Dad post-op Day 2 4:30

After concerns about his kidney functioning and fluid, the decision was made to move Dad to the icu for close monitoring. The thoracic surgeon on call this weekend has been excellent and was able to get things moving very quickly.

He has a chest drain in now and a tube to remove the gas from his stomach. Both of these procedures have greatly improved his breathing and level of pain. He's not allowed to eat anything while the ng tube is in, but he has been enjoying the wet sponges in his mouth. :)

Our pastor and his wife visited and dad really enjoyed seeing them. Dad has a long road ahead, and we appreciate all of your prayers.

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Cerebrocostomandibular Syndrome

If you happen to pick up the latest Reader's Digest, there is an article in there about Piper Breinholt , a four year old with CCMS. If you've been around here a while, you'll remember wayyyyyy back when we first received Abby's diagnosis that I was able to speak to Piper's mom, Reagan. The article is more about their story and not as much about the ins and outs of CCMS, but I think it's probably enough to get some people googling it and I'm hoping a few will end up here. Every once in a while, I give a blog post the title of Cerebrocostomandibular Syndrome so that it would show up in Google. My ever-present hope is that people will stumble across my blog and 1) be encouraged by the hope we have in Christ, 2) feel a connection with someone in a similar situation as them, or 3) get excited over the miracles that have been performed in Abby's life!! (a combination of all 3 is great too!) :) Notice that it's not to get famous and it ...

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Imagination Movers Photo Recap

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Life as a Leach

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