Caleb had another good night last night, he is starting to become more active and not really liking all of the tubes and machines that are hooked to his little body. The Nurses said that they were possibly looking at tapering down the ECMO machine last night, however Caleb thought he wanted to be a little more active thus causing his blood pressure to fluctuate a little bit, but the doctors did not seem to be to concerned about the fluctuation. Thanks once again to all of you for everything that you have done and all that you will continue to do in the future.
Wednesday, December 19, 2007
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3 comments:
He is sooo sweet!! So glad he is making "baby steps" each day in his progress. We love you guys and pray for you each day. Love the blog! We are here for you anytime! Love, The Simmons
THE KOOS FAMILY,
This blog is so neat! We love you all. Our thoughts and prayers are always with you. He is quite the little trooper and a cute one at that!!! Please let us know if we can help in any way!
Love, The Glover Family!!!!
He looks just like Brayden. Please remember we are just next door if you need anything. You have been in our thoughts and prayers. If Caleb is anything like his sibling he's a fighter, it will soon be a memory. Thank you for the blog...The Foremans
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