On our 18 week ultrasound they found a bright spot in the bowel, otherwise known as Echogenic bowel. This is sometimes a soft marker for chromosomal abnormalities, although we did the genetic testing and the results were negative. On Friday we have an appointment with the specialist, in which they will do another ultrasound to see if the spot is still there. If it is, we are offered the choice of an amnio for further answers. I know there is a risk of miscarriage and just wanted to see if anyone else has went through with this procedure?
Re: Amnio experiences or thoughts?
I hope that everything for your sake is okay. Good luck.
I had elective amnio despite no (low) risks on my Maternit21 blood test. We would not have done amnio solely to get the confirmation of low risk for downs etc (remember that amnio is a test, not a screening like the cell-free DNA tests). But, there is advanced genetic testing called a microarray that can be done with the amniotic fluid. If you do proceed, I would suggest inquiring about this testing (note it is very expensive so you'll also want to see if your insurance covers it). Amnio for me was not scary at all once I was in the actual room with my doc and perinatologist. I watched the baby on the screen the entire time and saw what they were seeing in terms of putting the needle as far away from the baby as possible. The needle "pain" itself was no more than a pinch, like getting the flu shot. Of course everyone is in a different market and has a different situation and relationship with their doctor, but, for us, my doctor had done thousands of amnios without in incident and had high tech equipment that set my mind at ease that I was in good hands (from what I read, much of the historic risk with amnio comes with doctor error).
My decision to have amnio is obviously a rather unpopular and unique one on this board, but if you do some reading around the interwebz, you'll find lots of stories about how modern amnio is no longer the scary procedure they used to tell us about -- pre ultrasound, they had to put the needle in blind and just hope they didn't hit baby (!!). That was not the case for me, and, if I understand correctly, is no longer how the procedure is performed (however confirming that could help set your mind at ease if you do choose to proceed).
Ultimately, remember that no matter what you read on this board: there is no "right choice" - only what is right for you.
All that said, the decision about whether to get the test, I think, was the easy part. Deciding how you feel about and what you'll do with any information you receive is the challenging part and that part that requires much exhaustive contemplation (with your SO if he is involved). My husband and I ultimately decided that "knowledge is power" and while there are things we may learn that will lead to more questions than answers with the microarray, we would rather know and be able to potential get our child whatever help it needs throughout its life than be behind the ball at some point wondering what's going on. I didn't find much other than horror stories when I tried reading about people's experiences with microarray (everything was either "this allowed us to assemble a NICU team at birth that saved my baby's life" or "this test lead to more questions than answers and my stress is now through the roof about when in life my child will exhibit traits of a syndrome he carries - I wish I didn't know.")
Apologies for the long post, but as someone who struggled to find many examples of others' experiences, I hope this is useful.
As for me, yesterday, my amnio results came back normal, confirming my low risk Maternit21 reading and we are currently awaiting the results of our microarray. So I cannot even say we made the right choice on doing the microarray, but the above is a window into the pros and cons we weighed as we came to our decision.
Whatever you decide will be what you are comfortable with for your pregnancy and baby. Read as much as you can, ask your doc lots of questions and make an informed decision is my best advice -- hard to beat yourself up either way if you trust yourself that you did your due diligence in coming to your decision.
Me: 34 DH: 36
Married since 11/11/11
BFP#1 10/5/13 MC 11/11/13 @9wks 3d
BFP#2 7/20/14 EDD 4/4/15
bfp 1 - m/c 1.31.11 @ 10 weeks
bfp 2 - baby born via c-section on 5.4.12 @ 37 weeks
bfp 3 - blighted ovum/d&c on 4.13.13 @ 8 weeks
bfp 4 - 3rd IUI, very late BFN with super low P, c/p
bfp 5 - natural bfp while on lupron, baby born via RCS on 4.27.15 @ 39 weeks
bfp 6 - surprise! baby born via RCS on 11.13.16 @ 38 weeks
bfp 1 - m/c 1.31.11 @ 10 weeks
bfp 2 - baby born via c-section on 5.4.12 @ 37 weeks
bfp 3 - blighted ovum/d&c on 4.13.13 @ 8 weeks
bfp 4 - 3rd IUI, very late BFN with super low P, c/p
bfp 5 - natural bfp while on lupron, baby born via RCS on 4.27.15 @ 39 weeks
bfp 6 - surprise! baby born via RCS on 11.13.16 @ 38 weeks
bfp 1 - m/c 1.31.11 @ 10 weeks
bfp 2 - baby born via c-section on 5.4.12 @ 37 weeks
bfp 3 - blighted ovum/d&c on 4.13.13 @ 8 weeks
bfp 4 - 3rd IUI, very late BFN with super low P, c/p
bfp 5 - natural bfp while on lupron, baby born via RCS on 4.27.15 @ 39 weeks
bfp 6 - surprise! baby born via RCS on 11.13.16 @ 38 weeks
Me: 34 DH: 36
Married since 11/11/11
BFP#1 10/5/13 MC 11/11/13 @9wks 3d
BFP#2 7/20/14 EDD 4/4/15