Blue Sky

the hunts in prague


This is Eliza.

She used to have cancer.


Today we crossed the finish line. There is no sign of cancer in Eliza’s body. Her chest X-ray and MRI are clear. Her AFP level, the liver marker they’ve been testing in her blood, is down to a normal level for a child her age. Her ENT physiology is normal, and she passed her hearing test with flying colors. She’s finishing a test of her kidney function this morning, but the doctors aren’t expecting anything from that.

Now cancer is sort of the gift that keeps on giving. So we’ll have monthly outpatient checkups for the next year, then the frequency will gradually go down for the next few years. The rate of recurrence is very low after successful treatment like Eliza’s, and it’s even lower after 2 years. But we trust in the living God, not in numbers. “He delivered us from such a deadly peril, and he will deliver us” (2 Corinthians 1:10).

There will be more for us to say, more thanksgivings to offer, more stories to tell. Today, with tears, we are just so grateful. God has given Eliza to us a second time. He has preserved our family through the valley of the shadow of death. He has given us an army of pray-ers and helpers. He has humbled us by showing us how little control we have. He has reminded us over and over again that nothing, not even cancer or fear or death, can separate us from the love of Christ.

Here we raise our Ebenezer: Our daughter is well. Our God is faithful. Amen.



Hoping for a finish line

Eliza and Melissa are in the hospital tonight, getting ready for several big tests Monday and Tuesday. These include imaging scans (MRI, CT) and blood work to confirm that there’s no sign of cancer left in her body, and several benchmark tests to check for potential side effects of her chemotherapy.

If all these tests are normal, we’ll go into a rhythm of regular outpatient scans. We haven’t heard at what interval those will be yet.

Please pray that all the news is good this week. All signs point that way, and we are eager for a formal status change: done with treatment, regular checks to make sure we stay that way. Pray for no lasting side effects from chemo: for healthy kidney function, no hearing loss, and for E’s immune system to build itself back up.

This is sort of a finish line, and it feels like we’re crawling across it. As lots of people have told us, the adrenaline carries you through an actual crisis; it’s the aftermath that can really get you. We are so tired and weak. We’re eager for normal life, but not ready for it yet. E is basically still not supposed to leave the house, so daily logistics are tough. Our awesome boys are feeling some fallout from all the stress of the last few months. We keep committing to very simple things– Yes, I can meet you for lunch on Wednesday. Yes, M can buy flowers for our church Thanksgiving dinner.– and then having to bail when something happens. Nobody’s putting any pressure on us, but we still feel useless.

So the Hunts are still a mess. A grateful mess, and sometimes a hopeful mess.  I was frustrated and depressed the other day, with several things going wrong, and while running into the store looked in the back seat and saw Foard and Eliza holding hands. The things that are going well are much more important than the things that aren’t.

Please keep praying for us. Pray especially for Eliza this week, for good and accurate test results, and for us as we wait. Pray that we will enter God’s Sabbath rest and experience his peace.


If you’re feeling stressed, I invite you to gaze upon this picture of a baby in a pea coat.



No more port!

Just a quick note to say: the port is gone! We had to wait awhile because of an operation ahead of us, but when the oncologists noticed we were still there, they made some calls and got us in. After that, things were easy. The operation took less than 30 minutes, and Eliza slept through most of the time before she could eat and drink. Then she pretty much ate all afternoon, so we think she’s good to go.

When we started going to the oncology ward, it was mid-summer, before it gets hot here. Now it’s cold. Some of the same kids are there, but a lot of new ones. It’s so sad to see the ones in mid-chemo, and the freshly-diagnosed moms and dads trying to be brave as they learn the ropes. If you would, while you thank God for Eliza’s health tonight, pray for those families. Pray that their stories will go as well as ours seems to be.

Cancer is awful. And God is good. We are grateful for this big step for E today.

And now for something completely different: Foard made his own sandwich for the first time today. He was very proud. He has no idea how thrilled his parents are.

And now for something completely different: Foard made his own sandwich for the first time today. He was very proud. He has no idea how thrilled his parents are.

1 Comment

Out, @^&#ed port!

With the exception of the weeks after her surgery, Eliza has had a chemo treatment basically every other Tuesday since July. Every time, she would really hit a stride– eating well, gaining weight, generally happy– the weekend before, just in time to get knocked down again by those wonderful, terrible meds.

She hit that stride again this weekend, and today she didn’t have another round of chemo. Instead she had her regular weekly blood count, which showed continued good news. And tomorrow, she’ll have a brief surgery to remove the port that has delivered those chemo meds.

You’ll recall that our oncologist told us “I think you just have bad luck with ports.” The first one got a stubborn infection and had to be removed. The current one has flipped over repeatedly, so that it takes a surgeon coming in to make it usable. So we’ve had our share of frustrations with it, but the technology is really incredible. It has done its job, and now we are happy to say thank you, goodbye, and good riddance.

Other steps coming soon: At the end of November E will have another round of scans and tests. Some of these will be to verify that there’s no sign of any cancer left in her body. Others will be to look for any side effects of chemo: hearing loss, immune problems, etc. From what we understand, if all the news is good then, we’ll go into a pattern of regular check-ups, but be finished with treatment.

Again, all signs are good so far. The liver markers they watch in her blood are approaching normal levels, and falling each week (falling is good). She is happy, growing and getting stronger. Most days we don’t feel very fearful. I expect that if the tests in a few weeks are good, that will help us exhale. Please pray for us to trust that God will do what is best for us, whatever the circumstances are on a given day.

Pray for E tomorrow as well: for her not to be too fussy (she can’t eat before anesthesia), for the surgery to be quick and uneventful, and for them to send her home in the afternoon. Thank you as always for praying.



Just one more!

Eliza’s in the hospital today for her last round of chemo! We don’t know exactly what happens next– we know there will be frequent scans and tests for a while. But God willing, after tomorrow we should be in a check-up phase instead of a treatment phase. Unbelievable.

The surgeon came in and flipped her port without surgery again– we’re pretty sure our oncologist makes him do that to punish him for putting in a port that keeps flipping around. And she’s up to her highest pre-fluids weight yet– just over 9 kilos. The doctor was very happy with that.

Please pray for an uneventful rest of today, that the needle will stay still and not cause problems, and that the girls will be released tomorrow afternoon. And pray that this is the last cancer treatment Eliza will ever have to have.



2 pieces of very good news.

Eliza is home!


More importantly, Eliza had a clear CT scan today! So there are still liver numbers to watch, chemo treatments to go through, and miles to go before we sleep. But there’s no indication of any tumors in her body. As far as we can tell, she’s on the road to health. The LORD is a warrior; the LORD is his name.

She is so happy to be home. At dinner she just kept looking around at everyone and smiling. She worked more on crawling and was excited to see all her toys. She is THRILLED to see her brothers, and they her. Foard laughed and skipped around for the first 15 minutes we were home. M picked up Sam at school and he jumped up and down when he saw her.

The Lord has done great things for us, and we are filled with joy. The journey is not over, but today is a really, really good day. All of you have helped by storming the throne of God’s grace on our behalf. Thank you.

She goes in Monday for her next chemo treatment. We have a big weekend as Faith Community is organized as a self-governing church, and we also just want to be together, so we’ll probably have lighter updates for a few days. Thank you for continuing to hold us up in prayer.

The LORD of hosts is with us; the God of Jacob is our fortress.



Tuesday: last night (we hope we hope we hope)


Today Eliza had an ultrasound that showed everything looks good on her liver, and that it’s healing well. She also had some sort of blood test that meant we had to go to the Nuclear Medicine wing, so there’s that. And an ENT test that confirmed all her E’s, N and T are normal. This is especially good news because hearing loss is sometimes a side effect of the chemo drug she’s had.

Tomorrow she has a CT scan, which we hope will confirm there’s no sign of cancer anywhere else in her body. She’s had at least one of these, I think 2, and they’ve all been normal, so we’re expecting good news. (You can probably tell I’m preaching to myself some here.)

If everything is as we expect, she’ll come home tomorrow. Please pray this happens. We are so beyond ready to have our family together again. The boys haven’t seen their sister in over 2 weeks, except for a quick hug from Foard in the lobby yesterday. Melissa hasn’t been home for a week and a half. It’s time.

Most of all, please pray for the tests to be accurate and the news to be good. And pray for us to trust God, whatever the news is. He is a rock for our feet. He is good.