New Year...New Beginnings!

It's fitting that we will be going home with Abby in January. January 1st marks a new year and is often symbolic of new beginnings. The Leach family will certainly be starting over in many ways!

My New Year's resolution is to cherish the little things...when Abby looks at me with those big dark eys...when Caleb cuddles with me...when Becky lays her head in my lap...when someone sends me a sweet card...when students in my class give me hugs...

All of those "little" things are so very important to me! I hope and pray that I can truly cherish each moment and be thankful for everything God gives me. It's way too easy to get wrapped up in our situation and lose sight of the most important thing about Abby:

She's here!

As nervous as I am about bringing Abby home, I wouldn't change it for the world. I am so thankful that we get to bring her home!!

I would love to hear your New Year's resolutions as well. Please feel free to comment and let me know what they are!

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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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Life as a Leach

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