Rang the GP - she's pretty clueless - and I suspect the report mentions that I'm at high risk of having a Trisomy 18 baby even though the baby scan is normal. So no points on brilliance for GP or reporting radiologist. I'll stick with the research I've done so far, and get another detailed scan at 23 weeks, and then the growth scan at 30 weeks and thereafter.
The GP went on (on the phone) about seeing one of her colleagues for Genetic Counselling. What's the point? What will be will be. I guess everyone wants to know different things at different times. I'll take baby as he/she comes, regardless of poorly informed advice of health professionals that are insensitive to religious and personal beliefs of mere mothers. I'm clinging to the stats that 85% of babies with a single umbilical artery do JUST FINE. :smt023
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