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“Till He Come”
It was a week ago that I sat huddled under blankets in our den, fire burning, reflecting, praying, weeping. I was missing my Pappy whose birthday would have been the next day. I was longing to sit with my dear college friend who is walking through pain unimaginable as she watches and grieves the impending loss of a loved one. She and I had talked and shared and cried together that day, aching to accept the losses of this life with grace and trust.
I moved into the living room, to our old, antique piano with weathered ivory keys and a few notes that just never can quite be tuned. I needed music, not just mentally and emotionally, I needed to physically interact with it, to let my hands fumble over those keys as the tears fell. I pulled open my battered blue hymnal, the one that’s dog-eared and duct-taped, the one that I played from all through high school, the one I used as I played for church through my teen years. “Lord,” I prayed, “Just show me what I need to hear.” I opened it and let it fall to a page.
I started to play, reading the lyrics as I moved through the piece, unable to sing without my hoarse voice croaking, but then I could hear my daddy’s beautiful tenor voice singing as I played (what a sweet memory). I thought of my pappy, my nanny, of my friend, Kim, whose loss four years ago I still grieve, of my dear one who is tasting this grief in the waiting.
Oh, y’all… God knew what I needed to hear, of that “little while between… severed only till He come.” We’ll see our loves again one day.
I’m not even sure why I share this. I just hope these words bless you today, whatever you’re walking through. Death and darkness and the tomb only pain us for a little while. They pain us with a dark, weary grief, but I’m thankful for the hope that comes beyond.
“Till He come!” – Oh, let the words
Linger on the trembling chords,
Let the “little while” between
In their golden light be seen;
Let us think how heav’n and home
Lie beyond that, “Till He come!”When the weary ones we love
Enter on that rest above,
When their words of love and cheer
Fall no longer on our ear,
Hush! be ev’ry murmur dumb,
It is only “Till He come!”Clouds and darkness round us press;
Would we have one sorrow less?
All the sharpness of the cross,
All that tells the world is loss,
Death, and darkness, and the tomb,
Pain us only “Till He come!”See, the feast of love is spread,
Drink the wine and eat the bread;
Sweet memorials, till the Lord
Call us round His heavenly board,
Some from earth, from glory some,
Severed only “Till He come!”(~Edward H. Bickersteth)
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Remission: What Does This Mean?
“I don’t think we’ll step lightly into the new year ever again. But perhaps that is a better way to begin: remembering the staggering heights and the terrifying depths, with our eyes fixed on One Who never leaves us and is always good.” (~Christie Purifoy)
December held the quiet of the holiday season, basking in time together, quiet days, movies, hot chocolate and popcorn, a visit from my in-laws and then the season of giving. We enjoyed a Christmas Eve service with dear friends, Christmas day with my family and then piled into our RV for a week trip to Disney, our gift to our children this year. (More on that in a future post.) It was a much harder trip on me than I anticipated, even with a couple weeks off chemo so I would be stronger for it, but I relished the joy of watching my loves soak it all in. We returned home to cold and seeping into my bones along with that cold was the struggle of our reality. We faced an immediate PET scan to see what is happening with my cancer, then chemo began again after a five week break!
Y’all, my oncologist is pretty amazing. She called the night of the PET scan so I wouldn’t have to wait to let us know the good news. The PET shows no surprises. The cancer is staying suppressed.
I visited her two days later and discussed what exactly this means. What do I call it? What about treatment? Where do we go from here? Any changes?
She confirmed that I am considered in remission.
But what does this mean?
Well, I just so happen to have some bullet points to help. (Pardon the disjointed nature of this post. I am battling a raging headache today and thinking straight isn’t really happening.)
–Remission. This does not mean the cancer is gone. This means the cancer is quiet or dormant in my body right now. I will never be considered “cured” of cancer.
–Chemo. I will stay on chemo indefinitely (read that to say: for the rest of my life unless we choose to go off of it). This keeps the cancer quiet for now.
–Oral chemo. I take my chemo orally for 11 days, then I have 10 days off. I cry every. single. time. I have to start chemo again, because I know what this means for the next couple weeks.
–Roller coaster. The first few days of chemo are fairly “normal” (whatever that means), then I begin a downward spiral. By day eight, I am spending most of my days curled up with no energy, nausea, aches and pains. This lasts about five days, then the upward climb slowly begins back to “normalcy.” Then I have about a week where I feel fairly well.
–Normalcy. There really is no “normal” for us during the weeks off chemo. One day might be good and the next bad, or I might have several good days in a row. We plan for life around my chemo schedule; however, as I’ve said before, “our no is no and our yes is maybe.” Some days it’s all I can do to pick Ash up from track practice and find myself canceling plans with friends, other days I might be busy running errands and having coffee with a friend. I’m still learning what it looks like to conserve my energy for my family and our evenings together.
–Side effects. As mentioned before, fatigue, nausea, aches and pains are part of the side effects, so is depression, peeling hands and feet, chronic dry eyes, and insomnia. I am also suffering from chronic headaches (and finally able to return to therapy for those now that the new year has turned) and they sometimes turn into full blown migraines.
–Life. We work hard to make life as “normal” as possible. I try to be involved in the children’s school and their field trips. I run children to practices and games as needed. I spend many quiet days at home, curled up with our pup and books and my journal, a few loads of laundry, and small projects. We go to church and get together with friends (and I’m so thankful for friends who let me sleep on their couches!). We go camping and take trips (our RV is such gift to create home away from home for us). We just “live” as we are able. Sometimes this means Bri and the kids are going places without me, and I’m learning to accept that this is okay.
There is so much thankfulness and relief that chemo is working, that the diet changes I have made are helping, that the cancer is in remission. So. much. relief. Y’all, I can’t begin to even explain it. Brian once described our life to someone that it’s like living life with “an axe over our heads.” We never know when things will change, and life is still hard even when the good news comes, but the good news helps lighten the load.
We are choosing to look at life through the lens of faith and gratitude. We live the staggering heights and the terrifying depths. We see the axe, and it’s scary to see, but we also see, as a friend reminded me, “the hand that’s holding it, safely away until it’s time. His time. He won’t let it fall early.”
Thank y’all, always, for your care, your concern, your prayers.
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His Poetry
He breezed in the back entrance
carrying lunch
and discovered me curled up
on the couch,
tears streaming, and
eyed me
quizzically.“I love you.”
It was all that would pour
forth from my
full heart.
I laughed softly, then told him
I was inhaling poetry.He smiled and
sat down, he
listened
while I read stanza after stanza
of love, tragedy,
love, home,
and more love.He is not a man of many words
but he shares my love for them.
He understands
my desperation to read
them aloud
to hear words
whirl off my tongue.He is not a man of many words,
but he comprehends
the importance of them,
the exquisite magic of
poetry.He doesn’t write them
to me,
words,
he is not wired
that way,
and I don’t expect it
from him,
but he reads them
with me.And he writes countless words
with his life.I hear the rhythm of his
poetry every day,
lyrical verses
that tone constantly with
his love. -
Beautiful Moments
This past weekend was full of so much wonderful, so many beautiful moments. My Bella was in our little city Christmas parade wearing her red cloak, plaid scarf and matching braids, vibrant red in the night sky. She carried her lantern and waved excitedly. Her zest for life was palpable. After the parade it was the annual Christmas party in the office where Brian sublets, and we sat with friends and contentedly watched our children with their friends, and we laughed hard and long. A friend took me home earlier than my loves and I crashed on the couch until they arrived home late to drop exhausted into bed.
Saturday found us driving to northern Virginia for Brian’s company Christmas party and y’all, we were spoiled rotten and overcome once again with the joy of his work, the camaraderie of his co-workers, and the blessing of working for men who care deeply for their employees, both spiritually and physically. It was another night of sitting with friends, laughing hard and long and then heading to a hotel to drop exhausted into bed.
Sunday we rose late and drove another hour to Baltimore, picking up Starbucks and gifts for my childhood friend, Monica and her loves. I’ve written often about her family, about our friendship, and once again, her dear daughter has undergone major, life-saving surgery and they are worn within inches of existence. We hugged and cried and shared and laughed and then cried more deeply as I prayed over my friend. Dear Lord, how much can one family bear? We drove hours home to our own loves, wrapped up the evening with snuggles and stories. I began my chemo regimen that night and fell exhausted into bed again.
And Monday, the beautiful pushing of the weekend reared its ugly head. Mingled with the beginnings of chemo, the downward spiral began. This spiral is normal on chemo. How do I even explain? It’s the exhaustion of even moving off the couch, away from the warmth of the fire, to fix myself a sandwich for lunch… the nausea and vomiting, the aches and pains. Then the forcing myself to get into the car for errands or picking up my Ash from track practice. When days before I was celebrating and laughing, now I am fighting for deep breaths and wondering how I will make it to my children’s Christmas program. How do I maintain the normalcy of life?
A friend and I caught up for a few moments on Tuesday evening, happening to run into each other. “This new normal,” he said, speaking of his own cancer recovery, “We are realizing there is no new normal.”
Exactly. Life is disrupted.
But it is still filled with so many gifts.
I saw my oncologist on Wednesday, and as I left her office, tears leaked from the corners of my eyes. Not tears of fear, but tears of sadness. Sadness that this is our life… full of wonderful, yet full of so much nebulousness. I am weary of fighting this disease, of the chronic pain, of bone-deadening fatigue, of the constant work it takes just to have a “grab and go” breakfast, of never knowing how to explain to friends what our life really looks like, of the battle against hopelessness even when things are looking very hopeful. Because, y’all, this. is. my. life. until God calls me home.
And I cried because I so easily drift to auto-pilot and lose my desperation for Jesus. I don’t want good news like tumor markers dropping or a clear MRI to deaden my heart. I don’t want God to just be a go-to when life is hard. I don’t want to just run to Him when everything is caving around me.
I don’t ever want to lose my desperation for Jesus.
“It’s hard to remember, isn’t it?” my brother once said to me, “the goal of all this isn’t you getting back to where you were before. It’s getting to know Jesus more deeply.” He is such a wise, kind man whose heart is enormous, and I am thankful for him and for how he walks with me through suffering.
Good news or bad news, good days or bad days, I only want to grow in my desperation for Him.
Even as I struggle with the hopelessness of the day-in and day-out of all of this, God comes and gives me huge gifts like clear MRIs and seemingly small gifts like weekends of love and laughter. Only I have come to realize that the latter is really the bigger gift. The family, the friendships, the joy He brings in the ordinary day-in and day-out of life are magnificent. Every moment is important.
The news is good today.
And as I sit and gaze at the sparkling lights and dangling ornaments on our lovely Christmas tree, I am reminded of the good news that came 2000 years ago.
The beautiful moments I get to share with my children. The joys of deep friendships. Time away with my hubby. Time to grieve with my friend. These are all gifts, yes, but they are not what drives me.
Every moment is important, because every moment is from Him.
That good news has never changed.
This. This is what drives me. And it drive me to Him.
Our lives are at once ordinary and mythical. We live and die, age beautifully or full of wrinkles. We wake in the morning, buy yellow cheese, and hope we have enough money to pay for it. At the same instant we have these magnificent hearts that pump through all sorrow and all winters we are alive on the earth. We are important and our lives are important, magnificent really, and their details are worthy to be recorded…We have lived; our moments are important.
(~Natalie Goldberg, Writing Down the Bones) -
The Good News
Monday morning, they strapped me down in the MRI machine, arms pinned to my sides, plates on my abdomen, jazz music in my headphones. The tears leaked from the corners of each eye… tears from dry eye syndrome, tears I could not wipe, tears of disbelief as I looked at the dingy white cylinder above me. “Lord, really?” I asked, “Is this really my life? Seriously?”
I’ve had a lot of those moments these past weeks as we’ve waited and faced more scans, more diagnoses, more possibly scary results. The contrast dye from the MRI gave me a migraine, and I started chemo again on Sunday, so I am still very weak and nauseated. “Seriously? How did I get here?”
On Tuesday, one of my heart friends showed up with both my favorite coffee and my favorite flavor of gelato, warm hugs and two hours of deep conversation, tears, grueling struggle on both our parts, and truth spoken gently. We needed each other. We needed freedom to really share our lives. And we needed truth.
Yesterday she texted me. Read Isaiah 55. So I put my Bible app on audio and listened as the Word washed over me, words of promise about our covenant keeping God, words of peace. I let it go on and on and the voice read chapter after chapter. When Isaiah 58:11 was read I fell into a ball on the floor and wept.
“The Lord will guide you always;
he will satisfy your needs in a sun-scorched land
and will strengthen your frame.
You will be like a well-watered garden,
like a spring whose waters never fail.”“Could this really be true? Will I ever be like that spring?”
The truth is, I already am. God has never ceased to guide us. He has satisfied all my need in Jesus. He has strengthened me in my weakness over and over and over… and ultimately will give me full strength in heaven. And those springs whose waters never fail. Jesus. His Word. When I drink deeply of Him, I am drinking of living Water.
He, our covenant keeping God, has promised. Oh, for eyes to stay looking up on Him and not on the hard, the daily hard of constant pain and fatigue, of wondering how I’m going to do. this. again. today. How do I live in constant brokenness?
He will guide me. Always.
As I puttered around the house last night, wiping counters, picking up clutter from the day, the phone’s ring startled me, and when I saw the hospital’s number, I sank into the couch. Deep breaths. Do I answer?
Of course, I did.
“Angela?” his voice, calm and steady, tinged with its kindly southern drawl, “This is the doctor. I’m calling you about your MRI results. I know you don’t want to wait until your follow-up (December 9th, y’all!). And you need good news, don’t you?”
Oh, y’all… do I ever need good news!
They believe it’s a cyst. It’s a proteinaceous cyst, and it’s shrinking–down 4 1/2 mm! He wants me to have a follow-up in six months to keep an eye on it, but it appears to be nothing of concern.
Oh, y’all. I sobbed on the phone and I could hear the smile in his voice. I sobbed with Brian and my parents and close friends.
One friend told me, “My heart is racing with the joy!”
That is how we all felt. I don’t think I realized how heavy this was upon me until last night when I felt two hundred pounds lighter.
Do I ever need good news!
The truth is every three weeks when I see my oncologist, the rug could be pulled out from under us again.
But the truth is, I have good news. I had it all day yesterday and the day before and the day before. Even in the blackest, darkest nights of midnight cancer I have good news, because I have my covenant keeping God Who covers me with His wings and sent His only Son for me. For ME!
We live walking on tenuous ground, yet we stand on a solid rock.
We are basking today.
In good news.
Thank y’all always for your heart, your love, your prayers. This cancer road is long and hard and never-ending. You are harbingers of joy and strength as we continue through each day. I am humbled.
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All In
It was a gorgeous night for football practice. I curled up cross legged on my blanket and looked at the crescent moon just beginning to show its face. Crickets chirped and the chatter of parents surrounding me was a soothing sound. Across the field, one of the players on Bear’s team sat by himself while the boys scrimmaged around him. I had arrived late so I wasn’t sure what had happened… whether it was injury or disciplinary.
Bear, who usually plays center (that boy has an impressive hike in shotgun formation) was playing defensive right tackle instead. I watched as he ran, bringing down boys in tackles and never giving up on attempts. At one point, he crossed the field, dove after the runner with the ball, almost got him, rolled, got back up on his feet and trust me, if he had 10 more yards, he’d have had that boy down. I could hear his coach yelling, “Bear! Whoa! Way to be there, Bear!”
Over and over I could hear the coaches, “Give it all you got, boys”
“Leave it all on the field.”
“Good job boys.”
“All in.”
I heard the boys roar in response, saw them fist bump and chest bump and smack each other’s backs in encouragement.
As they played, one of the coaches walked over and dropped next to the boy sitting alone, and they talked for a few minutes. Then coach helped him up and carried him on his back to the sidelines and his mom. His ankle was wrapped, but he was joking with coach on the way over. It was a sweet and gentle sight.
The coach walked back out onto the field, yelling plays, pointing where kids needed to be, encouraging, commanding, leading. At one point though, he stopped the whole team.
“Guys. Stop. Be quiet. Do you see that?”
He pointed to the v-shaped gaggle of geese flying overhead, honking boisterously. As they watched, the lead goose fell back to the end of the line and another one took his place leading them southward.
“Do you understand what just happened?” Coach pulled the team in a circle around him and described the teamwork they had just witnessed. “They all work together and follow the leader. When he tires, he falls back and another goose steps up.” He pointed to each of them around the circle, “That is what a team should be. Work together, all moving together, watching each other and helping. You step forward when another can’t. You fall back and let others help. You. are. a. team.”
They roared together jumping up and down, waving helmets overhead, watching the geese disappear in the twilit sky.
This, y’all, this is why I love this beautiful game. I love the respect for authority, the leadership, the athleticism, the community, the dedication, the teamwork.
Oh, y’all, the teamwork.
All in, boys.
All in.
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The Pulled Rug
It has happened again. The rug. Pulled out from under our feet and we are upended. Reeling. Sad. Clinging.
I saw the doctor to finally get answers about the kidney stone, aptly named Stanley by a friend of ours. The good news, Stanley is gone. No. more. stone!
However… they see more on the ultrasound than they would like. There is a mass of some sort in the kidney. A small one, thankfully, but a mass. They are going to schedule an MRI (am still waiting on date for that) which should give him more of an idea of what we are dealing with. Top choices are: a cyst (but it doesn’t look fluid-filled), breast cancer metastasis, or a whole new cancer–kidney cancer (which would bring us up to five different types).
Reeling. Sad. Clinging.
Once they know more from the MRI, they’ll go in with a needle to deal with the mass. If it’s cancer, they’ll burn it up with radiation and then they’ll just watch the area. So it’s overwhelming, but not huge like some other news we’ve had.
I told our children. Y’all, I am so tired of seeing the fear, the sadness, the loss on their faces. So very tired.
Reeling. Sad. Clinging.
I am tired of the rug being pulled out from under us, but at the same time, I accept that this is our life. Incurable cancer does this to you without warning.
But here’s the thing. He puts it back. The rug, woven through with the tapestry of our lives. Our God puts it back. He doesn’t leave us floundering and trying to get our footing. And each time it is pulled from under us, we get to see the Rock we’re standing on. And each time He puts it back, the Rock feels firmer under our feet.
I wonder.
May I use some hopefully sanctified imagination here? After all, as Frances Schaeffer wrote, “The Christian is the really free man–he is free to have imagination. This, too, is our heritage. The Christian is the one whose imagination should fly beyond the stars.”
I wonder if that rug will sit on the floor of our mansion in heaven? I like to think that I’ll see it, that I’ll run my hands over it and remember His goodness…
“See that?” I’ll say, “That green? That’s the grass in which we smothered our bare feet, trying to taste the goodness of God’s earth. And that? That gold? That’s the gold of sunsets we watched out the window and marveled at His beauty. The black? That’s the inky darkness of long nights, of midnight cancer… but every black strand turns brilliant yellow as the light emerged. And this red? It’s the cut of every knife, every incision into my body, every needle prick, every scar. And the blue? It’s the water He gave me to drink daily through His Word. Look, there’s the pink of ribbons friends wore to honor me. This purple? That’s the laughter of my children. There’s a lot of purple in there. And white… the purity of my Brian’s love for me, an example of Jesus. And look, more red… Jesus’ blood shed for me. And this one, look how much of this clear strand there is. These are the unseen prayers of those who loved us, their tears. My tears are over there on that shelf in a bottle. Theirs are in bottles, too, but this rug is woven with them, too (I’m not sure how that works). And look at the brown and white and yellow in all different shades, these are the arms of those who carried us through. And all of it, a remembrance of His faithfulness to bring us through. Shot through with His mercy, goodness and grace. Isn’t it the most beautiful tapestry you’ve ever seen?”
I have sat with friends this week to weep, enveloped in hugs of care. I have poured out my heart and rocked in Brian’s arms. I have wiped the tears of my children. And held my dear friend, her head on my knee, my head on hers while voices covered us in prayer. We are held. And through it all, you are adding to the beautiful tapestry in my life.
Would you continue to pray for us?
I keep searching for the answers to my doubts
It’s like I’m caught between belief and wanting out
But there’s this promise that my soul just cannot shake
That I am loved despite the struggles of my faithAnd now that my eyes are open
I can see that I am stronger broken
You’re the mystery that I put my hope in
More I seek, the more I find
Don’t want to live like I’m an orphan with no bed
Still I keep searching for a place to rest my headBut I have all I’ve ever needed
Help me trust beyond what I’m not seeing
To be content with all this grace You’ve given
In my weakness You are strongYour grace is my sole sufficiency
Your power is made perfect when I’m weakJust want to shout it out for the world to hear it
That I’m His kid no matter what I’m feeling
I’m doubting doubts, I just cannot help believing
That I am loved no matter what
I am loved no matter what! -
Midnight Cancer
Midnight Cancer
is a bottomless pit
where voices echo
around and around
endlessly
repeating the same
prayer:
oh
God…Sooner or later, midnight
cancer changes to
morning
cancer,
brighter,
more hopeful.
Somewhere in the sun
rises warm and round.
Birds are singing.After a while,
morning cancer melts
into afternoon cancer
where it hides among chores:
cut the grass
clean the downspouts
drain the noodles.Later, the house falls silent
and even the dog is asleep.
There might or might not be rain.
Without a sound
you are falling,
arms wide and circling.
It’s midnight
You have cancer.~Mary Braddish O’Connor from her collection “Say Yes Quickly.”
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Protection
A repost from years ago, because I need the daily reminder that He is with us:
The children love to climb the ladder to our attic and explore. I needed a few things so I asked for their help, happy to incude them in our daily tasks. The boys were up top grabbing the items we needed and handing them down to me. Bella-girl stood on the ladder with me behind her holding her so she wouldn’t fall. She began climbing down, and one of the boys began moving things back into place, finishing their job and not seeing what was coming…“Don’t! Don’t! Don’t!” I heard the other boy shouting, insistently, almost fearfully.
It was too late.
Looking up, I saw it rolling. A barbell with weights on it. At least 20 pounds of metal and bolts and pain falling towards us, right on top of her.Then I heard her screams as I pinned the weight beside me with my bad arm (I don’t know how) to the back of the ladder.
The boys’ faces, white, peered from the attic hole and Bella’s wails of “Oh, it burns! It BURNS!” pierced. I grabbed her with my left arm, the weight with my right, and climbed down the ladder, trying to soothe her screams.
“Is there blood?” she asked through sobs. I was terrified to see what had happened.
I looked.
No.
In fact.
There was nothing.
From a human standpoint, I have no idea how she was uninjured.
The weight must have only grazed her lip.
I don’t know how.
But I do know how.
It was God’s protection over my child.
And it was protection over the heart of a little boy who didn’t see the weight he accidentally knocked out… over the heart of another boy who saw it coming but couldn’t stop it… over the heart and body of a little girl who could have been horribly injured.“Mommy! Mommy! Mommy!” she kept saying it over and over, like a mantra. She just needed me close. Then she finally said, “If you hadn’t been there…”
“But I was, dear girl. I was.”The illusion of control, as my sweet friend, Beth, says…
I like to think I have it.
I don’t. And it’s moments like these in our ordinary days that remind me I am not in control of anything.
But He is.And He spared my girl today. He spared all of us.
It’s the daily reminder I need. That He is in control. He is guarding and protecting us.
Honestly, I shook for at least an hour after this happened. I hyper-ventilated in the bathroom and called Brian to talk me down from a panic attack.
What might have been attacks me and plagues me still…As I look back over my life, there is so much pain, so many falls, and I find myself crying, “Jesus! Jesus! Jesus!” like a mantra. I need Him close, “If YOU hadn’t been there…”
I hear His whispered reply…
“But, I am, dear girl. I am.” -
This Beautiful Ache
It’s days like these that make me ache.
I ache with the sweetness of a simple day, curled up with my Brian for the morning together, tinkering around the house and running errands “just us” before the children come home. It makes me realize how much I am looking forward to his retirement and us having long days of togetherness. I told him this after he picked up a prescription for me, giving me time to rest in the car. He laughed and said, “We’ll be just like your mom and dad, puttering around and going everywhere together.” He couldn’t have offered a higher compliment. I love the way my parents love.
I ache with the struggle to even dream about the future. This month is two years of living with Stage IV metastatic breast cancer. At diagnosis, most MBC patients are given two to three years to live. Only 15% live more than five years. How do I dream about a future when these are my odds? I can’t tell you how many times I am asked about when I will be done with treatment, when I will feel better, when it’s over, and I have to face my reality yet again and answer, “Never.” Treatment ends when we choose to stop or when I die. How do I dream when this monster threatens me every single day?
I ache with the gratefulness for life. As of right now, treatment is keeping the cancer suppressed. We don’t know how long it will stay this way, but it’s suppressed today, and I am living life with my loves. I am having days like today with my Brian. I’m reading more and more articles about women who are beating the odds, of how MBC is still incurable, but it’s becoming more treatable. My oncologist told me of one of her patients who has been on my same oral chemo for over ten years now. I want to groan about ten years of feeling this way, but then my heart beats with thankfulness that this is even a possibility.
I ache with the kindness of friends. Friends who bring warm pasta with fierce hugs. Long chats with friends who understand suffering and for the truths we speak into each others’ lives. Friends with whom I can dream and talk about our bucket list of things to do together, who aren’t afraid to plan with me and dream with me, even though they know my fear of dreaming, who make me feel normal. Friends who text just to see how I’m doing and to tell me how they are.
I ache with the fear I have some days. The what if’s? I fear for my children as I watch their fragile strength. I want someone to tell me they’ll be okay. If I am gone in a year, they’ll be okay. I want to hear from someone who knows, and then I look at my own father who lost his father suddenly at a young age, and I know. I know they’ll be okay. My Brian will be okay. It would devastate but not destroy, but I fear for the devastation it could bring.
And I ache with the hope that conquers the fear and the struggle. The hope that is deeper than life here and points me to life eternal. The hope that has justified, and sanctifies and will one day glorify. The hope of “what is” instead of “what if?” The hope that isn’t about odds and is about soul healing (and sometimes body healing, too). The hope that anchors my soul, that points me to the blessings I have… a cup that overflows.
And I ache with the tenderness of it all. The beauty of simple life with a caring man. The beauty of watching my children grow and live. Oh, y’all, nine years ago, the first of four of my diagnoses came. A dear, dear friend, who has walked with me since the onslaught began, sat with me days ago and said to me, “Ang, we begged God for time for you, for time with you. Look how much time He’s given. We beg Him for more, but look what He gave.” And I wept with her over His wonderful goodness.
I ache with the color of flowers on my porch and turning leaves in golden sunsets. I ache with the warmth of long evenings over glasses of wine laughing hysterically with friends over the antics of our children. I ache with the quiet nights curled under new fuzzy blankets with Bella girl’s head on my shoulder, arms intertwined with hers. I ache with the pride of a mom watching her boys run and tackle and seeing the joy on their faces. I ache with the comfort of Jesus, how He has walked this way before me and never, ever turns His back on me. I ache with not just the truth that He won’t turn His back, but with the truth that He can’t, because He keeps His promises to hold me fast.
Yes.
It’s days like this that make me ache.
There is so much in this life that makes me ache.
Some days the ache is deep and hard.
But today, the ache is beautiful.
“What makes the desert beautiful,” said the little prince, “is that somewhere it hides a well…”
(~Antoine de Saint-Exupery)







