Caleb had some friends over the other day to play in the sprinklers and have lunch. They had the BEST time just running through the slip-and-slide and splashing in our kiddie pool. It wasn't anything fancy, but they all had fun! You know you've done something right when your son tells you this was the best day ever as you were tucking him in thaqt night. Caleb gives up a lot these days, so I'm glad that it was a good one for him. He deserves it!
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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