So things got crazy REAL fast on Thursday morning. Matt and I had been on Ella duty for 3 nights in a row because Eli, Ella, and I got our nurses sick. I was up early Thursday morning and was getting ready to say goodbye to Matt and Ella as I was leaving for work and then Ella started to throw up. Ella's heart rate tanked to the high sixties and low seventies which was a little lower than usual. Now all of this is all pretty normal up to this point, but here's where it got nuts... Her heart rate wasn't going up like it normally does after vomiting, so Matt and I thought that it was an issue with the pulse ox's measurement. We switched the pulse ox probe to the other foot... same results... weird. Opened and placed a brand new probe on the other foot... same results... weirder. Matt and I look at each other and say, well, now what?! We definitely didn't want to give her compressions and she was acting similar to her norm, just a bit more sleepy. So we agreed it was time to call 9-1-1. I was on the phone with the dispatcher for a while and they were at our house within a few minutes. During those few minutes, our home nurse showed up and we all quickly started gathering everything we thought we'd need at the hospital. Let me tell you, we thought we had to pack out a lot of stuff when we had a less complex baby, Eli, but Ella has taken it to a whole new level. We made sure to grab the normal stuff like diapers, wipes, the baby bag, extra clothes etc. but we also had to grab the trach supplies, medication box, suction machine, pulse oximeter, ambu-bag (what we'd use to do CPR if needed), oxygen tank/connectors, travel ventilator, HMEs for the ventilator, formula and feeding pump, electrical chords for all of this and the list goes on... While we all gathered her things, I called Ella's cardiologist, Dr. Hill, and explained that we had to call 9-1-1 and then broke down crying. I handed the phone to Matt to have him explain it all to him. I quickly pulled myself together as the fire engine rolled in sirens and all.
The paramedics showed up and we immediately told them she has Hypoplastic Left Heart Syndrome and explained what her oxygen sats should look like, explained what had happened, and asked if we could be transferred to Sutter Sacramento. They made a couple of calls and said that they'd be able to take us there which was a HUGE relief. The hospital here wouldn't have known what to do with her anyway. So Matt, dressed in his work clothes and ready to go to work himself, got in the ambulance with Ella and the EMTs. I was planning on driving behind them but was then told I could go with them as well. So I grabbed a shirt for Matt and some comfortable shoes (because I was wearing heels, a skirt and a nice blouse for work) and we were on our way. Ella, by the way, was so curious about everything and just kept looking around at the equipment in the ambulance then took a little nap to gear up for the ER.
During the ride, we handed the EMT the binder that we take everywhere that explains everything about Ella. He looked over it and couldn't believe all that she's been through. Our tough little chicky. 😊 He then proceeded to tell us that he was on his way to work this morning and got a call from one of the other EMTs asking if the call was for his family BECAUSE HE LIVES IN OUR APARTMENT COMPLEX! WHAT?! Small world... So he quickly turned around and called his wife panicking because he has a kid ELLA'S AGE!!! So he wasn't sure if the call was for his son! SO NUTS! What are the odds?! It's nice to know we have an EMT a couple of houses away now! We continued on our journey while Matt measured out her meds and I suctioned Ella and chatted with the EMT about her.
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| Matt in the ambulance with Ella |
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| Just hangin' out in the ambulance 😂 |
After we arrived at the ER Ella's heart rate was stable in the high seventies to about eighty, which is still really low for her. She is normally around 110 when awake and high 90s when asleep. We walked into the ER and were greeted by a friend that is one of the heads of the respiratory department at Sutter. It was nice to see a familiar face. We got into the room and they wanted to get an IV line put in just in case they need to deliver any rescue meds and to get blood work done. Well, I think I've said this before in our blog, but Ella is a tough poke... The first poke was done and she was TICKED. Her heart rate jumped up to the high 140s to low 150s and stayed there for quite some time. Matt jokes now that if that ever happens again, we just need to pinch her or poke her with something to get it back up. They had to call in multiple nurses/IV therapists, poked a total of 6 or 7 times, and still couldn't get one that would work to draw blood from, which really wasn't a surprise to me.
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| Silly little girl. |
The PICU has been slammed so they had to move some patients around to get Ella in. Five or so hours later we were taken to the PICU where we were greeted like celebrities! Everyone kept saying, "We're so sad you're here, but so happy to see you!" It was like we were at a big ol' family reunion. By this time I was completely wiped out and had a mean headache. All of the exhaustion from staying up the three nights before and then the stress of the morning had all sunk in and I had to lay down. I ended up falling asleep on the couch in Ella's room while Matt explained everything from what happened... to how much she eats... to how far to suction... to what size diapers she's in now. I woke up about 45 mins later and the headache didn't subside. I quickly remembered that we had Ella's meds with us and she has aspirin! HAHA! I took some and quickly felt better. Matt and I hung out for a while then my parents showed up with all of our clothes, pillows, etc. that we would need to be able to stay the night. We left them with Ella and drove to the Ronald McDonald House to check in. We were so thankful they had spots open, often you get placed on a waiting list and have a couple of nights in the hospital before you get a room. We went back to the hospital and then left around 9:30pm. That whole day we were greeted by nurses, RTs, doctors, surgeons, PAs, and Child Life staff. It was fun for us to show everyone how much Ella has grown and how well she is doing overall (even though we were in the hospital 😂). We even had some people say, "I'm impressed this is the first time we have seen you! Way to go guys!" Almost everyone commented on how much hair Ella has now and how many teeth she has gotten. She flashed her big toothy grin at everyone as they came to visit her.
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| Our crazy-haired child still feeling a bit under the weather but as sweet as can be. |
When we returned to the PICU Friday morning, we rounded with the doctors and got a lot of pretty BIG NEWS. First, we knew Ella was sick and tested positive for rhinovirus (which is the fancy name for a cold). Then we were told that Dr. Hill and Ella's surgeon, Dr. Watanabe, were talking about having Ella go in for a heart cath to check out a lot of stuff: the pressures in her heart and lungs, how many collateral veins have opened up, what the status of the blood clots are in her neck, and most importantly, how big the IVC is. The inferior vena cava (or IVC) is a large vein that carries the deoxygenated blood from the lower and middle body into the right atrium of the heart. Now you may be wondering why the IVC would be getting measured, and we did too at first... There is a possibility that Ella may be going in to get the "third" surgery, the Fontan, much sooner than we anticipated. The third surgery uses the IVC. Dr. Watanabe visited us on Thursday night and we could tell that the wheels in his head were turning, but we didn't exactly know why. Come to find out, he and Dr. Hill talked the next morning and because of Ella's size, Dr. Watanabe wants to do the Fontan soon to get her out of the risky interstage. Now mind you, we had been told it would probably be in the fall of 2019 then we were told it may be closer to when she is 2 in the spring of 2020, but now we are looking at a possible surgery this April. Maybe this is why God had this all happen, if Dr. Watanabe hadn't seen Ella I believe we'd still be on course to do the Fontan later in the year.
Whhhhaaaatttt?
Matt and I were shocked! We couldn't believe it. We were a little excited and want Ella out of this risky interstage period. And because of the clots in her neck this period has been extended longer than normal due to not being a candidate for the "second" surgery, called the Glenn. As exciting as this could possibly be, we are also kind of scared. Back when Ella was going through her first three surgeries, we didn't know her as well so I found it a little easier to handle it all, but now that we've had her home for so long and built more of an attachment to her, I am a little nervous to go and relive all of the scary moments and everything that comes with a child's open-heart surgery. Just the thought of seeing her intubated through the mouth again freaks me out a little. But I know God has a plan for her and we have been through so much that I am almost calloused enough where I feel like I can get through almost anything at this point.
The other topic that we discussed was if her IVC is not large enough (at a 15 or higher), we would aggressively work to get her off of the ventilator while in the hospital!!! The PICU doctor doesn't relaly see a reason as to why she even needs the ventilator. We've even been taking her off to do certain things (for only seconds, but still!) and it's like it doesn't even phase her. The doctor even mentioned doing it during this stay, but then remembered she was sick so we better play it safe and wait until she's back for the cath. We even talked about an ideal situation of Ella having the Fontan, getting intubated through the mouth, taking out the trach, and LEAVING. IT. OUT. What?! Could you imagine?! No interstage? No trach? Sounds waaaayyyy too good to be true... Now, Matt and I are certainly NOT holding our breath for this to happen, but that would be best case scenario and would completely change our lives. But I am holding on to the fact that we will get her off the ventilator soon and that alone will change a lot about our lives. And as we've all seen through Ella's life, God does big things and things that we don't expect. So we shall see! Yippee!
We made a tentative return date of April 15th (while I'm off of work for Spring Break) to do the heart cath and see what will be the next steps. So we have 6 weeks to keep this girly growing and strong at home.
After all of that news, we went into Ella's room and saw her big smiley face. We were told we could leave as soon as all of the discharge paperwork was filed and then we'd be on our way! We did a trach change, chatted with Dr. Hill a little more, cleaned out the Ronald McDonald House, ran an errand to pick up a supply for Ella's trach stuff, and then we left around 4pm.
Fast-forward about 15 hours we got everything loaded back in the car, plus Eli 😉, to head down to Sacramento for the Donut Dash, a Child Life fundraiser. We weren't sure if we would take Ella out of the car because it was pouring rain, but it lightened up and we ended up all going and had a blast. We ran into a lot of friends from the hospital and they were so excited to see Ella there. It made me so happy to be able to finally get outside and do something "normal" (I hate that word now) for a change. Ella rode in her stroller like a champ, smiling along the way, and we feasted on donuts halfway through the walk. Here are some pictures from the event...
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| Ella all snuggly and ready to go! |
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| TEAM ELLA (minus the Bestelmeyers, Tomlinsons, and George Newman!) |
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| So excited for donuts! And yes... Eli somehow managed to eat all 6 donut holes without us realizing! |
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| Ella and I with Sarah from Child Life (who is amazing by the way) and Dr. Falco! |
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| Woo Hoo! Donut Dash baby! |
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| Some of our favorite PICU nurses and Dr. Falco!!! |
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| We got to see our other heart warrior buddy, Everley, too! Check out that pose! |
Love,
Jillian
