Terrified
Excited
Dread
Concern
Exhaustion
Thrilled
Disbelief
Did I mention... Dread
I so don't want to be here. I so never wanted to travel this path. Every parent has a dread, a fear, an uncontroled worry. When MEB was little, mine was Spinal Menningitis. I was sure every fever was going to be permenant brain damage and death. My sister-in-law was afraid of choking and cherrios.
This sort of fear transfers to something else in Cancer World. We all fear relapse. It is something you worry about all the time and it never leaves your mind yet we are all sure that we have said the special prayers and done the right dance and purchased the right organic vegetables and relapse will never get your child.
Then we all have lots of individual fears. Feeding tubes, pain killers, germs, fungus, colds, chicken pox, plague, witches, the usual.
Mine was transplant. I was so relieved when Mary-Elizabeth went into remission, did not relapse, and made it through treatment. It was not smooth sailing, it was a rough couple of years full of weird side effects and long term side effects and hives and shortened tendons and loss of gray and white matter but there was no transplant.
It was such a relief that we never faced that battle. I saw those room, the weiry parents and exhausted kids. While our children were sick, somehow they were sicker, so much sicker. It made me so sad. I would see the dark rooms, the nurses gowning up and numbers of people in and out. Then the kids would disapear. I would wake up and there would be a room, previously closed for days, wide open and empty, the child and the activity would be gone. It was so so scary.
We are so so ready for this and yet so not ready. I guess we don't have a choice so we will go and do this.
Right now we are working on surviving the 5 days of chemo.
Mary-Elizabeth is awake and talking.
Twenty Years, Two Hundred and Forty Months, Seven Thousand Days, and Three Hundred Days. Since we started chasing Leukemia.
Blog Archive
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2011
(97)
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November
(20)
- So No Remission for Us.....
- Back Again..... But Progress has been recognized.
- 10 Hours in.... More to go
- The R Words
- Chef Walter Speaks and I reply.
- Almost Home
- Home After 6 Days.
- So, Treasures are Falling From the Sky
- Lookemia is sort of Like Living in Seattle and bei...
- This is me trying to get the Chef's Attention
- 11/11/11
- Chef Walter and I are going to be friends.
- Things I Never Wanted to Know aboutj Platelets.
- Time Certainly Passes when you are not having fun.
- Crane Folding and X-File Watching
- So...... We enter Cord Blood World
- More Cord Blood Information.
- Turkey Day 2010 and 2011
- Gravy Boat Envy
- Thoughts on Transplants
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November
(20)
3 comments:
A beautiful young woman. Here's to the absolutely best chemo week possible. A day at a time.
Oh Sally and Mary Elizabeth - you're both so wonderful. Maggie
You and M-E have the strength to do this and you will both get through it. As you say, you do not have a choice. Now is the time of the long march. Just keep you head down and put one foot in front of the other. You will be out of Siberia sooner than you think.
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