Wink from Heaven: Fluffy

Saturday, November 8, 2008

Fluffy

I just love fluff-- Caleb fluff. His little body is so fluffy and completely snuggable! His little feet are so cute and pudgy- I love to rub those sweet little feet! His fingers look like little potbellied people, and I love how his knuckles are little dimples in his hands. And oh the cheeks, those soft round cheeks! They are so irresistibly kissable. Even Caleb's hair is as puffy as a dandelion, blow on it and make a wish! Thank you for being so fluffy, Caleb, and for reminding me that a little bit of fluff is a good thing!

3 comments:

Amber said...: Oh the smell of your own little people's cheeks is amazing. His cheeks look so warm and kissable.
He is one loved little man..xx; November 9, 2008 at 4:07 AM
Becky said...: LOVE this picture. He is darling. His hands actually remind me of Ben's. I LOVE 'em. A little fluff IS a great thing. :); November 10, 2008 at 2:53 PM
Unknown said...: Now dandelion fluff will forever make me think of your sweet boy. Thanks. You all are in our prayers. We love you!; November 10, 2008 at 10:15 PM

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.