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.

A Time to Speak

A Time to Speak

Last year around this time, there were things that I found upsetting in modern politics. As I sat in Church in an hour of prayer, I laid it all out before God and asked, “Should I speak?” And I very clearly felt Him say no. It was not the time. I didn’t understand why, but I obeyed.

I think perhaps now I understand why He asked me to wait. I think it may be because I was at the beginning of what turned out to be a year-long (and ongoing) experiment. See, I’d never been one to read the news—it was too depressing. ? Instead, I’d rely on my news-rabid husband to keep me informed. But last January, I’d felt the need to break that old habit…but I wanted to do it right. I decided that I would read news from a deliberate variety of sources. Especially when a big event caught my attention, I would seek out both the liberal and conservative perspectives on it. My husband does this daily and also reads foreign news, so as we discussed things, he would add in the perspective of international news outlets. (He still spends a lot more time reading the news than I do!) Last year, my opinions were not very well-informed, which means they weren’t all that well formed, either. They were emotional responses—not as reasoned as I wanted to think they were, and not nuanced.

In this year of deliberate reading, I discovered something. I discovered that it was very easy for me, a lifelong Conservative, to pick out the liberal bias in a piece, and after I acknowledged and then dismissed my own knee-jerk reaction to it, I could read the actual information contained with objectivity. It was more difficult in conservative pieces, because their bias is my own. I had to work to be able to pick that out and examine the facts.

Although, I also discovered another interesting thing—that as I perceived Conservative politics (from my perspective, I know you may not feel the same way!) deviating more and more from my own long-held beliefs, that bias in Conservative news began to strike me in a new way. I was angry. I was upset. It felt like a slap in the face that made me do something very strange—it made me want to turn away from it entirely.

That was bizarre. While I have new understanding of many liberal views, there are also key issues where I still very much disagree with the usual lines…but this knee-jerk reaction was pushing me toward them. And then I realized why it was.

I felt betrayed. And when you feel betrayed, a frequent emotional reaction is to want to turn completely away from the perceived traitor. This is why couples who go through divorce can so quickly go from love to hate. Once I identified this emotion, I was able to sit back, evaluate my actual, continual core principles, and realize that the appropriate response was not abandonment…but healing.

That’s the journey I’ve been on in this last year with modern politics.

Now—I’ve long had a policy. As a Christian novelist with a growing platform, a core tenet of my interactions with the public has always been “don’t talk about politics.” It’s a guaranteed way to alienate half your readership—because there are Christians on both sides of the political aisle. But as American politics continue to spiral into snarling shouting matches, I found myself again at a place where I wanted to speak.

This time, it was different. This time, it was because of a few stupid memes. Now, another key tenet of mine is “Don’t argue with people on Facebook,” a corollary of which is “Especially don’t argue with memes.” ? But these particular memes struck me because they were cruel…and they were shared by people I know personally. Now, this is nothing new with these particular people (again, people I know in real life, in my hometown). But on this particular Friday night, it brought me to tears. (Granted, I’m super emotional right now after my second cancer diagnosis, LOL. See my post called “Given to Tears.”) Not because of the political opinion—but because of the attitude of disgust and bitterness and hatred from these people who I know love Jesus. That brought me to tears. It wasn’t worry, it wasn’t anger. It was sorrow.

And responding from sorrow…that’s very different from responding from anger.

I asked again, “Lord, is it time to speak?” And this time, the answer was very different. This time, the answer was yes. That night, I woke up at about 2:15 and, as often happens to me in the middle of the night, my brain clicked on. (This is where most of my books are plotted, LOL. In the dark of the night, when I should be sleeping. Now you know my secret.) I lay there for the next four hours working through what He would have me say—what would glorify God and also lay my heart bare. What would not invite argument, but rather dialogue. I crafted and recrafted the words in my head. I prayed. And as David eventually woke up in the morning (LOL), I told him my thoughts, and the tears came again.

Again, not from anger, not from worry. From sorrow. From grief.

So I got up and I wrote a Facebook post. It was five pages long, LOL. THAT wasn’t going to work, so I had ChatGPT recommend where to cut and tighten, and I ended up with a far more reasonable two pages. In this post, I spoke directly to my MAGA friends (though I didn’t name names). I did something I don’t do—I talked about politics. I shared my own stances and opinions, from the perspective of why I feel betrayed by my party, and more, why I feel betrayed specifically by these people—these people who helped raise me, who are the ones who taught me how to follow Jesus, who taught me what I should look for in politicians. Who, from my point of view, are now not only defending things they once taught me to despise, but who are mocking those who disagree. Am I misunderstanding them? I really hope so. (I had a lot of people who chimed in saying, “Do you consider me MAGA just because I voted for Trump? Because there are a lot of things I have problems with, I just made a decision based on these key things.” My answer to them is, “No, you’re not the ones in particular I was addressing, though I do really appreciate your perspective! I was addressing those who defend everything he does.”)

I didn’t set out to convince anyone of anything—not my goal at all. I set out to be vulnerable. To express why I feel the way I do, to share how I’m interpreting their actions, and to ask them to weigh in and correct me where I’m wrong, explain the things I just don’t understand, and to help me see their point of view more clearly. I love them. I don’t want to judge them (but I had been…which ain’t cool. I know that.). I want to start healing this wound in my own heart, and also healing this rift that is growing within the Church.

What followed were thousands of comments, both from my MAGA friends and from a lot of people who feel the way I do but thought they were alone. People from all sides—from the left, from the right, and from this weird place in the middle of current definitions where I find myself—who had given up speaking because they were afraid of being attacked. The comment section, and my private messages, became a place where they could engage honestly and openly and without fear. It was overwhelming, I’ll be honest—I spent that entire Saturday answering comments and messages—eight long but beautiful hours. When I woke up on Sunday morning, there were about 360 comments, many of which were my own replies, and when I left for church, I had about 50 yet to go through. After church and nursing home ministry and lunch and a nap, I went back to my computer to hit “refresh,” and there were 900 comments, 600 of which I hadn’t read.

I’ll admit it–I panicked, because I hadn’t been there moderating. And yet the newest comments, from total strangers, many of them even from around the world, were to the effect of, “Wow, I didn’t think conversations like this could still happen. This gives me hope.” It gives me hope too. =) The comment section did eventually devolve, and I know of at least two cases where people were hurt and only seeing ugly, bullying comments, and they were baffled by how I was saying it was good…and I get that and regret so deeply that this happened to them! I will share one particular experience about how it resolved soon. And I will also say that I learned how tricky it is for anyone to see a full picture when algorithms are in play! I kept getting notifications like “Jane Doe + 56 others tagged you in a comment.” When I clicked on it, it would show me that first comment, but none others, and short of clicking “all comments” and scrolling for an hour to try to find one in particular, by which time more had come in…I simply couldn’t see them. I imagine it was the same for others, who were alerted when they were tagged, so if they were targeted with bullying, that would be all they saw. Which wasn’t at all what I intended.

But in general, as people checked out (understandably) it was often with comments to me thanking me for the tenor of the original post and conversation. Even with ugly sneaking in at the end, many people agreed that it was beautiful. It was healing.

And I realized that it isn’t enough. It’s the proof of a concept, but one that needs to continue. Because friends, we can’t continue like this. We can’t continue refusing to hear things we don’t like, dismissing any view not our own, and embracing those knee-jerk, emotional reactions that tell us if someone disagrees, then they’re not really a Christian. That if someone disagrees, they’re evil. If someone disagrees, then we should dismiss them entirely. More, we can’t continue growing angrier at each other, letting the wounds fester. That isn’t what God wants for us, and I know we all agree on that!

Ours is a world of nuance. How can it not be? We serve a God who is at once so simple, able to be summed up in a single sentence: God is love. And yet so infinitely complex that our human minds will never grasp His intricacies and mysteries this side of Heaven. We serve a God who is both perfect Justice and perfect Mercy. His creation is just as complex. And fallen humanity? Hoo, boy! There’s nothing simple about how to untangle the mess our sin has created in this world.

And so, in the next few posts, I’m going to keep speaking—and you can expect me to continue to do so. Not to be political—I may discuss current events, and I’m of course coming from my own perspective—but to invite dialogue, to dig down not only to the heart of issues but also into our own hearts, and to grow our mutual understandings. Because I will be the first to admit that I do not understand ANYTHING fully. I am keenly aware of how my own opinions shift as I learn more. So if my opinions change, why would I try to convince you of them? I’m just hoping you’ll want to come along on the ride of discovery and learning and deepening our own understanding, with the goal of better seeing the nuance of those complicated issues and also of each other’s hearts.

I’m going to break these into multiple posts (because this one is already long), but I’m going to publish several of them all at once. If you’d like to engage, you’re welcome to do so at any time on any of the topics. As I publish them, I’ll be adding links to each topic at the bottom of this cornerstone post.

I hope and pray that whether we’re in the same place or different ones, we can be open and vulnerable like that Facebook conversation was at the start—because I love you. You, my readers, are my whole purpose. You are the reason I get up every morning and write the stories God has put on my heart. I don’t love you because we agree—I don’t love because we’re on the same “side.” I don’t love you because I think you’ll echo back to me my own beliefs.

I love you because you are so precious in the sight of God. Most of you know Him and love Him (I know I have some readers who aren’t there yet, too). So most of us are starting from the same place…but that doesn’t mean we’ve taken the same journey or are viewing things in the same way now. And that’s not only okay, that’s beautiful. That means we have so much to learn from each other. It’s no coincidence that Jesus invited both Zealots and tax collectors into His inner circle. Two diametrically opposed positions in that world—both of whom could bring those opposite politics to the Lord’s feet and love Him.

I want us, the Church, to begin healing. And that requires conversation. Not shouting matches, not debates, not trying to win or be right. Learning. Truly learning the other points of view, truly seeking to see others’ hearts.

You’re going to find other people who are standing exactly where you are—and you’ll realize you’re not alone. You’re going to find people who disagree with you—and who can show you things you’d never considered before. You’re (again) going to find people who disagree with you—and who need to hear what you have to say. You’re going to be confronted with uncomfortable truths, no matter your opinions. And you’re going to have to wrestle with them. Because denying them doesn’t achieve anything but the hardening of our own hearts.

I hope you’ll come along on this journey with me. If you’re not up for it, that’s okay. I get it. Maybe it isn’t your time to speak yet. But if it is, and if you do, I pray you’ll join me in the spirit in which I’m opening this dialogue, and I pray you’ll be vulnerable and share your thoughts and opinions and stances. I need to hear them. I need to understand where you’re coming from. I still have so, so much to learn—I know that. And since you’re human, I bet you do too. ?

A year ago, I was angry and wanted to hold people accountable. This year, I’m grieving, and I want to heal. Are you ready for that, too? Then please, come along.

In one of my next posts, you’ll find my story as I shared it on Facebook. In another, I’m going to pause to remind us all of what makes for constructive dialogue, and I’m also going to equip us with something I sure need—a logical fallacy toolkit. The purpose of that will be to give us the tools and words to help us identify why certain arguments feel “off” to us, which in turn helps us know how to respond. I’ll be using examples of them straight from my social media feed. And from there, we’re going to start talking about some of the hard topics and hot button issues we’re confronted with every day right now, from immigration to Greenland to abortion.

And I’m doing something else too. I’m opening up a place to talk about these things live. If there’s enough interest, I’ll be hosting Zoom chats with my husband, in the tradition of Benjamin Franklin’s Junto club or the Maryland founding fathers’ Wednesday Club—where we talk about things that matter from a place of vulnerability, desire to learn, and love and respect for each other. No “winning,” no “agreeing to disagree” (I hate that phrase! LOL). Just earnest, open communication between people who love God and crave that unity in the Church that’s sorely lacking right now.

I’m calling this “The Common Room.” Historically speaking, that’s the place in an inn where people would come to gather—to share a meal, to learn, to talk. We’re going to be emphasizing what we have in common (our faith, our love of God and of the home here on earth He’s given us, and also of each other), and we’re going to be learning from each other when it comes to differences. So I’ll also be sharing the “rules of engagement” for these meetings. ? I hope you’ll come. If you’re interested, please fill out this super-fast form so I (a) know there’s enough interest to warrant it and (b) can send you the Zoom link.

And so, this post will end with this message: if you are liberal, I love you for your concern for your fellow man. If you are conservative, I love you for your adherence to core principles and belief in the sacred. If you are moderate, I love you for trying so hard to strike the balance between the two. If you are confused about it all, I love you for your self-awareness and admission that there’s just too much to take in. No matter where you stand right now, your perspective matters. Your views are not only valid, they are valuable. Come be seen. Come be heard.

Come be healed.

(*A quick note–when this posts, I’ll be in Morgantown for my next chemo infusion, and my website does hold comments from first-time posters for approval, in order to weed out bots. So if you comment but don’t see it pop up immediately, that’s why. I’ll get online as soon as I’m able to approve anything that’s waiting. I just don’t want you to think any delay is intentional or aimed at whatever you might have shared!)

A Quick Guide to My “Hard Topics” Articles

Is America a Christian Nation?

Is America a Christian Nation?

I don’t think anyone could argue against the assertion that America’s foundational documents are greatly informed by Christian principles…but are we truly a Christian nation?

read more
A Soft Answer

A Soft Answer

A soft answer really does turn away wrath–and one that seeks to understand rather than be understood can make new friends. I can prove it.

read more
Why Now?

Why Now?

Should I be worrying about these things while I’m fighting cancer?

read more