In order to avoid a Facebook overload, but keep our families and friends informed without non-stop texting and phone calls...

I created this blog to tell the story of our Baby Boy arrival into the world as a premie.

My water broke March 22nd at 26 weeks pregnant and our Max was born March 25th just before 2:00 in the morning.

Tuesday, November 27, 2012

Surgery

Maximus was born with a CCAM in his lung, as a reminder we didn't know this until he was born though they can sometimes be detected on ultrasounds. This is a random event 1 in 300,000 babies are born with them, and his has nothing to do with his prematurity, nor did it cause his premature birth. A CCAM is a fluid and air filled mass similar to a cyst. From his CT scan on November 2nd we learned that it  was oddly shapped and the largest 'bubble' was 1.5cm and the smallest 'bubble was 5mm. They decided that they wouldn't know exactly what to do until they actually got in there. They also learned that there was a large blood vessel 'feeding' the cyst that they would have to be very careful about to avoid too much bleeding.

Monday was surgery day and the initial plan of action was to do a diagnostic Laparoscopy, Thoracotomy, and lobectomy (removal of his bottom right lobe)  of his right lung, in addition to repairing his inguinal hernia. At the last minute the surgeon told us wanted to avoid a Thoracotomy because the recovery and risks will be milder the other way.

They took him back at 2:35 pm and told us to expect him to be done at 5:30pm. We waited in the surgical waiting room after we got our sleeping arrangements figured out. We got a message around 5:30pm telling us he was ok, stable, and they weren't quite done yet. We got the same message at 6:30, stable and they would give us another update in an hour. At 7:00pm they told us he would be heading to the recovery room soon and the surgeon would come meet with us in a few minutes.

The surgeon explained that they had completely deflated his right lung during surgery in order to get the best look at the CCAM. Maximus struggled with that and had some respiratory distress. The surgical team worked hard to keep him stable, but they decided they needed to do a Thoracotomy after all. I'm really really glad they told me this afterwards, but the surgeon reassured me that they never let his oxygen drop low enough to cause any sort of damage. He also explained that the CCAM was rather difficult to get out of the incision site, but they were able to get it taken care of. He told us to give the nurses 30 minutes and if we hadn't heard from anyone (the waiting desk was closed by this point) that we should walk to post-op and ask them where Max was.

At 8:00 on the dot we walked down to find him, and a super nice nurse lead us to the PICU (Pediatric Intensive Care Unit) and we walked in to find them finishing getting him settled. It was the most awful feeling of Deja-vu to see all those familiar machines and monitors, but at least I knew what they all meant and what to expect from them. He was, of course intubated and swollen. He was covered in bright orange stuff and was a little pale, but he was perfect and handsome and peacefully sleeping. He continued to sleep while we got updates and everything was settled before we had to leave. They told us they would be extubating him at 6:30 am so we set our alarms for 5:45 to make it on time.

As I learned from our time in the NICU things always change and they decided to extubate him early so we were surprised to be able to see his face again when we walked in at 6:30 am. It was a hard and blur of a day getting him eating again, keeping his pain at bay, and making sure he knew we were there. I am eternally grateful for every person who has ever decided to be a nurse, because it has got to be such a hard hard job. The doctors decided he was doing so very well, he didn't need to stay in the PICU and he could move to his own room on the 3rd floor in the Pediatric Surgical Recovery Unit. We had to wait until a room opened up, but he was ready whenever one opened up. This was a HUGE surprise for us because we had been told he would spend 3-4 days in the PICU and only go to a room before he was ready to be discharged.

Around 4:00 pm while we were getting Maximus ready to eat again his nasal canula came out and fell on the floor, since he had been at 100% on the lowest setting his oxygen machine would go the RN decided to see what would happen if we left it out.
That was over 6 hours ago. That's right, for the first time in his ENTIRE LIFE Maximus is breathing completely on his own.  If he keeps this up, he may not need to even be on oxygen during the day anymore. The thought of bringing him home without being hooked up to an oxygen tank makes me want to cry.

He's hoping he stays oxygen free all night!

3 comments:

Amanda and Chad said...

you guys have had the craziest year! i just can't say enough how strong & amazing you, solomon, and evalynn are. this just makes me so happy that things are going good... and hallelujah about the oxygen! you will have to keep me updated on that... i hope he keeps breathing on his own :)
love ya!

Sarah Wilson said...

OH HAPPY DAY!!! I am so glad he is doing so well. I know it's been rough and scary so happy he is on the up and up.

The Brindley's said...

I love love love this!!!! Amanda is right, you are sooo strong! And OMG he is a cutie!!!