After a two and a half hour visit with a specialist and U/S tech, little Max has been confirmed to have Gastroschisis. However, the good news is that there is absolutely no chromosomal abnormalities that they could find (FI and I decided against an amnio).
When I tested positive for NTD, what the nurse did NOT tell me was that the same test also shows an indication for the gastroschisis. So all that worrying and panic attacks about both that AND spina bifida was for absolutely nothing.
I will now have to go in for ultrasounds every three weeks as well as my appointments with my regular doctor every four weeks. I also have to set up an appointment with the surgeon and what not at the Children's Hospital of Wisconsin about delivery and what our game plan will be.
Max will have to go into surgery as soon as he can (if he's healthy enough for it, around two hours after birth. Otherwise it would have to be a couple days after). Then he'll be in the NICU for 6-12 weeks. Of course, there are more risks involved before birth, during birth, and of course during/after surgery. I don't really want to bore everyone with the details.
But I really want to thank everyone for the help and support during this last week. It's been mentally draining and just... Thank you for all the prayers. You have been a wonderful group of women.
Re: Update from the doctor.
I am glad that the issue is limited to just the gastroschisis!
Sounds like they have a plan of attack and baby will be just fine, what a relief!
Indeed. It was so relieving. He will most likely be smaller than a healthy baby his age, but it shouldn't anything to really worry about. But they want to monitor like crazy.
But I guess that just means I get more pictures =D
Thank goodness for a very positive prognosis!
I am sending you all of my positive vibes. I just know that if you and DH can stay positive, you can find the light in this entire situation.
Best of luck with everything you're about to encounter.