Hi all
I’m hoping some people can share some similar experiences and maybe help put some perspective on mine.
I went for a growth scan on Wednesday (36 weeks) followed by a consultant appointment (already under consultant care for BMI and family history of pre eclampsia) - in the consultant appointment I was told I had “a good amount” of excess fluid and would need to see fetal medicine for another scan.
In the moment I didn’t really take it in properly or ask the right questions, but the fetal medicine words raised alarm bells. Luckily I had a midwife appointment booked the next day. At the appointment with the midwife, she explained it was called Polyhydramnios, and that my deepest pool was 9.8 and AFI 34.8 which I understand to be quite high, but now I literally cannot stop panicking about there being something wrong with my baby.
My questions are how could this have been normal at 32 week growth scan but all of a sudden high at 36 weeks? Does this mean it’s less likely to be a genetic problem with the baby? I tested negative for GD but I suppose it could have developed even though I feel well. Would they have picked up genetic issues with the baby in other scans? I’m so nervous for the fetal medicine scan and now can’t look forward to the birth. I’m already booked in for an ELCS 39 weeks due to other reasons.
any words of advice would be so greatly appreciated.