Caleb & Company: Singing Lullibies

Thursday, July 3, 2008

Singing Lullibies

This has been one of my favorite moments with Caleb lately.

5 comments:

Shanana said...: Oh my gosh! How sweet is that? That is so cute!!! Melts my heart!

I love the yoga routine. If I haven't seen the pretzel in real life, I would've never believed it!; July 4, 2008 at 3:17 PM
Mommalynne said...: "Oh my gosh!" is exactly what I thought of to say. What a precious moment! You both sing beautifully!

The yoga looks very fun and he does it so well. thank you for sharing.
Lynne; July 11, 2008 at 11:21 PM
Anonymous said...: Amy... So... I'm at work and about to cry now... that is the sweetest thing :); July 25, 2008 at 1:59 PM
Caleb's Co. said...: I just love these moments with Caleb and am so happy to share them with you all.; July 26, 2008 at 3:12 PM
Anonymous said...: That is precious! I love Caleb singing along and the occasional laughter on both sides :O) What a moment to be cherished!; July 28, 2008 at 9:38 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)