The longer one hangs out in Cancer World, the more apparent it becomes that it is not a wondrous, happy, healthy, healing place. It just isn't. No one exits without deep permanent scarring. The shocking kind that can be hidden, yet still exists under the long sleeves.
I often wonder if anyone is really interested in watching the Cancer World train wreck day after day, week after week, year after year. Does my writing help anyone? Do I do it because 12 years of living here have taken away my ability to write about anything else? Does my constant haranguing make people desensitized to the entire journey? Cancer World is simply a grind. An endless plodding grind.
One with an ambiguous ending.
People want happy endings, evidence of great triumph over adversity and life-affirming stories. The grim reality of Cancer World is there are no happy endings. Many many children die long horrible deaths. Some receive reprieves and believe they are done. Families celebrate "End-of-Treatment," "Cancerversarys" "One Year Off Treatment," "Last Dose of Chemo." No Hallmark card fits any of these situations. Very few children ever hear the words "Cure." They are told they continue to be "NED."
No
Evidence of
Disease
Many are told they are in "Remission" This is not a word that warms the cockles of our hearts. Simply a reprieve. Some are short, some are endless. We all live with the fact next word we will hear is "Relapse or Recurrence." We know cancer comes back with a vengeance. There is no way out. We are here for perpetuity.
Mary-Elizabeth is currently doing great. She seems to have settled into her little universe of side-effects. She handles the GVHD. She sees the endocrinologist. She manages her hot flashes. She weeps on occasion for the loss of the chance to have a child that carries her particular group of DNA. She is hyper aware of any changes in her body. A bump, a sneeze, a strange feeling of concern. She addresses each of them. I only try to put my worry in the way back of the fridge and hope it is not growing something disgusting.
Others have not been so lucky. We have met so many people over the years and know many many families that have come to the end of the road. They simply take their children home to die.
These deaths are painful and agonizing in so many ways. There is no way to describe the veiled anguish of every Mother's post. They put their best face forward and try to have something happy to say.
They acknowledge they are counting on God to perform a miracle and have their child with them again. Yet they know, they know all too well, the time of the last smile, the last breath, the last gentle kiss is coming. The sand is rapidly escaping the hourglass, and there is no way to stop gravity. The entire process is just overwhelming and excruciating.
Time does not heal the wound of losing a child. The pain does not lessen or diminish in few months or few years. This is a gaping, car-swallowing sinkhole kind of wound that never ever heals. The pain of losing a child remains forever. Life does not get easier, nor does the pain lessen.
The reason we fight so hard to beat such a demon is that somewhere in our mother souls we know. We know the depth of the love, the deep well that burrows into the center of the earth and out the other side to connect with the Universe. We know how much we love our children and losing them is not an option.
I ended the blog because I couldn't keep from talking about all the sadness that had been the last few months. There had been so many losses of such lovely children. Too many funerals, too many "Joyous Life Celebrations" too many deep sighs choking back tears moments.
I don't keep count anymore. I cringe every time someone celebrates the last dose of Chemo or the end of treatment. I just hold my breath for them. I know too much.
We were at the end-of-treatment to only have the monster return seven years post-remission and 57 months after the last dose of chemo. What the Hell!? She is now 5 years post-transplant, and no one is talking cure. No one has said we don't have to worry anymore. No one is saying much. I think we are all just waiting.
I certainly am.
Twenty Years, Two Hundred and Forty Months, Seven Thousand Days, and Three Hundred Days. Since we started chasing Leukemia.
Showing posts with label Bone Marrow Transplant failure.. Show all posts
Showing posts with label Bone Marrow Transplant failure.. Show all posts
Friday, May 26, 2017
Sunday, January 17, 2016
Bright Sides
"Look on the Bright Side"
I am sure I have said the phrase a million and one times. I am certain I have heard it a million and two times. It is sometimes said without thinking. It is in our repertoire of things we say when words fail us. It is an easy thing to say but a hard task to accomplish in most instances. It is okay to feel sad and afraid because sometimes horrible things happen. But the gift of time often allows for healing, understanding, and acceptance of any bad situation.
Sometimes there is no "Bright Side". Sometimes both sides of a penny are dark and gloomy. It is not always possible to happy about the fact your child has relapsed AGAIN, and the odds are similar to the odds of winning the Power Ball. I know there are times when news hits me in the gut so hard, I can not breathe. I am shocked in a time in my life I don't think I can be shocked by anything. It is so hard sometimes to ramp myself up to see a friend, or break some news to the family or worse yet, to your child.
I am not talking about our family. Things are going great right now. Mary-E is cooking along and will graduate after only four years of schooling. She will do so being ever so close to graduating with honors. She is ready to take on the world in one way or another.
But day after day, week after week, I am holding my breath, knowing this will never be a solid state of being. Many say to me "Look on the Brightside." "Don't dwell on what could happen." "Don't be pessimistic." While knowing each day could bring new cancer or a new side effect is not being pessimistic. A bit of well-placed pessimism is simply my reality. It is just that little niggling voice sitting on my shoulder reminding me to value and enjoy every day. It lets me forgive myself for my many imperfections, my never organized house, piles of self-reproducing laundry, my endless to-do list.
It makes me try harder to do things that make a difference in people's lives. It makes me balance what I want. I want to spend time with people that make my life richer and more interesting. My house is not perfect, but six people are coming for dinner. The lamb is a bit spicy but then why did God make sour cream?
The bright sides of my penny bring me back to this moment in time. This is where I stay, knowing the penny, no matter how dark, is still a work in process. There is a good chance it there will shine on both sides.
I am sure I have said the phrase a million and one times. I am certain I have heard it a million and two times. It is sometimes said without thinking. It is in our repertoire of things we say when words fail us. It is an easy thing to say but a hard task to accomplish in most instances. It is okay to feel sad and afraid because sometimes horrible things happen. But the gift of time often allows for healing, understanding, and acceptance of any bad situation.
Sometimes there is no "Bright Side". Sometimes both sides of a penny are dark and gloomy. It is not always possible to happy about the fact your child has relapsed AGAIN, and the odds are similar to the odds of winning the Power Ball. I know there are times when news hits me in the gut so hard, I can not breathe. I am shocked in a time in my life I don't think I can be shocked by anything. It is so hard sometimes to ramp myself up to see a friend, or break some news to the family or worse yet, to your child.
I am not talking about our family. Things are going great right now. Mary-E is cooking along and will graduate after only four years of schooling. She will do so being ever so close to graduating with honors. She is ready to take on the world in one way or another.
But day after day, week after week, I am holding my breath, knowing this will never be a solid state of being. Many say to me "Look on the Brightside." "Don't dwell on what could happen." "Don't be pessimistic." While knowing each day could bring new cancer or a new side effect is not being pessimistic. A bit of well-placed pessimism is simply my reality. It is just that little niggling voice sitting on my shoulder reminding me to value and enjoy every day. It lets me forgive myself for my many imperfections, my never organized house, piles of self-reproducing laundry, my endless to-do list.
It makes me try harder to do things that make a difference in people's lives. It makes me balance what I want. I want to spend time with people that make my life richer and more interesting. My house is not perfect, but six people are coming for dinner. The lamb is a bit spicy but then why did God make sour cream?
The bright sides of my penny bring me back to this moment in time. This is where I stay, knowing the penny, no matter how dark, is still a work in process. There is a good chance it there will shine on both sides.
Tuesday, May 19, 2015
Emily is Gone
Another one... Another Loss. It sometimes seems like a steady stream... She was a strong determined little girl. Her family was with her all the way..... Her family is exhausted and need lots of good energy sent their way. Sometimes when I post these things people tell me they are sorry for my loss. It is never about my loss... it is about the world's loss. We all are less for what has happened here.
Childhood Cancer is a tough one.
Childhood Cancer is a tough one.
Monday, May 18, 2015
Just Sent MEB to California for a Couple of Weeks ...... I am So So Lucky
As usual, this summer is not working out as I had anticipated. Thought the child would be working in Spokane but as it happens, she is on a different kind of adventure. Her summer is falling together with bits and pieces of this and that.
Camp Sparkle for Gilda's Club will take two weeks. It is a camp for kids that have had cancer somewhere in their lives. Moms, Dads, Sibs... They spend a week doing healing things. Fun things. They all love Meb because she knows, she knows what it is to have cancer and to have lost friends to cancer.
She is spending two weeks with her Uncle David, maybe more depending on how his summer goes. She is going to get to work in the office with his great assistant Donna and learn the business side of things. She is great at doing those sort of things and had lots of organizational skills.
She wants to spend some time with her Grandma in Eugene. Maybe for the Country Fair.... Maybe some time on the water somewhere in the Puget Sound, Maybe some time in Central Washington with a metal lathe and some cutting torches, Maybe.... The Summer is full of maybes... and Maybe that is okay.
I decided yesterday that Maybe this is just a great gift from the Gods. Maybe I we just need to settle an unusual summer, one not dominated by BMT fears. Maybe this is what it is supposed to be. I just keep receiving notices and reading posts about kids that will not be spending the Summer with their Mom's.
Our little world of Childhood Cancer is losing some bright futures right now. Young lives are winding down and people are just down right sad. No other word for it. Sad. Emily seems to be done after cramming so much into her "life list". This was the post this morning from her family.
Enjoy every breath your child can take with ease.
Camp Sparkle for Gilda's Club will take two weeks. It is a camp for kids that have had cancer somewhere in their lives. Moms, Dads, Sibs... They spend a week doing healing things. Fun things. They all love Meb because she knows, she knows what it is to have cancer and to have lost friends to cancer.
She is spending two weeks with her Uncle David, maybe more depending on how his summer goes. She is going to get to work in the office with his great assistant Donna and learn the business side of things. She is great at doing those sort of things and had lots of organizational skills.
She wants to spend some time with her Grandma in Eugene. Maybe for the Country Fair.... Maybe some time on the water somewhere in the Puget Sound, Maybe some time in Central Washington with a metal lathe and some cutting torches, Maybe.... The Summer is full of maybes... and Maybe that is okay.
I decided yesterday that Maybe this is just a great gift from the Gods. Maybe I we just need to settle an unusual summer, one not dominated by BMT fears. Maybe this is what it is supposed to be. I just keep receiving notices and reading posts about kids that will not be spending the Summer with their Mom's.
Our little world of Childhood Cancer is losing some bright futures right now. Young lives are winding down and people are just down right sad. No other word for it. Sad. Emily seems to be done after cramming so much into her "life list". This was the post this morning from her family.
We are losing our Emily. She is still paralyzed. I thought today would be the day, but this little girl is a fighter and came back to tell me how much she loved me, that I am the best mom that she could have asked for, and that she is so happy that she chose me to be her mom. She is not in pain anymore, but is struggling to breathe. Please pray that God brings her home to him, so she can dance in fields of flowers. And run and play with her friends Becca, Albert, and Sarah. And be greeted by my dad and her Nonna. This is heart wrenching to watch. As selfish as I want to be, I won't. I need God to answer my prayers!
This is a very personal time for us, I ask you please to respect our privacy. I have shared her for four years, i need this time for me. I am spending every second with my baby. It hurts so much to imagine that I will never have another hug or kiss from my girl. Or hear her say "mommy" the special way that she does. This hurts so damn bad.
Enjoy every breath your child can take with ease.
Subscribe to:
Posts (Atom)

