Miscarriage/Pregnancy Loss

Put off joining for a while. Intro

Sha259Sha259 member
edited October 2014 in Miscarriage/Pregnancy Loss
I put off joining here for a good while because first I was in shock, then I was busy healing, and then I was waiting for news. My back story. TTC since 2011, but found success during our first full cycle of IVF. Things were going great until 7w3d when I had a bleeding episode, no cramping. Baby's hb was slow, but still there, I was told to go home and be a vegetable. Next appt 2 days later still showed a hb, it was better, but still slow. I was told to take it easy and come back in a week. At 8w3d baby only measured 8w and had no hb. I had a D&C that Friday. It's been 3 weeks since the D&C, I physically feel better, and even started working out again. But today I finally got the results of our baby's chromosomal assessment. Chromosomally normal baby girl. I am devastated. They prepare you saying that miscarriage is normal, and usually caused by embryo/fetal chromosomal defect. They prepare you for future success. Now I know that my baby girl was likely fine, and there is something in me that did not let her thrive. I know I can't speculate as to what the reason for this was. But Ive got 5 embryos frozen and I am deathly afraid to transfer them now. I cannot take carrying and loosing another healthy baby. I have an appt to talk to my RE about the results and steps forward on Friday, I plan to suggest doing the genetic screening for myself, and possibly DH. Sorry this was long. It just sucks that any of us have to be here at all. My prayer are with you all as well.

Re: Put off joining for a while. Intro

  • I'm so sorry for your loss. Hugs to you.
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  • I'm so, so sorry for loss.
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  • I am so sorry for your loss. I was told that both of my twins were normal as well so I know exactly how you feel. ~Hugs~ Lilypie Angel and Memorial tickers
    Lilypie Angel and Memorial tickers
  • I am so very sorry for your loss. Just a thought to share... When I had my MMC back at the end of July, my RE warned me that the only problem with testing was that if it came back healthy female, with the type of testing they do, there would be no way to know for sure they tested fetal tissue and not that of the mother due to contamination and the fetal tissue still being so small. Apparently, it is unfortunately easy to do. In our case, the test came back with Trisomy 21, so we know it was the baby. I hope sharing this is not upsetting to you (I hesitated to post knowing it would possibly have been upsetting for me to hear after the fact), but I did want to mention it in case your Dr had not. Again, so sorry for your loss.

    *************Siggy Warning. Loss mentioned.************




    Me: 36, DH:37

    Married 4/2010, TTC since 7/2011

    Dx: Officially Unexplained (I have Polycystic Ovaries diagnosed via ultrasound, but few classic PCOS symptoms, he has mild MF issues. So... not issue free, but nothing so severe as to explain IF)

    I also deal with post-surgical Hypothyroidism following Thyroid Cancer in 2009, but under control with Levothyroxine

    4 months Clomid (thinned lining) and 10 months Letrozole (every indication that I responded perfectly)

    6 failed IUIs in 2013, 3 with trigger

    IVF #1 in March 2014

    ER 3/21/14, 31R/21F, 12 frosties!

    ET 3/26/14, 1 perfect blast transferred: BFN

    FET#1 5/28/14, 2 "beautiful" early blasts transferred. BFP!!

    Beta #1 (6/11/14) 798; Beta #2 (6/18/14) 7,966.

    1st u/s (6/25/14) showed 2 sacs, 1 empty & 1 with a beautiful little bean doing what it needs to do!

    EDD 2/14/15, missed miscarriage, DX: Trisomy 21. D&C 8/1/14

    FET#2 Transferred 3 embies, 2 looking pretty good, one not so much. BFN.

    IVF#2 January 2015, tentative ER 1/23

  • I'm so sorry for your loss. Take care of yourself.
    Married: 4/28/12
    BFP: 7/2/14 ;  1st US 7/21/14 Baby measuring 7w5d, HB of 138;  Discovered MMC 8/18/14 at 11w2d, baby measuring 8w5d, no hb ; 8/19/14 D&C
    image

    TTCAL December siggy challenge - Autocorrect Fails

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    | <a href="http://www.fertilityfriend.com" style="font-size:smaller;" >Ovulation Tracker</My Chart

  • Thank you all for your kind words and support.

    Actually, when my nurse called me with the news, she was shocked that they didn't take a vial of my blood to be tested as well in the case of this sort of result. At this point I don't really know if it would add any value to what we currently know, and would likely just cost us more money.

    My RE has agreed to do the repeat MC panel on me, maybe they can send another sample to be tested against the other results.
  • I'm so sorry.  Can I ask a question?  We asked for genetic testing of the tissue too...but I don't think I want to know the gender- I think that will upset my greatly.  Should I/Can I ask that they not tell me the gender?  Is this an automatic part of the results?

      Me:36, DH:37

    DS born 11/2012

    BFP 7/26/14, Missed M/C at 8 weeks, discovered at 10 wks, 6 days, D&C 9/22/14, Dx: Partial molar pregnancy

  • I am so, so sorry for your loss and the confusing circumstances around your situation.

    -----------------------------------SIGGY WARNING-------------------------------------


    Me: 31| DH: 36
    TTC #1 Since 07/2010
    DX: Unexplained Infertility
    TX: 
    IUI #1 on 7/3/14 100 mg Clomid + Ovidrel + IUI (44 million sperm, 1 dominant follie) = BFN
    IUI #2: on 7/28/14 100 mg Clomid + Ovidrel + IUI (23 million sperm, 2 dominant follies) = BFN

    IUI #3 on 8/22/2014 100 mg Clomid + Ovidrel + IUI (53 million sperm, 2 dominant follies)= BFP MMC @ 7weeks


  • I'm so so sorry for your loss. I think why this happened to any of us is the toughest question. I hope you find your answers.
    Me: 32 DH: 32
    Met: 4/25/2004, Married 8/14/2010
    Off BC 1/2013 TTC (actively) since 5/2013
    5/2014 started testing with RE, me:  HSG normal, normal AMH, no cysts; DH: great sperm
    Unexplained IF + unexplained anovulation (post-pill vs hypothalamic)

    7/2014 Clomid (monitored) + TI: BFN
    8/2014 Clomid (monitored) + TI: BFP #1: 9/12/2014, EDD 5/22/2015, MMC 10/11/2014 8w1d
    11/2014 Clomid + Novarel + IUI 12/5/14: BFFN
    12/2014 Comid + Novarel + IUI 1/3/15: ???

    **PgAL/PAL welcome**

  • @FigureSkater8‌ I think if you tell them ahead of time that you don't want to know, they can put it in your chart. In my case, I was 8 weeks along, and knowing the gender didn't change how sad I already was. But the normal result did.
  • I'm so sorry for your loss. I know exactly how you feel. When we found out we had lost a chromosomally normal boy it really tore us apart. It made me feel like I had done something wrong to cause the loss and like somehow the baby could (and should) have been saved.

    FigureSkater8 -- For us, knowing the gender made it more difficult to handle. It made it easier to picture all the experiences that we had lost. My husband, who isn't a crier at all, teared up when he heard the news and it still really gets to him.
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