Friday, March 30, 2012

Update on the update...

Carson is perfectly normal!! He does not have a vascular ring or anything else compressing his esophagus or trachea. He doesn't even have acid reflux, which he has been on meds for since he was 5 weeks old!! The dr, radiology tech and nurses at LeBonheur are the BEST!! The dr was training an intern so he was thinking out loud as the test was running. I was nervous about that at first and kept asking him questions. He finally told the intern that I was the "typical helicopter mom, hovering over her baby." LOL!! He later asked me if he offended me when he said that and I told him, "No" but that I was going to blog about it and asked if I could take his picture.

Dr. Young and Carson

Carson so was so good, as usual. He drank that Barium like it was kool-aid and stayed pretty still while he was being x-rayed. He has undergone lots of tests and procedures in his short life and he ALWAYS has a smile on his face...unless he's hungry...imagine that!! :)

Praise God that my prayers were answered and my baby is healthy!!! Thanks for all your prayers as well.

Wednesday, March 28, 2012

Some pictures...

I thought this picture was so sweet! Alex is such a big help. He was my first baby! I lived with he and his mama the first year of his life. He was holding Carson while I was getting LG's dinner and Carson's late afternoon snack ready. He is like their big brother!


Then, of course, LG could not be left out so she wanted to get up on the counter and get in the pictures too! She NEVER looks at the camera!
And then when I get her to look at the camera, Carson looks at her! LOL!!!


All my babies!!

Tuesday, March 27, 2012

Ahh Laaa

A little play on words. I told you in an earlier post that we call Carson, Laaa, because that's what he says when he cries so we call him Ahh Laaa in this picture:

Andy loves to put the burp cloth on Carson's head and make him look Muslim so when he brought Carson up to my work we had him pose with my Muslim friend, Noha. He doesn't look as good as she does in the head wrap, maybe that's why Muslim men don't have to wear them...hmmm, points to ponder from other religions. :)

Update

We got discharged from LeBonheur late Sunday afternoon. Carson sounded so much better after they sucked all that junk out of his nose and throat! He does however still have a wheezing sound coming more from his upper airway, which is of concern. I kept him home from daycare and took him to his dr's office yesterday for a follow-up. The two dr's that saw him said his lungs sounded good but they could still hear the wheezing in his throat. We are scheduled for an upper GI test at LeBonheur on Thursday to find out if there's anything pressing/squeezing his trachea causing the wheeze. It could be that he has a normal trachea and the bronchiolitis caused inflammation in it but at the other extreme, it could be a rare congenital heart defect called a vascular ring. This is where a vessel from the heart has wrapped itself around his trachea and is squeezing it. Some children who have this do fine with no intervention but in some cases, surgery is warranted. But we'll cross that bridge when we get to it. For now, we would appreciate your prayers that we have a healthy baby boy with just some tracheal irritation.


Here he is last night with his buddy, Alex. He looks HUGE in this picture. I mean, I'm not in denial that he's a big baby but he looks exceptionally big in this picture. :)


I know God is going to take of my sweet boy but of course, as any mother would be, I am nervous/anxious about the test. Please pray for me that I would be able to rest in God's plan for Carson, cast my cares on the Lord and not worry (Phil. 4:6-7).

Sunday, March 25, 2012

Dejavu...

We have been dealing with an upper respiratory issue with Carson for several weeks now. We have been back and forth to dr's offices trying to figure out what is going on. He has a lot of drainage and has recently started wheezing. He was diagnosed with bronchilitis a couple of weeks ago (as you may know from earlier blog posts) but has always been sent home.
Yesterday I took him in to the dr's office because he sounded like he was wheezing quite a bit more than usual. The dr checked his pulse oxygen level and it was 92. She gave him 3 breathing treatments and his pulse ox stayed at 92. She said it was like she hadn't done anything. She stared at me with a look on her face that I had seen once before...when LG was 4 months and 2 weeks old she was having the same issues and we were transported from that same dr's office by ambulance to LeBonheur Children's Hospital for an overnight stay. She was eventually diagnosed with bronchilitis and underwent several deep nasal suctionings to get all that pesky snot out. Carson is 4 months and 1 week old and that's exactly what happened again. We were transported by ambulance yesterday and admitted to Lebonheur for the night. They did a chest x-ray to rule out pneumonia and other respiratory problems. But like LG, he has been diagnosed with bronchilitis and has received the same suctioning to clean all that junk out of his nose and throat. The problem is babies can't blow and cough that stuff up so it settles in their chests and causes breathing problems. Today his oxygen level has remained around 99-100 so we are being discharged.
The pictures below chronical our journey yesterday and today. This was Carson at the dr's office getting his first breathing treatment. He fought it so hard at first that he passed out in my lap.
My friend, Alisha was kind enough to come get LG from the dr's office after we had been there for two hours so she could take her to get donuts and just to get her out of the office. LG was being so helpful and good but she was getting bored and that can spell disaster for a 3 year old. Thank goodness she came and got her before we had to ride in the ambulance.
Alisha wanted to hold the big baby before she left. The smile on his face was indicative of his attitude all day~happy except when he was getting his breathing treatment or nose sucked. Everyone has commented on how he doesn't seem to notice that he's sick.
This picture was taken in the ER in his cute little hospital gown. He fell asleep with his paci hanging out of his mouth~long, rough day for my little Laaa.
We finally got moved to a room after around 6 hours in the ER. This was Carson's "jail-like" bed. He has seemed relatively comfortable in it.
Different angle of the bed.
This was Carson after he got his nose sucked for about the 5th time. He hates it but can breathe so much better for a couple of hours after. I wish we had one of those machines at home! Those stupid nasal bulbs don't do anything! A nurse told me that she thinks they sell a little battery powered suctioner at Walgreens. I will definitely be checking that out ASAP.
This is the entire room which is much better than what we got when we came three years ago with LG. She was in the PICU and shared a giant room with about 10 other babies. We were not allowed to stay with her and that was agonizing, especially since she was our first child and we had never experienced anything like that before. Andy slept on that pull-out chair to the left and I slept on the couch in Carson's room.
The dr's and nurses have been wonderful!! They have loved on Carson and spent so much time with us, explaining things and just talking to us.
We should be discharged in a couple of hours. All in all, I'm glad we came here so Carson could get some much needed snot removal and so we could rule out any critical issues, but I think we'll all be happy to sleep in our own beds tonight.

Friday, March 23, 2012

The mind of a child

Last night as I was giving LG a bath, she said, "God is the bestest!" and I said, "Yes, He is. Why do you think so?" and she replied, "because he put me down here to you."

Wow!! God knew I needed that. I have been getting so frustrated with her lately. It's only because she's doing the stuff that all three year olds do but I just expect her to know better. I have been so lazy, not giving her the attention she needs and not taking the time to teach her about rewards and punishments. She is growing so fast and I don't want to miss out on this time. Advice to myself~slow down, take one day and a time, and enjoy your babies while they're still babies!!

Thursday, March 22, 2012

ENT again...

LG had to go to the ENT again yesterday for a follow-up (after a 6 week round of Dimetapp and 7 days of antibiotics). She did have some fluid still in her left ear but Dr. Cunningham said they look so much better than they did 6 weeks ago. He wants her to continue to take Dimetapp for 3 more months and then he wants to see her again to assess the need for a second set of tubes. I thought this part of the visit was funny:

LG had to get a hearing test. She was standing up so Ms. Sarah (the tech) squatted down so she could get the device in LG's ear so since Ms. Sarah squatted down, so did LG. So Ms. Sarah had to kneel down even further on the floor so naturally, LG knelt down even further. This is how the test was done:

Get low

Get Lower