Well, there haven't been any HUGE changes here. Oakley has continued to pee, so he hasn't needed any more dialysis. They removed his peritoneal dialysis catheter this morning. They've started to lower the pressure support on his ventilator as well.
He's still going to be intubated for. Few weeks more, but he's on the upward slope of healing.
His arterial stick line went bad, so they're poking him again. We made them switch back to his heels after coming in to his thumbs and fingers covered in blood...they poked his fingers from the knuckle up, I guess they don't know how to ask endocrinology where it's ok to poke?
His weight has been pretty steady, he was 8.4 kg's this morning after his procedure, and was the same yesterday.
We have been so fortunate this holiday, we've been adoopted by a group of people in Boise and by the NICU folks at Saint Luke's. We have been so overwhelmed with the love and support we continue to experience from home!
My parents and their international students have been in town the last few days, and Trevor and I have had good breaks from the hospital. We went to a huge outlet mall, tried to get into Canada (visa problems stopped us from going all the way in), and we're going to cook up a big Christmas Eve dinner tonight! It's been hard to balance spending tiime with Oakley in the PICU (we're limited to 3 people in his room at a time, including Trevor and I) and spending time with my family while they're here. We're going to spend all day with Oakley tomorrow, we hope to get a picture of him with Santa Claus!
We'll post pictures of Oakley with all his gifts soon, for now he's just trying to sleep, heal, and grow. We love you all and we covet your prayers.
Love,
Samanatha, Trevor, and Oakley
PS, we wish we were home with you all, and can't wait to make up for it double next Christmas!
Showing posts with label IPEX. Show all posts
Showing posts with label IPEX. Show all posts
Monday, December 24, 2012
Merry Christmas Eve
Tuesday, September 11, 2012
Well, last night was a tough one. I had been to a doctor's appointment that day, and was gone for much of the afternoon, but when I got back to the hospital, Oakley was playful and happy and had just eaten a little bit from a bottle. Trevor and I ate dinner, and then we all cuddled in on the window seat bed to watch some tv. We had noticed the back of the little guy's head is getting a little bit flat, so we laid Oakley on his tummy while we were there with him. Around 10, I fed him (after he got his Lovenox shot and was a little cranky), and he was scarfing. We have been nursing in different ways, because he was resistant to nursing a couple of weeks ago, so we are trying to make nursing a super comfortable and soothing experience. So, Oakley and I were laying side by side, while I nursed him, and he started acting like he was going to throw up. This is a fairly normal occurence for him, especially on Bactrim days (Bactrim is a med he gets on Mondays and Tuesdays as a prophylactic against PCP pnuemonia). I raised him up, and his lips looked like they were turning blue, and realized he wasn't breathing. I told Trevor, and he called the nurse while I tried to get Oakley breathing again. He started breathing after about 10 seconds, and the nurse came in to check him out. While she was there, he did it again for 10-15 seconds. It was really weird, because he wasn't acting like he was struggling to breathe, he just was acting like he forgot to...and he was super calm, just turning blue. She called another nurse in and they called the doc on call, and they hooked him up to some monitors to watch his heart rate and respirations and O2 saturations (the amount of oxygenated blood getting to his extremities). He was getting pretty mad, because they were checking his blood sugar, and poking him and prodding him to try to figure out why he had done this. We thought he might have sucked his zenpep down his trachea instead of getting it into his stomach, or that he had aspirated some of his food, or even that he was getting acid reflux issues. We put him on a foam wedge, but then he got a hive-like rash. He was given Benadryl to get rid of it. They wanted him to calm down, so they could get a better idea of what was going on. They had me hold him and rock him, and he nuzzled in to try to sleep, the Benadryl was definately kicking in. The nurses started talking and Trevor and I were joking about how Oakley sometimes does inexplicable things, and then they go away. His left leg that keeps swelling up and turning red or purple, his rashes that come and go, in the past he's had random fevers that go pretty quickly, etc.
I noticed he wasn't breathing again, and pulled him away from me to look at him and show the nurses. This time we blew in his face, rubbed his feet, shook his arms, but he still didn't start breathing. They called a code blue, and people rushed in from all over the hospital. They put on an oxygen mask and started pumping air in and out of his lungs manually. He had gone 30-45 seconds that time. Chaos ensued in his room. Respiratory therapists looked him over and poked and prodded, his pupils were checked by 5 different people, the ICU team came and looked him over and over. He was breathing on his own again, but was exhausted. He was breathing heavily and grunting a little, and his head was bobbing with his breaths. Trevor and I just attributed it to the Benadryl and the exhaustion, but they said they'd check him in 2 hours to see if he was stable enough to stay on the transplant floor or if they needed to move him to the ICU until they tested him in the morning.When they came back, he was breathing pretty normally, but they wanted him to go up to the ICU for the night just to make sure he was going to be ok. Trevor and I were exhausted, and wanted him to be able to stay, so we could get some sleep-he was on monitors now-but they insisted. They don't intubate on the transplant floor, that's something they only do in the emergency room or in the ICU, and they wanted him to be in an accessible place so there wouldn't be chaos if he needed breathing assistance.
We moved up to the 4th floor, giving up our suite-hopefully just for the night- and while the ICU team was admitting him and poking and prodding and examining-he woke up, and stopped breathing again. This time was different than before. He turned very pale, looked off and then went stiff as a board. His arms and legs were straight, and then he arched his back. They thought it was probably a seizure, and they gave him Adovan. They wrestled him down and got a bag on him, to get him breathing again, and decided to have a CT done on his brain immediately, instead of waiting until morning.
As we entered the CT scan room, he stopped breathing again, and they couldn't get him to start again, even after bagging him for a while. They decided to intubate him, which means they pumped him full of pain killers and muscle relaxers, then put a tube down his trachea for a ventilator to pump air in and out of his lungs. The first doctor tried twice (they had to take the bag off his face while they tried), then the second doctor tried twice. I don't know if there's a timeframe in which they have to call a code, but they called another code blue, and kicked Trevor and I out of the room. They sent a social worker to talk to us while they were intubating, and she incorrectly told us they were having to do chest compressions and bagging him while they tried to intubate him. That freaked me out. I asked her if he was dead and they were trying to resessitate him. She didn't seem to know, and Trevor and I got pretty scared. She came back in and told us they finally got him intubated, after 10 minutes. Instead of talking to her, I went back into the room and asked the doc if they really had done chest compressions, they told me no, his heart had never stopped, they just had trouble intubating him.
With Oakley intubated, and still having episodes, Trevor and I gave in to the realization that we wouldn't be able to keep our huge room on the transplant floor. We went down and packed up our stuff and loaded it into our car. After we got everything out, we had to drop a couple of things off in the ICU, and we wanted to see Oakley and meet his nurse (it was 7 am at this point, time for shift change). They wouldn't let us back there, because they were doing a sterile lumbar puncture, but they did let us know that the CT scan looked good. They were worried he might have a brain bleed or a blood clot, but it was clear. The lumbar puncture was to look for meningitis or encephalitis. Trevor and I went to our room at Ronald McDonald house, and I slept there for the first time in the 16 days we had been here.
We came back this afternoon, and met with the neurologists. They're the ones who will get to decide when Oakley can be extubated (which he needs to be before he can move back to the transplant floor). They did an EEG today, and they want to wait on the results of that before they can make any decisions. They think he may have had a seizure, but that it was likely caused by his blood sugar. They don't want to put him on seizure meds, but if his EEG comes back that there's a problem, then they will. He had an MRI that looked great, so we're really just waiting on the last test. They have kept him sedated the entire time, so he's been out for about 20 hours now. It's so hard to see him all hooked up to tubes and not get to hold him or see him smile. It's like reliving his birth and the first couple of days with him all over again, but it's harder, because now I'm used to being spoiled and getting to see his smile.
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| the face I'm missing right now |
The nurse and I just spoke, and Oakley's been fidgeting and seems uncomfortable, so they're starting him on a morphine drip to keep him further sedated. I am going to now spend the night at Ronald McDonald, and it already feels bizarre.
Tuesday, August 28, 2012
Sorry for the Delay; but we're finally in Seattle!
Ok, sorry for it taking so long to post an update for you all. We finally made it to Seattle, after a pretty hectic week! We were initially supposed to come here on Wednesday, the 22nd. We got a call on Monday afternoon letting us know that the PICU (pediatric intensive care unit) at Seattle Children's was full, so we would be delayed until Friday (They wanted to put Oakley in PICU because he has an insulin drip, and isn't necessarily stable on his drip-so he would have closer monitoring there). Trevor hadn't left yet (he was going to leave Tuesday evening, after his mom got off work, so it was ok-we even got to spend our anniversary together. Trevor, Mona, and Bill wanted to be there when Oakley and I arrived, so they convoyed up on Thursday, and Trevor dropped me off at the hospital with my overnight bag that afternoon. Oakley and I were supposed to head up on Friday morning at 9:30 to the airstrip and fly on a fixed wing Cesna to Seattle, courtesy of Air Saint Luke's. Friday morning at about 4:30, we got a call saying that they didn't have room for Oakley, and that they didn't know when he could get into a bed there. The Neonatologist and nurses at Saint Luke's were pissed-they had called the day before at 3, and there had been a bed, so the Doc asked the bearer of bad news why they didn't just have us fly up then. After several phone calls and angry conversations, Dr. Crichton got ahold of one of Oakley's Docs in Seattle and they decided they would just place him on the Hematology/Oncology floor, and he told her that he would lay in Oakley's crib if he had to, in order to ensure there would be a room for us on Saturday morning.
So we finally got to leave Saturday morning. It was the first time Oakley had ever been off the 2nd floor of Saint Luke's in his 4 months of life. He was looking all around and especially interested in the different light fixtures in the elevator on the way down to the ambulance. His first breath of outside air was super smoky-it tasted like campfire because of the crappy air quality being caused by the fires surrounding the area. He slept the whole way to the tarmack, and when we moved him from the ambulance to the little airplane, he got sun in his eyes for the first time...he didn't like it. We covered his face with a quilt that was given to us by the NICU, and loaded him into the plane. He was just on a little board, so the EMT transport staff had more room in the cabin of the plane than they were used to. I got to sit up front, next to the pilot and view us rising out of the smoke, and got to see Mt. Adams, Mt. Rainier, and Mt. Hood as we got closer to Seattle. It was awesome. Oakley slept the entire flight, and then on the ambulance ride from the airport to Seattle Children's. Once we got to the hospital, he woke up, and was again intrigued by the lights. We wheeled him down to the 3rd floor, and were ambushed by doctors, nurses, nurse practitioners, and mauled with loves from Trevor, Mona, and Bill. He was quite overwhelmed and cried for most of that. He hid his face in my chest and I fed him, and he calmed down a little bit.
Once things were calmer, we looked around his room, and the accomodations are amazing. We really wanted him to have a window, as he was in an interior room in Boise because of his immunosuppression induced isolation. Here, he has a window (which is above our bed/bench for Trevor and I), he has a balcony room that is all windows except the ceiling and beam, and he has a view out of both! He has a tree and can see an outdoor play area, so Trevor and I were pretty excited for him. Oakley is still a little vampire though. When we walked him into the sunshine in the balcony area, he may as well have hissed and burst into flames.
We have a lot more backstory to fill in, as well as a mushy post about how much we miss Saint Luke's and all of our family and friends, and how cool everyone at the NICU was/is as well as a giant thank you to everyone! So stay tuned, we'll get to it eventually...
So we finally got to leave Saturday morning. It was the first time Oakley had ever been off the 2nd floor of Saint Luke's in his 4 months of life. He was looking all around and especially interested in the different light fixtures in the elevator on the way down to the ambulance. His first breath of outside air was super smoky-it tasted like campfire because of the crappy air quality being caused by the fires surrounding the area. He slept the whole way to the tarmack, and when we moved him from the ambulance to the little airplane, he got sun in his eyes for the first time...he didn't like it. We covered his face with a quilt that was given to us by the NICU, and loaded him into the plane. He was just on a little board, so the EMT transport staff had more room in the cabin of the plane than they were used to. I got to sit up front, next to the pilot and view us rising out of the smoke, and got to see Mt. Adams, Mt. Rainier, and Mt. Hood as we got closer to Seattle. It was awesome. Oakley slept the entire flight, and then on the ambulance ride from the airport to Seattle Children's. Once we got to the hospital, he woke up, and was again intrigued by the lights. We wheeled him down to the 3rd floor, and were ambushed by doctors, nurses, nurse practitioners, and mauled with loves from Trevor, Mona, and Bill. He was quite overwhelmed and cried for most of that. He hid his face in my chest and I fed him, and he calmed down a little bit.
Once things were calmer, we looked around his room, and the accomodations are amazing. We really wanted him to have a window, as he was in an interior room in Boise because of his immunosuppression induced isolation. Here, he has a window (which is above our bed/bench for Trevor and I), he has a balcony room that is all windows except the ceiling and beam, and he has a view out of both! He has a tree and can see an outdoor play area, so Trevor and I were pretty excited for him. Oakley is still a little vampire though. When we walked him into the sunshine in the balcony area, he may as well have hissed and burst into flames.
We have a lot more backstory to fill in, as well as a mushy post about how much we miss Saint Luke's and all of our family and friends, and how cool everyone at the NICU was/is as well as a giant thank you to everyone! So stay tuned, we'll get to it eventually...
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| My little papoose, as he was getting strapped to his board |
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| Oakley and I, right after he got to leave his room! |
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| Owyhee Mountains, just above the smokeline |
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