I went in for an amnio almost 2 weeks ago. My husband and i are both alpha thalasemmia trait and the only way to know right now to whether the baby has major thalasemia is through amnio. And i will prolly be doing amnio everytime i get pregnant to because if the baby is a major thalasemmia it will give my baby and I some complications. They do ultrasound to locate the best place to do the amnio and to also make sur3 the needle is no where near the baby.
Oh, yeah, and of course, the only reason to do any of these tests, is if you consider abortion in case the test comes out positive...
Same here. I chose not to run this test, but did the DNA blood test - in Israel it's called NIPT. I guess your doc should know what it is. It's quite expensive, but I prefer to pay and not to put my baby at risk.
I have chose not to run the test. In my opinion the risk to the baby is to high for results I will find out when it is born anyway. My doctor stated that the only reason to do the test and know now instead is if I planned to abort and I don't so I chose not to.
Hi there, my results for Down Syndrome came 1/410 possibilities, so medium risk, and my doc said that I could do the amnio to be sure. But I didn't want to risk losing a healthy baby (1 out of 200 amnios end in miscarriage) or hurting the baby (a friend of mine had to have it done 3 times! In the first they actually stuck the needle on baby's leg, the boy now 10 years old has a big scar on his leg, but it could have been anywhere else in his body...)
So I opted for the DNA blood test, it's 99+% accurate and it tests several diseases plus DS. Non invasive, though expensive. It cost me about 1000$, but it's because they sent my blood from Europe to California, therefore increasing the price. Maybe if you are in the US it'll cost you less... I don't know, if your results are good, I wouldn't risk it. Good luck!