wookie130
Momma to H, O, & C
- Joined
- Jun 10, 2011
- Messages
- 13,471
- Reaction score
- 30
Just some background...I'm 35, and this is my 2nd "successful" pregnancy. I've been pregnant 4 times, with one live birth...my daughter, who is now a year old. I opted to take the MaterniT21 screening with this baby, due to my age, and the results came back stating that I have a normal healthy boy.
Fast forward to my 20 week ultrasound this past week.
Everything with little man looked great, except that the ultrasound tech stated that I have a 2 vessel cord, rather than 3...which she did not seem worried about, nor was my OB, in light of the fact that everything on the scan looked normal, and great. HOWEVER, I was then promptly booked for a level II ultrasound at University Iowa Hospital, nearly an hour and a half away, just so they could "check him again."
I then, made the mother-of-all-mistakes, and consulted Dr. Google.
And the words, heart defect, soft marker, genetic abnormalities, stillbirth, IUGR, prematurity, kidney problems, and low birth weight stood out to me. Over and over again.
First of all, in light of my perfect MaterniT21 results, what is the likelihood that he has some wierd undetected chromosomal or genetic problem? And the 20 week anatomy scan looked great, and no one seemed concerned. What does a level II ultrasound entail? How is it better or different than a regular ultrasound?
Needless to say, I'm very worried, even though my OB told me that the vast majority of SUA babies are born with no issues at all.
Fast forward to my 20 week ultrasound this past week.
Everything with little man looked great, except that the ultrasound tech stated that I have a 2 vessel cord, rather than 3...which she did not seem worried about, nor was my OB, in light of the fact that everything on the scan looked normal, and great. HOWEVER, I was then promptly booked for a level II ultrasound at University Iowa Hospital, nearly an hour and a half away, just so they could "check him again."
I then, made the mother-of-all-mistakes, and consulted Dr. Google.
And the words, heart defect, soft marker, genetic abnormalities, stillbirth, IUGR, prematurity, kidney problems, and low birth weight stood out to me. Over and over again.
First of all, in light of my perfect MaterniT21 results, what is the likelihood that he has some wierd undetected chromosomal or genetic problem? And the 20 week anatomy scan looked great, and no one seemed concerned. What does a level II ultrasound entail? How is it better or different than a regular ultrasound?
Needless to say, I'm very worried, even though my OB told me that the vast majority of SUA babies are born with no issues at all.