I am hoping someone can help me out.....I am expecting my second baby this August and already a proud Mommy to a beautiful little girl. I went in for my first appointment on Tuesday and they had mentioned doing an ultrasound on my next appointment for check for Down Syndrome and other chromosomal defects and my doctor had mentioned that I had done this with my first one but after asking some family members I did confirm I did not have this with my first one. Granted my first child is 7 (8 in September), so my question is.....is this a new test or something the doctor has seen on the screen and I should be worried about?
Re: Ultrasound question
Married May 2014
DD born August 2016
Baby #2 due December 2017
Our little lightbulb is on the way!
12 weeks 3 days
TTC since Oct 2011
Me: 33, hypothyroidism since 14, cleared all HSG, US, Pre-pregnancy panel tests.
Hubby: 36, testicular Ca, chemo April-May 2012.
Natural cycle IUI #1 with trigger and Progesterone Suppositories (Jun 2012) Neg
Natural Cycle IUI #2 with trigger and Progesterone Suppositories (Jul 2012) NEG
Aug 2012 - break due to needing a girls' weekend in Cape Cod
Natural Cycle IUI #3 with trigger and prednisone (Sep 2012) NEGATIVE
Switched fertility clinics - forced break Oct 2012
Natural Cycle IUI #4 (Nov 2012) no trigger, no progesterone, no prednisone (Nov 2012) - Neg
1st round Clomid Cycle IUI #5 (Dec 2012) - POS
I had it done with DD and have it scheduled with this one because of family history, so I didn't have to pay OOP. If it weren't covered, I don't think I'd opt to have it done.