Hi
An issue was picked up at our 20 week scan and, after having multiple scans, it was concluded to likely be an echogenic bowel (we received a different diagnosis I initially but doctors were not certain at that point).
We were offered an amniocentesis and did not know what to do but went ahead in the end due to the risks of Down syndrome and CF as an echo bowel is a soft marker for them.
Our bloods were also sent away to see if we are carriers for CF.
I am stressed beyond words, Down syndrome feels less likely (probably because I had no other markers and the combined test came back as the lowest risk but I know it doesn't completely rule things out). I am just so worried it could be CF.
Don't know why I am posting 😔 Saw lots of positive stories where an echogenic bowel was just a transient observation and went away in a few weeks.
Trying not to go crazy while waiting for results, CF results can take weeks and we should get results for the three syndromes either tomorrow or Monday.
I know that statistically speaking, it is more likely to be good news than bad news but it is so nerve wracking.
Thank you for reading