Wow, it's only been a week. The longest and shortest ever it seems. 7 days ago was one of the most stressful days of my life, and that first night was incredibly hard. Every day is better and better. If I didn't know that Joshua had surgery, I probably would never guess. He is back to his always charming self, and wants to spend his whole day gaming. He is still a bit limited in the things he can do. He really can't run around like a crazy boy, he can't go swimming and I have to force him to read. But I am back to limiting game time a bit. Next Friday we see the surgeon for his follow up appointment. He will have a few limitations for about six months, until the breastplate is fully healed. No lifting a heavy backpack (going to have to figure that out), and no contact sports or activities where there could be impact to his chest (like bike riding). Other than that, he can do normal stuff. Thank you all for everything. The prayers, positive energy, get well cards, evening meals and most if all, giving us the amazing gift of coming home to a newly cleaned house. We appreciate each and every one if you more than words can express.
Thursday, July 30, 2015
Sunday, July 26, 2015
Home
We are home!! Josh is having some game time. The one hour rule is kind of out the window for a little bit. After all of this, we are pretty much allowing most things!
Discharge day!
The talk is that we are coming home today. Strange thinking that he had open heart surgery less than 72 hours ago. All but that first day have been smooth, and medically the first day went great, it was just very emotional for us. Kids are definitely resilient! He is not back to 100% obviously. We still have work to do to make sure he continues to recover and is back to his crazy, goofy, adorable self soon. Thanks to everyone for the prayers, positive energy, friendship and kind words. It does take a village! I can't imagine being alone during all of this. I have amazing family and friends. Thank you from the bottom of our hearts.
Saturday, July 25, 2015
Good night
Joshua slept all night, even with the nurse coming in 4 times to check his blood pressure. Probably the first good night since we got here (even though that's only been 2 nights!). Today, I think the plan is to get him out of bed and walking. He really hasn't complained of any pain. I am amazed. Have a good day all. I will update if there is anything new.
Friday, July 24, 2015
Moving already
Out of the PICU and onto regular pediatrics.... Didn't think things would move so quickly!
Playing games
Josh only has 2 lines left. The central line in his neck, and one IV. Things are moving quickly. The chest drain was removed. He is now sitting up in a chair and playing........minecraft. you guessed it! Who would've though after open heart surgery he would be up and moving post op day 1.
And a big thank you to Marcia and Scott for the balloons and teddy bear!!
Foley gone!
The catheter was removed, and he is feeling relieved. He had his first sips of water, and the look on his face was pure bliss. Next, some pancakes and yogurt. He is starving!! Have to work on the lungs today. Taking those deep breaths and getting some good air flow. Still lots of milestones to conquer, but we are on the way.
Good morning!
It's been a long night. Josh seems to be very comfortable. No issues so far with the drain tube or incision. He is however, having major issues with the catheter. Somehow, he has been peeing around it. Still has tons of urine in the tube, but has been asking for the bed pan every hour or so. They plan to remove that this morning, and then I think he will really happy, and more comfortable.
The only pain meds overnight have been tylenol.
He has,food belly sounds this morning so it looks like he will be able to drink and eat today.
We don't know for sure, but hopefully today will be removal of a lot of the tubes. Good day!
Thursday, July 23, 2015
PICU
Joshua has tubes and lines everywhere. We counted 6. He has a central line in his neck, an arterial line, 2 IV's, a chest drain and a catheter. We are surrounded by awesome, caring staff. He wants to drink and is hungry, but no bowel sounds yet, so the best we can do is glycerin swabs, and lip balm. We are hoping that tomorrow will be some tube removal, and at least some oral fluids. He is in and out of sleep, which is good. He needs rest. He did ask to play on his tablet, which we would have allowed, but it needs a bit of charging. He is half watching Disney channel. We are expecting a sleepless night for us, just because I will wake up for every movement. We know that today is the worst, but we know every day will be better.
Resting
We have been in with him for a few hours now. The hardest thing for Dave and I is seeing him in any type of pain. They are keeping on top of it, but there have been a few times that he has woke up in pain, and that of course made me cry. Heis comfortably resting right now. It's going to be a long night. Tomorrow will be a much better day.
All done
We talked to the surgeon. All went well. He is off the ventillator and his heart rhythm is good. He is in the PICU noe, and we should be able to see him in a few min.
Hard part done
Surgery day!
Wednesday, June 10, 2015
The Verdict- Heart Surgery
We haven't received the call from the surgeon yet (just his cardiologist). The good thing is, that Yale Cardiology takes the results to the group, and a group of 10 cardiologists determine whether the results indicate surgery. It was unanimous. So while I can't tell you all when, as we don't have a date yet, it will be this summer. I am shooting for July so that he has lots of recovery time before school starts. Once we have a date we can tell you more. We do know that he will be at Yale for 4-5 days and home recovering for another 7-10. Mostly normal activities after 2 weeks. While we knew that this was probable, getting the news still hit me hard. I have my big girl panties on now. We will need lots of prayers, positive energy, blessings.. whatever it is you all do. Love you all, thank you for being my friends and support!!