• No Bad Endings

    It seems the past month has held wave after wave of life crashing around us. We’ve reeled and pitched with the tossing of each wave, but our ship holds fast, because our Father holds us. We tell each other this… look at what is true. I hear it from my Brian. I hear it from the lips of my own children as they wrestle with why God allows hard and scary things into our lives. But they know, we know, God is always, always good. He never changes. He is always with us.

    During our spring break trip, I sat with my eldest while Bri and the other two climbed a ropes course. We talked about life, school, friendships, college, the future. I asked him how he deals with my cancer. Always pragmatic, my Ash smiled. “It’s not like I can say, ‘Well, Mom, I think about it and you this many minutes every other day.’” We laughed. Then he opened up and shared his fears, his struggles and his acceptance, his faith. He threw an arm around me, “And you and Dad have never let cancer consume our lives. It’s part of us, but it doesn’t rule us. That’s a gift.”

    Oh, y’all.

    God’s mercy overwhelms.

    While we were in Atlanta, my Bella-girl was having a girl’s morning with my dear, dear friend. On route to meet us, someone ran a red light and t-boned my friend’s car on Bella’s side. They are okay. The walked away. Y’all, I’ve been told I have cancer five times. I’ve never been so scared as when we topped that hill and saw the lights flashing around a bent, broken vehicle. They are okay… they are okay. Bella still deals with pain (whiplash is no joke!) and some fear, but she is okay. And on her birthday last week, my tears of gratitude were deepened with the understanding of what could have been.

    Oh, y’all.

    God’s care overwhelms.

    Our trip during spring break found us sitting with old friends in Chattanooga, then Atlanta, then Gatlinburg. It was hours and hours of knowing and being known… of laying all of life out there and holding each other up, of speaking truth and sharing hearts, of just resting in friendship together, of loving conversations and playing games. Of time. Time together.

    And time together as a family was so much needed. We took long, lazy mornings together, sleeping in and drinking steamy mugs of coffee. We watched movies and read books. We took in some sights and ate at fabulous restaurants. We relished time away as a family, not without its arguments and frustrations, but still living the language of grace together as we forgive and move forward. We are always learning more—more of each other and more of God in our lives.

    Now we are home and there are track meets and Boy Scouts and birthday parties and Spring programs and behind-the-wheel and friends coming into town for visits. We keep moving forward.

    Oh, y’all.

    God’s love overwhelms.

    Last week I saw my oncologist. Even as we move forward, the sighs are heavy, friends. My tumor markers are rising, my liver levels are not settling, there is pain in my left side that is concerning. I have a CT next Tuesday (the 24th) and we will find out results and course of/changes in treatment on Thursday (the 26th). In two days, on Wednesday, I have an echocardiogram to see if there is damage to my heart from chemo. The nights are hardest. We walk with heavier steps as we consider what this could mean. But at the same time, there is still peace. I spoke with a friend Saturday evening and told her that there’s just been an overwhelming sense of gratitude for how much time God has given us together… do I long for more? Yes. Do I fear there won’t be? Yes. But as I dig deep in His Word—His very presence—I see yet again how sadness and joy do co-exist.

    So, here’s where we are. Reeling and clinging. Laughing and crying. Fearing and hoping. Holding on and living.

    My childhood friend, Monica, once encouraged my heart with the truth that for Christians, there are no bad endings. The past few weeks, I have settled yet again on that. Already, no matter what comes in this present life, we have what is best, for we have Christ. He rides in the vessel. He controls the storms. He is the hope, the sure and steady anchor for our souls. And He will guide us safely home.

    Oh, y’all.

    God’s grace overflows.

    (On repeat today:)
    Before the throne of God above
    I have a strong and perfect plea
    A great high Priest whose Name is Love
    Who ever lives and pleads for me.
    My name is graven on His hands,
    My name is written on His heart.
    I know that while in heaven He stands
    No tongue can bid me thence depart.

    When Satan tempts me to despair
    And tells me of the guilt within,
    Upward I look and see Him there
    Who made an end to all my sin.
    Because the sinless Savior died
    My sinful soul is counted free
    For God the just is satisfied
    To look on Him and pardon me.

    Behold Him there, the risen Lamb!
    My perfect spotless righteousness
    The great unchangeable I am
    The King of glory and of grace.
    One with Himself I cannot die;
    My soul is purchased by His blood.
    My life is hid with Christ on high
    With Christ my Savior and my God!

    (~Charitie Lees Bancroft/Vicki Cook)

  • Random Thoughts from Christmas Break

    It is the last Friday of Christmas break, and I find myself looking at the calendar and asking, “How is it possible that time, once again, has gone by so quickly?” We have basked in the joy of being together this season. We’ve filled our days full of friends and family celebrations, laughter and tears, good foods, skiing and snowboarding for Bri and the younger two, shopping, sleeping late and staying up to snuggle under blankets by roaring fires and watch movies. We’ve shared hearts and struggles and fought and forgiven and we’ve been intentional about just being together.

    Yesterday was chemo.

    I had an extra week in between treatments, and I am always amazed at how well I feel during that extra week. I was able to cook and clean and make meals for friends and get out and do things with my family that I wouldn’t have normally been able to do. And I’ve been able to do it well. In fact, I spent all day Wednesday in the kitchen, content in my happy place. I deeply grieve that loss.

    Yesterday was hard emotionally and physically. I was worn from chemo. I was sad because I have to do this—that this is my life—but as we sat with friends who are in in town for the holidays and shared dessert and our lives and the gifts that God has given, I was overcome yet again with just how very much we have.

    We learned during the holidays that my PET scan came back with no change. This is a good thing—a very good thing. This means my cancer has not metastasized to the bone in my hip and back like we had feared. While this doesn’t give answers to the pain I’m having, it does give the relief of no spread, and we are enormously thankful.

    We have settled into the relief this news brought. Having Brian here for the week has been wonderful. He’s worked around the house and played and shopped. This morning he took Bella and Ash at 6:00 (yes, that’s oh dark hundred) to deliver a gift to a girl we love dearly at the hospital as she awaited wrist surgery.

    This morning my Bella baked her brother’s birthday cake. We decided fairly spur of the moment for him to have a party with his friends tonight to celebrate his fourteenth birthday (which is Tuesday), and again I ask, “How is it possible that time has gone by so quickly?”

    Our Bear is so dear and so funny and so gentle and so kind, and we are thankful for each and every day God has given us with him. So we turned up the music loudly (The Greatest Showman—-wonderful movie and phenomenal soundtrack. We saw it over the holidays and all loved it. We laughed and I cried and then cried again and then cried some more, but it was such a good kind of cry. We’ve been playing the soundtrack ever since.) This morning Bella taught me new dance moves as she stirred chocolate batter, and she baked the cake and Bear cleaned the kitchen and vacuumed while Brian took Ash to an appointment and picked up groceries and I sat down to decorate Bear’s cake. Tonight ten 13- and 14-year-olds will descend on our home, many of whom call me “Mom.” The significance and beauty of that does not escape me, and I cry just typing it. What gift to know and love Bear’s friends so well.

    Earlier this morning I sat with another friend who is walking through struggles and trials and suffering unimaginable to me (we shared of the danger of comparing trials and the comfort of honesty and understanding), and as we talked about God’s goodness in the midst, how truth still stands, how He still has given us so much I’m struck once again at the wonder of it all. By the wonder of each day, the wonder of salvation, the wonder of the season, the wonder of how God became man and lived perfectly and suffered and died and rose again so that we could have life here on earth and life forever to come. I am struck by the wonder of these lives with whom He has entrusted Bri and me… our Bella, Bear and Ash… of each other… of our families… of our friends. We are entrusted to love.

    There are only a few days left in Christmas break. I know when Tuesday comes my heart will be sad. The children and I are already lamenting time gone by too fast (and Bear always laments school resuming on his birthday!).

    But, oh, y’all… all of this time is a gift not a thief.

    This time gives us togetherness. It gives us joy in the midst of struggle, beauty in the ashes, hope of life forever where the only time that will matter is that we have yet one more day with Him.

    This year has been a hard one for us, but it has been full of hope.

    It will not disappoint.

    Happy New Year, my friends… and wonders of His love.

  • Light Always Returns

    Today was a chemo day. I’ve lost track of how many treatments I’ve had. There is no countdown to when I’m done. There is no bell to ring as I walk out of the chemo treatment room for the last time amidst the hugs and cheers of nurses who have become friends.

    There is only, “We will see you in three weeks.” Or four weeks, because my oncologist is wonderful that way and scheduled my next chemo for after Christmas so I could feel well for the holiday.

    I feel it strongly. The howl of Advent. The longing, the ache.

    Over the Thanksgiving holidays we watched a movie together and during a voiceover, I found myself weeping (seriously, trying not to be a distraction) as she spoke something along these lines:

    Darkness is always there, but there is something that is worse than darkness. The truest darkness is not absence of light but the fear that light will never return… But the light always returns… Hope is real. You can see it.

    Oh, my friends.

    This describes the past year of my life. I have wrestled and wrestled this fear that the light will never break through the darkness.

    And now, as I face more procedures and tests and waiting…

    The howl is still there. Some days it’s so loud it’s all I hear… other days it’s quiet. But it is an achingly lonely longing for the restoration of the brokenness of this world.

    An achingly lonely longing.

    I often wonder what it was like during those years of silence before Jesus was born. What did they think? How did they feel?

    I imagine it was an achingly lonely longing.

    The howl of Advent.

    My biggest fear in all of my struggles with cancer has been that I would lose sight of Him. That the darkness would become so oppressive that I wouldn’t see the light.

    But the light always returns.

    Advent isn’t just an achingly lonely longing, it’s an expectant waiting.

    Expectant.

    Because hope is real.

    Light always returns.

    Today the light came in small ways:

    “Mary’s Song (Breath of Heaven)” by Hannah Kerr on repeat in my car as I ran errands early in the morning…

    My dear daddy, always my chemo buddy, sitting by my side sharing truth with me (and a lover of quotes, like me, sharing words)…

    Kind friends, remembering, texting me, sharing love, understanding my darkness…

    An oncologist who laughs with me and cries with me, who’s always on top of where I am and what I need…

    My mom, stepping in to fold that load of laundry I didn’t get to, driving children from school and to appointments…

    A warm “breakfast for supper” brought by a friend…

    And now, a quiet night together.

    He shows Himself in mercy after mercy after mercy as I wrestle over and over and over.

    Hope is real.

    Light always returns.

    Only His light.

    It’s never gone.

    I just need eyes to see Him.

    5E5E052E-C8DD-4F31-BCD9-69EE0F3C19DA

    (The next two weeks hold more procedures and scans and waiting. I tire of the waiting and wondering. Of my inability to be and do all that I long to do for the holidays with my loves. Will you please pray for good results? And for a heart like Mary’s who willingly bows in acceptance?)

  • The Pause

    “After all,” Anne had said to Marilla once, “I believe the nicest and sweetest days are not those on which anything very splendid or wonderful or exciting happens but just those that bring simple little pleasures, following one another softly, like pearls slipping off a string.” (~L.M. Montgomery)

    It seems this keyboard is a bit rusty these days. I’ve wanted to write. My brain sometimes thinks in essays full of vibrant color and ebullient words, but when I open my trusty laptop, it’s as if my fingers are paralyzed by my heart. Words. Stolen from me.

    I’ve been here before, but never this long, never so dark as I’ve wrestled and struggled and grappled with the day in and day out of living with Stage IV cancer.

    But my childhood friend, Monica, who knows a physically painful suffering far deeper than I, shared a nugget with me as we talked for hours over phone lines. “Oh, friend,” she sighed, “Don’t forget, sometimes the pause is just as important as the note.”

    Yes.

    The pause in writing, like in music, carries a weight of its own, and without it, the piece doesn’t carry the same wonder and beauty.

    I’ve needed a pause. I’ve needed quiet space in my heart for my family and close friends and me to grapple together. And frankly, to just live together, seeing the simple pleasures in each day and holding them close.

    Along the way our family has been given enormous gifts, huge pleasures, too… like four weeks out west together, slowly traversing in Merlin the Magic Bus, spending days seeing God’s grandeur, visiting old friends, curling up for quiet days in our home away from home, time together for which we deeply long. It was a phenomenal time, and with a three week break from chemo, I tasted and remembered for a short time what it feels like to feel well. I had forgotten, and the taste was delectable.

    We finished our summer at the lake with friends, a working vacation for Bri, a respite for me, a week of laughter and learning and playing for our children. Gift.

    Pause. Breathe deep. Exhale. Move forward to the next thing.

    School started along with cross-country races and Boy Scouts and volleyball and adjustments and piles of homework, travel for Brian, weekend trips and camping for Bear, wisdom teeth surgery for Ash, and chemo after chemo after chemo. We just adjust our sails every few weeks knowing I will be out of commission. I cry over missed field trips and I delight in events I can attend (I tried real hard last night not to be the blubbering mess of a mom when my boy lettered last night in XC). But I delight mostly in being here, a welcoming face for my children when they walk in the door or when I pick them up at carpool. The smiles on their faces when our eyes meet… simple pleasures.

    Honestly, the past year and a half, I’ve wrestled through a darkness that is terrifying, an anxiety that is paralyzing. And the cupped hands together in prayer, the bowing in worship tasting and seeing that He is good, the clinging to friends’ arms and weeping together, the sitting with my parents and working through the same fear after fear and struggle after struggle has been a necessary pause in the story I write.

    His story for my life.

    And I’m learning what I already know as I frantically beg, “God, I need you.” or “Stay my mind, dear Jesus, stay my mind” that He is here. Even in the darkness, He hears. He never leaves. Never forsakes.

    Right now I’m in the midst of tests and procedures routinely run making for long, hard days… any one of them could mean our lives change all over again. But it could also mean it all stays the same. Chemo. Feel miserable. Feel okay. Push through. Live the life God has given.

    That is the choice we make every day.

    To live.

    Today. Lovely today offers itself to us. Life. Together.

    Simple pleasures.

    Following each other softly.

    Notes.

    And pauses.

    Held close.

    (I have heard from some of you, wondering if I am okay, how we really are. Thank you for asking, for checking in, for cards sent to remind us we are not forgotten, for meals on the hard weeks. Thank you for pausing with me. Your care for us resonates.)

  • Where Is the Reverse Gear?

    The excitement in our home is palpable.

    We are so glad for school to be over. Oh, how I miss them when they are gone!

    I’m a little behind because of chemo this week, but I’m readying our summer basket and we’re putting the finishing touches on our summer list. We’ve even checked a few things off already! The past six weeks have been hard on all of us as we’re learning to adjust to my new chemo–what it takes, yet what it gives. I’ve been quiet here, needing space to process and grieve and accept all over again. We all have.

    But in the midst of it all, we anticipate and relish the thought of our summer days together. I’m shedding a tear over the passage of time. It seems to be speeding up these days. As Jack London said, “Darn, the wheel of the world! Why must it continually turn over? Where is the reverse gear?”

    As my Ash breezed into the kitchen yesterday, I looked up into his confident face as he draped his arm over my shoulder. He’s a full foot taller than when he started ninth grade. And it’s over, his first year of high school, where he gained insight and friendship and wisdom and confidence and maturity. My eyes welled with a mama’s pride.

    And my Bear, who flopped next to me, shining eyes, dimpled grin. “Exams are over.” He has stressed all week, this boy who struggles to test well and tries so very, very hard. Our eyes are level these days, and his arms that squish me in hugs are stronger, lean with muscle. His heart grows larger each day and he revels in adventures… even creating an adventure for himself and his class tonight, planning party food with his Grandma (Brian’s parents are here for a visit) so he can have capture the flag in the yard with his class and then a big bonfire. “I can’t wait to burn my Latin papers!” he laughs. I love having his friends in our home and I love watching him with them.

    And Bella girl, our last elementary schooler. She’s finished. Elementary school is over. She’s grown up on us despite our stern warning to the contrary, and as she settled into my lap yesterday at our lunch on the terrace, she tucked her head under my chin. “I’m so ready for summer with you.” Her girlishness is settling into a womanly grace and strength I don’t feel prepared for… yet I know I need to prepare her for. She has thrived in fifth grade and fills our home and her friends’ lives with kindness and beauty, compassion and empathy.

    My oncologist is working with our summer schedules to allow for travel times and to give me “good weeks” when it suits our summer plans best. I am so thankful for her.

    Even with cancer’s shadow in our lives, we are still chanting our summer mantra and filling our days full…

    The only option as I see it, is this delicate weaving of action and celebration, of intention and expectation. Let’s act, read, protest, protect, picket, learn, advocate for, fight against, but let’s be careful that in the midst of all that accomplishing and organizing, we don’t bulldoze over a world that’s teeming with beauty and hope and redemption all around us and in the meantime. Before the wars are over, before the cures are found, before the wrongs are righted, Today, humble Today, presents itself to us with all the ceremony and bling of a glittering diamond ring. “Wear me, ” it says, “Wear me out. Love me, dive into me, discover me,” it pleads with us.
    (~from Shauna Niequist’s “Cold Tangerines”)

    Yes, we are ready. And we heave deep sighs and look forward to pool days and learning new games and root beer floats and catching fireflies. To travel and concerts. To us being together. To growing up and growing old. (Y’all, what a privilege it is to grow!)

    To celebrating, really celebrating, this life we’ve been given, tasting the simple joys of ordinary days and the exquisiteness of new adventures. And to being thankful every day for the life our God has chosen to give us.

    Yes, as Hannah Coulter (one of my favorite reads) says, “This is [our] story of giving thanks.”

    Our summer basket is “almost” ready.

    And so are we.

  • “And More”

    “Oh, Marilla, looking forward to things is half the pleasure of them,” exclaimed Anne. “You mayn’t get the things themselves; but nothing can prevent you from having the fun of looking forward to them. Mrs. Lynde says, ‘Blessed are they who expect nothing for they shall not be disappointed.’ But I think it would be worse to expect nothing than to be disappointed.”
    (~L. M. Montgomery, Anne of Green Gables)

    There is a word in Dutch that we don’t have in English, voorpret. It describes pre-fun, the sense of enjoyment felt before a party or event takes place.

    I’ve watched my Bella-girl these past couple months as she has planned and prepared and anticipated her birthday party. She had a folder with sketches and artwork and plans. She looked through pinterest ideas with me, so she could create a beautiful table for her friends. She made lists of fairy garden supplies and tea flavors and hors d’oeuvres. She could. not. wait.

    Last week was brutal for me. I could not function. This wasn’t just a curled-up-on-the-couch kind of not functioning, this was an I-can’t-even-crawl-out-of-bed not functioning. She would curl in bed with me, and we’d scheme and plan. The invitations had been sent. The party was Saturday. It couldn’t be moved. What would we do?

    Bri was in Seattle for the week, and my parents came up to help us. They ran errands and bought food and Daddy scrubbed outdoor tables free of pollen and helped prepare the outside for her party. A friend mowed our grass. Another friend lent us her tea set to add to mine (inherited from Brian’s Grandma). Knowing I might be down from chemo, I had already asked a sweet friend if she’d make Bella’s cake. Mom helped make tea sandwiches and chopped veggies. I shopped with Mom one day for fairy garden supplies, and ended up sitting down in the middle of the store because I couldn’t go any further. Home we went, where I curled up again. Mom and I both ended up with colds, neither feeling on top of our game to put it mildly. You have to be kidding me?

    On Friday, sweet Bella girl had two friends spend the night. My parents had gone home and Bear was at a sleepover. I loved the sound of my home filled with giggles and late night stifled laughter. We ordered pizza and they prepared for the party, tying twine around napkins and creating name cards for each place. They prepped mason jars with straws and filled containers with fairy garden supplies.

    My fever spiked that night, so I got the girls settled and Ash hung out with me in my room to watch a movie. As he readied for bed, he came in to wish me good night. “Mom, you look miserable. What can I do?” I told him I just needed a good night of sleep, and he leaned down, kissing the top of my head, “Mom, if you can’t run the party tomorrow, you just tell me what to do. I’ll run it for you.” Y’all, that dear, dear boy… just imagine him running a fairy garden tea party for fourteen giggling girls! His heart is huge.

    I woke the next morning with no trace of cold, no fever, and just a tinge of laryngitis. Bear arrived home. Then Brian. Things were falling into place as the boys moved tables and set up canopies outside to prepare for the heat. A sunny 90 degree day! The girls worked tirelessly on decorations and food, chattering and laughing together. They covered the table with glittery twists of tulle and organized Brian’s grandmother’s tea set. Bear made an appetizer for the party while the girls ran off to change and do each other’s hair and wait for friends to arrive.

    IMG_0045

    IMG_0012

    Tabitha arrived with the cake, and oh, y’all… the cake. Tabitha not only created a wistful thing of beauty, she prayed over it, she knew words were my love language, so she filled butterflies with words that Bella could keep in her memory box. She went above and beyond, even stopping by the side of the road on her way to our house to pick poppies and add them to flowers she had chosen for our girl.

    IMG_0065

    IMG_0081

    IMG_0072

    Girls started arriving. Dear Gen, an older sibling arrived with her sisters. She came to be my helper, and joined Ash in carrying cups and plates and filling glasses and cleaning up when it was over. Ash climbed the swingset and watched the activities from his perch above. Bear hid in the house away from all the chaos, only coming up for air for food when we called. Bri filled our yard with joyous music.

    IMG_0127

    IMG_0036

    And thirteen girls descended on our yard to create fairy gardens to take home, to run and play with Coop, to laugh around a beautiful table and fill their hearts and bellies. They piled around Bella as she opened gifts and oohed and ahhed. Our neighbors (Bella just adores Miss Emily) joined us for slices of cake. I loved watching it all, sharing stories of how the lemonade pitcher was Brian’s Grandma’s (purchased before World War II–such a lovely heirloom), laughing with Gen, and reveling in the delight of the girls as they tried to figure out whether they should raise their pinky or not when they drank. It really couldn’t have been more perfect.

    IMG_0035

    IMG_0034

    IMG_0025

    IMG_0129

    IMG_0122

    I marveled afterward at all the hands involved. So many who stepped in where I could not to make Bella’s first party-planning event a success. Our hearts are so full.

    And Bella? Oh, y’all… sweet Bella. After it was over, she leaned into me, overflowing with gratefulness. “Mom?” she whispered, “It was everything I hoped for…

    And more.”

    Then she looked up, eyes sparkling. “I’m already planning next year!”

    IMG_0102

  • Frayed and Ragged

    Thursday morning arrived far too early with the insistent ringing of my alarm and my fumbling to find it, using every ounce of strength to not just chuck it out the window across the room. I rose in the dark with my son, who is perfectly capable of doing early mornings on his own and often does, but I like to make him some scrambled eggs and smoothie, fuel for his six a.m. track practice. Yes, he runs two mornings a week at 6:00 in the morning. Who is this boy?!

    I spent the rest of my morning curled by a gentle fire, taking the chill from our home, reading, sending my other two off to school, picking up clutter in the rooms that aren’t impacted by our renovation, doing a couple loads of laundry, playing the music from Beauty and the Beast far too loudly, and packing my chemo bag. Brian cut gorgeous white lilacs from the bush my childhood friend, Monica, gave me years ago, and I tucked them into a lovely vase. I thought I was doing okay.

    IMG_1127

    While folding my load of towels, my finger caught the edge of one as I lifted it and it ripped right through. There were already signs of wear, but nothing like this. I immediately crumpled. I sat on my bed, cradling a towel we’ve had since our wedding and sobbed, and I realized how frayed and ragged I really felt, how like this pile of twenty year old towels, my body has been slowly fading and wearing and weathering. My mind raced with how I could fix it. While I’m at chemo, I’ll get on Amazon and order some more towels–big, fluffy, fat towels that we can melt into, yellow and soft and sunny–and we’ll all feel better. And white ones for our new bathroom when it gets finished. I imagined hanging them on the line in the warmth of summer’s sun, and sighed happy sighs. At least, I thought, somehow buying new towels could fix something. I’d have control over something.

    You see, I have my days. Days where I just want a fix. I lament the way cancer often controls our lives. I leaned into Brian before he left for work, “I don’t want to do this.” I whispered, husky voice even huskier because of it’s teary thickness, “I want to just be done with cancer. I’m tired of fighting. I’m tired of battling to cling to my faith. I’m tired of always feeling like a failure because I can’t care for my family and home and friends the way I long to. I want to be done. I’m just. so. tired.” There’s my heart, in all it’s honesty. I. am. so. very. tired. of. it. all.

    My body and mind and heart feel as if they are frayed and worn like my towels. But I can’t just go out and buy a new body like I can new towels (ha! imagine if!).

    But those old towels, y’all…

    They may be faded in color and starting to fray a little, but they are so soft. They have spent years surrounding us in warmth, drying our bodies and our tears, they’ve snuggled babies and warmed snowy hands and feet coming in the door from the cold. When I pull them off the line or from the dryer, I inhale them, the clean scent of homemade detergent and freshness of citrus vinegar softeners. They’ve been part of our lives every day and put up with a lot of abuse, too. Snapping towels races through the house, being used as an extra when I run out of towels to use for rags, thrown on the floor for our feet when the mat is in the laundry. They’ve been substituted for hot pads, pulling steaming pot pies from the oven. They’ve wiped up spills on the counter, and held freshly baked cookies and breads and sat on laps when the napkins ran low. They’ve been clothespinned around necks and flown behind make-believe heroes and wrapped around silky red tresses, a bridal veil. They’ve been folded on pillows for guests and color coordinated in my linen closet.

    I guess those towels are kind of like us… we’ve softened, too, as we’ve aged. We’ve surrounded each other in warmth and brought comfort. We’ve not always treated each other well, but we always return to wrap our arms around each other in love. We’ve lived a whole lot of life. And sometimes we even smell nice.

    In case y’all haven’t figured it out, I’m pretty sentimental, so when those towels end up relegated to the rag bin, I’ll probably cry a little, because they’ve endured twenty years with us. That’s pretty amazing.

    I told my oncologist about my meltdown over towels when I saw her later that day. She kinda got teary, too. Then she told me how she admired my resilience and I told her Jesus was my strength, and she said she could tell. Then we laughed over my stories from our spring break trip. (How Brian and I did a Chinese fire drill in standstill traffic on a highway… y’all, we are. that. crazy…. while Matt and Amy cheered from their car behind us. How we high-fived when we stopped at 9:00 at night to eat at a Denny’s for all-day breakfast and none of our kids knew what Denny’s was. #momanddadwin… And how my doctor accidentally encouraged her kids to moon their friends, but stopped them before they actually did it.) Oh, she is such a good oncologist.

    IMG_1150

    My dad sat with me during treatment… six long hours at the cancer center. He offers to go every time (y’all, I cry just typing that… my dear daddy). All went fine. I’ve felt very flu-like for the past three days and everything aches deep in the bone. She gave me some high-powered pain meds to take if I need, which I really don’t want to do, but both she and my general doctor have encouraged me it’s okay to do if I need the relief. I took one Friday and one Saturday. I’ve been mostly bed or couch-ridden, but I’m starting to perk up a bit, and able to do a few things around the house. My Asher’s track meet was canceled for rain, so he went to work vacuuming for me, and my Bear took care of dishes and my Bella baked cookies to thank our neighbor for mowing our grass for us. I reveled in the glorious green of Spring from my kitchen window. I organized my Kindle books into collections and keep opening my Kindle every now and then to look at the three pages of categories instead of 50 pages of randomly filed books. Yes, y’all, I know there is something wrong with me.

    IMG_1152

    This morning I braided my Bella’s hair before church and hugged my loves as they went off to worship. I am waiting for a sermon to download, a series on Abraham and faith that my heart desperately needs. Like I wrote a few weeks ago, our hearts have desperate hands. That is still the case. And as tired as I am of fighting for life, of clinging to faith, of pain and struggle, I’ll push on in Jesus’ strength and pray I’m used for His glory somehow in all of this. After all, there is still lots of life to live for Him… and then, the life to come. Imagine the living there!

    And you know what?

    I never did order those new towels.

    The Lord God is the light of the heavenly Jerusalem; and is the “river of the water of life” that runs, and “the tree of life that grows, in the midst of the paradise of God.” The glorious excellencies and beauty of God will be what will forever entertain the minds of the saints, and the love of God will be their everlasting feast. The redeemed will indeed enjoy other things; they will enjoy the angels, and will enjoy one another; but that which they shall enjoy in the angels, or each other, or in any thing else whatsoever that will yield them delight and happiness, will be what shall be seen of God in them. (~Jonathan Edwards)

  • Strength for Today

    FullSizeRender-9

    The rain is pounding on our tin roof; the wind is buffeting and howling under the eaves. I want to hunker down, to hide, to let the tears flow today, to pour down like teardrops from dark clouds. I’ve shared heart and life over coffee with a friend this morning. And I have heard sad news today about another friend. That aching, heaving, cancer is horrible kind of news. I wrote her from my car while I waited for the rain to let up:

    I’m just crying along with those raindrops for you… I want to cuss (and I’m not a cussing girl) and scream and stomp my feet and just beg God to stop it! Please, dear God, stop it!!

    My Bear needed me yesterday… a lot. He shared stories of a handbell piece they performed. “Mom,” he told me, “It was a moving piece.” He told me of the story behind what they played, of the joyful start and fresh music of a girl living life, then finding out she had cancer, then thinking it was cured, then the sadness of the music as it returned and she passed; how the mallets hit the bells slower and slower until there was one final ring. He described the new tinkling of high notes, a brightness as angels came to carry her to heaven and home. His voice was husky as he shared. My voice could utter no words. We sat quietly in the car holding hands as music from my phone played around us.

    I’ve described it to friends. We are okay. We are just living life with an overarching sadness, but not an overwhelming sadness.

    Yesterday I saw my oncologist who went over the PET scan, and we discussed future treatment. Brian was with me asking questions that wouldn’t have even come to my mind.

    The PET scan, as we expected, showed no new growths. Except there is an area around my vocal cord that was “hot.” This means they see something, but they’re not sure what it is. My vocal cord is where this metastatic breast cancer all began… she is sending me to my ENT to get it looked at more closely, to see if it’s inflammation or tumor.

    No new growths is encouraging news. We are thankful.

    However, my tumor markers are still rising. What this means is that because she’s been so vigilant with me, they’ve caught growth early. My cancer is growing, it just hasn’t grown enough yet to show up on scans. This means we don’t know where it is, how extensive it is, we just know it’s there.

    But it’s small. Which is good.

    But it’s insidious, which is scary.

    After spring break next week, I will see her again and begin a new chemo. It’s one I’ve been on in the past and has been effective. It helps to know what we are facing. I’m just so weary. I’m tired of “doing.” I’m tired of suffering… of pain… of fighting literal death in my body.

    I hate it that cancer is so relentless, that I can’t sing anymore, that my bones are brittle, that my days are consumed with making the right foods and homemade soaps and oils, that my eyes water and ache constantly, and that joy is so. hard. to. fight. for.

    Yes, the rain pours down here. In literal and figurative ways.

    But God…

    I see blue skies rolling in from the west. And perhaps even a rainbow will appear.

    God’s faithfulness.

    God continues to give us yeses and nos.

    And both those answers are good. And grace.

    Because healing from cancer isn’t the answer. He is.

    Because healing from cancer isn’t enough. He is.

    So we thank Him for mercy in the fight.

    We have strength for today and bright hope for tomorrow, even on rainy days.

  • Another Man’s Shoes

    On Brian’s 40th birthday (am I allowed to say how old he is?!), I threw him a birthday party with friends from college and early marriage days. Twenty or more years of friendship. Six couples around a table celebrating and laughing and enjoying life together. Each year since, I’ve thrown the second or third annual “Brian’s 40th Birthday Party.” For his party this year, we surprised him by all (except one couple who couldn’t make it, *sniff, sniff*) going to a Drew Holcomb & the Neighbors concert with dinner beforehand.

    Y’all, these people.

    FullSizeRender-8

    I can still remember the guys as freshman who slept on couches in the house Bri lived in his senior year. Two of the girls were instrumental in me actually meeting Brian (I wonder if they even remember that.) Groomsmen and bridesmaids and attending each others’ weddings. College band gigs and camping trips that fell apart and soccer games that ended in too many injuries. The monthly theme dinners and long jeep drives, off-roading in the mountains. Then children… between the six couples we have 23 children…bleary-eyed days of figuring this parenting thing out and having gatherings that ended much earlier because we had to get home to bed.

    We have, as Drew Holcomb sings, “walked miles in another man’s shoes.”

    Yes, they have walked miles with us, grieving with us, rejoicing with us, and carrying burdens with and for us for longer than we could have imagined it would be. And we gathered last Wednesday night. We traveled over the mountains to dinner, talking of work and life, still figuring out this parenting thing, only this time instead we were talking of soccer games for our children, track meets, school trips. Instead of toddler foibles, it was relationships and colleges and how. the. heck. do we do this?

    Some of us grabbed dinner together before the show, sitting outside on a cool spring evening to once again celebrate, toasting Brian and life and friendship. We ate long and leisurely, steaks and venison and crab cakes. We joked with our waiter and one another and we forgot, perhaps for just a moment, that a PET scan was awaiting me the next morning. We just breathed in life.

    And the show. Oh, y’all, Drew Holcomb is a mix of Americana, folk, and roots with all kinds of relationship built in. At one point we were all on the balcony together, and I watched my friends in front of me, her head on his shoulder, whispers in each others’ ears… from behind, Jas, would lean forward the say to Brian, “Aww, yeah…” as a new song started. He’d talk about what chords the band was playing and he’d laugh in sheer joy. Brian belted out songs along with the band, and held me tight, as they sang of love and loss and hard roads. And I cried (of course) tears of gratefulness and sadness and joy.

    When it was over and we parted ways, there were long hugs, whispered, “I’m praying…” in my ears. Less than twelve hours later I’d be in a machine again, seeing where, what, if there was any spread to this monster that has attacked our life. Yet another mile for them to walk in my shoes.

    They’ve walked well with us. So few people I know have so many college and post-college/early marriage friends that remained in the same town together.

    We are so very, very blessed.

    Here’s to Brian’s next annual fortieth party.

    Thank you, my old friends, there truly are no words.

    There’s a “good light shining in you.”

    (And thank you, Drew Holcomb & the Neighbors, for another amazing show.)

  • Desperate Hands

    The last time I wrote here was over a month ago, as I grieved the brokenness of this world with my sweet Bethy, my dear friend from college. Before that I was cautiously reveling in the news of continued remission. Thirteen long months of remission. It has been gift. I’ve been quiet lately, processing my own struggles and walking with friends in the darkness of theirs.

    Then last week happened.

    For those of you who don’t know, we received news that the cancer is no longer in remission and is active in my body again. My tumor markers are rising (tumor markers are an indicator in my blood of cancer activity.) Again we walk this life in what feels like an unbearable weight. Some of you have asked how we are, what the next step is, what can you do to help.

    As for how we are, sad seems like such a small word, but it carries heavy weight. We are so, so sad.

    Yesterday, I watched my boy climb off his team bus after a day long track meet hours away. I watched friends jostling and laughing with him, then watched him casually wave at them, then turn and casually wave at me, waiting in the car as he walked my way. He oozed a weary happiness as he settled in the seat beside me. We talked about the meet, about his day, about his tribe of friends. We laughed at stories and shook our heads at antics as we drove home. Turning in his seat, he asked, “How are you feeling, Mom? Was it a good day?” He always, always asks. He’s told me how he thinks about me at school. How every day his thoughts turn to me and he wonders how I am doing. I’ve pushed his arm playfully and said, “Oh, son, you’re so busy at school…” He interrupted with, “No, Mom,” those soulful brown eyes boring into mine, “Every day, I think about you.” He bears the weight quietly, but his head seems to bow lower these days.

    “Mom? Can we talk?” I look at the clock, time inching past ten. It is late already for me to be up, but he settles next to me as I pat the cushion beside me. I will never, ever refuse that question. He shares struggles and questions and what ifs and what about and how do I?… And we talk of the hard of this life and I point him to truth and open my heart and arms to a boy whose melancholy heart is full of a deep sadness. His brother sits near and listens, taking it all in, ready to be a confidante when I cannot. “I’m here,” we both tell him, “Whenever you need us…” Days later he is filling our halls with laughter, yelling up the steps, “Mommy, Mommy, Mommy! I love you, love you, love you!” when he arrives home from school. He is not quiet about my cancer. He asks friends to pray, he tells coaches, he shares with teachers. This is his life. He accepts it, but he grieves it.

    And our sparkle girl still sparkles. She does. She oozes kindness and joy in her classroom, on the track and gymnastics mat, in the kitchen as she whips up a batch of cupcakes, outside as she finds our neighbor to show her fairy gardens. I often listen to her in her room, singing quietly as she works at her desk hidden behind lace curtains busy with crafts. She is her father’s daughter, loving life with zest. She is a mix of sunshine and storm clouds these days. Not angry storms. Unlike the redhead stereotype, I can honestly only recall a handful of times I’ve seen her show anger. It’s the storm of tears, of “I’m just feeling really sad these days and need to cry.” And we cry and then she is moving onto the next beautiful thing with which she can fill our lives, fully of fairy dreams and flowers and music and books and friends. She has had the flu this week, and her neediness has struck a chord with me. She wants me by her side constantly, needing a mama’s love. Y’all, you know where the what ifs take me in this… and I cannot go there. I will not. I need not.

    My Brian, like my Ash, bears the weight of this quietly. He does what needs to be done and then some, checking in to see what I need before he moves onto projects or the ski slopes or a concert with a friend, outlets in the hard. Days after our news, he sat down wearily next to me, “I just feel down today.” he sighed. “Oh, baby…” the words from my lips, “Of course you do.” It comes out as a whisper. Three days before we had locked hands at the funeral of our forty-year-old friend, ravaged by this disease. We had sung truth through tears, that whatever our lots, it is well with our souls. This time it was our eyes that locked and no more words needed to be said as quarrels of the day before disappeared in the understanding of what this could all mean. And how the heck do we do. this. again? Y’all, I watch him as he works these days, and the lightness in his step isn’t there, and I think that is the thing that makes me saddest of all.

    As for me? I walk in a fog. Honestly, that’s the best way to describe it. Y’all, last week it took me three tries to put my shoes on the right feet. Three! I only have two feet! I was slicing cheese for crackers for my Bella girl, and the cheese kept crumbling and not slicing. I couldn’t figure out what the heck was going on until I finally realize I was using the knife upside down. Yep, sharp blade edge up. Every day I wake a few minutes before the alarm, and in the darkness of the morning, my first thought is, “Yes. You still have cancer.” And I have to accept it over and over and over again. I am scared of what the future holds. I know the hope of eternity. But the physical pain that I know I will have to endure terrifies me. Cancer is a painful disease, and I don’t mean the chemotherapy. I mean the actual cancer.

    It’s not just us reeling. My parents, oh, y’all, my dear parents. We touch base every day, even if it’s just to be sure of each other. Bri’s parents, our siblings, my brother’s voicemail that I just. can’t. delete. from my phone, my Uncle Sammy’s texts that make me both laugh and cry.

    I recently read a quote by John Piper on Psalm 63:8 where the psalmist says, “My soul clings to you.” (Incidentally, Psalm 63 has been my favorite psalm since I was a teenager.) Piper said, “The soul has desperate hands.” I’ve used the analogy of a roller coaster many times for our up and down life. We’ve done it before, hanging on for dear life. But, thank God, we hang onto the One Who operates this coaster. We are living in a quiet grief these days and our souls have desperate hands, clinging to the One Who holds us fast.

    ~~~

    On Thursday I will have a PET scan. My tumor markers have more than doubled, but they are still lower than they’ve been in the past. She did say we still might not see growth on the scan, or if we do it will be minimal. However, this gives us a baseline. April 5 my oncologist will meet with us to discuss where we go from here. There are options. Because she has been so vigilant with me, she has caught this early. Treatment will change, but I don’t know how at this point. What I do know is that the cancer is growing and we need to stop it! I am upping my diet, making even more changes. Adding new things in, taking other things out. I am filling my home (even in the midst of this seemingly never-ending renovation–that’s not a dig at Brian, by the way… he feels that way, too) with flowers, reading poetry, beautiful things to brighten my days, because I need beauty. I am understanding more and more how I am wired that way, and it brings healing.

    IMG_0923

    ~~~

    And what we need? Oh friends. The fact that so many ask is a gift. A friend visited me on Friday, bringing muffins for my flu-girl, a flower for me and some delicious organic mangoes. We sat with cups of tea and she listened as I grieved and vented and shared. “Angie,” she told me, “So many of us love you and want to fix you, but we can’t. We can’t make the cancer go away, but we can make life easier for you. What can we fix?” And her delicious laughter filled my living room. I loved her way of explaining this need–how our friends have to. do. something.

    Yesterday, piles of people from our church arrived, part of biannual Service Saturday where folks serve in various places. Ours was a “place.” And y’all, as I stepped outside I swear I heard the groaning creation of our yard breathe a sigh of relief. Weeds pulled, mulch placed, porch washed… some of the many things I’ve back-burnered to focus on the more important things that take my energy. I miss it. The feel of dirt sifting between my hands. I’ve dubbed one plot of dirt my space. A small corner where I can plant and grow and see beauty from my window… but I digress.

    It’s not just our home church friends that look for ways to help… we are so rich with friendships that cover years of life in various places. Over the past six months, we’ve been unable to attend our church because of an issue with mold. I have been unable to be in the building without getting sick. Over those months we have been welcomed into various churches each Sunday and sat with life-long friends and met news ones over and over and over. (And our children have groaned that we know someone every.where. and are still always the last to leave!). What a gift, y’all! To know people in so many places where we can worship God together. To be covered in such love. A couple of places truly became homes away from home as we are waiting. A friend from one of those places wrote in a letter to me, “We prayed for you in church… and it was so clear that the whole church body was yearning and reaching out to God earnestly hoping and praying for your perfect healing…”

    And our far-away friends. The phone calls, the tears, the ache to be together. Y’all, I have a friend driving four and a half hours tomorrow because she just needs to sit with me, and I with her. My Bri has a tribe of middle school friends (and some even since pre-school) that keep up with us, that ache for us, that care. Oh, y’all, we. are. so. rich.

    Again, I digress. Our needs…

    I’m really not very helpful in the way of what our needs are. Because of that fog I mentioned above, I really don’t know what our needs are. When something comes up, I might think, “Oh, I could get help with this.” But then the fog sets in and I don’t even know how to make it happen. Even something as simple as a text to our care coordinator can feel like a monumental task. It is the way of suffering. My friend, Zoe, came the night we heard the news. She sat on my couch with me and we grieved together. Twenty years of friendship. She is scared with me. As I talked about the overwhelmingness of it all, she asked questions, “What overwhelms you? How can we take this off your plate?” She enters into the grief, and because she does, her pragmatism is a gift not a burden. In fact, she took a burden off me that night, showed up the next week and spent hours shopping for me and dicing up onions and peppers so they’d be easy for me to access and cut the prep-work out of meals for me.

    I have a friend from church who is helping coordinate care for us. During my remission, we’ve not needed as much, but we know our needs will increase as we ramp up this battle again. She and I will be in touch. She will communicate needs. (Please let me know if you want to be on “the list” and I’ll let her know.)

    ~~~

    We. are. rich.

    In the midst of this, we are still happy. Not always. But we laugh a lot together. I drive a carpool of seven kids once a week after track, and I revel in those voices, their chatter and noise (although I am thankful it’s windows-down weather!). We still live life as we are able. We have sleep overs and movie nights. As I write, my boys are playing Battleship on the floor at my feet, and I’m yelling “You sunk my battleship!” as often as I can to drive them crazy. Coop follows us everywhere we go, nudging us relentlessly for love and being his goofy, furry self (and scaring me half to death with a couple seizures this week–but he’s going to be okay). Ash and I watch basketball and yell at the TV and compare our brackets (which are both pretty busted). We celebrated Bri’s birthday last week, and Bella wrapped his gift entirely in duct tape just to make daddy laugh because we all love his laugh. We do. It’s contagious.

    I make lists and we do chores and pack lunches and put laundry away. I love perusing pictures on Facebook and reading of all the goings-on in friends’ lives. I want to know how to pray for others. I love watching my former youth and college students… every day there is a tear. (How does a heart hold so much love for so many people?!) I really do love it. When I hit like or love or comment, I mean it. (I ignore all the other stuff, because I cannot. deal. with all the constant controversy. I just can’t.) We get together with friends even if the getting together means three of us sleeping on couches while Bri watches the end of the race (I STILL do not understand why you want to watch cars drive around a track over and over and over) and our children hang out in rooms beside us. We go to our home group and the boys go to their youth group and Bible studies. I have quiet days where I curl up with tantalizing books and read essays and listen to sermons and drink deeply of truth, knowing how I must continue to saturate in it, lest I push it away.

    So. I guess that’s where we are.

    Desperately clinging.

    Still living life.

    Abiding in Jesus.

    And thankful for what He’s given.

    Even in the hard.

    Because it’s all gift.

    Every day.

    This day.

    This we know to be true.

    “I want to abide in this day, to make my home in it; I must only tear my eyes from tomorrow and look around. For there is a wholeness to this day that I do not want to miss.” (~Christie Purifoy)

    (P.S. And after I read this to my family, my Bear says, “Amen!” Oh, y’all… the heartbeats of love only grow stronger.)