Hi Hun,

I know the feeling of shock you are in. I was 25 last year when I was told my baby had a high risk of a chromosome problem too as her nuchal fluid was high. We decided to have CVS testing done, instead of an amnio (which is what you are having I think) as it can be done much earlier but gives the same info. I think I was told my risk was about 1/30. Anyways fast forward and had the cvs and lost of other specialist scans throughout the pregnancy and my daughter was born healthy!! The fluid had resolved b 19 weeks which the geneticist told us that if the CVS results came back fine and if the fluid had resolved by 20 weeks and if they couldn't see any other defects at the morphology scan at 19 weeks then we had a very good chance our baby would be fine.

I really hope this is the case for you.
Big hugs xox