The Mini Mister is one tough little guy. He had a rough week. I will spare you the pictures of him on the ventilator. They are disturbing to me still. Having your baby on the vent, paralyzed and sedated isn't easy.
With Daddy before surgery.
Grammy and Grampy pre-op.
Welcome Family and Friends
Together we can shake things up, make some waves and have fun doing it!
Believe it or not...
The choice is yours!
Tuesday, January 27, 2009
Week in Review
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Shaking it up and making waves!
at
5:56 PM
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We are home
We are home. I'll have to post some pics soon. He needs to drink more but I'm bribing him with Sonic milkshakes. More later.
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Shaking it up and making waves!
at
3:53 PM
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Thursday, January 22, 2009
Mini Mister Update
The Mini Mister is off the vent but having a lot of pain and requiring a lot of pain meds. He will need to stay in the ICU for a couple of more days so they can monitor him for respiratory distress since he is on so much pain med. Please continue to pray for him. It is so hard to see him in so much pain. If you are on Facebook look me up. It is easier to update FB from my Blackberry than this website. My phone is my main mode of connection to the outside world at the hospital.
Thanks for all the prayers.
Sophie
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7:38 PM
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Sunday, January 18, 2009
My Joy
I laid down with Zachary this afternoon to take a nap but I can't sleep. I've laid here watching him sleep and memorizing ever adorable inch of him as the tears have flowed. I have never in my life wanted to do something for someone else. I wish I could take on this surgery for him. He has been through so much in his short little life. I have questioned him having this surgery a million times over. I know he needs it. I don't doubt God's sovereignty in this. He hasn't brought him this far to let him down now. I just don't want him to suffer, to hurt, to experience anything but joy. But, this week he will hurt. That is inevitable. I always wondered if people who adopt can love a child they didn't give birth to as much as one you did. I have to say, you can. With everything in me my love for this child is no different than that of my girls. He just came into our family in a much different way. He has been such an example to me. Life has dealt him blow after blow. He shouldn't even be alive. Life support was almost removed numerous times because it all seemed so hopeless. But, he is here and he is thriving. And by some miracle God brought him to us. There are no words that can ever express my gratitude to God for that. For allowing me the privilege and honor of being this child's mommy. But, Tuesday I will let him out of my arms into the arms of doctors I know well and trust completely. There will be ICU nurses, my friends, that will take care him will diligent love and care, and will also be there for me. He has been prayed over so many times and I know that the prayers for him will continue this week. God has something so amazing for this child. We all have a front row seat for it. So, continue to pray. Pray for this precious child. Pray like never before.
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at
4:36 PM
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Friday, January 16, 2009
Pray hard on the 20th
His big day is coming up Tuesday. He is doing so well that I hate the thought of ruining that but he needs this surgery. Here he is having fun with Yellow Bird. The girls love playing with him.
Aren't they all so cute.
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at
9:52 PM
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Thursday, January 15, 2009
Tuesday is the big day
I did the Mini Mister's pre-op today. Everything is all set and I have to say I'm getting nervous. Pray hard for our little guy. This will be a big surgery and I want his recovery to be quick.
Sophie
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11:28 AM
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Thursday, January 1, 2009
Funny!!!!
One of our ER docs did this presentation for the Christmas Party. It is so funny I thought I would share it. It is especially funny to those who went through IKE. You've gotta' learn to laugh.
http://www.bly.cc/ike
Enjoy!
Sophie
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Shaking it up and making waves!
at
10:29 PM
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