 40's AFC: 8
    BFP from Clomid/IUI ~ Pre-e and IUGR during pregnancy ~ DS born 9/4/12
    Feb./March 2013: AMH less than 0.16 (undectable) and AFC = 4;
    BFP from supps ~ DS#2 due May 2014

    May 2014 January Siggy Challenge:
    image
    image
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