My gynac wrote this test for me at my last visit and i forgot to ask her properly what its for. Now im a bit anxious googling it. Can someone explain in simple words what it checks?
I got mine done and the wait for results made me so nervous! Did others also feel anxious? Mine came low risk, the doctor was very reassuring about it.
Its a simple blood test in the first trimester, nothing to fear. They combine it with the nuchal scan and give a low or high risk result. If high they suggest further tests, thats all.
My doctor explained its a blood test done around 11 to 13 weeks, usually with an NT scan. It checks two markers to estimate the risk of certain chromosomal conditions in the baby. Its a screening, not a final diagnosis, just gives a risk level.
Its an optional screening test for the babys health. Some couples do it, some skip, depends on age and history. Best to discuss with your gynac whether its needed for you.
Just a heads up its a paid test and prices vary by lab, so ask the cost beforehand. We did it because of my age. Worth asking the doctor if its recommended for your case before spending.
