It’s been two + years my dear friends, the Lefkows, have endured a battery of Leukemia treatments for their little girl, Ashley. I’ve blogged before about cancer since I know many who are fighting cancer, have lost the fight to cancer, or have lost a loved one to cancer. So this is for Ashley and her journey. Normally I would say, “Hey cancer- knock, knock, mother f****r”, but this is about a 6 year old girl so I will keep the swear words to potty talk only.
Hey Cancer, you’re a poopy headed, boogery fart-face that needs to go down the toilet!
This week marks the end of her treatment, the end of daily chemo pills and weekly/monthly trips to Children’s Hospital to access her port. The end of a lot for her mom and dad and big brother. But the start of something wonderful. Life as it should be.
I remember September of 2009, the text I got from her mom, my good friend Christin- it said, “she has Leukemia”. My knees buckled and my head started to swim. I have no idea what they were going through on that day. I can’t imagine getting that call from the doctor. Immediately they began her treatments, surgeries and making Children’s Hospital in Seattle their reluctant, second home.
There were late night fevers and trips to the ER, oh, on Christmas EVE mind you. There was the ongoing and whole summer of surgery and C. difficile. If you don’t know what it is- Google it. Nasty stuff. There was the steroids. Which was like having a pot smoking teenage wrestler in your house in the middle of the night with the munchies- 2 am nachos, sliders, ramen noodles, scrambled eggs, hash browns and waffles, for a SNACK!
The good thing about something awful happening to your life is that there’s a bunch of people that will come to help you. The Lefkows used all their connections and community that was there for them and turned it into a foundation to help others. Within months after starting treatments at Children’s, they began Ashley’s Team. A non-profit that gets video games, dvd’s, iPods, and other games and toys of entertainment for patients and their families. It’s not research, it’s not ground breaking medicine, but it makes those 72 hours, 12 hours or even 4 hours, that much better for everyone involved with the treatment of a child. Can you imagine what it’s like sitting in a hospital for 8 hours while your child is waiting for test results and you have their siblings with you bored out of their minds? Me neither. And God help me that I never do.
They used their company, Bacon Salt to promote a Bacathalon fundraiser that raised thousands of dollars for Ashley’s Team! It was a crazy bacon-eating contest, tricycle riding obstacle course of madness and Makers Mark, but hey- it worked!
Little girls should be able to play, to wear their hair long and pretty in braids and pigtails if they want to, instead of wearing non-itchy fleece hats on their bald little peach-fuzzed heads. They should get to go to a playarea or a birthday party without worry of infection. They shouldn’t have to worry about the sore on their leg that’s gotten infected. (oh that’s a whole other story!) But there’s millions of families dealing with this very crap. And for that I am truly sorry.
The blessing of Ashley’s story is that all her treatments at Children’s worked with textbook effectiveness. They can gratefully say she is cancer free. Which is like telling Leukemia it’s a poopy-headed fart-face. See ya Mother Fucker. Oh crap- and I was SO NOT going to swear!
But for today, it’s hooray for Ashley and her family of Christin, Dave, and her super awesome brother, Dean (7) to say- We did it.
I love you guys.
If you want to contribute to Ashley’s Team check out their website http://www.ashleysteam.org
Families need financial help for uncompensated care, if you’d like to help with this you can donate to http://www.miraclehouseguild.org
If you’d like to check out Bacon Salt, they’re pretty cool too. http://www.baconsalt.com