We called the pediatrician and they said to take him to the ER. No messing around with babies! That's for sure. So that's what we did. We went at about 3:30 pm. Ev had to be at the church at 5 pm to take the youth to Youth Conference (no way out of that either). We were trying to figure out how it was all going to work b/c 5 rolled around and we still hadn't heard back from the doctor. We had no idea how the rest of us would get home after Ev left us. Only having one car is a little rough at times! Maybe that's an understatement. Ev called the leaders at the church and told them he was going to be late getting there. The doctor finally came in and said they were going to admit him over night so they could do some tests and really try and figure out what was going on. So with that said...Ev was able to just leave. We called the Granthams and asked if they would watch Brampton for the night (Thanks a ton!!!) and Ev headed to the church at 5:30 pm.
At the hospital they did a urine and blood test. They also took some x-rays of his chest to see what was going on. We were taken to the children's hospital and put in the nursery. Cardston had 2 other little roommates. One baby...a little boy...was named SPARKY. Funny huh? Cardston was put on a monitor so the nurses could watch his heartbeat and oxygen levels. He also had a little IV put in. So sad. Cardston did pretty well with his breathing for the first part of the night. The doctor came in and asked some questions...she then told me what she thought was going on...REFLUX. Well at about 10pm he started having some labored breathing and his oxygen level got to about 84. They prefer 95-100. Anything lower is not too good. They paged the doc and she came and took a look. She was concerned and wanted to do a lumbar puncture (testing spinal fluid) to make sure it wasn't meningitis. They started him on 3 different antibiotics and we were then just awaiting the results of the test (48 hrs). Friday morning rolled around and come to find out they wanted to do more tests. Cardston had an upper GI barium swallow test done (to see if he had any reflux) and the cardiologist came and did an echocardiogram to look at his heart. Boy...my poor little baby was sure put through the ringer. It was all a little frightening just b/c they couldn't figure out exactly what was going on. But...thankfully the Lord answered many prayers. Come to find out the upper GI test showed that he has severe reflux. Cardston doesn't spit up...it just comes up to the top of his esophagus and causes him to gag and choke. He even gasps for air at times. Nothing too serious. They put him on pepcid and told us to keep him elevated to help keep everything down.
After two days of being in the hospital, I was sure excited when they released us on Saturday afternoon. I could hardly wait to sleep in a bed and have my baby free from all the stinkin' cords. Here are some of the pictures I took to remember this crazy event. I do have to say that I am so grateful he's healthy and able to be at home with us. I can't imagine having to do something like that long term. That is just too rough on a family.
17 comments:
Steph, you poor thing! I am so sorry about all that! I am so glad he is doing okay, though. Take care of everyone! We love you!
Oh Stephanie! I am so glad to hear that all is well now! Tyler loved holding onto Carters legs too how cute, and funny.
Oh Steph, I'm so sorry! I'm so glad everything is better now, hopefully it stays that way! Glad you are home! Been meaning to call to find out but didn't want to bother you. Love you guys!
The poor little guy!! And your family too! That is so scary. I can't believe they had to do all that just for reflux!! I didn't know reflux could have a kid hospitalized either. Josh had severe reflux for 13 months (not to scare you or anything) but that was a long time for us but we never had scary moments like what you went through. I agree, it's tough on the family when any child needs to go through stuff like that.
Glad you are back home and things aren't as bad as they seem. He's just so little to already be on meds, it's sad:( Take care!!
sorry lady, that is the saddest/most traumatic story ever. poor little guy!! glad you got to come home, good luck getting everything back to normal.
I have another family I know who had a son who had the same thing. But much worse. This is their blog if you go back to december 2007 they have the whole adventure.
http://mamahen15.blogspot.com/
I hope those YM had a good camp out :)
Jessica Finnigan
WOW super scary!! I am so sorry! Tessa has reflux too. She spits up like crazy and has a lot of discomfort with hers. she is on a special formula, takes previced twice a day, and something else for the pain 4 times a day!!Totally do the propped up thing for at least 20 min after he eats. Also, you can get this wedge thing that is for their bed and it props them up while they are sleeping, my dr. told me to get it. I am glad to hear that he is ok now and at home!
Oh my goodness! I'm so glad Cardston is okay and that they figured out what it was and you were able to go home:) You are such a good mom. I hope you have no more ER visits for a long, long time or ever!!
Poor little guy! I'm glad that he's safe and home now. I can't imagine how uncomfortable it must be to have to stay overnight at the ER.
His little striped outfit is so adorable...at least you had his looking good (even if he didn't feel that great :o)
Oh man girl!!! I'm so sorry! I'm glad everythings turning out okay. What a crazy year. Wish I was there to help out. I'd say next time, but lets hope your ER visits are done!
Uck! That sounds like a nightmare. it was when douglas was in the hospital at 14 months. I can't imagine an infant. So, how has the medicine been working?
Crystal-
To be honest I can't really tell if the meds are helping or not. If anything it seems like it is worse. But I'm not sure if that is b/c I am more aware. The pediatrician said that the med was really mild and that we can up the dosage in 2 months.
Love the new header!! So cute and so boy friendly!
Wow, that's so scary! I'm so glad it turned out alright. I'm sorry you and Cardston had to go through that. I hope he's doing better now!
hey, how do you do decorate your blog? I have been wanting to do mine but I dont know how to do it.
How is your little on doing? Oh I was going to say make sure that you over feed him. That makes it worse. give him just what he needs when he gets more than he needs he will spit up more. Well I hope he is going ok.
We did that super fun ER trip with Hadley at two weeks old too. They did a spinal on her as well. SO scary. I'm glad they figured out what the problem was!
hey steph! i just got read these posts, and am sorry about your little one having reflux. You know that Ben heiner had reflux, right? They bought a special wedge/bed insert that put him on an incline when he slept. I don't know much about it. I hope you are doing ok.
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