Caleb and me on his 2nd birthday
He had Down Syndrome and severe heart and lung defects, as well as extremely low muscle tone. He amazed the doctors by living three and a half years. The most he ever weighed was 22 pounds. He could say a few words. He never walked or crawled, but he was very loving and cheerful. He enjoyed worship music, and would bounce on his seat and clap his hands and shout, "Woo Hoo!"
The time he was in the hospital when he was 20 months old, we were told there was nothing that could be done for him and they expected him to die right away. That was when we were playing the praise music. A few days later, the heart doctor was shocked to see him smiling and bouncing a rubber ball against the wall.
We had many happy days together, and then many sad ones as his health began to decline again.
I had a "professional" tell me I should put him in a facility and forget about him because he would have a negative influence on his brothers and sister. I cannot even describe what a tremendous blessing he was in my life and in theirs.

