Ava Winter Grace Dillon
Born at 4:12pm on March 3rd, 2010
7 lbs. 11 oz. & 21 in. long

Taken less than 5 minutes after her birth.

Cutting the Cord with the NICU team. Including a whole team of people from the NICU there were no less than a dozen people on hand for the delivery—primarily because of the concerns about the blockage in her digestive system.

Trying to get a bit of much deserved sleep in the NICU. This shows just a few of the cords they have to place on her to monitor things. She has a total of about 5-7 different cords coming off of her at any given time—placed mostly on her hands, feet, and lower stomach.

Hanging out with Mr. Ducky the Duck.

Our whole world in less than 8 pounds. Notice the amazing amount of hair on her head. Every NICU nurse that has seen her has made some sort of a comment to the affect of “what a beautiful head of hair she has!” We couldn’t agree more!
Mark here again. I should have had this post up sooner but we’ve had a flood of additional checks, tests, and follow-ups since her birth. It seems every department has their own set of required follow up requirements for Ava and Melissa. In between everything else we also had to move all of our stuff into a postpartum room on another floor of the hospital. The main reason for this post being so late though is we’ve wanted to stay right next to Ava’s side as much as possible. She is currently residing in an NICU (neonatal intensive care unit) room with around 6 other babies with the entire room being overseen by a whole staff of world-class nurses and doctors. While every single doctor and nurse we’ve come in contact with has been outstanding, it’s still hard to leave Ava all alone in what must be such a scary place for her. And as I mentioned above, she has a bunch of cables, cords, and sensors attached to her so they are able to monitor everything. Here is what we want everyone to know, though. There appears to be absolutely nothing wrong with her aside from some sort of partial blockage in her digestive system. What this means is it is NOT the complete blockage (duodenal atresia) they thought it was prior to her birth. She is peeing and pooping just like any other 2 day old, which the doctors told us would not be possible. She is also starting to breastfeed, which the doctors also told us would not be possible. We haven’t shared this with many people (mostly on account of it not changing our opinion about Ava) but also worth noting is the doctors told us about a month ago Ava had a 1 in 3 chance of having down-syndrome. At this point we can say with absolute certainty she does not have down-syndrome. In addition to all this, Melissa was also able to deliver Ava without a c-section, which multiple doctors didn’t think would happen. I only mention this as a testament to the goodness of God and as a thank you to every single one of you who have lifted up prayers for her in the past 9 months. THANK YOU from the bottom of our hearts.
We did have a few scary periods in what turned out to be the 18-20 hours of labor—the most scary of which involved Ava’s heartbeat dropping drastically and the doctor sending out a department wide page for an emergency c-section. A flood of other doctors came pouring into the room then proceeded to rush Melissa very quickly toward the surgery center while at the same time informing me I “wasn’t able” to follow them. As her stretcher left the room she was calling my name and I couldn’t do anything at all—I couldn’t even go with her. I’ve never been so afraid in my entire life. In the end Ava’s heartbeat returned to normal right before they were about to begin surgery and they proceeded to monitor her very closely until she was delivered. Again, this is a testament to all of the prayers spoken throughout the past 2 days and testament to the unfathomable goodness, mercy, and grace of God himself.
To summarize. Ava is beautiful. She is happy (most of the time). And she is unbelievably strong. Melissa did an unbelievable job with the labor and delivery. And I can say with complete confidence I am by far the weakest of our now 3 person family. If you can please keep Ava in your prayers tomorrow. They will be running some more tests to see if a surgery will still be necessary and if so, what type of surgery it will be. The possible surgeries still sound fairly straightforward but this doesn’t change the fact that surgery is something we would prefer to avoid altogether. Please pray for complete healing for Ava’s body. I will likely be writing about another miracle tomorrow afternoon. Melissa sends her love to everyone and I promise her blog will be back to it’s previous glory once she takes over the writing again. She’s still trying to work her way back to full strength and could still very much stand to benefit from your continued prayers. We’ll also have some more photos of Ava up soon. And I’ll do my best to get an update out tomorrow soon after we hear the surgeon’s opinion. Think that’s all for now.
Love,
Mark