Thankful Thursday

Last week, on Thanksgiving, I told you I was thankful for the love that these two have for each other.

Here's the proof.

This week, I'm still thankful for that. They are so sweet together!

In other, unrelated news, my lack of posting has been due to an issue I've been having with Google saying I have used up my photo storage allotment. After a week of trying to figure out a way around it (without deleting precious photos from my blog!), I broke down and paid for the cheapest subscription. Since it took me 5 years to fill up the free allotment, this storage should last me a while! It's still frustrating though. :(

Comments

Danika said…

You don't know me, I found your blog from someone else's (hope that doesn't make me sound like a freaky blog stalker!). I have never commented, but I enjoy reading about your life and I'm thrilled Abby is doing well!
I recently ran into the same space issue problem with my blog and my tech-savvy bro-in-law found a free workaround solution! I found your email address on your blog profile so I will email it to you. Hope it helps! Happy Holidays!
~Danika

November 29, 2012 at 5:28 PM

Mary Lou said…

Julie....
Hi. Remember me? I am sorry for no longer commenting on your Blog. However, I have still been reading it!! Faithfully. ;-D
I am so pleased with how far God has taken you with Abby.... What a doll she is!! ;)
I love the Christmas-themed look on this Blog.... Plus you updated pictures!! ;op

November 29, 2012 at 7:53 PM

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 ...

Bath Time Photos!!

As promised, here are lots of photos of Abby's first bath. Caleb was supposed to be in bed, but the bathroom is right next to his room... "I'm not too sure about this..." Once she learned how to splash, she was all smiles! Her first good hair wash! Gotta protect the trach! She really liked getting water poured on her head. It was cute! Smiley (and bubbly) for Daddy while he dried her off. All clean!! (Note the Lysol wipes in that last picture. They are NEVER far away!)

Imagination Movers Photo Recap

Seriously, The Imagination Movers were so much fun! They played lots of their own music, with some classic rock mixed in for the adults. There were also quite a few jokes and references to Baltimore, which was kind of fun. The whole night centered around this robot named Rock-o-Matic, or "Rocko." This is Mover Scott, and he wears Wobble Goggles that help him see new ideas. Caleb and Abby have a pair of goggles too. :) There are 4 main Movers that are part of the TV show, but they have 2 extra movers to play instruments and do back-up vocals in their live tour. Abby finished up her feed before the show started so that she would be free to dance! My dancing queen did NOT want to sit in my lap. The row in front of us was empty, and that is where she stood almost the entire show--dancing the night away. My Imagination Movers Caleb did his share of singing and dancing too. He knows m...

Life as a Leach

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