Our Growing Baby

Sunday, January 19, 2014

Oliver's Birth Story

Hey all, I know I have been pretty silent in sharing the details on the arrival of my sweet baby boy. I swear to you that when I got to the hospital, I was planning out the blog post in my mind the whole time. Per usual, though, when I am planning things everything seems to go exactly the way I never expected, so I have been putting off posting until I was A. out of the hospital and B. had enough story not to leave you hanging (completely). So, here we go…Oliver's Birth Story:
6:15 Thursday morning, I woke up to discover that my water had broken, but I was having NO contractions, so I thought maybe I was crazy. And I had just had a prenatal appointment on Wednesday where my doctor told me I was 80% effaced and dilated to a 1 (and still 2.5 weeks away from my due date), so I wasn't expecting action any time soon. But I called the hospital and asked if I should come in. They said "yes" and we were off (well after I spent a good twenty minutes trying to remember my check list of things to add to the hospital bag before we went). We got checked into the hospital around 7 AM and they double checked me to make sure that my water had in fact broken (which it had) and to see how far I was dilated. I was at a 1.5 (I think they just said .5 to try to make me feel like I'd made some progress in the 20 hours since my last appointment). To move things along, they got me set up on an IV. After about three hours, my contractions were starting to get pretty painful and so I had them bring in the anesthesiologist to do my epidural. After he took care of that, I was feeling great so Tommy and I started watching movies and playing cards. 
Around 1, I was measuring at an 8, which I was very excited about. Literally right after the nurse left from checking me, I threw up, so she checked me again cuz she said sometimes that can actually help you move along. Yep, I was at a 10 and ready to push. So they called the doctor and it took him an hour to get there and then I started pushing. I only had to push for 15 minutes (which was crazy amazing and not what I was expecting) and our Oliver was here!
 Pretty quickly they realized that his breathing wasn't as strong as it needed to be. He was breathing, but they were recording his breaths and they were staying right at 80 (they're supposed to be between 90 and 100), so they had me do skin-to-skin contact with him against my chest for a couple minutes and then said they were going to take him to the NICU to take care of him and thought he would only need to be there an hour or so to get his breathing where it should be. I had Tommy go with them to the NICU while I ate some dinner. A few minutes later, the doctor came in and told me that Oliver's breathing was getting under control, but he was exhibiting some behaviors that made them think he was in distress. Only a few minutes after the doctor left, Tommy came in and told me that Oliver had HIE, which is a condition where at some point in utero or during delivery (they don't really know which), Oliver's brain wasn't getting enough oxygen. The lack of oxygen can lead to strokes, brain damage, or death, so they were taking immediate action to put him into a cooling blanket for a 72 hour, medically induced hypothermia treatment that is supposed to slow down the body's functioning while they correct his levels and allow his brain to develop without getting damaged. What we learned later was that Oliver was very borderline--they debated doing the treatment or not because his case was not very severe, but he did have some symptoms that made them decide treatment was the best option to make sure that he wouldn't suffer brain damage. They also told us that the best results come if treatment starts within 6 hours of birth, and they got him started in the first hour, so that was really good. We had Tommy's uncles come to the hospital and they gave us both a blessing and then they let us into the NICU to give Oliver a blessing. Me and Tommy were really worried we were going to lose Oliver at this point, but in all of our blessings the spirit was so strong and we both looked at each other after Oliver's blessing and said we knew he was going to make it. The neonatal specialist then came up to us and said she was very optimistic that he was going to make it and that she thought there was only a 20% chance that he would suffer any brain damage and, even if he did have brain damage, it may only be in areas of the brain that wouldn't impeded his development, but make it necessary for him to create connections in a different way then we normally do. We felt much better after talking to the nurse, though brain damage was still very high in our minds.
The cooling process was no fun for us or for baby. Oliver was pretty heavily sedated the whole time, which was pretty sad. We were happy that it was helping him just sleep and not be super aware of how uncomfortable he was, but it was hard to look at my shivering baby who I wasn't really allowed to touch since touch is uncomfortable/painful to babies when they're that cold. His oxygen levels were up and down a lot during those three days too. It was pretty emotional every time we went to visit him and I was constantly counting down the hours until they were going to warm him back up.
Now that he's off of cooling, he is doing a lot better. His breathing and blood/oxygen flow has dramatically increased, way faster than the doctors had expected. We got his MRI and EEG results on Friday. The EEG showed some slight abnormalities in the frontal lobe, but they are pretty sure that it is just from irritation because the MRI was normal (no areas of concern in the brain). They are going to do another EEG before Oliver is discharged in order to make sure the abnormality isn't a sign of seizure activity, but they are pretty sure it's not since he hasn't shown any signs of seizure activity. We are very happy the MRI was normal! The doctor said we'll just have to continue to watch his development for the next couple years and work with a neurologist to make sure everything is normal.Yesterday they had to put him on a lighting blanket for his jaundice and they already took him off because his numbers had gone down where they needed to be. At this point, we are working on nursing and digesting. They're steadily increasing how much they are feeding him when I'm not there and letting me try to nurse twice a day. Yesterday he did really well with nursing and has been digesting almost all of his food, which is great. I am very impatient to get nursing down because I am very, VERY impatient to get him home, but he has been doing so well and we have been so blessed. We're so thankful for all the answers to prayers we have had the last 10 days and are so thankful for our Oliver James.
 Here Oliver is sleeping in his Daddy's arms…^
^ Oliver loves to have his hands up by his face and he also loves to keep his pinky, ring, and middle fingers up on his right hand…Here he's throwing up a gang sign (Tommy says it's his Cave Creek sign)
^ Look at my happy baby!! I love his awake time, it's so great to interact with him now that he's off that stinky cooling blanket

10 comments:

Ashley said...

Wow! Definitely not the way anyone wants to start out parenthood, but you guys have done amazing with everything! So happy he's better, can't wait till you can take them home! Love the gang sign. Guess I should return the cooling blanket I bought for you as a baby gift. Sounds like you don't like them!

Unknown said...

He is adorable. What a story. I love that you knew from the spirit that Oliver would be just fine. I love you and Tommy. What wonderful parents to sweet little OJ. I can't wait to hold and "squeeze" him.

Unknown said...

Ashley your comment is funny.

Kimberly said...

THanks for sharing. It is crazy that even with all these details, it is just the surface! Even since you wrote this, he has increased in his nursings, gone down on his oxygen, and decreased the heater... and I love him even more everyday!

Kingpin said...

So Happy things are going better. What a little cutie. Hope he continues to get stronger.

Jason and Kenna said...

That first picture of him looks total Blodgetto. Yep, Kimbers, everyday is going to be better and better and different and different and then sometimes hard, but overall better and better. It is crazy how much he is changing and getting stronger I'm sure. PRetty amazing to have front row seats for the show..

LOVE from the Brockstars.

RaeAnn said...

that one kimbers comment is from me! and I hope you can find time in between feedings and sleeping to post again, because he is already so changed from these pictures!

Jason and Kenna said...

Hey how big was he??? I need stats stat.

Alisha said...

I love that you are blogging. So glad that Oliver is okay and progressing each day. Thanks for writing all about your experience!

Alisha said...

BTW he is so cute. By the looks of it I think our kids will get a long someday :)