Wink from Heaven: Show and Tell

Thursday, October 21, 2010

Show and Tell

Tomorrow I am helping Matthew's class with a Halloween art project.

His teacher e mailed me to tell me that Matthew would like to "Show and Tell" Caleb while I'm there.

I was touched.

Matthew isn't self conscious about his little brother.

He is proud.

He knows how special he is-

and when you experience something extra special.

You want to share.

I know just how he feels.

11 comments:

Colleen said...: That is so sweet!; October 21, 2010 at 9:50 PM
Anonymous said...: How lovely! I would be very proud of Caleb too!; October 21, 2010 at 10:07 PM
shirlgirl said...: Will look forward to hearing about your "show and tell" at school. I'll bet everyone will absolutely love your sweet Caleb and want to kiss those beautiful cheeks.; October 22, 2010 at 5:14 AM
brigette said...: What a sweet brother he has!!; October 22, 2010 at 8:25 AM
Tara Bennett said...: I wish the whole world could share in Caleb's goodness. It would be a better place. I'm so glad you get to give that experience to those kids... they are lucky.; October 22, 2010 at 9:17 AM
Amanda Thrasher said...: oh my goodness.. that is so precious!; October 22, 2010 at 9:28 AM
Becky said...: ME TOO! I know how that feels. I'm so grateful he "gets it".; October 22, 2010 at 6:29 PM
The Kings said...: That is SO cool!; October 22, 2010 at 10:58 PM
Kel said...: Ooh! I also look forward to hearing the details of show & tell. How awesome for them to be together at school!; October 24, 2010 at 1:56 PM
Cami said...: I came upon your blog through a mom that I met at the pediatrican's office. I was reading about your sweet Caleb; my daughter also was born without her right globe and optic nerve. She too has hydrocephalus. Interesting about the two of these special kids....
If you want to meet her, email me so I can add you to our blog; it's private.
camisaari@msn.com
Thanks for sharing your story! It is nice to not feel "alone" sometimes.; October 26, 2010 at 9:14 PM
Unknown said...: Awesome. Just awesome.
XO; October 27, 2010 at 7:04 AM

Prayer for Caleb

(written by Caleb's Grandma in her weekly column -2008-)

In my family we have a secret code to communicate our love for each other when we are out in public. We wink. When one of us is about to perform or speak, we look for a family member’s face in the crowd. Then we wink at each other. Closing one eye and winking is our secret code for saying, “I love you. You can do it. You’re wonderful.”

About three years ago, my grandson Caleb was born into our family. He must have known before birth that he would never be able to speak to us because he was born with one eyelid permanently closed. So, he is always “winking” at us, always communicating, “I love you. You can do it. You’re wonderful.”

Caleb has one eye lid permanently closed because he is missing one of his eyes . . . and he is also missing his brain. All the doctors said he would die soon after birth. They were wrong. Caleb is three years old. He is a medical miracle. The doctors say he can’t see, hear, speak, think or move. Those who know and love Caleb understand he has his own unique way of experiencing the world and communicating his love to those around him.

After Caleb was born the hospice people told us to buy a burial plot and continually warned us of his imminent death. We soon learned you can not live well in a state of fear and sadness. We decided we could spend Caleb’s entire life anxious and scared he might die at any moment, or we could celebrate each day we were blessed to have him with us. In the beginning, my daughter April celebrated Caleb’s birthday every week instead of every year with balloons and cupcakes because we simply did not know how long we would have him with us. We stopped the cupcakes after we gained ten pounds, but the celebrating goes on.

We all prayed for a miracle when we first learned about Caleb’s condition. We got one. Caleb’s birth, life and mission have had a deep and lasting impact on our lives. His spirit, eternal identity and most of all the loving, individual relationship he has with each of us is truly a miracle. Because of Caleb we know that each of us has a divine purpose and that the physical body is a sacred gift we should never take for granted. We better understand the worth of a soul and the resiliency of the human spirit.

Caleb’s five year old brother Matthew said, “Grandma. The doctors said Caleb was going to die, but he didn’t. That’s the first miracle I ever saw!”

Sometimes Caleb’s baby brother Mitchell pulls out his feeding tube while they hold hands riding together in their double stroller. Sometimes the only intervention that can get Caleb’s heart rate up is when his older brothers Josh and Matty crawl in his crib, hug him and sing, “I am a Child of God.” ...If you have a moment please offer a prayer for the little boy who has never been able to utter a single word and yet has taught everyone who knows and loves him – all the secrets of a rich and meaningful life.