and now we march
Yesterday's visit with the specialist confirmed the suspected diagnosis: the wee one has hydrocephalus.
Because of all the reading and preparation I had done before this appointment I already knew quite a bit about this condition. But we were still hopeful that maybe somehow the initial sonogram was incorrect. This was not the case, as the hour long level 2 ultrasound confirmed the previous finding.
I was really strong, and did not break down until the very end of the consultation with the perinatologist. At that point, he said to me "It's alright to feel upset. It IS scary, and when parents don't seem upset I usually have to explain things over again because it means that they didn't understand." He also told us that we'd probably feel a lot better once we meet and talk with the pediatric neurosurgeon who would be handling our case once the baby is born, since the surgeon is the person who maintains contact with the families and does all the follow up, even years after. He told us that this particular surgeon has patients with hydrocephalus who are now well into their teens and beyond, so he'll be able to give us a better picture of what to expect down the road. That was comforting news. But we won't be meeting him until next month when we have our next appointment with the specialists to have another ultrasound and monitor the baby's development.
Until then we are grateful that the most recent ultrasound showed no other indications of anything else out of the ordinary - specifically, they looked for other indications that the wee one might have trisomy 13 or 18 (which he said are generally "incompatible with life"). The doctor warned us that things might arise later in development, but at least for now, the rest of the baby looks wonderful. To me, the baby looked perfect.
So now we just do all we can to help the wee one grow big and strong, and give it every chance we can. And try not to have too many break downs while we "wait and see."

