A Peek Inside My Fridge and Cabinets

I have really found a love for the glass Lock-and-Lock products. I put a lot of leftovers in them so that I can put them right in the oven or microwave. I've bought a few more rectangular pieces, in addition to the pieces I was given through L&L Supporters, and I also have some round ones from my last shipment. They are well-used!

The plastic ones store a lot of different kinds of things...ie: chocolate gold coins that I use during "School Time" with Caleb! :)

All our various types of jelly...

Look closely here...that round one in the background is extremely useful! I just got it recently (it's part of a lunch box kit, actually), and I am pretty much always using it for something. The ones in the foreground are holding celery and cucumbers for Caleb's snacks. There's also one (without a lid) that's cut off on the left. We put thawing milk in there!

I have a snack drawer for the nurses, but found that putting entire boxes of snacks would mean that about 1/2 of the box would go stale and be wasted. Since then, I've started splitting the boxes in half and putting them in two Lock and Lock containers. Since they're airtight, they don't go stale! It's worked really well and then we don't waste food.

This is Caleb's snack basket (I have a "Snack Shop" where he "buys" snacks...I need to blog on that sometime!) Lots of Lock and Lock in here because the stuff doesn't go bad this way!

In case there was ever any doubt, I definitely do use Lock and Lock on a daily (hourly, minutely...) basis! It's a part of my everyday life. :)

Comments

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

Search This Blog