Here Is the Christ Child

Here Is the Christ Child

Where was the Christ Child?

He wasn’t in the palaces, bustling with servants, feasts in the halls, music in the chambers.
He wasn’t in the temple, where the incense was burning and the well-written prayers soaring upward.
He wasn’t on the road, where watchful eyes were waiting for the victorious Messiah to arrive and deliver them.

He was in the manger, swaddled in His mother’s arms, animals gathered round.
He was there, in tiny, delicate baby arms and legs, waving a greeting.
He was there, sleeping after the miracle of his birth.

But let’s not be mistaken–that night wasn’t silent.

The angels were singing.
The shepherds were running.
The heavens were ringing.

As God
became
FLESH.

As the infinite
stepped
into TIME.

As the Savior
put on
humanity.

Where will you find the Christ Child this Christmas?

It might not be in the hustle and bustle.
It might not be in the feasts and songs.
It might not even be in the services of worship.

But it’s okay.

Take a breath.
Be still.
Listen.

He’s there.

He’s there in the quiet moments.
He’s there in the shimmer of light from a tree.
He’s there in the laughter of children.
He’s there in the pitter-patter of your pet’s steps.
He’s there in the snowfall.
He’s there in the whistling wind.
He’s there.

Right there, beside you.

And He’s whispering, “Come.”

Come. Let’s adore Him.

The king of all ages.
The prince of peace.
Emmanuel.

Come.

 

Merry Christmas!

My Characters on Stage!

My Characters on Stage!

Part of me wanted to share all about the ballet of Christmas at Sugar Plum Manor the moment I returned from Colorado at the end of the November…but I decided to share health stuff first. And then I figured I’d save this one for the week before Christmas, because it’s just so festive and fun.

So here we go! The rundown on how awesome and amazing the Colorado Springs trip was!

First…I was excited, y’all. I had an appointment at the hospital in Morgantown the day before we left, to get the staples removed from my head before traveling (ahhhhhhh, relief!), and by the time we left the hospital at noon, I was pretty much skipping my way everywhere I wasn’t dancing. As David said, “That’s when you started vibrating.”

I was excited to see my P&P girls. I was excited to explore a place I’d never been. I was excited that my good friend Karlene, whom I haven’t seen in years, had decided to make the 8-hour drive from Utah to see me and the show. And of course, I was sooooo excited to see my characters come to life!

Thursday, we drove over to my parents’ house around 7 and joined them for the 2.5-hour drive to the airport. We flew out of Dulles in DC, had an uneventful flight to Denver, during which I got the synopsis written for my next novella from Tyndale (you’ll hear more about this in the new year!), which left me feeling great. We had a fairly long layover in Denver before our very-short connection to Colorado Springs (it was cheaper to fly to the Springs than to Denver, otherwise we just would have driven it), which gave us time to enjoy some delicious pizza in a little Italian restaurant in the airport whose staff was fantastic.

Hilariously (or not?) that second flight sat at the gate for an hour while they tried to deal with a weight and balance issue. It was a tiny little plane. And eventually, they had to ask someone to volunteer to take another flight. Or, as we joked, “They actually kicked someone off!” Once we were airborn, it was practically a blink and then we were in the Springs. It was dark and raining by the time we landed, so that 20-minute drive to our rental house was a little not-fun, but then…then we arrived.

So this was our third retreat with the P&P group, in our fourth year. (We had to skip last year’s thanks to cancer.) At the first retreat, there were 5 of us. At the second retreat, there were 12, but not all at the same time–we broke it into half-weeks for those who couldn’t do a full week. I think the most there at once were 9. This time, there were 15 of us (this does count spouses and my parents), by my count at the Saturday night ballet. And from the moment we entered, there was a definite air of celebration.

The house was gorgeous, a historic one with tons of bedrooms, gorgeous old fixtures (clawfoot tub, old kitchen sink…just darling), and so much charm we just couldn’t get over it. (Great job picking it out, Caroline!) I thought, when I walked in, that the owners or management company had already decorated for Christmas, because there was a cute little tree decorated on an end table in the living room, miniature stockings hanging…but no. Candice (the official “in charge of retreat” member of the group) had packed it all in her checked bag! Yep, she brought a Christmas tree with her, with nutcracker ornaments that we all got to bring home, and those stockings? They were for us! Each one had our name on it, and she added stickers and bookmarks and a pocket prayer quilt each night.

Our previous retreats have been “creative retreats,” where we work on our creative projects during the day and then hang out and socialize from dinner onward. We knew that wouldn’t work for this one, so instead it was just three straight days of laughter, sightseeing, exploring, talking, eating, baking, seeing the show, playing games, and just generally having the BEST time. Seriously, I don’t remember the last time I laughed that much.

We went to the US Figure Skating museum on Friday, Zoomed with some of the ladies in the group who couldn’t make the retreat on Friday afternoon, which was SUCH fun too–and we got to meet one of our newest members and put a face and voice to her name, which is always amazing! We set a date for our members-only tea party book club for The Christmas Book Flood too. Friday evening, Cali Hannah made us a fantastic dinner (at this retreat there was Hannah F from California and Hannah A from Texas in the house, plus Hannah Currie from Australia who came to the shows, so we had Cali-Hannah, Texas-Hannah, and Aussie-Hannah there–it was hilarious! Also, those first two Hannahs were my first two P&P members when I started the group!). After dinner, we played Fishbowl, which was HILARIOUS, and then did a white elephant style book exchange.

This gets its own paragraph, because, hello–BOOKS! 😉 We each brought a book to share, wrapped and anonymous. We had sheets printed out to give hints about the book, and since this was a group of friends, Caroline (who organized it) came up with a rating system specific to us. The romance meter was guaged by Bethany, who usually likes only one Disney-style kiss in a book; the violence meter was by Julie, who doesn’t care for such things in her stories. Two little details that just made my day because they spoke to how we’ve become such a family. (My poor mother, who isn’t officially in the group, had no clue what those meant, LOL…) We set a rule of 3-steals-only and a book was locked in, and I am happy to say I got to be a third steal and take my first-choice book, mwa ha ha ha. Though I would have been perfectly content with the one I’d first opened, had someone not stolen it from me. 😉 It was also fun to read the vague descriptions on the books and identify about half of them, which I’d already read and so knew well enough to guess. It was also rewarding that the books I brought–I totally cheated and brought two, The Lost Girl of Astor Street and The Secret Investigator of Astor Street with their new, matching illustrated covers, by my best friend, Stephanie Morrill–were also stolen the maximum number of times.

Also on Friday, the fantabulous Candice surprised me with sugar cookies decorated to match the book! (Purchased, LOL. We made many cookies while there–well, Deanna made many cookies while there, LOL–but these specialty ones were purchased by a local baker. See the photo carousel for pictures! And they were as delicious as they were gorgeous!)

Saturday morning a bunch of us went to Garden of the Gods. My group was the “can’t do to much or we’ll pay for it later” group, so we picked and chose where we explored, and it was breathtaking! We ended up at one point just settling on some rocks with an amazing view of Pike’s Peak and lots of birds to watch and just fell into chatting again. We saw two horse tours go by, so that was fun too. Then back to the house in time for lunch, because the first show was at 2:00, and I intended to be there!

So…socially awkward author here. I’m great at being “on” when it’s for a purpose, and as long as I was standing there signing books, I knew my place, LOL. But once all the books were signed, I had a few minutes of “Okay, I’m just gonna stand here at the table and blend in with the concession workers, I guess…” But I needn’t have worried. The families of the dancers soon picked up on the fact that I was there, and there were folks who came JUST to see/meet me, so that was such fun. I personalized some books, took some photos with readers, and then my husband ushered my vibrating-with-joy self into the auditorium and we found our seats.

The show…THE SHOW. It was simply AMAZING. That first time, I watched with curiosity, constantly asking myself, “Now how are they going to handle this bit?” And then watching their choices and going, “Ah! Perfect!” (I mean, obviously there was no frozen river for Mariah to fall into, and they had to make plenty of choices about what to leave out versus keep. But I 100% approve ALL those choices!)

Mimi McKinnis did the adaptation, and she did it brilliantly. (THANK YOU, MIMI!!!) The performers were so much more than I’d envisioned–not just dancing, which they did so well, but acting. The leads were all so expressive, their faces perfectly portraying the emotional journey for each character. I love how they showed backstory, especially with the story of how young Mariah and young Cyril wrote the story the cast later performs…the story that we know as the Nutcracker. And so when familiar Nutcracker music began to play? I got a completely idiotic grin on my face and just couldn’t shake it.

Also…SO MUCH PURPLE! Obviously, this purple-loving girl was thrilled to see all the purple lights, the purple costuming Mariah wore, and so much more.

During intermission and after the show, I was out at the table again, signing and personalizing books. I met more readers, more families of dancers, and after that first show, some of the dancers themselves.

And here’s the funny thing. For me, it was both humbling and ecstatic to see my characters live and breathe, so to my mind they were the stars. They were the people giving the gift–to the audience and to me. I was a little starstruck to see Mariah and Louise, Fred and Professor Skylark, Cyril and Soren all right there in front of me, living and breathing and smiling, in gorgeous costumes. To my mind, they weren’t just student performers. They were something more. They were dreams come true.

Of course, to them, I was the author who brought this fun story to them to begin with, and they approached me with wide eyes and bouncing excitement, asking me to sign their books, take pictures with them, and give them hugs. And it struck me, then–how there’s never just individual creating. It’s co-creating. We create first with our creative Father, the Creator of the universe. And then we create with those around us. As an author, I create with my editors, my cover designers, my marketing team–and my readers. As dancers, they create with their bodies but also their fellow cast, their director, their choreographers. We created something together, something bigger than what any one of us could create on our own. And it was beautiful. So, so beautiful.

I stayed there between the two shows, since there was only about an hour to kill, and then my people all showed up, so more giddiness ensued. The performance was just as fantastic, and afterward we got a group picture for P&P.

It was also after that second show on Saturday that one of my favorite moments happened. Jackson (who played Cyril), Anna (who played Mariah), and Lacy (who played Professor Skylark) came over to meet me, and Jackson pitched me a sequel. Hannah Currie was there and caught a photo of it (also in the image carousel below!), which I absolutely LOVE. On Sunday, before that final show, we got a group shot with the whole cast and me, and after that, Jonah (who plays Fred) and Jackson told me a bit more about their idea, and it just made my day. My weekend.

I made a thing that got these kids so excited, they wanted more. I wrote a story that captured their imaginations. I gave them a plot for a show they so enjoyed, they wanted to do it again, see what happened next. For this creator’s heart, that’s just…amazing. It shows me, yet again, that it’s bigger than me. It shows me the power of story, and how I’m just one participant in it.

It shows me why it’s worth it. Why it matters. Why it’s important. After one of the shows, another of the dancers, Ellie, found me to reiterate exactly this, which brought tears to my eyes. That my story matters. My writing changes lives. 

Before each big scene, there was a voice-over narration that told a bit about the story we were about to see unfold through dance, and in the second act, most of the lines were taken straight from the book. And guys, tears filled my eyes again as I heard my words over the speaker-system. As that narrator’s voice spoke about choosing to embody joy, choosing to cling to the miraculous, choosing not just to plod through life doing the expected, but to live, to live with cheer and happiness and delight, my heart just overflowed with exactly that. Because this ballet did exactly what the whole point of the story was–it brought people together and gave them a reason to celebrate.

At the end of the show, it’s Christmas music they’re dancing to, and the audience was invited to sing along to “O Come, Let Us Adore Him.” Such a wonderful final call to leave us with–the whole point of the season. The whole point of everything.

There were readers who came to every show just to see me, and to you–thank you. It was so, so wonderful to meet you all, to sign your books, to give you hugs and take photos with you.

To Mimi and the entire cast of the show, you have made my year. My decade! I will never, ever forget the joy of sitting in your audience and seeing our story come to life. Anna, Mariah will always have your face in my mind from now on, and we’re still talking about how you conveyed so much with your eyes. Jackson, you were an even better (and taller!) Cyril than I had imagined, and I loved watching you bring so much humor to the role. Corban, you played an awesome Danish lord with the gravity that suited him…and then the discovery of joy that made him into a hero too. Lacy, your crazy and expressive Skylark was a brilliant adaptation of my slightly-nutty old man, and you lit up the stage each time you stepped onto it. Lauren, I know it was against your happy nature to keep from smiling so long as you played my grieving Louise, but when you finally could let that smile shine, it moved my heart and was such a moment of victory! Jonah, when Fred hoisted that key high and then jumped into the toy line…I still laugh when I imagine it. Jessica, you are SO much nicer than Pearl, who you played so very well, and I love the guys’ idea to give you a redemption story! 😉 Also, all those pearl accents on your costume were just genius. Natalie and Dustin, when you brought the backstory to life, it was sheer delight! Ella, Rachel, Megan, Olivia, Ellie, Evie, Adeline, and Catie…all those Nutcracker callbacks, the mice and Mouse Queen numbers, the flowers and dewdrops and Sugar Plum Fairy and Nutcracker prince…more moments when I was grinning like an idiot.

I realize I’m writing a book here, because words can’t quite express how awesome it was, so naturally I have to pile more and more on to try to convey it. 😉

After the final show on Sunday, my friend Karlene came back to the house with us. A couple of the girls had already left, so she ended up crashing there for the night, thanks to snow in the passes on her drive home. Which was lovely. We ended up having a hair-braiding party in the kitchen (which was hilarious too). We told final stories. We exchanged final hugs. I had one final night of not-sleeping (I could NOT turn my brain off the whole time I was there–I was like a 5-year-old at Christmas for 5 days straight!), and then it was off to the airport ridiculously early, and my euphoria finally, finally began to settle down into contentment.

I knew I’d crash when I got home. Seriously, I was running on pure adrenaline, barely sleeping, from Thursday through Monday, I was darting around, I was talking a mile a minute, I was running up aisles and down stairs, I was making a whole lot of jazz hands in an effort to show my enthusiasm, and “vibrating for days,” as David said. It took me a solid week for this introvert to recover, LOL.

And as my mama wrapped her arms around me Sunday morning in the still-dark kitchen of that so-charming rental house as we waited for the men to come downstairs, she said, “It was so good to see you with your friends. So good to see your joy.

And that’s what it was. A weekend of friendship. A weekend of euphoria. A weekend of giddiness. A weekend of laughter. A weekend of discovery.

It was a weekend of joy. Pure joy. And that is so fitting…because that’s what Christmas at Sugar Plum Manor was all about.

And good news! 😉 You can purchase the recording of the show and see for yourself what a fantastically amazing job Fidele Youth Dance Company did in bringing it to life!

On His Will and Our Ill

On His Will and Our Ill

“It’s never God’s will that you’re sick. Jesus healed everyone. Just claim that healing.”

Several times both through my original cancer journey and this latest drama, I’ve heard this. And well before my own health troubles, I’ve heard it too. Have you? Or perhaps this is what you believe?

I think it’s something we need to talk about. Because I know how I react to it emotionally, and I also know how dear friends and family have reacted to it. Personally, I always find myself thinking, “I understand your belief, and I know you’re saying this out of love and faith. I, too, believe Christ is our Healer, that He can heal anyone. But saying that He will choose to heal me if I just have faith enough is not helpful.” I’ve never said this to an individual before, because the last thing I want to do is lash out when someone’s trying to speak hope to me. But it has lingered in my mind this time.

So let’s ask the question. Does God ever will our ills?

Many people say, “Of course not! God wills only good for us!” And that is absolutely the truth…but I don’t think it’s the full picture. I don’t believe that God wants disease or illness for us, I don’t believe He sends them to us…but I do believe they are an inescapable consequence of our fallen world and that, because God in His omniscience knew this world would fall, He’s made a way not just to deliver miraculous healing in some cases, but to use our ills for His glory in ALL cases…if we let Him. 

First of all, we have examples like Job, where God did indeed will and explicitly allow Satan to bring hardship including disease onto His faithful servant. Now, God did not send the disease. But God did allow the disease. And though, yes, Job was eventually delivered from it and went on to new health and wealth and joy, we can also be certain that he still died eventually. And that would be after he spoke to God directly.

In the New Testament, we know that Paul had some undisclosed issue (most scholars I’ve read assume it was a physical ailment, though of course we can’t know for sure) that he prayed three times to be delivered from. And what did God say?

My strength is made perfect in your weakness.

We also see in the Epistles that new Christians were very confused as to why some of them were dying. Didn’t Christ’s wounds heal them? Weren’t they supposed to live forever? But they weren’t. They died like everyone else. What did that mean? Was their faith false?

Of course not, and Paul explains it all to them, making it clear that eternal life is for now given to the soul, and that the resurrection of our bodies, our flesh, will come later.

And we also need to look at the two thousand years of Church history. We know that every Christian to come before us has died. And we know that they didn’t all die from violence or martyrdom. That many–most–died of some disease or another.

So taking all of this into account, I would have to say that, questions of will aside, we all do get sick, and the majority of us die of some sickness or another. Is this God’s will? Or is it all Satan?

Questions like this feel not only tricky but dangerous. Because obviously God’s perfect will was for man not to sin, and hence not to die–EVER. Which would include no sickness. But mankind did sin and DOES sin, and so we introduced death into the world. And given that God created this world, created man, created free will, knowing all along what would happen, I think we need to accept that there is nuance to the will of God. That while He would love for us all to be perfect as Christ is perfect, imperfection is part of His working will. That includes our sin, our brokenness, and also our diseases.

Which brings us back to today. Do I believe God afflicts us with disease? No. Do I believe that God can and does still give miraculous healings? Absolutely. But I also believe that those people who receive them will go on to die, likely of some different disease, at a later time. We will all die. For many of us, we’ll be sick first. This is reality, and given that there are no 2,000-year-old people still walking around, our faith must take that into account.

For many, many Christians, living with ongoing suffering, with chronic illness, is reality too. And this is not a lack of faith. But I’ve spoken with so many suffering friends who have been told that if they just believed more, they’d be healed. And I grieve with those friends over the guilt this puts on them–a shame they do not deserve.

Because you know what? God uses our pain for His glory. When we are weak–sick, injured, dying, suffering, exhausted–He’s still at work. He is strong, and His strength can shine through us. When we are weak, we are quite often better at sharing the heart of Christ than when we are well. When we are weak, our hearts are more vulnerable to the pain of those around us.

Christ chose to suffer, after all. He could have called down the angels. He could have miraculously healed His own wounds. He could have walked through the midst of the people who came for Him, as He had done before. But He didn’t. He chose instead to be subjected to the most painful suffering humanity had been able to devise. It wasn’t disease, obviously, but it was intense agony. He suffered it for us.

I cringe every time someone says I (or someone else) just needs to claim healing because Christ healed all the sick, and if we have faith, we can claim it too…because this argument effectively says the opposite too: that if you’re sick, if you die of disease, you must not have faith enough for healing. This is dangerous, friends. This is judging people for being what humans have been since the Garden: MORTAL. This is unrealistic and hurtful to those who are already suffering. I have met quite a few people who left church and nearly left the church because they have a chronic illness and were told they could just be healed if they believed.

Friends, there is healing beyond the physical, and that is what Christ wants for us most of all. You remember the story of the paralyzed young man who was lowered through the roof by his friends, right? Do you remember Jesus’s immediate reaction? He says, “Your sins are forgiven.” The faith of this man and his friends did not immediately garner a physical healing–Christ knew his REAL need, and that was salvation of his soul. That was what He offered first, from His heart. It was the snarky thoughts of the onlookers that spurred Him to give a visible sign, a visible healing.

I know that young man rejoiced to leap from his mat. But what do you think really gave him the most joy–use of his legs for another decade or two, or an eternity in Heaven with his Lord? 

Every week in Mass, there’s a part where the priest holds up the host and says, “Behold, the Lamb of God. Behold, He who takes away the sins of the world. Blessed are those called to the Supper of the Lamb.”

And the congregation answers with another Scripture, but with a single world that reflects on our own situation, every day, rather than the centurion’s. We say, “Lord, I am not worthy that You should enter under my roof. But only say the word, and my soul shall be healed.” The Scripture, of course, says servant. But we say this as a recognition that we do not come to Jesus every day, every week, to ask that a servant and friend be delivered of a fever. We come to Him every day, every week, to be delivered from the sins that plague us. It’s our souls that He heals every time we ask–fully, completely, eternally. It’s our souls that most urgently need to be cleansed from disease. 

The test of our faith is not whether or not we get sick, suffer, or die. The test of our faith is how we get sick, suffer, and die. By which I mean, how do we handle it? Do we make the best or the worst of it? Do we affix our eyes to Christ on the cross as we’re suffering, asking Him to take our pain and join it to His world-changing sacrifice, or do we complain about everything and cling to despair instead of hope?

Because yes, the world is watching. And while a miraculous healing might win hearts…so does God-lent strength amidst our trials. God can be glorified through our healing, but He can also be glorified through our suffering.

In this world, we will get sick. And whether or not our Lord chooses to heal us, our part is to cling to Him through it. Our testimony is not whether or not we are healed this side of Heaven–our testimony is whether or not we’re pointing to Heaven through it.

A friend recently reminded me of a passage from the little freebie I make available to newsletter subscribers, The Heart of His Brother. This is just a chapter that’s part of the Secrets of the Isles series, about the older brother of the Tremayne siblings who we never meet in the books because he’s already passed away, but whose memory and legacy is a very real part of Oliver and Beth’s story and even has a profound effect on Bram, hero of book three, who is a visitor to the Isles. Morgan was always plagued by disease and always knew he would die young. But he chose to live life in a way that made every moment count. My friend quoted this passage to me, and I think Morgan’s reflections here sum up my own beliefs rather well (and this was written years ago, well before any of my own health struggles):

“This infirmity, whatever it is,” he’d said to Beth, “is not from God. But He will use it. He will redeem it. He made me to be as strong as Oliver, and though my body betrayed that, He will perfect me in some other way, if I let him. For everything I cannot do, there’s something I can, that I’ve only discovered because of my limitations. And if I fail to do that, if I wallow in the ‘not’ instead—well, that’s my own fault, isn’t it? The Lord made me to praise Him. If I can’t do it with a leap, then I’ll do it with a shout.”

We should never stop praying for and believing in miracles. I absolutely, one hundred percent, believe that God can and still does deliver those miraculous healings. How can I not?

He’s already given me the most miraculous healing of all. He’s already forgiven my sins, taking my dying soul and restoring it to perfect life in Him. My body? He can heal that too. But if He doesn’t, then I will trust. I will trust that He can work more glory through pain and disease than He could through miraculous physical healing. I will trust that there’s still something I need to learn about Him that I can only learn here. I will trust that a healing received in Heaven is no less real, no less miraculous, no less beautiful than one given on earth. And I’ll know that I will see that there because He’s already granted that MORE important healing.

Pray for healing, friends. Always. But also remember that healing is never perfected this side of heaven. Lazarus went on to die a second time–bodily. But that is no cause for despair. Remember the words that Jesus told Martha outside that tomb:

Jesus said to her, “I am the resurrection and the life. Whoever believes in me, though he die, yet shall he live,  and everyone who lives and believes in me shall never die. Do you believe this?” (John 11:25, ESV. Emphasis my own.)

Do we believe this? Do we believe that, though these earthly bodies fail for now, in the way that matters most, WE SHALL LIVE? That day, Jesus raised Lazarus bodily from the grave. In another day, He’ll raise us bodily from the grave. It doesn’t matter if we were already sick and died. It doesn’t matter if we stink or have decomposed entirely, if our bones have been burned to ashes even.

When the Word that created the very universe says, “Come forth!” that’s exactly what we’ll do.

Because the only death that matters is death of the soul–and if we believe in Him, that’s the death we will never taste. The only healing that ultimately matters is healing of the soul–and if we believe in Him, that’s the healing that we can know. Every day. Every hour. Every minute.

So to my friends with chronic illness; to my friends with terminal disease; to my friends who suffer every day in a body that has betrayed that perfect vision, know this. You are already healed. And healing of the soul…that takes far more faith than healing of the body. That is the work that only God Himself can do. Physicians can stitch these limbs back together, perform surgery, do such amazing things to prolong physical life.

But the Great Physician is the only one who can give that most miraculous healing of all–the healing that makes us ready for eternity.

I don’t know if my cancer will ever spread, if it’ll come back again someday, if I’ll die of disease eventually or something else entirely, if it’ll happen in a year or a decade or a century. But I do know this.

I am already healed. 

The Health Update

The Health Update

I’m writing this over Thanksgiving weekend. Since Xoe is home, that means I’m back at my desk in the kitchen, where it’s chillier than I’d like in the winter…but where I have a fabulous view out the window. The winter birds are now hopping around–always there, in reality, but so much more visible this time of year when others have migrated away and the trees are bare.

I see the blue jay, big and bold, flitting from one branch of the tree to the other. I see the cardinal, hopping from the roof of our old Jeep to a bush. Flashes of color in a world gone brown, frosted with white. I’m not, generally speaking, a fan of winter. But there’s such beauty in it–in glimpses, if not in a riot.

Chances are good that you’ve already seen my update on social media or in my newsletter, if you’re following my journey in real time. But I know some might have missed it and others only follow my blog, and still others are likely to find it later, when they come here searching for things as they put their foot to their own journey…so I’m writing it here too.

It was cancer. The tumor they cut out of my brain a few weeks ago–it was cancer and, not surprisingly, the same cancer I had before. HER2+ breast cancer, metastasized to the brain.

Now, this obviously isn’t the news we were praying for. But it was the news I was braced for. When the surgeon said that’s what it looked like to him, I kinda sighed and mentally said to myself, “Okay. He could still be wrong, but…okay. We’ll go from here.”

There must have been some confusion as to who would call me with this news, because no one did, in the 2.5 weeks between when the tissue went off to be tested and when I came back for more appointments and consultations. I know my family were chomping at the bit, but honestly…I was okay not having that news hanging over me when I went to Colorado to hang out with my Patrons & Peers girls and see the ballet production of Christmas at Sugar Plum Manor. (I’ll be telling you ALL about this soon!) We got back on Monday, November 24, and on Tuesday, November 25, we headed back up the road to Morgantown, for a CT scan, a Gamma Knife consultation, and a follow-up with my neurosurgeon.

When we sat down with the physician assistant in advance of the doctor coming in and she said, “So you know the pathology now” and we said, “Um, no, actually,” she looked genuinely shocked and taken aback. And quickly gave the news everyone had been dreading. “It was cancer, consistent with the HER2+ breast cancer you had last year.”

On the surface, this is bad news. Obviously we’d have preferred it be something benign. But amidst that bad, amidst that brown of winter, there are plenty of glimpses of color.

It was one tiny, isolated spot, now removed. Usually when they see metastasis in the brain, it’s a lot of spots, everywhere. Usually, it’s come through the lymph nodes and is elsewhere in the body. Usually, they Gamma Knife them away, yes, but also start talking about palliative care.

This isn’t the usual case.

Thanks to that routine MRI, we found it super early, and it was isolated. It’s not in the lymph nodes (which means it had to have traveled to the brain last year, when it was in the lymph nodes, and just wasn’t fully wiped out by chemo in 2024. It must have been one or a couple cancer cells that multiplied after treatment stopped). It’s, now, nowhere

The PA referred to it as oligometastasis, which means a very limited spread of the disease. It also means it’s treated very aggressively, with the goal of eradication. (This is not true of widespread metastatic disease, where the goal is prolonging life and keeping it in check but not elimination.) This is GOOD NEWS. As my oncologist put it on Wednesday, “There is so much to be thankful for here. Right now, we have no evidence of cancer in your body. That means it’s tricky, in a way–because we’re going to be trying to measure a disease that isn’t there. But that’s good!”

Right now, the plan is as follows. On December 11, I’ll go in for Gamma Knife radiation. This is a super-targeted dose of gamma radiation pinpointed to the spot where the tumor had been. The goal here is to take care of any tiny little cancer cells that didn’t come out with the tumor itself during surgery. The only side effects of this kind of treatment are some tiredness that day from the twilight sedation they use to keep me still, and maybe a headache from the frame they use for the same purpose. No biggie. I’ll be back up and operational next day, and it’s an in-and-out sort of thing, like other radiation treatments. Despite the word “knife” in there, there are no knives involved. 😉 That’s just used to indicate how precise it is. A radiation scalpel.

The following Wednesday, December 17, I’ll head back to the cancer center to start my blocker treatments. These are similar to what I had after surgery last year, aimed at specifically blocking the HER2-protein that feeds this cancer. They refer to it simply as in-Her2. (Way shorter than its technical name, LOL.) There are possible side effects, ranging from nausea/diarrhea to hair thinning to a rare lung disease, but I’m hopeful that since I responded so well to that previous treatment (with NO side effects at all), that it will be similar for me with these.

If this were widespread metastatic disease, these treatments would be forever. But when my oncologist came in last Wednesday, he said with a big smile on his face, “Oh, no! Not in your case, not necessarily. We’ll do it for a year or two and reevaluate. You might be able to stop. We don’t want to treat you forever for a disease you don’t still have.”

This is where the tricky part comes in–how do you measure what’s not there? And I am praying for that kind of tricky, LOL! That it won’t come back.

From a storytelling perspective, this makes perfect sense. That God made a way for us to catch it early, so that we could take care of it. So that I could have many more years with my family. So that I could have many years to write many more stories. So that I can have the opportunity to grow old with those I love.

Will my life be that story? I obviously don’t know. But I feel like that’s the way things will go. (I am keenly aware that feelings do not dictate reality, LOL, but that’s the bone-deep peace I have right now, anyway.) I will do what I can, medically speaking, to destroy and block this cancer. And I will walk forward, confident that there’s still a lot of life yet to live. I will sign book contracts. I will write others’ stories. I will savor each moment with my kids, my husband, my parents, my grandparents, my sister, my friends.

And I will thank God for that pituitary tumor that necessitated the MRI.

Which is funny, right? When I got the news about that tumor in 2022, I was dumbfounded. Terrified. Even knowing it was benign, I also knew how it was affecting me, and it knocked me for a loop. It felt…so…big. Everything felt so uncertain. I hated that tiny little microadinoma, hated what it had done to me, hated all the questions it made me ask.

Now? Now, I think about that tiny little growth on my pituitary gland and realize it may have saved my life. This tumor they just removed was asymptomatic–too small for me to see any effect from. They don’t do routine brain MRIs to check for cancer spread, not unless you have symptoms to call attention to something. The fact that I even had a brain MRI…the fact that I had it at that precise time, when the tumor was just big enough to be picked up, not big enough to cause symptoms…some would call that good luck, good fortune, an amazing coincidence. I call that the timing of a loving Father God.

Even so, I can grant that this has changed me…and I dare to hope and pray it’s changed me for the better. I’ve certainly noticed that tears are closer to the surface. Usually, I’m a cry-twice-a-year kind of girl. Now I’m swiping at my eyes every few days. And you know what? That’s okay. Because it means it’s easier to weep with those who are weeping. Easier to mourn with the mourning. Easier to appreciate each gift of a day.

On Thanksgiving last week, we went to my sister’s, along with everyone else in the extended family (or so it seemed, LOL). Her house was bursting at the seems. Some years, my dad asks everyone to say something they’re thankful for. This year, he joked that if he did that, we’d be standing there until it was time for dessert. But I had my gratitude there, in my heart and in my hands. And he said, “But while I have the floor, I’m going to say something.”

And he looked over at me, this man I’m so like. And his eyes were glassy, and mine went glassy too. I can’t see my dad cry and not cry with him, it’s just impossible. I’m weepy now just remembering it. I knew, obviously, he’d be saying something about the trials of the last six weeks and how God was getting us through them. I just didn’t know what, in particular, he would say. Know what he did?

“I’m so thankful for my daughter’s rock-solid faith. I’m so thankful that, all these things she’s gone through, and she not only hasn’t faltered for a moment, but she’s there inspiring so many other people.”

Cue me wiping at my eyes.

Next week, I’m going to be musing about these things we suffer and whether they’re God’s will. About my emotional reaction when people say this disease (any disease) isn’t from God, and that we need to claim healing. I don’t want to steal all I’ve already written for that one. 😉 But I will say this, here.

Cancer has given me a view of life I didn’t have before. Cancer has shown me how precious it is. Cancer has opened me up to depths I hadn’t known before. Cancer has drawn me not only closer to God but closer to you.

I guess technically, I’m officially in Stage 4 Cancer…without any cancer left in my body. It’s a funny thing. And in the back of my mind these last six weeks, I’ve wondered what I might write about this new perspective, maybe for a book someday. It wouldn’t just be about inspiration to get through your own sufferings.

It would be about the view of life from where I’m now standing. The View from the Stage, this Stage 4 I prayed so fervently to avoid. I’m not sure yet of the subtitle. Something about living boldly? That’s not quite right. Embracing life? That’s closer. Regardless, something about the lessons we learn from a place of suffering, whether it’s from chronic or terminal or acute illness.

I didn’t want to stand here–no one ever does. But so many of us end up on this stage, looking out over our lives, looking out at the crowds around us–some still healthy, some suffering too. We end up looking forward to what could be our end. Sometimes it’s closer than we thought, sometimes it’s still decades away. But we catch that glimpse of it. And it changes us.

It can make people frightened. It can make them bitter. It can make them tired, oh so tired. Sometimes we see the long path ahead and dread those long, aching steps.

Sometimes we see it, and instead decide to treasure each step we get to travel. Because the winter is always going to be brown and cold–that’s its definition. 

It doesn’t mean we have to focus on the color that’s missing. We can still focus on the color that’s there, flitting from branch to branch. Those flashes of red and blue as the birds dance about, unhindered by the cold. We can still cling to the beauty, treasuring it even more when it’s glimpses instead of a riot.

This isn’t my end. The road ahead of me is still stretching out for years, I believe that. But I’m also not going to relinquish the view I’ve found here on the stage. I’m going to treasure every moment of beauty. I’m going to listen for every birdsong. I’m going to let the tears come, and I’m going to smile through them.

And I’m going to remain, always, so, so thankful. Because I’m not standing here alone. I’m surrounded by those I love. I’m joined by others on their own journeys through suffering and trial and challenge. And most of all, I know that this stage isn’t an unmoored, floating thing. It’s in the Father’s hand. And that’s exactly where I want to be.

Give Thanks in…

Give Thanks in…

When the sun shines bright and warms me,
When the wind is gentle on my face,
When the world is awash in Your splendor…
I give You thanks, O Lord.

When thunder shakes my world,
When the waters rise and overwhelm me,
When the winds shake my foundations…
I give You thanks, my Savior.

When joy fills my heart each morning,
When my arms are filled with embraces,
When songs burst from my lips…
I give You thanks, my God.

When tears are always burning my eyes,
When my arms are empty and grieving,
When sobs wrack my frame…
I give You thanks, my Sustainer.

For when the sun shines bright,
I get a glimpse of Your face.

When the darkness rolls over me,
I know it’s Your hand, providing shelter.

When I see what You have given me,
I rejoice in Your kindness.

And when I feel the pang of lack,
I know it’s a new opportunity for You to surprise me.

Lord, I praise You.
That in my pain,
You have a purpose.
That in my heartache,
You’re writing a new song.
That in my weakness,
Your strength shines.
That in my joy,
Your Son is reflected.

No matter the circumstances,
Today and every day,
I will thank You.

Because though those things around me change,
You do not.

You are so, so good.
So, so able.
So, so faithful.

You are Love.
And I am blessed to be Your child.

Strange Timing

Strange Timing

Sometimes, God’s timing just leaves me astounded. Even when it’s something that, to most, would seem small. I had one of those moments in my writing world just after getting that call about the lesion on my brain, and I wanted to take a few minutes to tell you about it. To tell about how God provided exactly the outlet I needed…and more besides.

Princess Iraja from Amazed
Awakened Book 3

Allow me to introduce Iraja. If you’ve read Awakened, then at the end you may recall a baby named Bleu. Well, 150-some-odd years in the future (keeping in mind that my magically Awakened people in this series are very long-lived), Iraja is Bleu’s wife of 34 years. (If you have not read Awakened, the point of this introduction has nothing to do with that story world and everything to do with my life. Bear with me, LOL.)

Several weeks ago, as I was diving into book 3 of this fantasy world, Amazed, I was debating which points-of-view I wanted to include. I knew that obviously I would have my heroine, Aziza. I knew I would have the king of Ellas, Stefanos. I knew I would have her hometown would-be sweetheart, Galenos. And I knew I needed one more, a POV to represent another part of the world. I’d already decided Prince Bleu and Iraja would be in Ellas during the story.

I’d also already decided that Iraja was dying. Oh, I created a fictional, fantasy disease for the purpose, linked to the oddities of this world. Nothing real. But it was fatal. It had to be, for the purposes of my plot. This isn’t a spoiler—they know it when the story starts, know she has only months left to live. So I was debating which of them would be the more poignant POV—the one about to lose her life or the one about to lose his wife.

I shared the debate with my husband and my P&P ladies, and ultimately I decided to go with Iraja’s perspective, largely because that kept a balance of two male and two female POVs in the book. Happy with that, I started the story.

Prince Bleu from Amazed
Awakened Book 3

Then came that phone call you’ve all heard about by now. The one that said I might have Stage 4 cancer. For weeks, I sat in a place of not-knowing. First, I didn’t even know if I was riddled with the stuff again. They thought it likely it was in my lymph nodes. It could have been in my bones. It could have been everywhere. (It’s not, but I didn’t know that yet.) As David and I drove home from that oncology appointment, where my doctor talked to me about palliative care, assuming this was what the tests would reveal to be necessary, I said, a bit stunned, “This could be the thing I’m going to die of.” And I wrestled with the reality that is always true but just became more true. My days are numbered. They always are, yes, but then I felt it.

And this was when I opened up my document and realized that the next chapter would be Iraja’s first POV. And friends, though I am not a crier and certainly not when working, tears stung my eyes. For one moment, just one, I hesitated. Did I really want to write this now? This? A woman struggling with her own mortality and how to say goodbye to her family?

Then I realized that, yes, I did. More—I had to. I realized that, first, when I decided a week before to make her my fourth POV character, God had nudged me toward an outlet. A way to work through and express my thoughts, my feelings. My fears and dreams. To wrestle with what I might leave undone and what I desperately wanted to do. To remind myself that even now, He should be praised. Even now, especially now, I need to embody love above all, as Iraja does. And I also realized, even after those tests proved that whatever is going on, I do not have cancer all through my body and am probably not dying any more quickly than usual (LOL), that He provided a way for me to have an insight into this woman that I otherwise would not have had. Which seems trivial. Silly.

But it’s not, not to me. It’s critical. Crucial. Because I know very well that there will be readers facing down their own struggles, their own life-altering diagnoses when they pick up this book in the future and think to escape their own world into one completely fabricated. And I want to give them a point of connection…and hope. I want to help them fasten their eyes on the Lord, as writing it helped me to do.

I was hesitant to mention this coincidence of timing to David—because while I was at peace with all this, it was harder for him. Which, again, reminded me of Iraja and Bleu and how I’d already decided they would be. Iraja, who had always known her Awakened husband would outlive her, who would stay young while she grew old; who had wanted decades more with him but trusts that even this is part of God’s plan for her life.

And Bleu, who is breaking. Bleu, who loves her so deeply and can’t imagine what life is going to look like without her. Bleu, who knows he likely has centuries left to live, and they look like a barren wasteland spreading before him without the woman he loves.

Over the last few weeks, there have been so many times when my precious husband pulled me close, rested his head against mine, and said, “You have to be okay. I can’t do this without you.” In those early days, all I could do was hold him. All I could do was promise, “If it’s Stage 4 cancer, then I’ll just set some records, right? On how long I can survive on these meds. I’m not giving up, honey. I’ll fight. I intend to have years and years left. We’ll get to our fiftieth.” And he’d bargain, “Seventieth. No—seventy more. We’re both going to live to be over a hundred.”

Over the last few weeks, every time I open up that document on my computer, I’m amazed (ha! Title of the book…) anew at how even this, this small, tiny, inconsequential thing, was planned so perfectly by the Father. Even this, He helped me set up in advance so that my heart would be more peaceful and my story richer.

Every time I write Iraja into a scene, whether it’s her POV or someone else’s, I see this woman choosing life even as she’s dying, choosing love even as she’s spending her last months on enemy soil, choosing faith even as her dreams are cut short…and I realize that’s who I want to be, whether I have a year or a decade or a century left to live. I want to be the person who embraces her enemy and sees in him a friend—and so, makes him one. I want to be the person who cries her tears and then fastens on her smile. I want to be the person who will change the tides of a story—not by sheer brute force, like her magical husband can do with the literal tides in this fantasy world. But by the power of her love.

So here’s Iraja. A princess-by-marriage in a fantasy kingdom, so very much unlike you and me in our real, humble world. But also very much like us—a child of the King of kings. Beloved of the Father. Chosen by our family. A woman who makes a difference not with power but with acceptance, with love, with a determination to see in others what God sees in them. Iraja is who I want to be.

Here’s Iraja, whose perspective helped me understand my own, as I stared one possible end in the eyes. 

I pray that, someday, when you read her POV, she’ll minister to you as she did to me. And you’ll remember that even in the small, tiny, inconsequential things, God’s hand is always at work.