Looking for comrades..
Has anyone else been seeing genetics for genetic screening complications? Looking for support. We found out on Monday that our integrated prenatal screen was positive at a risk of 1 in 2 for DS. We worry that if it isn't DS, what could be causing such abnormal biomarkers. We are strongly considering ending the pregnancy if a major anomaly is identified (for a number of reasons.. It is a heart and gut wrenching thing to have to consider. but please, I am only saying so to avoid comments and encouragement about life with a child with special needs, which we aren't finding helpful right now..)
My husband and I have spent the past few days in a haze of grief and worry. I know that very often the IPS screen is a false positive but I work in obstetric care myself and have never seen a 1:2 and I feel the risk is quite a lot higher that most positive screens... Tomorrow is our first genetics appt. I already know we will opt for an amnio. All of the waiting has been awful...
Today especially I have been feeling very lonely. I see all these rosy pregnant women moving forward with their uncomplicated pregnancies. Even though it was just 3 days ago that I was one of these women, I already miss my biggest worry being about how I would handle those early weeks as a new mom.. And now I feel like a shell, dry lips and big black circles under my eyes from a screen that doesn't feel like a screen when the result is that stark.
Wondering if there is anyone else in this boat and can share their advice or has a story of a woman with 1 in 2 risk..
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