Wednesday, March 31, 2010

The Angels Are Calling


This is a photo of a little boy named Caleb who is in our ward. He looks perfectly normal and acts just like any other 4 year old, but last week his doctors told his mum they don't expect him to live much longer than a week.

Caleb was born with heart complications, and instead of having 4 heart chambers like the rest of us, he was only born with one. He has been on heart medication since he was a baby and has been in and out of hospital quite a few times in his little life. Now his doctors have reached a point where there is nothing more they can do for him. Every day his heart is getting weaker and it could be any day or night when his heart will simply stop beating.

This is the saddest news I've heard in a long time. Its been hard to get off my mind. It is devastating for the family as they never expected Caleb's life would be so short. I've been thinking to myself all week how I would feel if someone told me one of my children only had 5 days to live... it would be such a 'heart sinking' feeling. It has made many of us in the ward realize how we sometimes take life, and the people we love, for granted.

Our Ward has really pulled together to do all they can to help the family. Last weekend Tony organized a small service project to clean up the family's yard (he's their hometeacher), the Young Women visited Caleb at home and sung him Primary songs, and nearly half the ward has taken turns at cooking the family dinner. It is such a great feeling of unity and love when everyone goes the extra mile to help and support each other through tough times.

This weekend the Wiggles did a show in Auckland. Caleb got to personally meet the Wiggles and during their concert they sung a couple of songs dedicated just to him.
Caleb and his mum;


I have a friend named Alice who is a balloonist. So I told her about Caleb and asked her if she would make Caleb a big fancy balloon to make him smile. She made him a monkey and a 'big smiley boy' and last Sunday we took it over to his house. It definitely made him smile, and a week later it is still standing by his bed. He won't let his little brother touch it and he proudly shows it to everyone who comes into the house to visit.


The doctors prognosis of him only having a week to live has already passed, so fortunately for Caleb and his family, he's been granted a little more time. Now it's just a waiting game. He is playing with his brother at home just like normal... NO ONE would ever know there is something so wrong (although he is always telling his mum he is really sick and very tired). At least for Caleb - who doesn't fully comprehend his situation - he is enjoying his last days at home with his toys, surrounded by all his cousins, grandparents, aunties and uncles.
Caleb with one of his cousins;


No family wants a 'storm' like this one, but it sure does remind the rest of us how fragile life is. And it reminds us that something we have today could be gone tomorrow.

Time for a tissue!

2 comments:

Jen Kesler said...

So sad!

Christy said...

That is so sad... I got a lump in my throat. It so makes you grateful for what you do have