Wednesday, April 28, 2010

Tuesday/Wednesday...

I have to be honest. I haven't been posting on my blog because I am trying to decide who I am writing this blog for. Is it for me? Is it helping me cope? Is it for all our friends and family? Or am I just throwing all of my emotions and feelings out on the internet for people to read and think "oh what a sad story" and we become more like fish in a fish bowl? I think I feel this way because I know many "friends" that are reading this blog but not once have I seen a comment from them, an email or a phone call. (Sorry this is just how I am feeling) I haven't completely come to an answer on this yet but I have come to another possibility of the reason for this blog. This blog may help other families that find they are in the same situation. I have found a couple blogs that I have stumbled upon and find myself crying but yet thankful that I came across it. So for this reason I think I will continue the blog but maybe not everyday... for now.

Tuesday was a very hard day for me. It was nice because I was able to stay at the house in the morning to kind of put some things away at the house, do laundry, dishes, clean out the fridge (man there was a lot of spoiled things in there!) and just try to have a half normal day. Of course I headed to the hospital in the early afternoon. Now I know that there are a few nurses reading my blog and I am totally ok with that. However, it has had me pondering if I should write about this next thing but anyone who knows me knows I don't hold back a lot so here it goes. Tuesday morning Mark called the nurse to see how Ethan was doing. He was doing worse than he was in Seattle. So this got us talking and thinking. We realized that in Seattle they had Ethan swaddled nice and tight the last few days that we were there and he was doing awesome. So we decided to ask the nurse if they could do that here since it seemed to help him in Seattle. She told me no. The reason for this is because they can't cover the temperature probe that is connected to the machine and is stuck to his belly. Well this really didn't make sense to me or Mark. So I was a little upset with it. I waited until the next nurse came on (which I was glad to see it was a nurse I have come to like) and asked her about it. She said that we could try it but it couldn't cover his temperature probe. Yeah, at least she is willing to try it. So we swaddled his bottom half and he seemed to do really good for the rest of the night.

So Wednesday morning I set my alarm so that I could call the same nurse to see how he did throughout the night. She said he had a really good night and that they were able to keep him swaddled. Great! So I decided to go to the hospital right away so that I could make sure he was still swaddled when I got there since I knew the nurse who told me no would be his nurse again. Well he was swaddled and he was doing really good. She said to me "yeah the blood we gave him yesterday must have done it for him." Well I am not a nurse or a Dr. so I don't know if it was the blood or the swaddle that made him do well but I do know from a little research that swaddling is GREAT for newborns and if it is great for newborns why wouldn't it be awesome for preemies that have to work that much harder! So he was swaddled up until 4pm when I fell asleep for his cares only to wake up to her telling me the temperature probe was saying that he was cold so she had to un-swaddle him. Ahhh so much for sleeping I guess. I just don't understand how Seattle could have no problems with swaddling him but Great Falls does. She told me that it has to do with hospital policy. Well, this is my baby and after they were telling me long term side effects that may OR may not happen (which is probably obvious to most of you as I have read about it but since no one mentioned it to me about OUR baby I put it to the back of my mind) I feel like we need to be more involved in how he is cared for.

5 comments:

  1. Mom and Grandma JolovichMay 1, 2010 at 3:33 PM

    Leah,
    You are your mother's daughter. When you feel that someone is not treating your children right, your mama tiger claws come out. There is nothing wrong with that. You have every right to say what you feel is best for Ethan. I got your back honey!
    Love you, Mom

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  2. I agree with your mom! Screw hospital Policy, you're that child's mother, you make the call. And for crying out loud... swaddle him on top, swaddle him on bottom, and leave his dang temp probe exposed... Do they want him to do well or not. He obviously does better being swaddled, ummm DUH!!!! Keep fighting for him! He needs a great mama like you! ;)

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  3. Maegan and David DunnMay 2, 2010 at 7:50 PM

    I agree with your mom and Lori! The nurses swaddled both of our kids in the hospital and if Ethan likes it, I say fight for it! He doesn't have a voice yet, so you are his voice. Fight for what you think is best for him...If they did it in Seattle, I don't see why they can't do it in Great Falls... Lets put the baby's comfort before hospital policy huh?!

    And just to let you know, we are following your blog religiously...and have shared it with our friends and family. You guys will have an incredible story to share with Ethan when he gets older because you documented all of your experiences on this blog.

    You guys keep on fighting (always) and keep on writing (as long as it works for you) :) Lots of love to you all!

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  4. Liz, Mike N EllieMay 5, 2010 at 7:00 AM

    Leah, I know that I may not comment like I should...but sometimes its hard to come up with words. I cannot imagine one day in your shoes. So just know that even if I don't comment, I still am thinking about you, Mark and Ethan. You cross my mind EVERY SINGLE DAY!!!! I talk about you a ton and my good friends ask about you and your strong little man all the time. We hope this week is going better and Ethan is making strides daily!
    Love from Iowa:)

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About Me

This blog started as a hobby for many reasons. It later became a way to keep the family up to date on our micro preemie baby, Ethan. Now as Ethan is nearing the 8 year mark with a little sister of 5 years I am finding a new reason to document on this blog.

Last year we were told by the school that Ethan had cerebral palsy, a blindspot and dyslexia. That is what started it all. I started taking him to doctors to find out what was going on and why this hasn't been discovered before now. In April 2017 we were told that he has executive functioning disorder. What the heck is EFD I thought?!?! After the doctor explaining it to us he basically said that if we don't start making changes now he could fall into the ADHD or possibly the autism category. Ok... so now what? What can we do?!? Well this blog is my way of documenting it all not only for me but also to help others find their way thru similar situations.

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