Our LO's heart stopped beating at 17 weeks or so. I found out at 18 weeks when no heartbeat was found on an ultrasound (I had some intuition that something was wrong, that's a whole other post). My cervix was closed up tight though, like my body didn't recognize what had happened.
We had a bunch of blood samples taken and had his little body taken away to be autopsied. I was also told they would need more blood from me once my hormone levels are back to pre-pregnancy levels.
I was warned that at least half the time, there is no cause that anyone can determine.
Just wondering if anyone who had a similar loss ever got any answers and if so, please share if it's not too difficult. Unfortunately, I heard a lot of 1st tri loss stories from my birth month board (blighted ovum, molar pregnancy, etc.) but I don't know anything about 2nd tri losses, I guess I never thought I would ever need to know. :-(





Re: 2nd Tri Loss - Reasons/Causes?
So sorry for your loss. My DS was born sleeping at 26 weeks. Autopsy revealed CMV (cytomegalovirus). It's a type of mono infection that I was exposed to during pregnancy. I worked in retail at the time and its impossible to know who may have shared the virus, but I was obviously not immune and it was terminal for the baby.
After I noticed a lack of movement I called my midwife who requested we report to the hospital to be checked. Ultrasound confirmed a lack of heartbeat and I was induced 2 days later.
Well, my situation was a bit different but it was a 2nd tri loss. My son was alive and healthy, up until literally a moment before delivery. I could feel him moving right before he came out, but when he did- he was gone.
I went into labor unexpectedly, and we never got an answer why. I had an uneventful pregnancy and also no issues w/ my 1st baby. Their unofficial diagnosis was pre-term labor and/or incompetent cervix. It's a "what came first" scenario- did my cervix dilate causing me to go into labor, or the other way around? They found nothing wrong w/ the baby, the placenta, or me.
First off, ((hugs)) and I am sorry for your loss. I mostly lurk here but I had the exact same experience. Our son's heart stopped beating at almost 17w for no identified reason at all. I only knew b/c I had an at-home doppler and after 2 days of not finding the hb after hearing it for 6 weeks, I asked to come in. An u/s revealed a 17w fetus w/ no heart beat, perfect fluid, and no abnormalities/cord issues. I chose to have a D&E and have him tested, and he was absolutely perfect in every way, nothing wrong, no infection. Since I am homozygeous MTHFR, I was already taking Lovenox and baby aspirin so it was def. not a clot or anything like that.
They told me the same thing -- 50% of the time there is no explanation. Being the type of person that I am, always needing something to "fix", this was and still is very difficult for me to come to terms with. Not knowing why is something that will bother me for the rest of my life. I am not a person who takes comfort in the "God has a reason" answer. It made TTC again very hard because there was nothing to change or add or test or u/s or treatment that we could do to assure it wouldn't happen again. There was no statistic that whatever happened only happens say, .5% of the time. I just had to fly by the seat of my pants and hope for the best, which is not something I do well. I had a lot of anxiety issues during my pregnancy for our rainbow baby and honestly, it was all too much for me and we are now done having children.
I hope you get an answer and the Dr.s are able identify what went wrong. And I am so sorry you are going through this.
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