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I am doing it. I am starting the blog that has been in my head for a few weeks now. This blog is the story of my daughter, Sydney and how we, as a family cope with her heart problems. Sydney has a heart defect that will most likely require open-heart surgery. This will be about her progress, her struggles, mine and Jordan's struggles as we try to help her, what her days are like, and most importantly-the miracles, big or small, that occur in our daily life.I believe that my daughter was born with this heart defect for a reason. We are supposed to learn from this experience so I am using this blog as a way to write my thoughts, fears, worries, and joys that come as we help our daughter heal. There are days when I feel like I have so many different emotions that I am going to explode and fortunately a blog will keep me from doing that! Lucky for you. You are welcome to read this blog even if I've never met you! Feel free to make comments, tell your own story, laugh, judge me on my mothering, or to just cry. Whichever suits you best for whatever reason is fine with me! Enjoy the read...

Wednesday, August 18, 2010

Dear Sydney,
I can't find my camera so I can't post any picture but as soon as I find it- I will put them up. I promise.

Well, lets just jump straight to the good stuff. You are now home from the hospital! You were doing so good that they sent us home on Sunday afternoon. I literally felt a weight lifting off my shoulders as we walked out the hospital doors. You were in the hospital for a total of 5 days- which is great because they originally told us to plan on staying for 7-10 days. You are so strong.

You were sent home on 5 medications. Two of them help you to basically pee out all of the fluids that are still in your lungs. Another one is to keep your blood pressure down. Your heart is used to working exteremly hard and the dr.'s said it will take a while for it it to realize it doesn't have to do so much work anymore. Another one is for the thrush that has decided to camp out on your tongue. Because you were on antibiotics for the first two days in the ICU it caused your body to react in such a way that a fungus-y white stuff started growing in your mouth. You were also sent home with a prescription pain killer but you haven't needed it. You have been using children's tylenol for the past 4 days. I am so amazed that you haven't been wrenching in pain. Instead you smile, kick your legs, try to roll over, and giggle. What a sweet girl you are.

I have noticed dramatic changes in you since your surgery. The first thing everyone notices when they see you is that you have color in your face now. You aren't pale anymore! You have rosy cheeks and a pink tint to the rest of your body! Oh, how I love it! You have so much more energy! Your legs are getting stronger by the day and your naps only last about 15-30 minutes and then you are good to go. (15 minutes is an extremely short nap but hey...at least you aren't sleeping all day!) You used to have a little cough and that is completely gone now. I love it! You used to cough so much that it would make you vomit and since your sugery you haven't vomited once. Wow! Your appetite has sky rocketed! On the drive home you drank 4 bottles in 4 hours. It was amazing! Your Dad and I just kept laughing because we couldn't believe it! Your weight gain has also increased. The day that we left the hospital you clocked in at 10 lbs. Today you went to the pediatrician and you weighed exactly 11 lbs. Whoa! I am so proud of you. I can't wait for you to have rolls going down your thighs and arms. I also love that I can't feel your heart pounding every time I put my hand on your back. You used to work so hard just to be able to breathe and now that's not the case anymore.

Something that I keep thinking about is what the surgeon told us after he finished your surgery. After he was through explaining that the hole in your heart was bigger than expected he said "God must want your heart to be beating because it's still beating." He was surprised that your symptoms weren't worse than what they were. He said that you were in the stages of heart failure. I don't even want to think about where we would be if your surgery was a few weeks further down the road. You obviously have some important work you need to do on this earth, Sydney. I feel so blessed.

Your incision looks good and strong. The surgeon did a perfect job at keeping it in a straight, clean line. It's not a messy scar by any means. The pediatrician took out your stitches from your chest tube today. You didn't even cry. You are proving to me everyday that you have a high pain tolerance. Which is a blessing for all of us. I hate to see you in pain. It is so hard to watch.

You are an example to us all, Sydney. We love you so much. I'll be sure to update you more frequently now that we are home and settled in.

Love always and forever,
Mom

7 comments:

Jeff and Aubry said...

Yay - Way to go, you guys!

Jed and Kera said...

Yahoo!! I was going to text you today if I didn't see an update on here. I'm glad I don't have to bug you. Wow that little Sydney is a special little thing! 11 lbs!! Wow!! Dalton is 15 1/2 months and weighs double that. He is in the 22%. I can't weight to hear where she is in weight gain the next few months. I also can't wait to see a picture of her rosy cheeks...color in there face is such a BIG thing. I know just by when Dalton was first born and was considered "failure to thrive" he was very paste white and sad looking. I think it's so cute that she had so many bottles on the way home! She'll be drinking 4-5 oz at a time in NO TIME! :O) I hope you and Jordan are sleeping better now and are able to relax somewhat. I'm sure it's hard to relax but I can only imagine the amount of stress you two have had to put on your bodies. I love ya girl! Still in each of our prayers.

Chelsee said...

Wahoo!!! So happy that she is doing so well. What a strong girl! She is truly blessed and watched over. Sounds like she is an amazing girl! Hope that things continue to go well for you! Can't wait to see pictures of her. Soon she'll be as big as Joshua. He's about 14 1/2 pounds now and eats 7 oz 4 times a day.

Mama Bean said...

CONGRATS!!!!

The Tibbitts said...

We are so glad that she is doing well. What a strong, sweet little girl you have. What a relief it must be for you and your family to have such an ordeal almost over. You are an inspiration to us.

Unknown said...

How exciting that she's recovering so quickly! It must feel so wonderful to see the change in her. I love how you're so excited to see her chubby roles come. Too cute :)

Jen Gillespie said...

WOW! What a strong little girl. And such a miracle. I cannot wait to watch her grow and she what amazing work she has on this earth. Love her extra long for me tonight.

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