Getting ready...

Since the last time I have posted we have had many many many check ups,  several scares that included midnight drives to Houston, and tons of prayer.  All of the check ups have led to one thing.  Another heart cath.  Ethan's o2 numbers are sticking around 77.  He is constantly huffing and puffing to catch his breath when he is up walking/running around.  He's scaring me to death but he's always done that!  Day after tomorrow we go for a dental check up.  As soon as he is dentally cleared, we call his heart team to see if they can get him into the cath lab before May 31, which is when he is currently scheduled.  The F word (Fontan, but I got you thinkin didn't I) will happen sometime in the next 6 months depending on the results of the cath.  His one heart valve is very very leaky and it's keeping him from being able to keep up like he was.  BUT...he has learned to hit a ball off of the t and can play catch with his daddy.  For these two things we are especially grateful.  Tomorrow is the first Sunday of the month.  In our church, we fast on the first Sunday for something that we are in need of, or to give thanks, or for another reason as determined individually.  As always, Ethan will be the center of ours.  He is an amazing little person and we pray that he continues to thrive.

Summer in Review

Now that I've had a couple of weeks to come down off of the summer I have decided not to give you the normal "sorry I haven't written in a while" mess and just come on out with it's been too busy to keep up! ;) As you can see from the picture, Ethan adores his little sister. The first picture is his first time to meet and hold her when she was just two hours old. The second was taken outside of our church on August 1st on her blessing day.

June was a whirlwind of Zoo camp, new dance class schedules, two birthdays, a trip to Austin for Nolan's specialists, etc that ended with a trip to Schlitterbahn Galveston for some fun in the sun (or as much fun as you can have in a double floaty two weeks before having a baby with an almost two year old freaking out because the waves are too high in the wave pool). It was actually really fun! The last thing in June was a check up with Ethan's cardiologist. He's doing really well but he's getting winded when he is playing a lot faster. And his 02 numbers are starting to trend down. When he first had his glenn he was 85...now he usually is around 78-81. When his numbers are consistently below 75 his Fontan will be scheduled. With his current rate of decline we will be looking at surgery sometime int he next 18 months. This is where you tell me to breath and that it will be ok...I'm really scared about his Fontan...

July was the most fun I think. The 4th was spent with family and ended with watching fireworks over the pond behind the zoo. Then it seems like no time passed until the 13th when sweet baby Natalie arrived by c-section. She is a doll. Ethan has been so good with her. He always wants her to have her suckie (pacifier) even when she doesn't want it. Some good friends came and gave me a huge helping break for the first week home as Richard had to work that week because almost all of his vacation days were spent on Ethan's procedures earlier in the Spring. Sadly, that's all I can remember of July because recovering from a section with 5 kids and no sleep leaves your memory very fuzzy. Suffice it to say that July was good.

August was a whirlwind of school clothes shopping and school supply shopping and meet the teachers (all three campuses in two hours...why they scheduled them all at one time is beyond me!). Everyone has adjusted to the routine of school fairly well even if the application of school rules is a little beyond a couple of them...

Ethan doesn't go back for another check up until November. His numbers have been above 80 for the most part int he last week so I'm going to keep my fingers crossed that he will continue to be unripe for surgery. I'm not ready for it. He just gets so tired so fast. And it is taking him longer to recover his breath. When he gets tired it can take days for him to adjust. School starting hit him pretty hard. He enjoys being a semi-only child for a few hours each day, but getting up earlier, even though he's going to bed earlier, is making him more and more tired. In a way I wish his appointment was tomorrow so I would have some answers, but all in all I only want to hear about good news right now.

Cath follow up

Finally had Ethan's cath follow-up with his surgeon yesterday. We got chest x-rays, echocardiogram and EKG...all came out fine. He has good flow over his stint and his saturations are level. He's now staying between 78-82...just going to be his new baseline...it's dropping slightly by a few numbers from where he was after his Glenn surgery, but that is to be expected as he grows. Those saturation numbers will let us know when his body is ready for his Fontan surgery. We will have to go back every so often as Ethan grows to open his stint further and have that artery grow with him...it just doesn't do it on it's own! So, we're going to become very familiar with Cath procedures and Dr. Ing over the next few years and for the rest of Ethan's life...

We'll meet with Dr. Altman, Ethan's cardiologist, on June 25th and repeat every procedure that we had yesterday to make sure that everything is still going well. We're going to have to baby his heart until the next surgery...basically keep a very close eye on his saturations and activity level. I'm very grateful that his next visit is at the end of June because Ethan's little sister is scheduled to arrive by c-section on either July 13th, or July 20th depending on her growth.

As always, thank you for your support and prayers on this and every step of Ethan's journey!

MRI/Cath update

It's been too long since I updated. Things have been busy getting back into the home schedule and getting my older kiddo's nerves calmed down after the MRI, emergency hospital admission, and Cath. Everyone is settling down and things are running as smoothly as you would expect with the stress level. Ethan got to come home the day after his cath but through a comedy of errors (that's the nice way of putting it) we weren't able to get him into echocardiography. So he went home without one. His second x-ray came in beautifully and he is doing well. We did find out when we talked with his cath surgeon that it wasn't just his pulmonary artery that is undersized. HIs whole right lung and all the arteries leading to it are very undersized. This means we have a brand new diagnosis of hypoplastic right lung to add to his already two line long heart diagnosis. This explains why his 02 desaturates with exertion. Now that he has his stent he is slowly getting faster about pinking up for us when he sits down. In the past few days he has started to sit down when he is gasping instead of just keeping on. He's learning his limits. Which makes me happy and sad at the same time. No 19 month old should have to limit his activity. We'll just have to keep a close eye on him like we have done since the day he was born to watch for even small changes in his saturations or his activity. There is really nothing else they can do other than hope that the stint will encourage that lung to grow more now that it has better blood flow. We're now one step closer to his Fontan surgery, but have also staved it off because of the bandaid that we just got in the cath lab. I'm so grateful that he hasn't had to have his Fontan early as his chance of survival at this point is just flat scary. I am also very grateful for the prayers and well wishes that I have received through my internet connections. I couldn't do this without my Heavely Father and you!

Done!!!

It got too busy to update last night so I'll do my best to remember everything this morning! The artery ballooned open beautifully...and then it went right back to how small it was before...so Ethan has a brand new stint in the right pulmonary artery. I even have before and after pictures that I will have to post when i can scan them in at home. He came out of anaesthesia really well...minimal fussing and very thirsty. He's swollen because of the IV fluids they pumped him full of and his kidneys are releasing the fluid with a single dose of lasix. We held him in the recovery bay for two hours and then got moved downstairs to our home away from home, 15th floor of West Tower. His pressure bandage was removed a little after one this morning and he finally slept soundly at 4. they came in a little while ago for another chest x-ray and we are waiting for those results now. He will have an echo cardiogram and be started back on his aspirin (which is his only heart medication currently) before we are discharged later today. Hopefully I will be able to update a little later after we know more. For right now we are grateful that yesterday is over and that he is doing so well. Thanks for all the prayers and well wishes you guys!!!

Balloon time!

Got the update call a few minutes ago..They are now attempting to balloon his pulmonary artery...we are hoping that the artery responds and doesnt' shrink back too small after the balloon is removed. If it shrinks too much they will place a stint. We are starting hour 4 for surgery now...but should have another update within the hour...

Heart Cath...Finally!!!

We arrived at the hospital this morning at around 8. We left Lufkin at 5. We were back, checked in and in the holding bay for Ethan's heart cath at 9. He was supposed to have his cath around 10. They finally took him to the back for his cath at 3:15 this afternoon. That was a long long wait. He was so good waiting! He played with toys and didn't complain once even though I know he was starving. He hasn't eaten anything since 8:00 last night! At 5:10 we got the update that he has a cath in the femoral artery in one leg, a sheath in the femoral vein in the same leg, and a cath in his coratid (spelling) artery in his neck so they have access to all areas of his heart...I'm thinking they had to come at it from both angles because of his PA band but I will confirm this. Thank you for your prayers for Ethan! Please continue them! And also please add the little girl that was case' # this morning. They had to do twice as much in her cath as they had planned and she is back in CVICU....not a fun place to be. More to come soon...