Dear Self: Grace In Hindsight

[originally posted in 2019 as A Letter For The Minute Before]

Dear 2012 Self,

Tonight, you are about to climb into bed – utterly beyond caring after days of worry – too tired to do more than collapse. 


I know you saw how Chase’s hand shook when he was taking off his shoes in the hallway tonight. I know you saw it and it stopped and so you doubted yourself. I know you’re secretly really angry because the doctors aren’t listening to you and don’t know.


It’s okay.


Everybody wishes they could see things more clearly at times. Everybody wishes other people had the answers when they haven’t a clue.


Tomorrow morning is going to come earlier than you think and it’s going to bring the answers you’ve been wanting so desperately, but they will come with a price. A big one. Chase is in more trouble than you think he is.


So sleep deep tonight. And when Darcy comes into your room in just a few hours, listen to her the first time – she knows what she saw. 


[Oh, and for the love… put on a bra before the firemen and paramedics walk through the door – you’ll wish you had it on all day.]


Kiss everyone extra sweet and hug them all a little tighter when you tuck them in. Everything you know right now is going to twist and vault like a bad case of vertigo.


You are about to find out that you’re both weaker and stronger than you think. And that God’s love and grace is worth it all – despite all the times you will scream and fight and hate Him just a little bit for what will feel like unanswered prayer. 


We know Chase was the accident baby. The one who showed up despite the birth control. But I think you’ve always known in your heart that he was special. And we’ve confirmed it a thousand more times since you first thought it when you held him tight at birth.


So sleep deep for these last few hours before everything changes. 


This isn’t your fault. It’s nothing you did or did not do. That’s not how this works. 


It’s okay to cry. And believe me, because it seems crazy, but joy will come when you least expect it – even as you sob.


Give yourself grace and be real because it’s about to get really intense. 


Life is precious.

Sending you a big hug from 2022 – 

Your Ten-Year-Older Self

A Brief History Of A Long Road

DO YOU EVER WONDER HOW IT ALL STARTED…??

On Sunday, Chase’s marks ten years of cancer fighting. TEN YEARS is quite the journey, dear ones, isn’t it? In case you’ve joined us more recently, or in case you’re curious or it’s been a while… here’s what brought us to this place:

Just before dawn on Tuesday, July 31, 2012, a six-year-old Darcy woke us to complain that Chase – only two and still in his crib – was “moving around and won’t stop”. 

“El…! You need to come here! Chase is having a seizure!” The mix of deadly calm and worry in Bob’s words propelled me from the bed before my eyes were fully open, heart racing. 

And just like that, we woke to the first day of a completely different life, never to return to the one we had known ’til then.

Within hours, we would learn that there was “a large mass” shoving one half of his brain into the other (causing the seizure) and that the hospital we had been taken to by the ambulance wasn’t equipped to deal with cases on this level.

By noon, Chase had been transferred downtown to the brand new Ann & Robert H. Lurie Children’s Hospital of Chicago facility. 

Within hours of the transfer, we had learned that he was having near constant invisible seizures and he was moved to the intensive care unit. 

By early Thursday morning, 48 hours later, we had signed papers, said goodbye, and handed our little boy to a team of neurosurgeons.

The surgery was mercifully short as brain surgeries go (under four hours), but the news was a worst case scenario: While the initial tumor had been successfully removed, Chase’s lead neurosurgeon gently explained that the pathology was not only deeply malignant, but also highly aggressive, and that he had actually visualized cancer cells all over the top of his brain…too numerous to be removed. The scans backed up the doctor’s assessment. There was cancer all over the brain, in the spinal fluid, and lining the spinal column. 

The plans were placed, the words were guarded, and nobody expected Chase to survive his third birthday. 

But he would…

The next nearly two years brought seemingly endless complications, procedures, and days spent living in the hospital. We moved in with my parents, who cared for our other three children. Chase went through so much chemo, so many days of radiation, and bag after bag of transfusions – so many interventions that Bob and I l have since lost count.

He finished treatment sixteen months to the day after starting and immediately began extensive therapies to improve his quality of life. 

He could speak, but he didn’t understand what words meant. 

He wasn’t growing.

He couldn’t hear well.

He couldn’t see well. 

He had almost no short term memory.

And we were informed that these would most likely be just the beginning of side effects. 

There were routine scans every few months.

A year later, the MRI picked up a small growth and we battled relapse fear – another MRI after six of the longest weeks of our lives showing what was most likely a radiation damage and he was diagnosed with benign tumors/cavernous malformations.

The next summer, he was officially diagnosed with significant hearing loss.

The following spring, he had two separate surgeries to remove cataracts and try to improve his vision. 

Three weeks after the first cataract surgery occurred in 2016, Tyndale House Publishers published my labor of love – “Chase Away Cancer” – the story of those first six years and some of the lessons we’d learned along the way.

We settled into post cancer complications and life.

A little over two years later (after the longest season of only routine appointments and few emergencies) an MRI pick up strange thyroid growths and in the last week of January, 2019, Chase was diagnosed with thyroid cancer and had his entire thyroid removed. 

A few months later, Chase had his first visible seizure in seven years. 

Only weeks later, his thyroid site showed cancer in a couple of surrounding lymph nodes and despite a full body scan showing the spread to be contained to the thyroid area, Chase was scheduled for radioactive iodine therapy two weeks before Thanksgiving. 

Since that time, despite frequent health anomalies that seem to require lots of appointments, tests, and even occasional surgeries and procedures, Chase continues with his two-cancer diagnosis – the primary never having relapsed, the secondary having been stopped from spreading. 

We have no idea what comes next. Although we will be meeting with a genetic specialist in September to try and better understand why Chase’s body succumbs to proliferating cells the way it does and if we can possibly protect him from ever having another diagnosis.

His story has been shared from teary hospital rooms to history-packed halls of the White House. And if we’ve learned one thing in ten years, it’s that Chase is a precious law unto himself, a broken, beautiful story that only God himself knows completely.

As always, thank you for coming on this journey with us. 

Moment by moment. 

[Chase’s family includes Dad (Bob), Mom (Ellie – who is the primary writer on CAC), older sister Darcy (16), older brother Aidan (13), and younger brother Karsten (10)] 

THANK YOU

See us running and hugging and freaking out a little? …crazy joy smiles on our faces?

Today, that’s what we’re doing because 1) our miracle boy turned 12 years old yesterday, and 2) because you put together the MOST AMAZING action in the last two days.

In less than 48 hours, the Chase Away Cancer community and friends gathered OVER $13,000 for Lurie Children’s Hospital and the Anthony Rizzo Family Foundation in honor of Chase’s 12 years!

You guys!

YOU DID IT!!!!!

I wish you could have heard the gasp Chase let out when I told him the news.

Dear ones… this was a VERY GOOD THING that happened this weekend.

From the bottom of our hearts –

THANK YOU

Moment by moment

[all photos: Margaret Henry Photography]

Waiting Well

Up until 5:30 on November 2nd, I could have told you Chase’s appointments and the general expectations through the end of this 2021 year. Everything was laid out…scheduled… neat, even. (…as much as we ever get with Chase)

But on November 2nd at 5:30, right as I was in the kitchen making dinner, I got a call from the oncology team, the result of which was that Chase needs more blood work and an MRI of his liver and kidneys. 

Dear ones, it’s a long and complicated explanation full of damages and inexplicable issues, and I’m sure everything will unfold at some point, but suffice to say that there is a chance that his liver is struggling through transfusion-related damage. And while they’re looking at his liver in the scan, they want to look at his kidneys too, because there is a noticeable growth there.

It’s more than possible that this is just a precautionary measure, and the growth is benign, but the news definitely surprised us. And honestly, it’s hard to hear that anything is growing in or on Chase – ever. 

Since that phone call, our minds have gone a hundred places and our hearts beat a rhythm of post trauma. And if I’m being honest, I’ll probably continue to vacillate between “don’t be silly, it’s nothing!” and “they said the spot in his thyroid was nothing too” until the tests are done and read. 

And that, oh that… that done-ness is a ways ahead of us yet. For reasons that only God himself knows, the earliest scan date is December 21st. So we will move through the holidays, through Chase’s birthday, through these next weeks in a season of more-than-usual waiting.

How we long to not just survive the wait, but thrive in the wait – to truly wait well.

The Saturday morning before I received the call from his team, I took Chase for early blood work and it was freezing, rainy, and dark. When I voiced worry and weather-complaining words, Chase said this, and it feels timely: 

“Mom, don’t worry. Jesus has lighted our way in the dark. He will do it again. It will be okay.”

And really…there’s no better reminder: He is light in the darkness and peace in the wait. It is well with our souls and our wait.

So we’ll sit with this a while longer…

Moment by moment. 

While my plan is to keep a chipper attitude and show God that I am a good student so he will bring my waiting to a close, God wants something even better for me. Rather than end my waiting, he wants to bless my waiting.”

Betsy Childs Howard, Seasons Of Waiting
[Chase wearing my glasses to make us laugh]

When Easy Is A Lie

Two years and a lifetime ago…

It was in the middle of a vortex of cold air sweeping through the January winter, the days dark and frigid, when we got the news. The results of the biopsy were in.

It was cancer. 

Again. 

In those first minutes, we reeled even though in a strange way, we had been expecting it. And in those first weeks, we heard one sentence stated a dozen ways and we believed it:

“This is the easy cancer”. 

In a way, this is a clinically supportable thought. The sheer number of days spent in the hospital, the number of moments we walked to the edge of life and back when Chase was two and fighting brain cancer – it doesn’t even compare. And yet…

Today is the second anniversary of Chase’s second cancer – a cancer that still sits in his body, making it outlast the actual time his brain cancer sat throughout his body by a good eight months. And these two years have been heartbreaking and complicated in so many unexpected ways.

You see, the problem with the word “easy” is that it is an immeasurable concept. There is no one-size-fits-all when it comes to the complicated complexities put before each of us. And the use of those types of words always end up pushing me down and hollowing me out. 

If it was supposed to be easy and it doesn’t feel that way, then there must be something wrong with me, right? 

And then I take those wrong, hard thoughts into the day with me and I walk into the processing, the tears and the pain not only unprepared, but feeling inadequate in all ways – because it wasn’t supposed to be this way. It was supposed to be “easy”.

And perhaps that’s the true cruelty of that word – “easy” – when life isn’t (and it almost never is), then my focus invariably turns to that second phrase:

“it wasn’t supposed to be this way”. 

But very few things from the start of the world were ever supposed to be this way .

“Easy” makes us sit with our doubts.

“Easy” is ripe ground for seeds of discontentment.

“Easy” is sorrow incarnate when it comes to the table of suffering.

There is no easy. 

Dear ones, I believe with my whole heart there is only ordained.

And it’s in relinquishing the “easy” word that I find peace. …not in this life, to be sure, but in hope. 

With hope, the hard melts and reshapes. It never disappears. Life is hard and broken and will be until I see Jesus with my own eyes. But hope is the banquet at the table of suffering.

Hope is rich and beautiful even when the tears are rolling down my face and my heart is crying out “two years of this that was supposed to be easy…?!” 

Hope holds me up when I weaken.

Hope comforts me when I weep. 

Hope means purpose even in cancer … and second cancers.

So throw out the thoughts of “easy” with all its frustration and futility and “What’s wrong with me?” questions.

And hold on to hope with all of it’s “God is good even here” truths. It won’t be easy, but then again, “easy” was never a part of the story. And what a story it is…

Moment by moment.

“Why am I discouraged? Why is my heart so sad? I will put my hope in God…”

“…each day the Lord pours his unfailing love upon me.”

Psalm 43:5a, 42:8a