I am writing today from my home away from home, Joe DiMaggio
Children's hospital. Most of you know about my son Josh, a leukemia
warrior. He is two years, one month and twenty four days into his
battle. In his current phase of treatment, we return to the hospital
every 84 days for our "long day," which consists of a spinal tap with
chemo (methotrexate) flush and a second (nasty) dose of vincristine.
The spinal tap is necessary because oftentimes, the leukemia cells lurk
in the central nervous system, but are too tiny to detect. The
methotrexate is supposed to take care of that. But the central nervous
system is where those damn leukemia cells will most likely reappear in
the case of a relapse. So, every 84 days, I wait with my nine year old
son while he is sedated, and then I wait to hear that (fear #1), he has
woken up from the sedation and (fear #2) I wait to hear nothing. For a
week. Because hearing nothing means that he has not relapsed. After
seven long, worry-filled days, that fear is shoved as far back in my
brain as possible. Until spinal day rolls around again.
Today,
another fear is at the forefront of my mind. Josh's oncologist is
concerned that the treatment of his central nervous system is actually
damaging him. He has back pain and periodic numbness in his legs. If
there is damage and it is bad enough, they might stop this part of his
treatment. They might stop the treatment that is preventing a relapse.
That is saving my baby's life. And that scares me to my core. So, Josh
laid down on the MRI table, kicked me out of the room and left me to
pace. And worry. And pace. And worry. And pace.
Leukemia is
often dismissed because the cure rate is so high in kids. I've been
told it's not "real" cancer. But it is the number one childhood cancer
diagnosed. I'm talking about thousands of kids who are diagnosed each
year. And hundreds of those kids die every year.
Tiffany died at age 16 after a bone marrow transplant.
Taylor is forever 12. She, too, succumbed after a bone marrow transplant.
Logan, 12, was in the same phase of treatment as Josh. He got the stomach flu, became septic and passed away in his sleep.
This
is the fear I live with daily. And I will live with this fear until the
day I die, or the day a cure is found. I will run until that day. With
your help and with your dedication, we will win this fight. We WILL find
a cure. My family is counting on it.