Caleb & Company: Passing the Time

Thursday, February 12, 2009

Passing the Time

With Caleb staying home sick today, we found a few ways to pass the time. Check out some of our entertainment...

(Don't forget to pause the music on the right-hand side if you want to hear the video better)

Hope you had as much fun watching as we had hangin' out :)

3 comments:

Alicia said...: Seriously...He is so darn cute!!! We missed you today!! But...we still went to Rubio's...as Jeff probably told you about the crazy girl that came up to talk to him...yeah...that was me :-) We thought about buying lots of food to freeze so I can eat it while my kitchen is torn up :-) But...we didn't!! It did make for a yummy dinner tonight though!; February 12, 2009 at 10:55 PM
Unknown said...: Awww I love the videos. I missed you guys today, but I hope you both are getting some rest and feeling better :) Have a good holiday weekend!; February 13, 2009 at 1:32 PM
Di said...: Honestly, the best moments in parenting occur when you're just "hanging out". I hope he gets better soon!; February 16, 2009 at 11:30 AM

The latest "Calebism"

12/17/11

Last weekend we were at the MDA Holiday party. He opened up the gift they gave him and it was a set of toy cars. He exclaimed, "Hot Wheels! They're so awesome 'cuz their wheels are so HOT!!!"

I can't believe I forgot to put this one on here!!! A couple of months ago we ended up in the ER with Caleb - he had the flu and just had a rough night. While we were there he saw a nurse pass by in the hallway. He stopped mid-sentence and said, "Whoa. She is so beau-tee-ful. I think I want to add her to my collection."

Don't forget to check out Calebisms Archived at the bottom of the page.

What is Ullrich Congenital Muscular Dystrophy?

In June of 2007 Caleb was diagnosed with Ullrich Congenital Muscular Dystrophy (UCMD). This is an extremely rare form of Muscular Dystrophy - to date there are only a few hundred documented cases worldwide. It is considered a slowly progressive and life-limiting form of MD.

This does not mean that hope is lost. There is new research being done for this disease, as well as many other neuromuscular disorders. In the last 4 years, Caleb's Crew has raised over $65,000 for the MDA and designated all funds to go towards research for UCMD.

Please click on the links below to find out more detailed information regarding UCMD, as well as to support the MDA and Cure CMD, two wonderful organizations.

Thank you,

Amy (aka Mommy)