Looking for prayers, encouragement, shared experiences, or whatever you can offer. This is a lengthy vent but I needed to write it out. At 22w we had our second level sono anatomy scan. They found a couple abnormalities in the brain. Her right lateral ventricle was measuring enlarged, just over 10mm and they saw a dangling choroid plexus. The nurse looked at the sonographers notes and literally said “I don’t even know what that second part means” and recommended coming in for a rescan two weeks later. She said she’d show my OB when he returned from surgery and if he didn’t think I needed to rescan, she’d call. Well, that left me with nothing for two weeks but Dr. Google. Fist off, as an OB nurse, it seems she should have at least been familiar with that terminology as a quick Google search found all kinds of information. Unfortunately it ranged anywhere from “my baby had this and it resolved itself” to “marker for Downs” to hydrocephalus that could require a stunt in your infants brain or inhibit their communication and mobility. It’s been a rough couple of weeks paired with moving and interviewing for a promotion. I immediately went off of my anti-depressants because it was the only thing I could point to that was different from my first pregnancy and I found one article deep in the internet that said SSRIs may impair brain development (I know that rationally speaking all pregnancies are just different and trying to find something I’ve done won’t result in anything. My OB and prior research also said my meds would be more than fine to stay on).
Yesterday we we had our rescan. They found the same issues and said they want to refer me to a Maternal & Fetal Medicine specialist. Said they have higher level sonos and are the experts that will be able to talk about what these things mean and next steps. We immediately walked into the specialist since it was downstairs and asked for their soonest available appointment. When I handed the receptionist my referral she said “are you doing okay?” And the vibe in there is fairly somber, will all of the literature about the doctor referring to her helping out with complications and high risks. Our appointment is for Tuesday morning. I know there’s nothing I can do until then, but it feels like forever. I know we were chosen to be her parents no matter what and she’ll be exactly who’s she’s meant to be, but I hate not knowing and feeling helpless that I can’t do anything for her.
I know every pregnancy and experience is different, but curious if anyone has similar brain scan results and what your story was. Or, If you can’t relate, feel free to share whatever form of encouragement you can.
Re: Referred to a specialist and scared.
June 2016 - CP
2017 - Medicated Cycles & IUI's
IVF w/ PGS - January 2018
FET #1 - April 2018 - BFN
ERA Cycle May / June 2018
ERA Biopsy June 2018 ~ Results: receptive (no change)
FET #2 - July 2018 - BFP
U/S #1 7wk1d - HB 144 U/S #2 9w1d HB 166
Anatomy Scan 1st 11/2/18 2nd AS 11/19
EDD March 28, 2019
Baby Girl born 3/26/19