Caleb & Company: Caleb Standing

Thursday, May 8, 2008

Caleb Standing

Here's a video of Caleb standing TOTALLY independently. There are no strings attached or any special effects...Just our amazing boy!

8 comments:

Shanana said...: So amazing! What a cutie bug!; May 8, 2008 at 10:21 PM
Anonymous said...: I love it. He already has Jeff's rhythm.; May 9, 2008 at 7:46 PM
Anonymous said...: Adorable! You two are such delightful parents. Thanks for sharing your joy!

Kelly; May 9, 2008 at 8:01 PM
Maddy said...: Such a sweet smile this brought to my face...Thank you
XOXOXO; May 9, 2008 at 8:36 PM
Ben said...: Caleb,

You loves to see me standing.; May 10, 2008 at 7:50 AM
Shanana said...: The boys were so stoked to see this video. Happy Mother's Day!; May 11, 2008 at 8:39 PM
Val Krasner said...: Bravo to Caleb, Mommy and Daddy! Caleb's smile is so sweet! Thank you for sharing this momment with me!
Love,
Val; May 11, 2008 at 10:53 PM
Caleb's Co. said...: Ben, I can't believe you speak Caleb! Thanks for all your support, everyone!; May 15, 2008 at 7:58 PM

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)