When Planning Feels Brave

When Planning Feels Brave

For most of this year, I felt caught in a sort of limbo…a kind where I didn’t want to plan anything. I knew surgery would be looming at some point, I have infusions every three weeks, I’m considered immunocompromised—all of that severely limits what I can do. Or rather…what I felt I could do.

But there’s a phrase I’ve heard over and over again from my team—from my oncologist, from my surgeons, from my radiation oncologists. And it is this: “You have to live your life.”

It’s never said as a rebuke, always as encouragement. When I mention that maybe I’d like to do something and ask if it’s possible, that’s what they say: “You have to live your life.”

The first time I heard it, back during Chemo Treatments 1.0, I didn’t fully appreciate what it meant, because at that point in time, treatments had an end date. Of course I would live my life, in between chemo and surgery and radiation. I’d squeeze things in, with the knowledge that soon it would all be over and life—full life—would be waiting. So while we didn’t get to take a summer vacation, we took a Christmas one. My spring retreat had to be canceled, but we did a fall one.

This year, though, the encouragement lands differently. This year, everything has felt less certain, even with clear scans. And since the summer, I have had other words spoken by my new oncologist playing through my mind, hovering back there waiting for the moment to pounce again: “It’s not a matter of if it comes back, it’s a matter of when.”

Those words have been like a specter hovering in the corner of the room. And they solidify every time talk turns to the future. Planning anything feels a little bit defiant—I will go to the Christy Award gala and the Read Write Rendezvous, even though it means rescheduling an infusion—so take that, cancer treatments! (To which, of course, my team says, “Of course! Go! You have to live your life!”)

But then, when conversation turns to plans farther out than a few weeks or months? It doesn’t just feel a little bit defiant. It feels…brave.

We’d like to retire down here. That’s what David and I were dreaming of when we were at the beach in September. We love Hatteras Island. The bookshops there feel like home. The locals feel like neighbors. And we feel so close to God there, we feel like healthier versions of ourselves. We would love to retire there someday.

But “it’s not a matter of if it comes back, it’s a matter of when.” The words bully their way forward. And in their wake comes the inevitable question: Will I live long enough to retire?

I don’t know the answer to that question. The truth is that none of us knows the answer to that question, but I’m very keenly aware of that lack of guarantee. With Stage 4 cancer, they don’t talk about 20-year survival rates. They talk about 2-year survival rates. Maybe 5-year survival rates. Even knowing I’m NOT typical Stage 4, that’s all the data they have to give me. And that’s…scary. It’s sobering.

And as someone who has always loved to plan, who had her whole life sketched out by middle school (and hey, I’ve stuck pretty close! Marriage + kids + homeschool + write novels = Roseanna’s Dream Life), it’s disconcerting, to suddenly have that check on my dreams. To have a caution light that blinks on whenever my mind turns to the future. To be constantly wondering what plans I dare to make.

Because that’s what it feels like. A dare. It feels brave. It feels courageous.

I want to say “It feels like faith.” But I’m going to draw a different line there—because I’ve come to realize that faith can’t just be faith that I’ll be miraculously healed and will live decades more. Faith means He’s with me no matter what; to live is Christ and to die is gain. I pray He’ll give me more time…but I trust that if He doesn’t, then it’s because the time He gave me is sufficient for the work He wants me to do here on earth.

So no. It doesn’t feel like faith that everything will work out the way I want it to. It is, instead, an act of courage in the face of the known-unknown.

This is something I was almost afraid to talk to my husband about, because he (understandably) doesn’t like conversations that hint at my death. But last month when I was having a bad day, we went for a walk, and I confessed this feeling to him. How planning a vacation had felt a little bold, how planning next year’s retreat feels a little defiant, but how planning for the future…that requires bravery. I admitted the questions that are always there, now, in the back of my head. We talked through the doctor’s statements that led to that hovering specter. We talked through how hard it is to feel like dreaming itself is out of reach in some ways. We talked through the frustration of not knowing whether my scans are clear because the problem is gone or because the treatments are just holding it off until The Next Time.

No one told me about this part of cancer. No one told me that part of the grief, part of the struggle would be the loss not of the dreams themselves, but of the feeling that I could dream.

And I’m not ready to give that up. I will not cower. Because while faith can’t be “I trust that everything will work out like I want it to” faith has to be, “I trust that He’ll be with me, whatever comes, and that He wants me to live life in pursuit of Him and walk out my calling as long as I’m able.”

So I will sign that contract for book releases that take me through 2030, and I will do it with courage. I will dream about that “someday” with my husband, and I will do it with bravery. I will reclaim what health I can, and I will dream my dreams, and I will live my life.

I will live it more aware than I ever expected to be of how finite it is. And I will find the gift in that—the blessing in the unexpected grief. Because it makes me appreciate each moment I have. Each moment I live out loud. Each plan I make and see through to fruition.

And that…that feels like faith. That feels like hope. That feels like joy.

It doesn’t give me certainty…and it doesn’t require it. It gives me something better. It gives me freedom. Freedom to accept whatever the Lord has in store. Freedom to stand tall in the face of that foggy future and bravely say, “I don’t know if it will actually happen—but I know I need to dream it anyway.”

It gives me freedom to dream into the unknown. And that is what I will courageously cling to as long as the Lord gives me breath.

43 in Review and now 44

43 in Review and now 44

For the past quite-a-few years, when my birthday rolls around, I do a “However-Many Things” post—with the number matching the year I’m about to turn.

This year, while I have enough “things” in mind that I could no doubt make that list, I didn’t really want to break them out into individual “things,” given how interconnected many were. So instead, I’m approaching it a bit differently and taking my reflections month-by-month.

Because it has been QUITE a year.

August

I thought, last August, that it was time to regain my health and walk boldly into my future. I signed contracts for an unprecedented SEVEN books to complete in 2026 (maybe eight, if I can squeeze another fantasy in this fall). I was feeling good and ready to prove it. August, my birth month, was full of the usual August things—moving Xoe back into her dorm, wrapping up summer pursuits, and, for the first time in 15 years, NOT starting a homeschool year. That was both weird and rewarding, to realize we were really, truly finished!

September

In September, we spent two weeks in Avon, North Carolina, part of the Outer Banks, which was a lovely beginning to 43. One week was vacation—the second week was a writing retreat. Because I had The Island Bakeshop due, which is set in Avon, so how fun to write it on location!! While there, I got to hang out with an OBX bookstore legend, GeeGee, the owner of Buxton Village Books…who passed away just four months later. I didn’t know her nearly as well as many locals and visitors, but I will always cherish the hour I spent in her shop, signing books and just chatting life with her. I finished my manuscript while there and got it turned in on time. (The Island Bakeshop was the first book I finished in the last year.)

The view of the sand dunes and ocean from Avon, NC

October

Then came October. It was time for me to begin writing Amazed, my third fantasy romance, and I launched into it with outright glee. As in, when I was brainstorming the word and mythology, I literally skipped out to the living room to tell David what I’d come up with, and then danced back to my computer, him laughing at my clear delight. I was so excited for this story. I’d had the broad strokes of it planned for YEARS—it actually predated my Awakened world, but I folded it into it when I realized it would work so well. I’d been working on the characters in my head for a long time too. The hero and heroine from that first idea, but then I realized that Bleu (son of the characters from book 1) had a role to play, and as it unfolded before me, he and his wife, Iraja, took on new life too.

I knew one of them needed a point-of-view. I debated which. And I already knew their story—after thirty-four years of marriage, Iraja (who is not magical and so has no special healing or longevity, unlike the magical people in this world) was dying. I came up with a totally fictional disease called the Desert’s Kiss—a disease of the lungs, caused by a particulate in the desert sands of her native Soltierra. So which POV would be more poignant? I put the question to my P&P ladies, asking “The woman who knows she’s losing her life, or the man who knows he’s losing his wife?” We decided on Iraja. And I got to work. The first six chapters came quickly.

Then one day, David and I drove to pick up a press run of books—Love in the Castle Library by Ann Swindell (fabulous book, by the way—if you haven’t picked up the In the Castle Library series yet, you totally should!!). We enjoyed the drive to the FedEx Freight facility in Pennsylvania, loaded the boxes into the car, drove back to the office, and set about getting all the pre-orders into the mail. That’s what I was doing when my phone rang. The call that changed everything.

The results from a routine brain MRI I’d done the week before were in. I had a tumor in my cerebellum.

You probably know the story by now, if you’re hanging around here. My breast cancer had metastasized to my brain. And for the next two weeks, as we hurried back up to oncology, as they scheduled scans, as we had those scans, as we awaited results…they were the scariest two weeks of my life.

And they were also, in some strange way, the most blessed. Because when you’re staring into eternity, everything looks different. Everything means something different. Everything shifts into better focus. That was also when I realized the next chapter waiting for me in Amazed was Iraja’s first chapter. The dying woman. That was what I was supposed to write next. At first, I wondered if I could do it. And then I realized it was God’s perfect, strange timing. Though my situation and Iraja’s were nothing alike in most ways, I did a lot of processing through her, not just then but throughout the next months. God knew that her part of the story was exactly what I would need.

We soon learned my circumstances weren’t as dire as the doctors had feared…but even so, it was still a return of cancer, and that’s what has dictated the rest of my year. They feared cancer was all through my body, but it wasn’t. Just that one, small spot. There was some argument as to whether to remove it or just hit it with special radiation called Gamma Knife.

November

Well, in November, I had brain surgery. I never thought I’d get to say that! I was supposed to be teaching a class at the ACFW VA online writers conference that weekend, but instead I was in the hospital recovering from neurosurgery—though, go figure, they only kept me one night! That night was also the Christy Awards. I didn’t have a book up for anything, but several friends did, including one of the books we’d published (Protector by Megan Schaulis—which is also an amazing book, and you should RUN to buy her series if you haven’t read it yet!). I really, really wanted to watch the stream and was really, really afraid that I’d forget.

So, hilariously, my first conscious thought after waking up from the anesthesia was seriously, “Don’t forget to watch the Christy Awards!” I then proceeded to joke with the nurse in Recovery, whose request for transport for me kept being cancelled in the system because of a glitch, so she called David to assure him I was fine and on my way out—and that I was “an absolute delight”—and then took me to my room herself.

I was able to watch the award stream on my laptop that evening, and guys—though I had no book in the running, I was touched to tears when the contenders all turned on their mics at the start to say hello and I heard someone shout, “We’re praying for you, Roseanna!” I’m assuming that “someone” was Susie Finkbeiner, because when she won her category and came on to give her acceptance speech, she gave me another shout-out that brought tears to my eyes. Susie was one of our early authors at WhiteFire—we published her first two gorgeous contemporary novels, and then she began writing historicals first for Kregel and then for Revell. I count her as a dear friend, and to realize that I was so present in her heart that day was just…beautiful.

Two weeks later, my stitches were out, you could barely see the evidence of the surgery through my hair, and I was on a plane to Colorado Springs, to see the ballet performance of Christmas at Sugar Plum Manor. We paired it with a retreat for my patron group, the Patrons & Peers, and fifteen of us crammed into a beautiful historical house and had a long weekend of fun, fellowship, and joy. We played games, we explored the area, we talked and talked and talked, we ate cookies, we laughed, we braided each other’s hair…and I “vibrated for days,” as David said. I was so keyed up (and my head was still so sore that I couldn’t find a comfortable way to lie down) that I barely slept, but who needed sleep?? Between seeing all my girls and seeing MY STORY ON THE STAGE (!!!!), I was on cloud nine.

Then came Thanksgiving, a visit with Xoe, and the knowledge that my treatment was just getting started. At my sister’s for Thanksgiving, there was quite a crowd. Some years my dad does the “Let’s go around the circle and say what we’re thankful for” tradition, but with so many people, he joked that we’d be there until Christmas if we tried it. So it was strictly volunteer, and he got us started. And got me crying. Because one thing that will always make me tear up is seeing my dad cry, and he was quite teary-eyed as he looked at me and said, “One thing I’m thankful for is my daughter’s rock-solid faith.” He went on to say how much it meant to see that not only was I not faltering with all that was going on, but that I was shining the light of the Lord for others through it.

Gracious, I’m getting teary just thinking about it now. Onward!

December

December actually kicked off with something amazing—I learned that The Collector of Burned Books had been named Christianity Today’s Fiction Book of the Year. There is only ONE category for fiction in their book awards, which means every single novel submitted, across all genres, compete against each other. I knew my publisher had submitted Collector—they’d sent me a note when it was short-listed. But I had zero expectations of winning, so when that email came in, I was floored and delighted and so very grateful. And Tyndale sure knows how to celebrate! They sent me sugar cookies with my book cover and the award “sticker” on them, as well as a gorgeous floral arrangement. More than once I just had to pause and praise God for leading me to Tyndale and putting that story on my heart to begin with. I felt so incredibly blessed, especially given that this came in the midst of all those initial “brain tumor” treatments.

Because just a few days later, I had the Gamma Knife radiation to hit the spot where the tumor had been and hopefully kill any remaining cells. It’s a one-shot treatment, not too scary aside from the lovely frame they attached to my head. So the funny story there, though—it’s basically like an MRI machine, but stillness is even more critical than for a scan, since they’re sending those gamma rays at your head. To help relax you, the nurses pipe in music. They asked me what I wanted, and I said, “instrumental Christmas.” I didn’t want anything with words—I planned to brainstorm a Christmas fantasy novella while in there, so no distractions, thanks. (Yes, that’s me—why not come up with a story idea while having your brain irradiated??)

Well, for the first half of the scan, there was no music. I figured they forgot, and that was fine. I was happily brainstorming Celebrated. Then the music started…and then it started again. But different music. While the first was still playing. They had inadvertently opened two different YouTube Music windows and had them both going, and it was probably fifteen minutes before they realized it and shut one of them off. I found it highly entertaining and made a game of following both of them (when not ignoring them in favor of said story). We had a good laugh with the nurses afterward.

I had another appointment in Morgantown the next day, so we stayed in a hotel up there that night—which was good. I had a killer headache from the frame, but it went away after a nap and some Excedrin. That evening, my P&P ladies were doing our annual Christmas ornament exchange via Zoom—I’d brought mine with me. My “secret elf” had gifted me a gorgeous Swarovski crystal snowflake ornament, which was just GAH. I had a tiny little one my aunt had given me many years ago, which I had long claimed as my favorite ornament. This year’s was a bit bigger and a different design (each year they make a unique snowflake), and having a second made me decide that this is a fabulous thing to collect, LOL. And before the party started, I started writing that novella I’d been brainstorming.

I finished it that weekend. So it’s safe to say a few gamma rays didn’t hinder my creativity any. 😉 (Celebrated was the second book I finished in the last twelve months, quickly followed by Something Old, Someone Knew, one of my Guideposts mysteries. That brings my count up to three.)

We had a wonderful Christmas. On the way back from picking up Xoe, we met two of my P&P girls for lunch, which was a great kick-off to the season. I got lots of books. =D And my husband gave me an Ember Wave, which is a personal air conditioner/heater you wear on your wrist. This to help me with the hot flashes I’ve been having courtesy of chemo-induced menopause. It’s so cool!

Over Christmas, I decided to write something just-for-fun and randomly wrote a short novel, Consecrated. Which gives us the back story of Bleu and Iraja, as well as a fun look at my desert kingdom, Soltierra, and the Calm Water mer I’d developed in Celebrated. (So that’s book number four in the last year. And brought my 2025 word count up to 773,400ish words. Um…yeah, that’s pretty cool!)

Another fun make-the-best-of-it from December—I had trouble getting my wedding rings off for the Gamma Knife procedure. So we decided to get new rings for our 25th anniversary year. I got them from Sateur; they’re lab-created gems, so a fraction of the price, and I absolutely love them. But I didn’t want to spend much, because I intend to get back into my originals. (I have deliberately put on weight in advance of my next reconstruction surgery, which is why they stopped fitting.)

January

Said ring arrived in January, the same day that I had my first chemo infusion. Originally we’d planned to start them in December, but new studies said there should be at least three weeks between radiation and this Enhertu treatment, so we began on January 7. I did not at all mind not starting before Christmas! But phew—that first treatment was rough. I was sick for a solid two weeks afterward.

At the end of January, Xoe took the ASVAB (Armed Services Vocational Aptitude Battery); she wants to join the Army after she graduates from college and do officer training. She scored a 95! We are SO PROUD!!

In January, I also wrote The Christmas Courier, which will be out this October. It was such a fun novella, inspired by a true story of two French Resistance workers. I can’t wait for everyone to read it! (Book number five!)

In January, I also had my first (and, let’s be honest here, probably ONLY) viral Facebook post. It ate up a whole week of my life, and though the comment section got away from me, it was also beautiful proof that we CAN still have conversations—even on Facebook—when we don’t see eye to eye.

February

February started with something not so pleasant—my reconstruction failed on my right side, and when I reached out to my surgeon’s team with a “Hey, is this normal?” I was met with, “You need to report immediately to the hospital for emergency surgery.” Um…yay? Definitely not how I planned to begin the month, but it wasn’t really that bad. Though this was the first time I had to stay in the hospital more than one night, and I found it hilarious that it required more of a stay than brain surgery. For my second night, the long-term wing “stole” me and took me up to a beautiful, enormous room with a window, which was lovely. It was also humbling, when my usual joking around with the staff led to one of them saying how refreshing it was to have a patient capable of laughing with them, because most of the patients up there were in too much pain for that. Insert all the prayers for those people!

Also in February, my baby turned 18! How is it that I’m now the mom of two adult children?? It seems like just yesterday I was “homeschooling [my] two small children” (excerpt from my old bio, LOL), and now here we are. Man, time flies.

My infusions continued to be pretty horrible, with me feeling sick 2/3 of the time. The PA I see at each appointment was awesome though, trying new medications and dosages, working closely with the pharmacist to try to make things better for me. And the hair thinning…not fun. Every time I touched my head, I came away with three or four strands of hair. I was constantly picking them off my shirt, brushing them off my neck, and showers–ugh! Dozens of them. I won’t lie—it took an emotional toll.

Inspired by that viral Facebook post, we also reached out to our pastor about hosting conversations in person on hard topics—you know, the topics people usually avoid in mixed company, if they don’t want an argument. We wanted to encourage questions, concerns, and civil discourse. Our pastor loved the idea and wanted to do it for Lent, so we very quickly put it all together and started Friday night dinners and chats.

March

In March, I had my 3-month MRI and PET scans, and since they were both clear, my oncologist dialed back the “nasty” part of the chemo cocktail. Yay! But excited as I was, it didn’t make an immediate difference. I was still sick 2/3 of the time…so he dialed it back again, and that did the trick.

Our “Common Ground” meals and talks at church continued through March. We didn’t have a ton of people come, but it was a great group that did, and we had some wonderful conversations. One of the biggest blessings to me personally, though, was getting to know Cathy, the lady who runs the kitchen at church. Every Friday we arrived an hour before anyone else and talked and got to know each other while we heated up soup and bread. What a wonderful time of connection! Cathy and her husband have been members of the parish for 70 years, and I loved hearing her stories.

In March, I wrote Secrets by the Sea, which will kick off a new Guideposts mystery series called Beach Rose Cottage Mysteries. I was so excited to get to be the first author in this series and had a blast setting up our Cape May world. When edits came back on this, my editors called it “nearly perfect” and only had very minor suggestions and tweaks, which made my day! (Secrets by the Sea was my sixth book since last August.)

Also in March I started working in earnest on The Translator’s War…but I soon realized I wasn’t going to make my April 1 deadline. For the first time in my 55 books, I had to ask for an extension, though I was determined to only need an extra week. See, that first week post-infusion just kept knocking me for a loop. If I was already super-engrossed in a story, I could keep working, but if I was trying to get into a story, my brain just kept saying, “Nope, I’m sorry. I’m offline. Please try again later.”

April

But with April and Easter, I did indeed manage to get The Translator’s War finished, and I was only five days late—and since those days fell over the Easter holiday and my editor had taken a few days off surrounding it, I was relieved to see that I hadn’t actually put her behind at all. Phew!

And this story, guys…I love all my books. But there are some that just take hold of me and don’t let me go, and this is one of those. So was Consecrated, and so was Amazed (more on that soon). My characters in this one, the adventures they found…I don’t know. There was just something special about them. Of course, I never know how a book actually is when I finish—I’m too close to it. So I turned it in and hoped for the best, and when I met with my editors at the end of April to discuss it, I was thrilled (and relieved, LOL), when they declared it my best-yet book (“which is a high bar to clear,” they said) and literally had three suggestions, all of which could be handled with a few sentences. (The Translator’s War was my SEVENTH book of the year! Pretty sure that broke my record…)

In health news, in April the hair loss stopped, which I was SO happy to see.

May

In May, my hair began to regrow, that receding hairline filling back in. I have no words to express how happy that made me, LOL. Infusions still left me exhausted for a week and nauseous for 7-10 days, but not as intensely as before.

Xoe came home from college in early May, but this year she only stayed with us for about a week before moving into our other house (which we’d been using as an office for the last twelve years) with her best friend. She and Willow have been enjoying “adulting”—mostly. Less so when they hear strange noises or when snakes get into the house (yeah, that happened in July…). She’s only about ten miles away, so still “home,” but I’m glad she’s had this opportunity to be on her own but with her best friend.

But it’s also a big deal…because given her plans to join the Army after graduation, that means she probably won’t ever live with us again. Oh, she’ll be home—holidays, breaks, and then leave. But it’s a new chapter. A bittersweet one.

Given that she wasn’t going to be in her room this summer…or likely claim it fully again…I decided to actually make myself office space in a way I have never done. There’s still a bed in here for when she’s home, but I bought myself a desk (also a first) and some gorgeous shelves and arranged the room how I wanted. I LOVE the space!

In writing, May saw me turning my attention fully back to Amazed. I’d written a bit more in it in April after turning in The Translator’s War, but I really needed to buckle down and get it finished. But y’all…this book was getting long. I knew what I intended to be my midpoint twist, but I didn’t get there until 90,000 words in. Okay, I thought, so it’s not really the midpoint. Maybe it’s the 75% twist… But, um, no. It ended up 192,000 words. For those of you unfamiliar with word counts, that’s twice as long as my Imposters series books. More than three times as long as my Guideposts mysteries. It is, in fact, the same length as A Stray Drop of Blood. But it’s what it took. So far, all my readers have said that, if anything, it could have been longer and not to cut a thing (I mean, words here and there, sure, but no content. Yay!)

And I poured myself into this book. Much like The Translator’s War, it completely consumed me when I was working on it, the characters gripping my heart. And given what I already told you about Iraja, it should be no surprise that I found myself working through a lot of my own thoughts and fears and the truths God had shown me through her. Because of this, it felt intensely personal, and I have been way more hung up on this story than usual, all but biting my nails as people read it. Thus far, all my early readers and editors have called it “Amazing!” Phew! (Amazed is the EIGHTH book I’ve written since my last birthday! And while, yes, two of those books were novella/short novel length, I think the ridiculously long length of this one more than makes up for it, LOL.)

June

In June, David and I celebrated our 25th anniversary with a trip to Quebec City in Canada. It was a wonderful trip to a gorgeous city, and we thoroughly enjoyed ourselves. We talked through his issue with Amazed (that Iraja line hit too close to home for him…and he demanded short stories where we see some of the adventures she and Bleu had in their thirty-four years of marriage, rather than jumping straight from happily-ever-after in Consecrated to “and now she’s dying” in Amazed), brainstormed those short stories, and also brainstormed book 4, Alight.

When we got back, it was time to nose-to-the-grindstone on my NEXT book that was due, A Storm to Still. This biblical fiction for Guideposts is for their Women of the Psalms series, in which we take a psalm and write a story that could have inspired it. Mine is based on 107, which tells the stories of different situations that God delivered people from—from wandering in a desert waste, to illness, to imprisonment, to a storm at sea. I decided that was just a map for a story right there! I pounded it out and turned it in a few days in advance of my July 1 deadline. (Which makes A Storm to Still my NINTH book. NINE. N-I-N-E. Even I think this is insane, LOL. But good!)

July

So Guideposts got me edits back on that bib-fic six days after I turned it in. And we think I’m fast!? I laughed. And was glad to see they didn’t actually want my revisions until August, because I was not ready to look at it again quite yet.

They actually came in the same day as line edits for The Translator’s War…the same day I was in Morgantown for my next round of scans. I had both brain MRI and full-body PET scan, and both were, yet again, CLEAR! Praise God!!

Also on that day (what a day!) I got some other good news—Tyndale was offering me a contract for three more novels plus another Christmas novella, all WWII settings. Given that I’d only pitched them two books and the novella, I was surprised and delighted to see that third “mystery book” on there too. =) I read the email from my agent after my final scan of the day, as I was waiting for David to walk to where they’d let me out, and I greeted him with a ridiculously large grin. And what really made my day was a sentence from my editor, saying Tyndale was hoping for a long-term partnership with me. That did my heart good!

And just two days later, I learned that Awakened had won first place in the Faith, Hope, & Love Readers Choice Award for the Speculative Fiction category!! This is the first year I’ve entered any awards myself in well over a decade, so this was a lovely surprise (and comes with both a physical award and a cash prize, so that’s fun.) Given that Awakened was my first fantasy, it’s also just a bit of confirmation that, though this is outside my norm, this book-of-my-heart that I’d used as “vacation,” the book that helped pull me out of burnout, was good.

August

And so, here we are, back in August. Year 43 has reached its end, and I’m ready to embark on Year 44. And as I look back…it’s crazy. It has been the most insane, horrible, amazing year. One that had the scariest weeks of my life…and the best. Because God showed himself to me in ways I’ve never before known. He held me so close. He poured out his Spirit into my heart and soul and life in ways that still amaze me.

Eight months of this year have been consumed with chemo infusions, ten of them with cancer treatments. I’ve had two surgeries, plus that Gamma Knife radiation. Including brain surgery. A third-to-two-thirds of my time, I’ve been sick and exhausted thanks to chemo.

And yet it’s been the most productive year of my life. NINE BOOKS! And right around 700,000 words. I got to see one of my stories on the stage. I got to visit with my amazing P&P ladies. I had a viral social media post. I’ve won two awards (and have two finalists in the Carol Awards too—that awards ceremony is in two weeks, so we’ll see how The Collector of Burned Books and The Christmas Book Flood do in that one). I’ve got new contracts waiting and so many fun stories on the horizon.

I’ve gotten to watch my kids step into their own futures. I’ve gotten to plumb new depths of love with my husband (that second diagnosis, man—it made us cling to each other in all new ways). We were able to get more involved in our church through those Common Ground meetings, and I was able to carve out some physical space that brings me joy every day.

God has shown me so many things in this last year. He has been so good, so faithful. And as I close it out, I can’t help but think that though I have no idea how many years are ahead of me (we never do), what I do know is that I want to draw closer to Him in each one. I want to walk worthy of His call. I want to work faithfully for Him. I want to spent 44 as I spent 43—safe in the palm of His hand.

Emotional Roller Coasters and Too Close to Home

Emotional Roller Coasters and Too Close to Home

I live in the mountains, so I’m accustomed to journeys having their ups and their downs. Uphill climbs and downhill coasts. I’m accustomed to valleys and mountaintops, to breathtaking views and challenging curves.

Life is a lot like those mountain roads, and I’ve definitely found the cancer journey to have a lot in common with them too. Nothing proves it more than my experience a couple weeks ago.

First came the high week–I had my brain MRI and full-body PET scan, and both came back clear. No evidence of cancer, praise God. My neurosurgeon deemed it a good enough report that he doesn’t think I need another one for six months (as opposed to the three-month schedule I’d been on since October 2025). Good news! I was thrilled, and since the week was full of other good things too–the release of The Spy Keeper of Marseille, a new contract from Tyndale, Xoe getting her drivers license, Awakened won first place in the Faith, Hope, & Love Readers Choice Award, and I sold the audio rights to Fathomed, so that will soon be out in audio–I was in a super good mood.

Of course, I know those good weeks don’t last forever. And I got my first glimpse of it when I had my follow-up appointment with radiation oncology a week after the scans. It was overall a very encouraging appointment, don’t get me wrong. I really like my team, and they are always so informative and build me up. But she said something that just really struck me: “We’re always going to be monitoring you closely.”

This is a good thing. This is what I want. But it also just really hit home–that this journey has no end, not for me. There’s not a point where I have reached the destination of “cancer free” and just get to go on with my life without looking back. I will be having regular scans forever. There’s no “looking at it in the rear view mirror” for my journey. Metastasis means a whole different category.

And my category is a strange one. It’s called Oligometastasis, and it’s not your typical Stage 4 (though it technically is Stage 4). It means that there was one isolated metastasis, and it can be treated aggressively, with a goal of curing it, of eradication. Usually with Stage 4, the goal is containment. So as metastasis goes, it’s the best case scenario…but it’s also rare. As in, there are hundreds of cases, not the many, many thousands. Which means no protocols in place.

Which means, as my radiation oncology team put it, my treatment is a conversation, and I have a voice in it. Which is also great…until I feel like I don’t have a voice in it. And that’s what happened at my last infusion. See, my original oncologist has moved to a different city, and I was put with someone new. I will miss Dr. Safi–he was not only a great doctor, he was personable and kind and genuinely cares about his patients. He was the kind to make a plan and then send a message saying, “Wait! I just read a new study that came out the other day, and we need to adjust the timing of this.” He was also the kind to come into an appointment and say, “I’ve been looking up your books. You’re very popular!” which just made me feel seen. Because that was something he did on his own time, in an effort to know me better.

But I was fully prepared to like my new oncologist too. I was expecting a long first appointment with her, because that’s how it usually goes, with them asking me to tell them in my own words about where I am and what I’m going through. This one didn’t do that. She was in and out in five minutes the first time. Last time (our second appointment), after these scans, I was prepared to engage more, and I asked about the plan now that we had two clear scans under our belts. Dr. Safi had said we’d do treatment for a year and then reevaluate, that maybe we’d do up to two years, but that he didn’t want to commit me to a lifetime of treatment for a disease I no longer have–that the risks of complications from treatment have to be balanced with risk of recurrence. This new doctor, however, just said, “This is forever. You can’t ever go off treatments. It was in your brain, we can’t risk it coming back. With Stage 4, it’s not a matter of if it comes back, it’s a matter of when it comes back.”

Cue that roller coaster plummeting so fast that I felt my stomach bottom out. Because while forever had been discussed at first, it was not where my original oncologist had settled and so not what I’d been thinking for the last eight months. And my team had just reiterated two days before that this was NOT typical Stage 4 and COULD be treated for a cure. I pushed back. Reiterated what Dr. Safi had said. But I didn’t feel like she was hearing me. She just kept saying, “This is protocol.” I asked, “Could we talk about spacing them out more in the future, at least? Because this cycle is hard on me.” To which she said, “There’s no protocol for that.”

My husband is usually the one with all the questions, but he stayed silent. Because, as he said afterward, “You seemed like you were barely holding it together and just wanted her out of the room.” He wasn’t wrong. I was fighting tears, and I continued to fight tears the rest of the day. Thoughts I have never entertained began bombarding me. Thoughts like:

What is the point?
Why am I doing this?
Why am I considering a big surgery to give me a body I’m more comfortable in, if it’s guaranteed to come back?
How many years do I even have left?
Am I seriously going to be dealing with this forever? Feeling sick 1/3 – 1/2 of the time? Being so depleted of energy?

I let myself feel all those emotions. I went to my infusion, and the nursing staff helped without even realizing it. Just by asking personal questions. Smiling and laughing with me. They even brought in a backpack of goodies that a local middle school team puts together for cancer patients, filled with blankets and socks and lotion and lip balm and even a Starbucks gift card. I messaged my friends asking for prayers and explaining the emotional crash, I called my mom and whined, LOL.

I slept on it. And then I messaged my physicians assistant who I adore, who promised to be with me through the transition to the new doctor, and I told her about my concerns at the lack of continuity. She promised to arrange meetings between the new doctor and the old, and to talk to them both, and fully understood my concerns. That helped. And this being me, I am seriously incapable of staying “down” more than a couple days. I bounced back and was soon laughing about it, confident we’d work it all out.

But man, this roller coaster. The twists and turns, the loop-di-loops, the ups and downs. It’s hard. And there’s nothing to do but ride it, and to cling to the safety bars of faith, and to work through all the emotions.

One of my biggest “work through” methods in the last 9 months since this new diagnosis has been my stories. Especially Amazed, my third romantasy, which will release in December. I already wrote about this a bit in a post called “Strange Timing,” in which I shared that as I was developing this story, I created a character whose sole purpose was to die. We know she’s dying at the start of the book, this isn’t a spoiler. It’s the whole reason she and her husband are in the kingdom it’s set, to soak in the healing waters of their mineral pools–one of the few things that can relieve the symptoms of her (totally fictional) disease.

I’d developed this character and story line to progress the plot of my world. I decided to write her POV in large part to keep a good balance of male/female points-of-view. What I didn’t know when I decided on that was that I’d get my new cancer diagnosis just as I was getting to the point in the story where I was writing her first scene. I was literally riding home from the hospital after my oncologist told me I had Stage 4 cancer (and at the time, before all the scans, they assumed it must be all through me, they didn’t yet know it was just that one tiny spot) and would likely be on treatments for the rest of my life, when I realized the next scene I had to write was Iraja’s first scene. As in, the dying woman.

For a moment, I wasn’t sure I could do it. Then I realized that God knew. God knew what I would need to process my own emotions when He put this idea in my heart and in my head. That strange timing was His timing. And so, I poured myself into it. Though Iraja’s story is nothing like mine in pretty much every way, she became my way of exploring and expressing all the emotions I was dealing with, all the wrestling with my own mortality.

So as I’m sure you can imagine, I was a little nervous as people began to read it–my editor, my husband, and the “alpha” team of my P&P ladies, who volunteer to read the first draft. One of the questions I asked them at the end was “How was the Iraja line? Sufficiently poignant? Does it need any work? Was she as lovable as I claimed she was? (LOL)”

Thus far, everyone has unanimously agreed that they love her, love her line, and it was SO emotionally impactful.

Everyone, that is, but my husband. When I told him my editor said the book wrecked her in the best way and she was bawling (in the best way) and she LOVED the Iraja line, and she wanted no major revisions, David’s response was, “Really?”

Um…uh oh. When these notes came in, he’d just finished reading it two days before, and we hadn’t had time to talk about his thoughts yet. But it was right before we left for our anniversary trip, so I knew we’d have countless hours in the car. And we talked through a lot on that trip. Not just his thoughts on the book (he thinks we need some short stories about Iraja and Bleu’s adventures together, to come between their happily ever after in Consecrated and Iraja’s diagnosis 34 years later in Amazed–and I’m cool with that. I’ll be writing a trilogy of short stories for them entitled Beloved, in which we’ll see Raji making friends of enemies and changing the world with her loving outlook), but also his struggle with it.

Because it hit too close to home for him, which is totally understandable. While I used the story to process all those emotions, they hit him hard. Especially because in the story, Iraja tells her Awakened husband, who likely has centuries left to live, that he must live. He must move on, because she knows somewhere out there is the fated match like his parents have. That she can’t hold his “forever.” And as David held me close one night, he said, “That better not be you saying that to me. Because there will never be someone else for me.” To which I replied, “Their story is not our story. The emotions are mine, but not the details. Yes, I want you to live if I go first–but that doesn’t mean the same thing.” We had to work through it. We had to hold each other close. We had to wrestle together.

And there is so much of that in this journey. There is wrestling with emotions and realities and might-bes. There is prayer and there are tears and there are victories we embrace with both hands. There are ups and downs and twists and turns, and it isn’t a ride I can just get off of.

But there is also new depth. New discoveries. New Truths the Lord is so gracious as to show me.

These last couple weeks especially, I’ve been thinking about the legacy I will leave behind, whenever the Lord calls me home (hopefully many decades from now!). Will people still read my books after I’m gone, or will Roseanna M. White just fade away when I’m not putting out new stories? I look at the ECPA bestseller list, and I see those books that have been on it every month for literally decades (looking at you, Redeeming Love, LOL) and I see that I’m not on there, and I wonder…does it matter? All this work I do–does it matter? Will it last?

I can’t know if it will last. But I do know that it matters. I know it because people tell me so. It matters now. It matters for you. So I will keep writing, as long as the Lord gives me words. I will keep pouring myself into each and every book I put out, because what is the point otherwise? I will take my pain and my questions, my yearning and my discoveries, my faith and my hope, and I will put them into the stories of brave French Resistance fighters, of gentle-souled princesses with fatal lung conditions, of mystery-solving restoration historians, of beach shop owners learning to open their hearts.

I will write. And I will fight. And I will live. And I will love. I’ll keep bringing things close to home…and I’ll stay on the roller coaster. Because it’s just my beloved mountain roads, taking me on a journey. And oh, the vistas from the mountaintops. Getting to those views is always worth the plunge through the valleys.

Health Update April 2026

Health Update April 2026

It’s been a while since I’ve done an update on the blog, though I’ve sent out notes in my newsletter, so I thought I should take a moment to do that, now that I’m through the first six infusions.

I’ll admit it–they’ve been worse than I was hoping and praying. Not nearly as bad as full chemo, don’t get me wrong–but not great. I know I shared how my heart sank at my first infusion, when they, first of all, called it “chemo,” while in my head I’d been thinking of it as a blocker treatment more than an aggressive one, and then when they gave me all the anti-nausea pre-meds and refilled my Zofran. Well, as it turns out, I’m particularly prone to nausea with this cocktail. =/

Up until the fifth infusion, I was experiencing about 10-11 days of nausea, five of which also saw me fairly exhausted. Not ideal–given that my treatments are 21-days apart, that meant that half of my time was spent feeling fairly lousy. I had to write my Guideposts book, Secrets by Sea, during one of those stretches of icky, which wasn’t fun. Zero stars, do not recommend. 😉 I pushed through, though, and got it done…and was all relief when my editors came back and called it “nearly perfect.” Phew! But you can be sure I planned the writing of my next book, the one due to Tyndale around Easter (currently entitled The Memory of Freedom, though that could yet change), to NOT fall during a post-infusion week! (I just had my editorial meeting on this manuscript too, and am ALL RELIEF and praising God that they had only very minor notes as well. Yay!!)

In early March, I went in for my three-month scans, and I am ecstatic to report that those were CLEAR. No cancer cells spotted anywhere in my body, including my brain. Which is, of course, a HUGE praise!!

After those results, my oncologist dialed back the “nasty” parts of the chemo cocktail (this is called Enhertu, specifically targeting the HER2+ cancer cells, and the only treatment with good brain/blood barrier penetration, so my only real option). We were all hoping that would mean less nausea and hair loss, but…I didn’t honestly see any change in either.

For my fifth treatment, they gave me some new meds to take at night (Zyprexa, which was first developed as a drug to treat schizophrenia, but which, in micro-doses, is also used for both insomnia and nausea) and then a steroid to take in the mornings a few days after infusion. The nausea was definitely improved, though not gone by any stretch–it only lasted 7 days, though, and wasn’t quite as intense. Though the steroids gave me some swelling in my hands and feet, which my oncologist didn’t like. He cut the steroid again on my sixth infusion.

And that’s the one I just had last week. He also dialed back those “nasties” again, in the hopes that the nausea would be cut back to just a few days. And praise God, that’s exactly what I’ve seen! My stomach was still feeling a bit “off” on Friday and Saturday following the Thursday infusion, but not bad. And by Sunday, it was almost normal (though I still took my Zofran preemptively). Monday, though still tired, I felt perfectly fine and didn’t even take the Zofran. So YAY! I think it’s safe to say that this dial-back has been effective in the nausea-department, which is so great. I can handle a few days of tired and a weekend of “meh” when it comes to my stomach. Such a huge improvement! And such a relief, because it’s been rough.

Again, this is nowhere NEAR as bad as the full chemo of summer 2024. But it has its own challenges. First is the ongoing nature of the thing–because in 2024, I knew I only had 6 infusions. We counted down. We had that end always in sight. Now, though, I don’t honestly know how long this treatment will go on. A year, most likely. But we’ll have to pause for surgery, and I don’t know if that “year” is including the pause or if, however many we “miss” during it, will be tacked on at the end. I’m a very fringe case–in the best way, treating a disease no longer in my body–so there’s not a clear procedure here to follow. We’re winging it.

I also readily admit the hair loss is getting to me. Complete hair loss is unlikely on this course, so I certainly don’t want to shave it off like I did when I lost half of it within three days in 2024. But as someone who has always had very thick hair, seeing thin patches begin to emerge hits hard. I’ve bought some lovely wide headbands that help cover it and might just take up wearing hats–by which I mean cloches and fedoras and maybe a newsboy. I’m not a ball-cap girl, LOL, but I’ve always loved those vintage styles and already have several! Who knows, maybe I’ll even break out my 1940s fascinator that I wore to the American Library Association Convention last summer with my 1940s style dress. 😉 Don’t put it past me!

The most encouraging thing with this latest infusion, though, is that David has said, “You seem more you than usual after treatment.” Often, that first week or so afterward, I’m so tired and nauseated that I guess I feel “dimmed,” let’s call it. Not my usual, ahem, sparkling self. 😉 Which my darling husband, of course, hates to see. He’s described it as “you feel so far away.” But not this last time, and I am so, so grateful for that.

Oh, and a quick funny! So with the Patrons & Peers this year, we’re doing monthly Zoom chats on my backlist titles. We’re finishing up the Culper Ring Series now, and it has been SO long since I’ve worked on these that I had to reread them. I had Circle of Spies with me at my last infusion, and my nurse came in and said, “Oh, whatcha reading?

It was a little embarrassing, honestly, to be like, “Oh, my own book.” LOL. But also SO funny how her eyes went wide and she leaned in to see my name on it and was like, “Oh wow, that IS your book! That’s your name on the cover!” So I explained it was book number 5 of mine, and I just turned in number 55, and it’s been a LONG time, so I had to reread before a book club chat… and she just got more and more excited and dashed out of the room over to the nurses’ station to look me up and was shouting to all the other nurses about it. Which was hilarious. I told David, “Gee, maybe I should always be reading my own book when I’m at an appointment.” I think next time I might bring in a goody-bag filled with a variety of my titles. I sure have plenty to choose from these days, for any taste. (I did take my oncology team copies of several over the years, but I hadn’t ever brought any into the Infusion Center, given that I rarely have the same nurses, that team is so big.) Anyway!

My next scans are scheduled for July, and again, we fully expect those to be clear. Between now and then, I have my next appointment with my surgeon in late June, at which point we’ll determine if I’ve healed enough from my emergency surgery in February to proceed to the next step for reconstruction, which will be the intense diep-flap surgery, where they take flesh and fat from my stomach to recreate the breasts.

But before THAT, David and I will be celebrating our 25th anniversary on June 17, and we’ve decided to take a trip to Quebec City for the week. Our original plan was to go to Europe for this one, but my oncology team advised against any flight of more than 3 hours, given that I’m immunocompromised, so…we figured we’d better stick to North America. David looked up cities with the most European feel on our side of the pond, and Quebec City topped the list. I visited once when I was 15, for a French Club trip, and really enjoyed it. I’d originally said, “Oo, let’s stay in the Chateau Frontenac!” it being the most iconic hotel in the city. Then I looked at the prices, LOL, and realized we could get a really nice AirBnB for a quarter of the cost. So yeah. We’ll be doing that and can go tour the Chateau if we want. 😉 But mostly our goal will be to wander, sit outside of cafes and people watch, read, relax, and just take in the charm.

Thank you all, as always, for being so faithful to remember me in your prayers. I am always so, so touched when I hear how many people have me always on their prayer lists, and their church’s prayer list, and their small group list, etc. I feel your prayers, my friends. And I know God hears them. He has been so, so good to me. I know this is just a season–perhaps longer than I’d like, and man, am I looking forward to the day when I’m not just waiting for the next THING–the next infusion, the next surgery, the next scans. I’m looking forward to being able to strengthen my body again and to feel good. I believe that day will come. And in the meantime, I’ll keep on clinging to His hand and resting secure there. I’ll keep on doing my work and writing my stories and finding the joy in the everyday miracles He gives me.

And I’ll keep on praising Him and thanking YOU. Because I can’t imagine traveling this path alone.

The Images of Ourselves

The Images of Ourselves

In The Christmas Courier, my holiday novella that will come out in October 2026, my heroine thinks this about the hero:

“It wasn’t that Daniel was particularly handsome, probably. He wasn’t not either, of course. He was just…Daniel. That strong, sharp nose, the dark brown hair that was somehow always in need of a trim, even right after a trip to the barber. The mouth always so quick to smile, that she’d dreamed for so many years would kiss her.”

I loved writing this part, because it’s so true, isn’t it? Madeleine, the heroine, has known Daniel literally all her life. And she’s loved him all her life too, in one way or another. She doesn’t love him because of how he looks–but because she loves him, she loves that appearance too. And as for her? Madeleine was self-conscious when she was younger, constantly teased for not being fashionably slender. But Daniel had always told her she was beautiful.

And so, she believed him. Even though she didn’t necessarily love how she looked, she learned to see herself through his eyes, and so she became confident.

This is one of my favorite things about writing romance. Sometimes my characters are traditionally beautiful. Sometimes they’re not. But always, always, always they are seen as beautiful in the eyes of the one who loves them. Sometimes, much like Mr. Darcy’s view of Elizabeth, that grows and changes over time. Sometimes, they see immediately what others don’t. Sometimes, they’re immediately struck by that overt beauty and have to dig down beneath it.

Whatever the story, whatever the character demands, in the end, they all end up at that place where Madeleine in when she looks at Daniel–the place I am when I look at my husband. The place he is when he looks at me.

The place where you see all the features, and they stop adding up to pretty or handsome or ugly or beautiful or any other such label. And instead, they add up to mine. They add up to the one that I love. And once they’re that…well, beauty is a side effect.

It’s probably no coincidence that I wrote Madeleine and Daniel this way, as my body is yet again going through chemo-related changes. I can admit that it’s not easy, and there are moments when I’ve been struggling. 

When I was undergoing full chemo in 2024, I told a friend who was on the same journey, but a month or so behind me, that I found losing my hair to be worse than having lost my hair. I felt better once I’d shaved it, but those days of it coming out by the handful–those were HARD. 

Well, I’m now in a perpetual state of losing. Complete hair loss isn’t expected with my current treatment, but “thinning hair” is my reality right now. Which means that every day, I’m seeing it. Every day, if I touch my hair at all, I come away with two or three or four strands in my fingers. Every time. Day in and day out. It wears on me, yes. I don’t like it.

And sometimes, when I look in the mirror, that’s what I see. The thin patches, the receding hairline. I see the lack of what I usually am. I see the disfigurement from my last surgery. I see the evidence of two years of not enough energy to exercise like I used to.

But you know what happens then? I turn away from the mirror, and I walk out into the room where my husband is. And every time, he looks up at me with eyes of love. Every time, he smiles at me and says, “You’re so pretty.” It doesn’t matter what my hair looks like, or any other part of me. He sees me. And so, I see me too. Just as I see him. The eyes and the dimples and the grin that I love, yes–my love. 

When we think about our self-image, how we see ourselves, I think most of us have probably given some thought to seeing ourselves for who we are, not just how we appear. And I’ve certainly reflected on how we need to see ourselves as God sees us.

Lately, though, I’ve been so grateful that He gives us people who love us, to help us with that. God sees us through the eyes of love–and that’s how we see those we love best too. We don’t love them because they’re beautiful–but they are always beautiful because we love them. And so, the same is true for us.

We are beautiful because we are loved.

I’ve needed that reminder lately…maybe some of you do too. So there it is. It doesn’t matter if you’re classically gorgeous. It doesn’t matter if you’re in shape. It doesn’t matter is your hair’s falling out or if you’ve been changed by surgery or if you have acne or scars or anything else. You are created in the image of God himself, and you are beautiful. Walk in the confidence of that.

A Holy Week of Suffering

A Holy Week of Suffering

Holy Week has long been the most precious week of my year. Even in high school, this was the week that brought my focus fully onto Christ in a way nothing else ever can. This is the week that inspired my first novel, A Stray Drop of Blood. This is the week when my hubby and I started dating. This is the week, especially the end of it, when we enter into Maundy Thursday and Good Friday, when I pause normal life to focus on the enormity of what my Savior did for me.

The fact that the Triduum (Holy Thursday through Easter) is also the biggest celebration in the liturgical year is one of the things I immediately loved about the Catholic tradition. In the Baptist church we spent fifteen years in, David and I were often left feeling let down by the disinterest in this holy time, when we wanted to do something each day and…no one else did. So we created our own traditions, but they never felt quite enough. Well, I can say in all honesty that the daily services and masses definitely feel enough. They are enough. They are, in my humblest of opinions, the most beautiful services to be found. The washing of the feet on the Thursday…the focus on the cross and fasting on Friday…and the candlelit vigil on Saturday…gah! I LOVE THEM.

This year, though, will be different for me.

This year, my Holy Thursday starts in an infusion chair in the cancer center.

Tears fill my eyes as I type this. Because, friends, this is not how I want to be spending my Holy Week. I want to be focusing on Him, not the churning of my stomach. I want to be thinking about the cross, not my exhaustion. I want to be celebrating His miraculous resurrection, not trying to drag myself out of bed.

As I realized that this, my fifth infusion of Enhurtu, would be on Holy Thursday, I very nearly reached out to my oncology team to say, “Could we postpone this a week, so that I don’t have to be sick over Easter?” Because the last four…they hit me hard. Even after my clear scans (praise God!) meant dialing back the nastiest part of the drug cocktail, I was still fighting exhaustion for five days and nausea for ten. Last cycle, the week following infusion, I didn’t feel much like me. My brain was a bit foggy. I felt subdued. It was hard to joke (my standard response to pretty much anything), hard to be creative. “You feel so far away after an infusion,” my husband said. And I knew what he meant, because I feel it too. Me, my personality, my spark, is so subdued in those days. I hate it–but it’s the reality.

I didn’t make the request, for a variety of reasons. But as I settled that in my mind, it made room for more thoughts. And they are this:

Maybe this is the perfect time to not feel like me–because maybe then I can focus more on HIM. Maybe this is the perfect time to be raw, emotional, and weak–because maybe then I’ll understand a bit better how HE felt. Maybe this is the perfect time to be suffering–because oh, how HE suffered.

Maybe I need to pause and realize that these holy days are not about me making them enough. They’re about HIM making them enough. Enough to fill me. Enough to sustain me.

Enough to save me.

This isn’t the Holy Week I wanted. But I pray it’s the Holy Week I need. I pray that as I sit in that infusion chair, I can reflect His light. I pray that as we experiment with a new med regimen to try to get the nausea under control, just enough me is there to cling to Him. I pray that as I’m no doubt fighting exhaustion, I can put myself in the garden with the disciples who succumbed to it too, and I can hear my Savior’s bid to pray with Him. To be there with Him. To watch with Him, because His time had come. The hour was nigh.

And all creation held its breath.

Whether we feel it or not, these days are so precious. Because we are pausing to remember the most amazing miracle. The Word who spoke the world into being, the Word that came among us, the Word that was silenced will ring out again in victory in a few short days. And all creation will shout with Him.

I pray that, whatever your traditions, our Lord meets you in a special way this coming weekend too. I pray that we, who are always held so tenderly in our Father’s hand, will be moved in new ways as we contemplate the suffering of our Brother, the sorrow of His death, and the joy of His resurrection. I pray we, too, rise anew with Him. On Sunday and every day. 

This weekend, I will likely suffer–just a bit. I’ll probably be tired. I’ll probably feel sick. And I’ll give it to Him, who suffered unto death. Who sweated blood. Who was beaten, lashed, had a crown of thorns pressed cruelly to His brow. Who suffered the most agonizing death ever devised by man, and who did it willingly.

For you. For me.

He stretched His arms wide to the world, by His own choice. 

And He defeated that suffering. Won the victory over death. And promises us all that even though we’ll encounter suffering of our own, there is a purpose. And it is Him.