Hi everyone- we are in our second trimester and we have a had a few little scares, but have survived so far. My wife went for her 16 week check-up last week and had some blood taken. The nurse called today while she was at work and told her there were some "abnormalities" with the blood work... aka a heightened level for DS (1 in 5). The nuchal and blood work in the first tri came back fine.
The nurse wanted us to meet with the genetic counselor on Friday to get some more info, more blood taken, and another US. I called the nurse back (wife was upset) and told her that we needed to get in there ASAP as we can't wait nearly a week and go through Thanksgiving not knowing what was going on... we have our app. tomorrow.
My question to all of you is- has your nuchal come back fine, but then "abnormalities" show up later on and if so, what was the outcome? The nurse suggested the "Harmony" test, but since it is so new, she doesn't know much about it. From what I've researched, it's just blood work that measures with 99% accuracy the 13,18, and 21 chromosomes.