had my nt scan today, which was fine except that the baby's bladder is swollen. apparently 90% fix themselves and 10% required intervention.
i really need to hear that someone else has been in this situation... we have to wait until 2 weeks tomorrow to see whether it has improved or not and then decide about invasive tests as it is a marker for chromosome defects. don't know what to do and am out of my head with worry....
just for background, my first baby died of a non-hereditary (ie random) chromosomal defect so am totally panicked.
please help...