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From what I understand, choroid plexus cysts are actually fluid filled pockets of space within the part of the brain, the choroid plexus, that makes cerebrospinal fluid for the brain. They usually appear in the second trimester (most people find them during their 18 week scans) and are often gone by the third trimester. These cysts are found on anywhere from 1-3% of all babies and do not affect the baby's brain's function or the baby's personality.
There is quite the debate over these cysts. For some time, these cysts were associated with a higher than average risk of Trisomy 18 (I think the highest I saw was an increased risk of 1:300, although that was from dated data). But, with no other abnormalities to indicate Trisomy 18, many doctors now believe that the risk of miscarriage from an amnio is higher than the risk of a genetic disease. Often, the only recourse needed is to do a thorough ultrasound to check all major organs, etc. and wait/watch. An amnio would come in to play if the detailed ultrasound showed some other abnormality.
I believe that Dr. Doom was under the old school belief that the risk was elevated for Trisomy 18. Then when he couldn't rule out the clubbed foot problem for one of the babies, and I was nearing the 35 age mark, he pushed the amnios.
Had Is.aac and I been the patients we are today (and more prone to research the hell out of EVERYTHING before we agree to a doctor's suggestion), we would have came home and likely not had the amnios done. Besides, by the time we went back for the next ultrasound, the cysts were gone, so the point would have been a non issue then anyway.
As for the guilt, I don't know why I continue to hold on to that. I guess it is my attempt to have a reason...a cause...something...anything to blame the whole clusterfuck that was that pregnancy. Yes, I know the doctor recommended the amnios. Yes, he did tell us the risks. Yes, he was the one in the know and we do have to trust the doctor's expertise to some extent. But, we ultimately made the decision to do it. I end up blaming myself because...at least there is a reason then.
Do I carry that guilt with me at a conscious level on a day to day basis? No.
Do I wish that everything went a completely different way and I had the voice to say no to that amnio that I wish I had? Yes.
Does the guilt still shows up on occasion to say hello? Yes.
I KNOW that I made the best decisions I could make at the time. I really do.
I KNOW I tried everything in my power to keep those boys in me as long as possible.
My heart still struggles there, though. Sigh.
I suppose it is a way to continue to punish myself for my heart's belief that my body failed.
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There hasn't been any conclusive reason to why my membranes ruptured. There are a couple of possibilities: 1) incompetent cervix in itself runs the risk of premature rupture, 2) the emergent cerclage also had the risk of premature rupture (infection was also a possibility, and we were all sick at the end. Don't know if the infection was there to begin with.), and 3) contractions that I didn't feel (I didn't really ever feel them even at the end before I delivered) that led to the rupture. Like I said, I had to have terb several times over that first day I was in the hospital for the rupture. Whether the rupture or the contractions came first is up in the air.
My OB was equally confused as to why Doom was saying to send me home. It makes me think all over again that he had really written that pregnancy off as unsaveable.
Sadly, I would have went home, too, had the OB not fought to keep me there. Thank goodness for him...he saved the boys with that call. I believe that with all of my heart.
This time, I will have the first course of steroids at 24 weeks as a precaution, with another series later in the pregnancy.
We're pulling out all the stops.
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I have a hard time with the memory of Doom's continued comments on whether the boys were genetically normal. I do think it directly affected how he dealt with my pregnancy the entire time. I strongly believe that he would not have "helped" us had one of the boys been genetically abnormal. Is.aac feels that way, too.
I don't get that feeling from him this time, though...his office hasn't even bothered to call me about the results from the screenings. I have to ask. It's almost like they don't even care what the results are now. (although I am sure that the results are there for them to check before we speak to anyone) It's strange. It doesn't make me trust him any more than I would have otherwise, though.
I feel he is one of those "fair weather friends" who is wonderful as long as all is going well. As soon as a complication starts to brew, I am sure he will be completely different. Sigh.
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Thank you for asking the questions. This really helps me clarify some things in my own mind, too.
The "punishing myself" part was an eye-opener...maybe just realizing that will help me combat those thoughts?




