I had my 13 week ultrasound last Friday. We were devastated to hear that our baby's Nuchal Translucency was 6mm which is far above where it is supposed to be. I was told that the cause of Nuchal translucency is Down syndrome 85% of the time and then given the option of terminating my pregnancy right after I was given the heart sinking news. I am now scheduled for an amniocentesis consultation on Monday. I am terrified of the results and am wondering if anyone else has had this very emotional and confusing reading?
Re: Nuchal Translucency
You could move forward with a cell-free DNA test (known under brand names as Materniti21, Panorama, etc) which is non-invasive. This is a simple blood test and carries no risk, however, it is not diagnostic but statistics show it has 99% accuracy of detecting Down's syndrome.
Alternatively you could get a diagnostic test to know for sure - a CVS or amniocentesis. While there is risk of miscarriage with these procedures, it is extremely low.
Definitely consult with your doctor on what that measurement means as far as risk ratio goes and what all of your options are. Wishing you the best.
I was offered an abortion at 28 weeks if I would have done the testing. I declined it because of the soft markers percentages and it being 3rd trimester when they found anything abnormal. Totally up to you but just know if it is downs as long as there are no major organ defects everything will be okay. I wouldn't change her for anything and one major perk of ds babies smile a lot sooner so we have been getting lots of real smiles at 4 weeks, where most babies don't do it for a few months.
I went through a little bit of mourning after we found out at birth. But I honestly know that she was sent to me for a reason.
It's okay to cry and be sad. The one piece of advice is not to look into the future too much because then thats when it makes you feel worse. I had to get past the is she ever going to marry or have kids? Because right now it doesnt matter and we just don't know anyways even if she wants to. Also with the way the education system is changing lots of the kids go on to get jobs and go to technical schools.
Depending on where you live get in touch with early interventions groups and ds support groups or places. They can help answer some questions.
With ds there are varying degrees and varying health problems. Some kiddos don't have any major issues and others do.
I am not sure if you are thinking about termination but think of it this way of the chromosome issues to have 21 is definitely not a death sentence for your baby.
Right now my hubby just constantly looks at her and just says how cute she is. He also told me a week after her birth that the day she was born was the best day of his life. So I am sure when your little one is born some of those fears will melt away.
Praying you find answers soon!