Quick update for the evening: Jude continues to do well! He had the following removed today:
- Central line
- Pacer wires
- Monitor for brain oxygen levels
- Oxygen
Our journey as a family through our youngest son's battle with congenital heart disease.
Quick update for the evening: Jude continues to do well! He had the following removed today:
Good morning! Just wanted to do a quick update on Jude. He is doing really well meeting all the goals the so far. Since surgery he has had the following removed:
We just returned to the apartment across the street from the hospital after a morning of tests and meetings. So far all results have turned out well!
This is Jude before we went to the room. He knows when we've entered the hospital and was already letting me know he didn't want to be there.
Here's a rundown of what Jude had to do in pre-op:
I first came across this essay last year in a book titled Maybe You Should Talk to Someone by Lori Gottlieb. It resonated so much with what I was feeling at the time (and still feel) that I have pondered over the words many times. Emily Kingsley wrote this in 1987 about her experience as a mom of a child with down syndrome, but it can apply in so many cases (in the book a woman who had terminal cancer identified with the passage). For me, it caused a complete mind-shift. I could either sit and bemoan the fact I was no longer going to Italy or I could embrace our new life in Holland. Yesterday's visit to Texas Tulips was a tangible reminder that our family now resides in Holland, and while it's not Italy, it is beautiful in its own right. I'm sharing it here because maybe it will help someone else like it's helped me.
Welcome to Holland
by Emily Kingsley
When you're going to have a baby, it's like planning a fabulous vacation trip - to Italy. You buy a bunch of guide books and make your wonderful plans. The Coliseum. The Michelangelo David. The gondolas in Venice. You may learn some handy phrases in Italian. It's all very exciting.
After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome to Holland."
"Holland?!?" you say. "What do you mean Holland?? I signed up for Italy! I'm supposed to be in Italy. All my life I've dreamed of going to Italy."
But there's been a change in the flight plan. They've landed in Holland and there you must stay.
The important thing is that they haven't taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place.
So you must go out and buy new guide books. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.
It's just a different place. It's slower-paced than Italy, less flashy than Italy. But after you've been there for a while and you catch your breath, you look around.... and you begin to notice that Holland has windmills....and Holland has tulips. Holland even has Rembrandts.
But everyone you know is busy coming and going from Italy... and they're all bragging about what a wonderful time they had there. And for the rest of your life, you will say "Yes, that's where I was supposed to go. That's what I had planned."
And the pain of that will never, ever, ever, ever go away... because the loss of that dream is a very very significant loss. But... if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things ... about Holland.
c1987 by Emily Perl Kingsley. All rights reserved.
We returned from Houston yesterday for Jude's check-up with his cardiologist. Since his regular cardiologist is still out on medical leave, we were assigned a new, temporary one. After a series of procedures including an echo, x-ray, EKG, and all his vital checks - all of which he loves (please note the sarcasm here), we had the fastest doctor meeting we have had yet (it lasted 5 minutes tops). The doctor said everything looked stable (which is good), except for maybe a new rhythm on Jude's EKG (possibly not good). Which meant Jude would need to be hooked up to a 24 hour EKG (called a Holter) and we have to return in a few weeks (the week before his scheduled surgery date) to have a repeat EKG and make sure there isn't a rhythm issue.
Thankfully, the Holter is something we could do at home and mail back, so we didn't have to spend another night in Houston (yay!). Also, we were pleased to be able to go home and no needs to move his surgery up due to emergent issues. Anytime we get to leave an appointment and go home is a celebratory day.
This photo was taken this morning right before we took off his Holter. Surprisingly, it didn't seem to bother him as much as I thought it would. We kept his onesie and pants on all through the day and night and he never messed with the wires. You can't see it below his leg, but there's a little box at the bottom that keeps up with all the inputs. We just tucked that part in his pants, so it looked like Jude had a little extra junk in his trunk for the last 24 hours 😂. This procedure is something Jude will have to do many times throughout his life. Because of his heart's anatomy, it is important to monitor his heart rhythms and head-off any issues. Hopefully, the anomaly that popped up yesterday on the EKG was just a fluke and not a sign of something more serious.
In the meantime, we are looking forward to spending Easter together as a family and celebrating Josiah's 6th birthday here at home next month.
Good morning! I know it's been a while since we updated last, but thankfully our lives have been relatively uneventful the last few months. Lots of quarantining at home, going to doctor appointments, and hibernating from the ice storm last week.
Back in November, when we saw the cardiologist in Houston, the plan was to get Jude presented in conference so his open heart surgery could be scheduled. We gave them a couple of months, so the team would have time to present, make a plan and account for the holidays. After not hearing from them by the beginning of the new year, I reached out just to check in. Unfortunately, his cardiologist broke her arm badly the afternoon of the day we saw her. She had to have surgery and had been out since that day. Which means his notes never got finished, he hadn't been presented yet, and his cardiologist wasn't scheduled to be back in the office until May. After lots of follow-up calls, pleading, and requests we finally got a consult scheduled with his surgeon at the end of January. However, the day before we were supposed to meet, the surgeon had a last-minute emergency surgery and we had to reschedule. That happens a lot at Texas Children's since they do lots of transplants and severe cases. Nothing to be mad about - I said lots of prayers for the family who had to take his spot, because if it's emergent that's never a good thing. We were able to schedule a tele-visit for the following week, which went well. We were able to talk to the surgeon, ask all our questions and be briefed on the surgery options for Jude.
The plan was to hear back from them in the next week or so to schedule his surgery. However, Mother Nature had other ideas in mind and sent the polar vortex. Texas was hit hard and the electrical grid was pushed to its limits, which means the hospital had to cancel surgeries and not much was done last week. But this morning, I finally got the called we had been waiting for since November - Jude is scheduled for surgery on April 22!
We are nervous/excited. Having this surgery will help improve his oxygen sats so he can breathe better, grow more, and live an all-around better life. But open-heart surgery is nerve-wracking. On top of that, we aren't 100% sure of the exact type of surgery they will be doing. And we won't know until they actually start the surgery. There is a very small chance that Jude will be able to have a bi-ventricular repair, which would entail the doctor fixing his heart to be rewired as it should be. In essence, Jude could live a completely normal life if that is the surgery they are able to do. However, the odds are very, very small that this type of repair will be possible. Most likely he will need a 2-step heart surgery called the Glenn and Fontan. The Glenn would be done in April and then another open heart surgery would be required to do the Fontan when he is 4-6 years old. This is not a fix, but rather a circumventing of the heart. Jude would still live a mostly normal life, but there would be limitations on what he can do throughout his life and health issues in the future. The bi-ventricular repair would be the optimal surgery, but we will be thankful for any help that he can get. One of the main reasons we have continued our care in Houston is to provide him this opportunity to have a bi-ventricular repair. There are only a couple of programs in the country that offer that as an option for his particular heart condition, and we want to give him the best opportunities we can.
Future plans include a cardiologist appointment in Houston in March just as a check-up. Since his cardiologist is still out (she had to have another surgery on her arm), it will be with a new, temporary doctor. It's super important that we keep him healthy leading up to his surgery (no fevers, runny nose, etc.) or he will have to rescheduled. For the winter season, he has been getting monthly vaccines to help prevent RSV and those go through April. For his surgery, we have to go down a couple of days before to Houston for pre-op appointments including COVID testing, blood work, X-rays, meeting the surgeon in person, etc. The average time in the hospital for the Glenn procedure is 7 days, followed by a week in Houston and follow-up appointments with the surgeon and cardiologist to make sure Jude is handling everything well before we return to Dallas. We are all hoping (his hospital team included) that this experience will be much smoother than his stay at birth.
In other news, Jude turned 1 year old on January 31! He now has 6 teeth (he decided to cut them all at once) and loves to grind them together (the noise that makes me literally want to climb the wall!!). He had a Developmental Outcomes appointment in January and is still in a good range developmentally. We will meet with them again in Houston when he is 18 months old. The dietitian has been helpful in making sure Jude is getting enough calories as we transitioned over to whole milk. He gets to drink Pediaure now, in addition to milk, which he likes. He has finally made it back to the 10% in his weight and is still barely on the chart for his height. He's gonna be a little short. 😊
Alex and Josiah are still attending school virtually and enjoying it the best they can. Our hope is that they will be able to go in-person next year, but it will depend on the number of cases and vaccine opportunities for them. (Jude will still have lower oxygen sats if he has the Glenn, which means it will be important to keep him healthy leading up to his next open heart surgery.) Alex will be starting middle school and is excited to be able to pick out his classes for next year. Josiah just keeps asking me how many days until his next birthday. 🤦🏻♀️
This post was a little longer that I originally intended, but wanted to update everyone. We so appreciate the kind words and prayers from everyone. Thank you for the love you have shown our family!
So I'm a couple of weeks late, but I wanted to share with everyone about the drive-through Christmas lights we went to while in Houston. During the day Jude and I had spent the afternoon at the hospital doing all his tests and seeing the doctor, so we wanted to have a celebratory family outing! After looking at a couple of different options for things to do that evening that were 1) socially-distant and 2) would keep Jude entertained, the vote went to Rudolph's Light Show. Houston has several different drive-through Christmas lights, but this was the original according to the Internet, so we decided to go with it.
First, here's the website for anyone interested: https://www.rudolphslightshow.com/
It's located at 19623 Bauer Road, Hockley, TX, which is about an hour from the Medical Center. It was rush hour, so traffic had some spots that were slowed down, but it really wasn't too bad. You can tell that a lot of people are still working from home based on how much lighter the traffic is during rush hour. The lights open at 6:30 p.m. and we arrived not long after that. Since it was a weeknight and the beginning of the holiday season, they weren't very busy. But based on their car lanes and organization, I imagine it gets pretty packed on the weekends. There were signs at the beginning to tell you which radio station to turn to for the music. We purchased our tickets online (you pay by car), so received a little bit of a discount that way. We just showed them my phone and they scanned the barcode and let us in.
It took us about 15-20 minutes to drive through each time, but I imagine when they are busier it would take longer. We have done drive-through lights before, both when Alex was a baby and Josiah was a toddler and they turned into disaster outings (i.e. screaming children for 45 minutes). But this time it was a really fun outing! I would recommend going during the week right when they open to help with the crowds if you have littles that don't like to wait. Also, there wasn't a whole lot nearby to pick up to eat, but we ordered pick-up from Cyclone Anayas closer to our hotel. It's one of my favorite Mexican restaurants in Houston (LOVE their crab nachos).
After the day of virtual schooling, Jude's doctor appointments and this outing we were tired, but so thankful for the family memories we got to make together. And thankful that we would get to go home the next day!