The actual surgery started at about 10:30. It will be around 6 hours from here. Updates are limited because they are only allowing essential personnel into this surgery. That's good in that it is limiting the risk of infection during a complicated surgery, but it means the family liaison doesn't get too much information. We are hanging in there.
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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"The actual surgery started at about 10:30. It will be around 6 hours from here." I am continuing to send virtual hugs, literal prayers and positive thoughts your way, Friend!! Hang in there, Mama!! ;)
"Stay hard, stay hungry, stay alive", Raelyn
PS. Thanks for the update!! ;-D