Thursday, November 29, 2007

Wednesday, November 28, 2007

Week 3 in Toronto

It's hard to believe that we've been in Toronto for 16 days now, especially after we were expecting to bring him home in just 7. Liam is now completely off IV, as his two most recent IV sites became inflamed. This is unfortunate, as the IV treatment he was receiving was fairly successfully bringing his drainage down. Now he is back to bottle feeds and is on a steroid, but he still isn't drinking much from the bottle (if I had to guess, it's because the special formula he's on isn't much to his liking). If he doesn't start drinking the required amount soon, he may have to get an NG tube put in (a feeding tube that goes through his nose and directly into his stomach), which he is sure to not particularly enjoy.

So please continue to pray for Liam. It's pretty humbling that so many people have been praying for Liam, so thank you for those who faithfully continue to do so. The waiting game continues...

Saturday, November 24, 2007

Another day

I was a bit worried that Liam might get ahold of his IV tubing and rip it out last night, a concern that I shared with his nurse yesterday. She told me it was pretty secure, and much to my surprise, he got through the night without ripping it out.

But he changed his mind this morning, and sure enough, he ripped it out. Luckily, Mary was there with a few minutes later, and found him crying and bleeding. So yeah, we're both pretty damned pissed off about that, and we let them know it. If he manages to rip it out again, I'll seriously consider having him transfered to another hospital. This is actually the second IV he's ripped out... a few hours after his heart surgery, when I thought he was supposed to be sedated, he ripped out his leg IV and his breathing tube (it was again fortunate that I was there, as none of the nurses in the room noticed, and I had to run over to one to get their attention).

To be honest, we've both been really disappointed with much of Liam's care at Sick Kids. Some of the nurses have bordered on being negligent, and we've had to complain several times; I'm sure we'll have to complain several more. I was expecting a lot more from such a highly-esteemed hospital. Some of the nurses have been outstanding, but it's clear that the shortage of nurses is having a serious effect on the care provided in Ontario. It's nice to not have to pay for medical care in Canada, but it's a shame that the care is sometimes complete shit.

Anyways, so Liam has a new IV in him and is doing fairly well all things considered. We don't have any new pictures, as he looks pretty much the same from the most recent pictures, except that his wound continues to heal nicely. Grandma and Grandpa Gerryts are coming to visit tomorrow, so the four of us are looking forward to that.

Friday, November 23, 2007

Still in Toronto

Whoops, haven't updated in quite a few days. Liam is doing well, but remains at Sick Kids due to his excessive drainage. The 5-day diet didn't bring down the drainage sufficiently (it actually went up yesterday), so today they put him on an IV (which he thoroughly enjoyed receiving). Apparently, the IV won't satisfy his hunger, so the next few days could be a pain. Hopefully it will do the trick and we can have him home by next weekend.

We were told by another mom that he will most likely have to remain on his special pre-IV diet formula for 6 weeks after we bring him home. The really bad news? It costs $28 per can. Yeah. So we'll see what happens with that.

For those curious about why he's still in the hospital, something in his lymphatic system was "knicked", which isn't all that uncommon. It causes his body to have a difficult time digesting fats, so the idea is to keep fats out of his body and allow the lymphatic system to relax and heal. So the heart surgery part of his recovery is going great; it's the accidental collateral damage that's keeping him in the hospital at the moment.

No new pics at the moment unfortunately, but hopefully by the weekend. His scar is looking surprisingly good.

Sunday, November 18, 2007

5 Days Down...

It's hard to believe that we've been in Toronto for nearly a week. Today Liam gave lots of smiles and was much more himself, cooing and flailing about (sometimes causing him to stop and cry for a few seconds, after which he would immediately resume flailing and cooing). But on the flip side, because Liam is draining more fluid than his doctors would like to see, he may have to stay as many as 5 more days, or even longer. While the issue doesn't sound overly serious, it's a disappointing setback, as we were hoping and expecting to come home any day.






Saturday, November 17, 2007

Day 4 After Surgery

Matt here, doing an entry for the first time in a long while. Liam seemed to be a bit more himself today, giving a few little smirks here and there. He finally got to see Zefram today for the first time since Tuesday, and smiled at him right away. I believe the only "hook-up" Liam still has is one of the drainage tubes, so it's cool to see him without the huge number of wires and tubes from 4 days ago. Once he's draining a certain minimum amount of fluid, he will be ready to come home. His incision looks better, but it's clear he's still in a fair bit of pain.

As a bonus, Liam also had visits from Auntie Lar and Grandma and Grandpa Gerryts today, so he had lots of love. We're anxious and nervous to have him home, but we're both obviously very happy that he's recovering so well.





This last one is of Zefram hanging out in Liam's hospital crib.
As you can see from his bib, he is a wiener. I mean winner.
And a superstar.

Friday, November 16, 2007

Day 3 after surgery

We received some surprising news today, which is that Liam may be able to come home as early as this weekend, because he's recovering so well. This isn't guaranteed however; it's possible he won't be home until next week.

Liam had another great night last night, but when I went to see him this morning, he was cranky and irritable. Mainly because the draining tubes are uncomfortable and he was hungry but couldn't eat because he was going for a heart echo. So after I had calmed him down and he was given his meds he was feeling pretty good; so good that I got 3 smiles out of him and he was just staring at me for 5 mins it made me cry. Out of sheer joy because he looks like my little lee lee again with a zipper down the front of his chest. But speaking of his heart echo, they're slightly concerned about two things they saw that Liam's pediatric cardiologist in Hamilton will have to keep an eye on. Something to do with a narrowing in the pulmonary valve and back flow from a valve. It's possible but uncertain that either problem could require another surgery somewhere down the road. So we ask that you continue to pray for Liam and his heart and his cardiologist in Hamilton. But before all that His nurse and I wheeled him down in his crib to where he had his heart echo, and he was very happy and content, looking at me and the nice sun shinning through the 4th floor. We went over a few bumps and he didn't like that so much, and he tried yawning and I could see that it hurt him, but he's a trooper.

They took out the central IV line in his neck. He does have a rash from the tape and pretty bad one but the air will dry that out, and he still has one draining tube in him which is still draining quite a bit of fluid. I asked his nurse if they were concerned about it and she the Dr's aren't, since it is still a good color and it's good that it is draining. So pray that, it clears up soon so he can return home. But it is all God's timing and his timing is PERFECT. But here are some pics of Liam 3 days after his surgery.





Thursday, November 15, 2007

48+ hours later

We cannot believe how great Liam is doing. It went from being in the CCU to not even 24 hours later to the 4th floor and now 48 hours later he is going to his own room. He is doing so well it's almost kind of scary. I spent most of the afternoon with Liam today and feed him his bottles and tried to burp him and hold him but he cried from so much pain and being uncomfortable that I got scared and nervous. So we just put him back in his bed and I fed him his bottle there and the nurse burped him but i have to leave the room b/c his cry breaks my heart. I've seen him cry to many time b/c of pain that I cannot handle that right now. I feel so bad for my little lee lee. I really miss him being awake and alert and himself. I keep praying for strength and it's granted everyday. But Liam is doing very well and I am so very thankful for that. So now that he gets his own room we can bring Zefram in and we can have as many ppl as we want as long as we aren't too loud and don't get in the way of the nurse that needs to come in and give him his med's and so forth and such. But we still need your prayers and support Liam still has quit a few more days of recovery and we need to get use to him again and learn him all over again. But here are some pics of Liam today. He is really starting to look like himself again. PRAISE THE LORD!!!!!!!




Wednesday, November 14, 2007

No more achy breaky heart

Liam is doing really well and he is getting moved from the CCU (critical care unit) to 4D so he's moving up which is a great thing, just means he's getting better. He is off the morphine and just on codeine which is another positive thing. It's just one awesome thing after another. Keep praying though he still needs your prayers as he recovers. He needs us more then ever. But here are some pictures of Liam from the past 24 hours. It will go from before the O.R. then when he came out of the O.R. and how he looks today






Tuesday, November 13, 2007

Our Little Mighty Mouse

Matt and I and of couse Zefram just came from visiting Liam in the CCU and he's doing really well. He Sats are 99-100 and he's doing so well that they already took out his beathing tube only 7 hours after his surgery. Well actually he decided to do that himself. He disconnected it so the nurse called the Dr and they removed it. He now has a little box over his head with some oxygen. I'm so thankful that God gave us Liam, he's out little fighter he's doing amazing. I wouldn't be surpised if he came home after a week. He's doing so well already. But we ask that you continue to pray as he recovers and for us and Zefram. Anywho from now on I will just update at the end of the day with one blog instead of 3...like today. HA! Well best be going back to the room since Zefram needs to eat soon and have a bath and I think we both really ready for bed too!

Happy that Liam's old ticker is fixed and he's good as new. I thank the Lord for all the strength that He's given us/me during this time.

Liam IS good as new

Well Liam is out of the O.R. after a 4 hour surgery and the surgery went really well and now is in the CCU recovering. I cannot thank Matt, my family that came here today and GOD who got us through it all. HE is an AMAZING GOD. I cannot believe the stregnth that He gave me today to pull through. Thanks for everyone that prayed and we ask you keep praying that he recovers and come home soon.

The Rikers

Surgery Day

Hello everyone we are about to leave to go to Sick Kids and wait the new if we are first or second today for Liam's surgery. Thanks so far for everyone that has been praying for us. We will keep you posted when we know how Liam is doing.

Friday, November 9, 2007

Ronald McDonald House

As Liam's surgery is getting closer we were trying to found out where to stay. We tried the Ronald McDonald house but we knew the chances of getting in there were slim. We knew there were hotels around the area where we could stay at but are VERY expensive and in no way could we afford to stay at a hotel even with the Sick Kids discount. My parents offered to help which is really great and nice of them but we didn't want them paying for our 2 week. But we prayed about and Matt called today and we got into the Ronald McDonald house in T.O. It's a 5 mins walking distance from Sick Kids. We have to be there at 4pm for a tour and an 'interview'. Pray that all goes well on the drive up and we aren't nervous but stay calm and remember to pray and breathe (the breathing part it for me)

Thanks again for your support and prayers

Wednesday, November 7, 2007

Liam and His Pre-Op Day

So we spent Sunday night at my parents' house so my mom could watch Zefram for the day and we could just concentrate on Liam while being at Sick Kids. We left at 5:15 am and despite some traffic and getting a little bit lost (stupid google maps) we arrived on time for Liam's first appointment at the blood clinic at 7:30 am, then we headed off to get an x-ray done and then went for an ECG. After that we did some waiting around for anesthesiology and Liam's surgeon. A nurse came to talk to us about what will be going on the day of his surgery and afterwards, and what time to be at the OR. It was a lot of information but glad Matt was there.

I finally feel ready for his surgery to be done. There is less then a 5% chance of Liam dying during surgery, which is my biggest fear. There are also other possible complications like a stroke and blood clots but at least we know what those risks are and if they do happen to Liam we are prepared. I think the more you know about it and research and talk about it the more prepared you are... well the most you can be prepared in this situation. But I feel at peace with it and I'm just at the point that I just want it done and over with. But after that long day and we were done at 2:30pm and home by I think at least 4:30. Liam slept the whole way home. It was a much needed nap since his were being interrupted throughout that day. Liam is up to 12lbs 14oz and 24 inches tall, or short how ever you look at it.

No pictures of the trip to Sick Kids; it was just one more thing to remember. Now Liam is doing well and his two bottom teeth are finally through. YEAH!!! :0)

Please keep us in your prayers for the next few weeks.

Saturday, November 3, 2007

Liam's Pre-Op

Monday, Nov 5, 2007 Matt and I will be heading to sick kids for Liam's pre-op. Going to be a long day but a long day that will bring much comfort. Liam will go for blood work and x-ray and we will meet with the surgeon and nurses. So pray for us as it's going to be a very busy day and Liam's been really cranky and teething. My mom will have Zefram all day. Thanks Grandma. So that will make it easier on us.