What Has Been And What Comes Next

It’s been a year since two dear ladies sat with me on a conference call and invited me to submit a book proposal and I’ve had to go back and re-thank them both for the honor I now understand that they were bestowing on me.

One whole year of writing and re-writing, editing and re-editing. Of bloody-looking files filled with red words and notes so prolific and desperately needed that Chase would come up behind me and exclaim: “Hey Mom, it looks like Christmas on your computer! It’s all red and white!”

One year of forming new bonds with a new family who have taken up Chase’s story as their own. They have prayed for him and prayed for me, and have cheered us on and even helped us find beautiful resolution to a story with no ending.

One year that we’ve all wrestled to “get it right” – and wow, is it beautiful. I filled the pages and they turned it into art.

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I cannot even begin to describe what it was like to put myself back in the rooms, on the ambulances, waiting during surgeries – all of it – and then to dig even deeper into the hows and whys. It’s both broken and strengthened me in so many ways to type the words “moment by moment” all over again through current life challenges and not just past seasons. Oh, God is good as He pushes me to keep seeing Him in all the craziness even now.

So, out of this process that I’ve begun to think of as a fifth pregnancy; after a long labor and delivery, there is birthed a beautiful new baby, if you will…

Chase Away Cancer: A Powerful True Story Of Finding Light In A Dark Diagnosis

My heart is full. I poured everything I had into these pages and they’re FOR YOU.

Where can you find Chase Away Cancer? Amazon, Barnes & Noble, Tyndale Direct, CBD, Lifeway, and more…

When will Chase Away Cancer be in stores? May 1st, 2016

How can I help? I’m so glad you asked! My heart for this book is to be an encouragement to others and also to help raise awareness about what it can look like on the inside of a cancer diagnosis.

So here are a few practical, hands-on way you can join me:

  • You can take to social media on behalf of the book: Please re-post and re-tweet anything I’m sending out – and don’t forget #chaseawaycancer
  • You can share the website with friends and family: My new BFF Rachel over at Tyndale designed the most gorgeous piece for www.chaseawaycancer.com, so now, when you go to the main address, it’ll take you right to book information complete with links to major retailers and beautiful pictures, bios, endorsements, free downloads, etc. It’s a work of art – check it out! Um, also? Free downloads. Don’t miss that part.
  • You can pick a special day to order the book: I’ve learned that sold books are counted not as whole, but by the week, so if you’re trying to figure out the optimal day to order the book, make it May 1st! If we raise the roof over this and hundreds of people are going crazy about the book on that date (and the following week), just think how many retailers and outlets will need to start thinking more about the topics covered within this story as they look at their weekly sales.
  • You can write a review of the book: After a certain number of reviews (50), Amazon will start to promote the book and suggest it to others. Um, yes, please!

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Promotion is not easy for me (just ask my realtor husband who has almost lay down and died multiple times with the crazy go-live-in-a-cave-and-not-talk-to-people-anymore things I’ve said over the years), but I’m stepping out of my comfort zone for you:

  • Because I believe God is good and that’s why I wrote this book.
  • Because I believe this book is full of things we all face in one facet or another.
  • Because I believe that if we all start talking about this story, then we all start opening doors and discussions to cancer, the goodness of God in trials, fear, faith, and so many other things.
  • Because maybe you know someone who needs to read this book even more than you do and you’re the one to put it in their hands.

You guys, I have no idea where this story is going to go, but I can tell you that the very first advanced copy went out on an ambulance. True story. Can you imagine…?

Moment by moment.

Giving What You Have

Photo credit: Tracey Rees

The bald one forgot his age again, insisting that he was barely five – even though he’s nearly half way through six.

The oldest brother wants everything perfect and keeps losing his glasses.

The sister is worried for the election and significant things like human injustice, but she only ever wants to talk about it late at night.

The baby who isn’t a baby anymore only wants to wrestle and get in trouble.

And somehow we’re out of spoons again.

The days come and go with the monumental tucked in-between little fights and insignificant things that seem huge in the moment. Homework to be done, medicines to be taken, clean up the basement… again…

How do we find significance in our mess and busy?

Photo credit: Tracey Rees
Photo credit: Tracey Rees

It was four years ago and a Good Friday. The house was cleaned, the children were cleaned, and dinner was almost prepared.

Those were the days in the condo and I feared having people over to the house because we had no storage and what you saw was what you got – everything was out on the surface. And with children ranging in ages from 5 years to 8 months, there always seemed to be stuff on every surface, half of it being decidedly gross. (those were in the days when Aid and Chase licked everything)

I was doubly afraid because my third-born was a wild card and didn’t fear the parental glare over bad behavior the way the others did. He was known for smiling, waving, and/or thumbing his nose in the general direction of manners and sanity.

Photo credit: Tracey Rees
Photo credit: Tracey Rees

And then Bob called and said he was running late and wouldn’t be home for dinner.

Great, just great.

I was making a desperate stab at hospitality and someone I didn’t know all that well was coming to dinner. Then we were going to have to try and make it out the door for the Tenebrae service – all the littles with only me to direct them. I was to be the herder of those with more energy than sense, those who were easily distracted by anything shiny. I could feel myself sweating.

And on top of that, what would this guest and I talk about? Having a conversation at dinner was an attempt at best and the chance of it being intelligible was severely lowered with only one parent at the table. I could just imagine the ensuing chaos. Ugh… People will post warnings about our family and our house. I’m just sure of it.

Then came the knock on the door and Tracey stepped into our lives.

She was already dressed up for the church service and I feared what would become of her beautiful light-colored outfit in my home. I could tell she was tentative and I was sure she probably thought we were crazy as I rushed around putting dinner on the table and the kids tried to be entertaining by putting together a series of banned activities for her amusement. “Miss Tracey! Watch me jump off this table!”, “Miss Tracey! Watch me stand on the chair!”

And then, as Tracey and I stood in the kitchen and made those first attempts at conversation between two people who don’t know each other yet, laying on a blanket near my feet; baby Karsten decided he would roll over.  

Photo credit: Tracey Rees
Photo credit: Tracey Rees

And that’s the moment everything changed. Suddenly, even though we didn’t know each other and the dinner was late and the kids were crazy, we were doing life together.

And then, as we sat down to our adventurous dinner, Chase leaned on Tracey’s shoulder and told her “I love you. I miss you.” And he repeated it throughout dinner, often leaning over to put his head on her shoulder. In those minutes, she became “his Miss Tracey” and to this day, both Tracey and I remember that time as one of blessing and also as one of his last more normal weekends before strange symptoms would indicate a brain tumor.

There is much to be said for the joy of shared experience in the knitting together of lives. I didn’t know Tracey before that day, but she was with me the first time my baby rolled over and one of the last times before Chase’s tumor started presenting itself. It’s taken a long time, but I’m slowly learning that these life-knitting connections are one of the most precious parts of opening my home or my life. What I have is yours (even the broken and battered stories) because all that I have is a gracious gift from God. I often hesitate and want to shrink from being around others because I want things perfect and neat before I invite someone in, and my life is rarely that way. So often, I seek to impress rather than to connect. But as I go through it all, I’m gently taught and re-taught that life and the living of it is a great gift and that I am most blessed in authenticity.

Never underestimate His beautiful plans for your broken life as you share it…

Moment by moment.

“What do you have that God has not given you?” 1 Corinthians 4:7a

(In addition to being a dear part of our family, Tracey is a gifted artist and photographer and has blessed our family with some of its most beautiful memories.)

Photo credit: Tracey Rees
Photo credit: Tracey Rees

Take Off The Bag

I first wrote these words on March 3, 2013 in the height of treatment and I marvel at some of the ways the awful cancer shows the goodness of God. His way are not ours…

A reminder for your day: whatever burdens you is not too big or great for The One who loves you.


 

Sixteen of Chase’s every twenty-four hours are spent attached to an IV bag. This bag, its carrying case and the pump weigh about as much as he does (when the bag is full) and he must drag it behind him everywhere he goes. In addition to the weight, the cord has a short range, so he can only walk about two feet before it pulls and strains; reminding him to pick up the burdensome piece again. The moment it beeps (a notification that the cycle is complete) is the happiest moment of his day and as soon as he’s detached, he immediately starts running and jumping…two things he really can’t do without causing harm when the bag is on.

However, there was a day last week when the IV pump notified it’s completion, and instead of the jubilant “My baggy’s done!!” that I usually hear, there was silence. I went to him and said “Chase, your bag is done! Do you want me to take it off for you?” He sighed and said “Not right now, Mom. I’m playing…maybe later.” He had become so engrossed in his play that he was no longer energized to remove that awful shackle of a bag.

And I suddenly saw myself in this encounter…

How often I struggle with fear and sin that -with God’s help- I could lay aside! I could find peace, find rest, and be free of whatever burden holds me. He comes to me, much as I came to Chase and says “It is finished, this can be removed…will you let me do that for you?” …yet in my foolishness, I am content to play while my worry and fear is attached to my very life vein because I am too preoccupied to see that He stands there -more able than I will ever be- ready to remove it.

“…let us also lay aside every weight, and sin which clings so closely, and let us run with endurance the race that is set before us, looking to Jesus, the founder and perfecter of our faith, who for the joy that was set before him endured the cross, despising the shame, and is seated at the right hand of the throne of God.” Hebrews 12:1b-2

Take off the bag. It is finished.

Moment by moment.

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Do You Want To Talk About It?

We sat curled up on the bed – just her and me – the only two girls in this whole house full of boys.

“Do you want to talk about it?”

Darcy’s nearly ten-year-old voice was calm as she described almost dispassionately what it was like to discover her two-year-old brother having a seizure when she was only six. And then, her tone changed and suddenly, like a full-fledged adult, a hand came up to her face as her eyes welled up. “I’m so sorry…I don’t know what happened. Sometimes I can’t talk about this without crying…”

Oh, how I know that feeling! Even when Chase is in the next room – living, breathing, and probably getting into trouble, the flashbacks can still take my breath away in an ordinary conversation. 

Darcy and I ended up talking for a long time and crying some too, and it lead to these words… Because sometimes I forget how hard this is for her, Aidan, and Karsten.

Aidan, Chase, and Darcy [photo credit: Jan Terry]
Aidan, Chase, and Darcy
[photo credit: Jan Terry]

For the “cancer” siblings: especially the littles…

Set the tone for understanding — To a child, sickness (of any kind) is contagious. I didn’t know this until we talked, but that early Tuesday morning when Chase was taken to the ER and Darcy and Aidan cowered in the shadows of their room, Darcy kept watch over two places. She told me she’d go to the window and check to see if the paramedics had taken us out yet, and then she’d go back and check on Aidan to see if he was seizing too. She stood in the dark of the room and thought it could be all of them…all of us. It would be some time before she and Aidan fully understood that cancer could not be caught from or given to another person. 

Presence can mean peace — They say nothing is worse than whatever you imagine and I think it may be true. We couldn’t always bring siblings to the hospital because Chase was in isolation so frequently, and our gut was to keep the very worst of diagnosis and treatment from them on some level, yet, Darcy told me that the times she felt most at peace were when she could either come to the hospital and see Chase personally, or when we’d FaceTime from our room in the oncology floor to Grammie’s house. She could see the IV cords and watch him vomit, but she could also see that he was alive and that was what brought her the most joy – just seeing he lived. 

Set the paradigm — This one is kind of interesting to process because Bob and I actually didn’t have the luxury of telling our kids Chase had cancer. We were completely separated from them for a full week and their grandparents had to tell them before they found out from a third-party as loving friends surrounded them in those first days.  But that being acknowledged, we’ve found (through trial and a lot of error) that explanations whenever possible can be very helpful. Whether it’s why Chase was getting gifts and special attention or why mom and dad seem so distracted, tired, or weepy, sometimes an age-appropriate conversation provided better understanding than pretending it wasn’t happening, brushing questions aside, or simply evening out special gifts among siblings. Our family motto has become: “There’s nothing we can’t talk about”. Hard, but good. 

Help direct emotion — Chase’s siblings cannot live through all that they’ve seen and not be significantly changed. Whether it’s memories of me laying on a gurney clutching their motionless brother to my chest or listening to kids making fun of a post-treatment Chase behind his back, there is a lot of fear, hurt and anger.  A lot. We spend a significant amount of time talking through how those feelings of fear or angry protection are a completely normal human reaction to what they’ve experienced, but it’s what they do with those feelings that will define them. We pray often that these things would make them and not break them, and that they would be strengthened in compassion and prepared to defend the weak because of what they’ve lived. And then we try and find ways to apply it to the every day.

Be prepared for deep feelings — This one surprised me and still does. Somehow, I expect that a lot of what we’ve gone through went over their heads. Not so – at all. They may not understand the word “terminal”, but they can sense it. There have been times that Darcy wanted to sit and talk and then others, like when she’s at school, where she hasn’t wanted to talk about Chase’s story at all, but she’s very aware of it and who she is in it. She explained that the kids don’t understand and the teachers all want to hug her and while she appreciates the love, both of those things make her feel very vulnerable. She doesn’t want to cry at school, but sometimes she needs to come home and just have a good cry over it.

Look for seasons of rest — Having a sibling with special cancer or neurological needs is as full-time for them as it is for us as parents. Whether it’s making a concession over parental attention, curtailed family activities, partaking in extra “cancer activities”, or interacting with a neurologically, emotionally, sometimes physically demanding playmate 24/7, I sometimes don’t even realize (in my own exhaustion) how tiring living with a cancer sibling is for my other kids. But Darcy could explain it to me; sharing how sometimes she can’t handle Chase anymore, but other times, she misses him and is slowly learning to listen to him when he demands her attention because he says things like “I’m a survivor, Dars!” (his pet name for her). And like adults, the siblings can have a layer of guilt over annoyance during a stressed family dynamic – especially when it’s towards a family member with a terminal illness. The guilt alone is exhausting.

There’s just no wrapping these things up. They’re messy and the dynamics continue to unfold as the kids change and grow and Chase lives on in his complications and joy. Some days are beautiful and could be used as parenting seminar illustrations and others feel like a complete wreck in which we need a bomb shelter rather than a house, but spending time with Darcy on this subject reminded me once again how good it is to just sit, talk, and pray together. We are not alone.

Moment by moment.

“Teach us to realize the brevity of life, so that we may grow in wisdom.” Psalm 90:12

The princess and the super hero
The princess and the super hero

Of Life, Lists, And Too Many Appointments

This past week, we finally finished up all of Chase’s follow up appointments from his January MRI.  I never get tired of seeing him interact with his doctors. This time, he brought his St. Baldrick’s cape (a gift from the staff for his ambassador year) and his new Spider-Man mask. He ran through the halls saying “Zoom! Pow!” until he tired of people talking to him, and then, stripping off his costume, he lurked in the clinic doorway and made silly faces at any doctors or nurses he saw in the hallway.  He also tried very hard to tell one of the doctors the new “knock-knock” joke he’d just learned from his kindergarten teacher (“Orange you glad I didn’t say ‘banana’?) and it was something of a fruit basket upset that was pure awesome and complete Chase. Life is never dull, that’s for sure.

Despite the good results of his January MRI, there are several continuing issues. After two years of stability, Chase’s hearing loss has gotten worse. Also, his growth has almost completely fallen off the charts – introducing conversations about the potential need for growth hormones. This is something for which Chase is potentially an excellent candidate, but something that also holds a very real threat of secondary cancers. (deep breath and lots of prayer…)

Before the end of July, Chase needs to do the following:

  • Have two separate surgeries on both of his eyes to remove treatment-induced cataracts that will leave him with the eyes of a 45-year-old (even after the surgery)
  • Have an echo to check his heart for chemo damage
  • Have a bone scan to check the age of his bones (a prerequisite for the growth hormone discussion)
  • Have a consult with his ENT to determine if he needs surgery to remove his ear tubes (they’ve been in for two years now and are showing signs of wear in his ears)
  • Possibly have an ear surgery
  • Have another audiology test to determine if he needs some type of hearing assistance 
  • Have blood work done for at least two of his doctors
  • Have a full brain/spine MRI
  • Meet with his neuro-oncology team
  • Meet with his neurosurgeon
  • Meet with his endocrinologist

And all of this is in addition to the behavior therapy consultations he needs, the IEP meetings, and the weekly speech, occupational, and physical therapy needs.

What a laundry list. I spent nearly three hours on the phone one morning just setting up appointments and coordinating with hospital staff and dates.  Currently, my calendar makes me want to go hide somewhere.

The danger in making a list public is that someone always has a longer and more complicated inventory of things to accomplish. Maybe it’s you. Maybe you’re looking at my “Chase list” and thinking: “Wow, she has no idea…” – and you’d probably be right, but I made this list up and wrote about it for two reasons…well, three, really.  

  1. Pray for us. The decisions ahead regarding growth hormone are not to be taken lightly and feel like some of the most weighty things we’ve talked about since the decision to radiate Chase’s brain.
  2. God is faithful. I need to remember this when I look at all the next few months will hold. He’s seen us through this far and He’s not about to stop now.
  3. Hug a cancer survivor.  Today, please.  This is what “survival” looks like. It’s a weird medical purgatory where you’re not really in treatment, but you’re definitely not out of needing help either.  So hug them close and tell them they’re amazing because the battle wounds are real and never quite go away.

Tying it in: Chase’s appointment list reminds me of my life. Too much, too complicated, too crazy… How do I reconcile all the broken? How do I best understand what God wants for me? …for our family? This is the moment by moment nature of it all. I need to lean in; seek Him. Thankfully, He isn’t done with me yet. …with any of us yet. The list is in His hands; life is in His hands.

“And I am certain that God, who began the good work within you, will continue his work until it is finally finished on the day when Christ Jesus returns.” Philippians 1:6 

Moment by moment…

{Below: some pictures from our clinic day at the hospital}

Calmly, the super hero makes his way through the metropolis...
Calmly, the super hero makes his way through the metropolis…
Chase taking a "selfie" with his Nurse Wendy, our family's brain tumor coordinator and a part of our heart.
Chase taking a “selfie” with his Nurse Wendy, our family’s brain tumor coordinator and a part of our heart.
Chase and his friend, Matthew, meet up and play "got your nose" in the Crowne Sky Garden after their appointments.
Chase and his friend, Matthew, meet up and play “got your nose” in the Crowne Sky Garden after their appointments.