Thursday, September 16, 2010

Training With Weights



Yep. It's that time again. In his dad's arms, my cute Jace is sleeping right now with a cold sweat and  body aches. Our Iron Man was under general anesthesia Wednesday morning by 7 AM to receive his Lumbar Puncture. [As a review, this means he received a chemo treatment into the spinal fluid (administered through his back), to reach the brain]. After his LP, we proceeded to Teton Oncology for him to receive the rest of his IV chemo through his port. We learned there that his WBC number is somewhat low; which I've come to learn means his daily oral chemo is just doing it's job. It's difficult for my heart not to freak out when I see the lab results and everything is flagged as L (low) or LL (really low!). But my brain (once in a while) kicks in and says, "It's ok Amy! This is what chemo is suppose to do!"  I'm just waiting for someone to invent chemo that only kills bad cells and not the good ones too. (Calling all brainiacs!)

Since Jace has been running around and appearing NOT sick, the common comment we hear (almost daily) is, "He's finished with treatments, right?"  We also hear, "If he's in remission, then why does he still have chemo treatments?" Because of the nature of Leukemia, he actually won't finish his chemotherapy for two more years. That's right, party people! We are all looking forward to the gathering we'll have in the fall of 2012 to celebrate "NO MO CHEMO!" right?? It's such a beautiful thought to be finished with chemo, that sometimes even *I* can push away the dreaded fear of Jace's cancer returning when the chemo stops...I'm actually not even going to go there tonight...because... Although Jace had to endure poison being pumped into his body, we were able to personally place TWO cancer bags that same day, and we are praying for our two new friends McKenzie and Dean.

I LOVED something Dr. Hancock said also. He explained that Jace will get so used to having low numbers, that it's like training with weights. In two years, when the chemo is finished (we hope forever!), the weights will be lifted, and he'll be stronger and faster than he ever thought possible. Sooo, training with weights is an interesting concept to me. Training AT ALL is sometimes a hardship. Who is with me on this one?? I can barely manage the 5 lb. trials that are thrown at me, let alone the hefty 50s or 100s.  As I watched Jace wake up so sick this morning, I wondered how I could just take his weights for an hour or two, so he could continue to sleep and not feel the nausea and discomfort chemo brings. But, we all know the truth; Jace wouldn't let me if I could. This Iron Man is training for something BIG!
Oh, and you might smile to know what Jace requested  for breakfast:  None other than....Olives.:) 

7 comments:

  1. Whenever I hear 'Olives for Breakfast', it will make me smile. Olives have taken on a new meaning.

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  2. We don't know each other but I found your blog through another blog and I have to say you have beautiful children! My best friend has a little 4 year old with leukemia and was diagnosed at 2 years old. She will be done with treatment in November. YAY!!! We are doing "Alex's Lemonade Stand" tomorrow and making a big carnival at our city park. The goal to raise is $10,000. I will add Jace to my prayers and I wish the best for your family.

    Erica

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  3. Your story is so amazing!!! We all have trials big and small and your strength is very inspiring!!!

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  4. Hi Amy- Haven't been here for awhile, it's Rylee's mom (Natalie). The cancer bags were such a great idea- totally helpful for those starting this journey we know all too well. I can relate so much to your posts...your words could almost come straight out of my own journal. It's amazing, but we're down to only 1 spinal tap left and 3 more hits of chemo. YAY! yAY! Hey, I'd love a copy of that picture from Relay for Life- can it be emailed? natalie-taylor@hotmail.com. Keep up the good fight!

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  5. Amy, you are such a great example. You are handling the 100 lb trials. Thank you for inspiring me and helping me handle the 2 lbers.

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  6. What a little stud! You and your family are still in Todd and I's prayers. Glad to see everything is going good. Todd and Suzy

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  7. I found your blog, through another blog given to me by my former Ricks College roomie who lives in Rigby! WHEW!! :O)

    My son, Oliver, who is now 9, was diagnosed with DIPG, terminal brain cancer two days before Christmas 2009. He's been with us for over a year which 90% of children diagnosed with this type of brain tumor pass within the first year and 10% in the second year post diagnosis. Every day is a gift...

    Cancer has flipped our world upside down and I am doing all I can to give it a run for it's money! I will be a part of the '46 mommas' (www.46mommas.com) 2011 team. Since 46 children are diagnosed with cancer every single day, we are going to be shaving our heads in Washington D.C. in September, Childhood Cancer Awareness month. By doing this, we hope to raise MUCH NEEDED awareness and funds for research to cure pediatric cancer.

    I will pray for your family as we continue on this road as well. I am grateful for the support I find via the internet, facebook, blogs, etc. It's nice to know that the feelings I feel are felt by a lot of us moms. Sad to be here, but trying to put one foot in front of the other every day.

    Love,
    Stacy Palmer
    www.oliverpalmer.blogspot.com
    www.46mommas.com (Stacy Palmer)

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