Remember our great night as a family? Here are a few pictures of our very normal, very average, very incredible family dinner. Please ignore the mess. We've been slightly preoccupied.
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 never wi
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p.s. Abby seems so alert, watching all of you at dinner, she is soooo adorable.!!
Thanks for the pics - especially the video of Heads, Shoulders, Knees and Toes! It helps me to see that Abby is just like any other little girl. She is so cute (as is Caleb!). Mrs B.