Saturday, June 09, 2018

A Parallel Life

Another day, another blood draw, another oncology appointment...

another life lesson to be learned.

Brad has often said to me, "This is the craziest life I've ever known."

Most days I just smile and shake my head at him. 

But today, I agree with him fully!

We are so grateful for God's sweet mercy! Brad's white blood count slightly increased from 2.1 to 2.4 and his neutrophils increased from .8 to 1.2. 

So he's out of the danger zone again, and he can say good-bye to his mask!

Wearing a medical mask in 95 degree weather is no fun AT ALL people!

Because his numbers have increased instead of decrease, we can also wait another 2 weeks until his next blood draw. And continue to pray that his bone marrow finally figures out how to produce more white blood cells.

In the meanwhile, Brad will do his best to rest and take care of his body, and I will do my best to keep him doing just that. 

As we were driving from the hospital, I could not help but think about how this cancer journey parallels a Christian life. The similarities suddenly struck me today.

We have made summer plans, but we know that Brad's numbers will determine whether we're able to fulfill and live out those plans. Each week we may have to adjust our lives in light of a blood draw or chemotherapy treatment or new symptoms of a possible infection.

"The heart of man plans his way, but the Lord establishes his steps." 
 - Proverbs 16:9

I am so much more aware at this moment, more than I've ever been in my life, that my life is not my own and the Lord will lead and do as he wills. He establishes our steps. I make plans, but the Lord is in control of all things.

And all will be for our good and his glory. 

My mantra has become...
“...if the Lord wills...” - James 4:15
 
So, we continue to try and live a (new) normal life...we make plans, but hold onto them loosely. 

Not only am I learning to use the phrase, "Lord willing," more and to guard my heart if summer plans have to be altered or changed, but I'm also learning how to be content with just knowing the very next step in Brad's medical journey.  

Brad and I were eager to talk at his appointment yesterday about whether he can still direct our church's VBS in 2 weeks or if we can go on our Aust family vacation in late July. 

But our oncologist doesn't know. 

We don't know. 

Nobody but God knows. 

We just have to be content with taking it one step at a time. 

God is giving us just enough light to see the next step on our path. He's encouraged our hearts by increasing Brad's numbers this week, but the final answer for VBS will be given on June 21, at Brad's next blood draw. Right now we can't see that step.

 "Your word is a lamp to my feet and a light to my path." -Psalm 119:105

One step at a time.  

That's pretty hard for the 6 month planner in me...

But it's good. 

So good for me. 

Whatever control I thought I had concerning Brad's health and recovery, I realize I don't. 

But I trust the One who does know. The One who lovingly leads and guides us each day. The One who is control of all things.

Wednesday, June 06, 2018

Life with cancer

As Brad and I were waiting to see his oncologist last Thursday morning, I was jotting down some questions I wanted to ask. My biggest questions were...

"Once his numbers are all within the normal range, how do we know his leukemia is dormant/gone/in remission? Will a blood test be the only way we will know for sure? Will signs of infection be our only clues that the leukemia is back?"

But, I wasn't able to ask those questions because his white blood count had dropped from 2.54 down to 2.1 (4-11 is normal) and his neutrophils had dropped from 1.48 down to .8 (2-8 is normal and below 1 makes him highly susceptible to infection) in just 4 and a half weeks.

The upward trend in Brad's numbers in April had given us hope that this medical journey might be coming to an end. 

But, as the Lord has seen fit, it hasn't. 

So, we have a short term plan in place. Wait for a week just to rule out that a virus wasn't the culprit of his low numbers...we had been living life normally, with visits from out of state family and friends, day trips to Pella, IA, and LOTS of neighbor kids running through our house. If his numbers are still low on Friday, the next step will be to do another bone marrow biopsy. 

And as I've been told since the beginning of March, the answers are often found in the bone marrow. 

After we get a pathology report from that, Brad's oncologist will be able to make a plan for what's next.   

So, unfortunately, we're back in the "waiting room".

Many of you have texted and called and reached out to us with prayers and words of encouragement. 

Thank you! 

So, how are we doing?

Overall, we're doing okay. I'm not going to lie...Thursday was a really, really hard day. But Friday morning, Brad and I were both up early, and we refocused and made plans for the new day. 

Last Friday was our kiddos' last day of school, and we decided to spend the day celebrating the completion of another school year! 

We started the festivities with a some pizza at a park.



 Then the kids rode the carousel at Union Park...it's only 50 cents per ride!


 



















The kids went swimming and played on the beach at Gray's Lake.





















And Brad and I got to relax a little in the shade. He always tells me to tell people that he's smiling under his mask!


Then we dropped off Sammy at Hidden Acres camp on Sunday afternoon. 

When Sammy first saw Brad with his mask back on last Thursday, she quickly stated without any hesitation, "I'm not going to camp. I need to be here in case something happens." As the oldest, she has carried a lot of the weight of family life at home in March and April. 

But no, sweet girl, you are headed to camp! You need to have a week to be a kid and not worry or be anxious about what may lie ahead.


As Brad continues to work from both home and church, preparing for his sermon on Sunday and VBS in a couple of weeks, the younger 3 kids and I have been busy with basketball camp, trips to parks, and some hot afternoons at the pool. 



 






















 
It's crazy how life continues to go on every day. There are moments where I only think about Brad's cancer and other moments when I'm busy doing things around the house or am out and about with the kids that I forget about the black cloud of cancer that hangs over our family. 

It's a strange, new normal. And it's something I'm sure our family shares now with many, many other cancer families out there. 

So, while we're in this waiting room and preparing for, perhaps, another round of chemotherapy and then a 4-6 week recovery, we work on house projects, spend time together, and make adjustments to plans in light of Brad's compromised immune system. 

I feel compelled, as long as we are on this journey, to not waste what God has for us in this battle against leukemia. If I believe, and I do believe, that God doesn't allow anything to touch us except what has been filtered through his loving hands, then there is good to be found in this. 

So, we place our hope in God, savor each new day, and live life in a way that makes much of the name of Christ.