I've named my kidney stone Rocky. He's quite comfy in my body and doesn't appear to have any intentions of coming out. I went to the urologist today (where I was the youngest person in the waiting room by at least 40 years!) and he said I will have to have it removed under general anesthesia and have a stent put in. Sounds like fun, huh?! The scheduler is going to call me tomorrow. In the meanwhile, I'm just trying to drink tons of water and learn how to coexist with my little friend.
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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