Hi!
I’m currently 12+5 and went for my scan today. The professionals in the room went into a ‘hush mode’ and me and my husband knew there was something happening.
We were told that the baby’s NT reading was above the normal range at 2.7.
We were whisked off to another room where a midwife explained what this meant. We were told that it could be a heart defect, a chromosonal defect or simply nothing.
I had my blood results back and I was 1 in 2000 for 21 and 1 in 10000 for the other 2. They’ve booked me in for a separate heart scan at 20 to see if there is a heart defect.
I am worrying myself senseless. Has anybody else had this? Any advice would be helpful. These will be the longest 8 weeks of my life
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Thank you!