Am I really going to blog?: Happy 4th of July

Saturday, July 4, 2009

Happy 4th of July

Last night we went to the fireworks display in Athens. We got there early for a picnic and to let Sam run around the field with some new-found friends. It was cool so we were dressed for fall weather.

Sam & Emily liked dancing to Hannah Montana which was playing on Samantha's iPod. There were some early fireworks going on behind us.

Sam loved watching the show.

She was very impressed by the grand finale.

This holiday has taken on different meanings for us over the years. In 2003, it marked Cameron's first day of remission. He had completed 3 intense rounds of chemo and was declared to be cancer free. In 2008, it marked 100 days post-transplant. In 2009, another first. Another holiday that he has been gone. 247 days.

1 comment:

Gina SampsonJuly 5, 2009 at 5:05 PM
At about 10:30pm I thought of you guys. I felt sad that you were having to get through yet another holiday without Cameron. So I did the only thing I could think to do . . . I said a prayer that the night would be blessed for you.

Looks like you had a great time. The pictures of Sam and Emily are great! Thanks for sharing them.
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I HOPE....

I hope you never have to hear the words, 'Your child has cancer.'

I hope you never have to hear, 'The prognosis is not good.'

I hope you never have to prepare to undergo radiation or chemotherapy, have a port surgically inserted into their chest, be connected to IV poles. Look at you with fear in their eyes and say, 'Don't worry Mommy, everything will be okay.'

I hope you never have to hold your child as they vomit green bile.

I hope you never have to feed them ice chips for lunch.

I hope you never have to watch the 'cure' you pray for slowly take away their identity, as they lose their hair, become skeletal, swell up from steroids, develop severe acne, become barely or unable to walk or move, and look at you with hope in their eyes and say,'It's going to be okay, Mommy.'

I hope that you never have to stay in the hospital for weeks, months, or years at a time, where there is no privacy, sleeping on a slab, with your face to the wall, where you cry in muffled silence.

I hope you never have to see a mother, alone, huddled, in a dark hospital corridor...crying quietly, after just being told, 'There is nothing more we can do.'

I hope you never have to watch a family wander aimlessly, minutes after their child's body has been removed.

I hope you never have to use every bit of energy you have left, with all of this going on around you to remain positive, and the feelings of guilt, sorrow, hope and fear, overwhelm you.

I hope you never have to see a child's head bolted to the table as they receive radiation.

I hope you never have to take your child home (grateful but so afraid) in a wheelchair because the chemo and radiation has damaged their muscles, 35 pounds lighter, pale, bald, and scarred. And they look at you with faith in their eyes and say, 'It's going to be okay Mommy.'

I hope you never have to face the few friends that have stuck beside you and hear them say, 'Thank God that is over with,'...because you know it never will be. Your life becomes a whirl of doctors, blood tests and MRI's and you try to get your life back to 'normal'. While living in mind-numbing fear that any one of those tests could result in hearing the dreaded words...'The cancer has returned' or 'The tumor is growing.' And your friends become even fewer.

I hope you never have to experience any of these things... Because...only then...Will you understand...

(author unknown)