The Light Around Me. Gauntlet Story Feast

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LightFinal

This week’s Gauntlet story is written by a young woman who shines her light and the light of Jesus through her own deep pain. I’ve learned to move from the shadows of fear and despair into glistening hope by watching her faith endure. In our community of suffering we band together and whisper to one another,

“Don’t be downcast, soon the night will come,
When we can see the cool moon laughing in secret
Over the faint countryside,
And we rest, hand in hand.
Don’t be downcast, the time will soon come
When we can have rest. Our small crosses will stand
On the bright edge of the road together,
And rain fall, and snow fall,
And the winds come and go.
And so we seek the light, my Friend,
Silken threads glinting in the gloaming,
Woven into heartbeat, breath and tear,
Sweet Jesus, always, ever near.”
–Herman Hesse

The Light Around Me
By Emily Dreyer

I woke at 2am with the left side of my spine, shoulder, and neck on fire. As I lay awake praying for the pain to calm, all my thoughts, doubts, and fears kept running themselves through my mind over and over again. Like some kind of horror movie that just won’t stop repeating itself, all I could feel and see was the pain of it all. I’ve found that even if you seem sane the day before, when it’s just you and your thoughts in the middle of the night it quickly becomes easy to question your sanity. Yet as I lay there I found my eyes were fixed on the cluster of glow-in-the-dark stars that I had stuck on my bedroom ceiling years ago. I couldn’t help but think about (as the saying goes) how “the darker the night the brighter the stars”. As I began to ponder this, I began to think about light and darkness. How does one stop the day from becoming night? How does one chase the shadows back into light? I do not know, and oh, how I wish I did. And though there may not be a way to remove myself from the darkness around me…I can still see the light.

I can see light reflecting off of my friends, the people I love. I can see the light shining through others even when they themselves cannot see it. I can see it struggling through a suffering friend who puts one foot in front of the other just to get through each day. I can see it radiating from another beloved soul even as she sits in the ICU while her daughter is in a coma nearby. I can see it shining off of a mom who can hardly take care of herself yet gives all of herself to care for her children. I can see it in the eyes of one who lost a child way too young after years of fighting for her life. I can see it through the smile of a doctor who is exhausted and discouraged yet who continues to fight. I can see the light all around.

What about when I can’t see the light in myself? Where do I turn when I can’t feel it piercing the darkness of my own pain? It is then I need to look to the light all around me. If you stare at the sun too long you’re left with bright spots in your squinting vision, and if you stay in the darkness too long it takes longer to adjust to the light when you see it. So maybe this is just a poor sort of analogy to some glow-in-the-dark stars on my ceiling. Or maybe it’s a way of acknowledging the darkness you are in, while taking note of and looking to the light around. It’s a way of realizing that anything that happens or has happened in the past, will be okay. Where the light is the darkness doesn’t really stand a chance. Where the Lord is the darkness will not prevail.

“I survived because the fire inside me burned brighter than the fire around me.” –Joshua Graham

Emily (1)

About Emily in her own words:

I was diagnosed with Ehlers-Danlos Syndrome when I was 10 years old after two years of declining health and searching for answers. In the almost ten years since then I have had 22 neurosurgeries including a brain decompression, tethered spinal cord releases, numerous lumbar shunts, and cervical and thoracic spine fusions. I live in Michigan with my family, love to read and write, listen to music, and spend time outside. You can read more about my journey at http://www.carepages.com/carepages/EmilyDreyer

SHARE YOUR STORY. If you are walking a Gauntlet or are close to someone who is and would like to contribute to our Thursday community please email me at mkayesnyder@gmail.com, and I will send you the instructions for submitting. Share with anyone you know who might like to join our Gauntlet Story Feast. (Please use the hash tag #GauntletStoryFeast when sharing so we can find and follow one another.) Our Hope remains.

Photography by Cindee Snider Re. Used with permission.

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Even Giants Fall. Gauntlet Story Feast

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8438288434_4149a61076_o (1)

This week’s story is a flashback written by my friend Cindee five years ago. Many of us are not just walking the Gauntlet on our own. We have genetically passed the DNA glitches to our children and are navigating this painful journey with them as well. It is heartbreaking to see them suffer. In families like Cindee’s and my own, there may be a sibling who has been spared. All the guilt and gratitude the well child feels along with fear and sadness for their brother(s) or sister(s) swirls into a vacuum of physical and emotional pain we never could have imagined.

God brought Cindee and I together last fall in the most beautiful place at the perfect time in both our lives. Her kindred heart is treasure. She has faithfully covered me with her prayers and words. During my last plasmapheresis treatments she sent me a card with a poem every single day. Before my last surgery she filled an entire journal with handwritten quotes, poems and verses. They continue to be balm for the wounds of my soul.

Today Cindee is at appointments all day with her daughter Meg. They had PT this morning then four hours in the research unit this afternoon. Tonight they are helping genetics and their PT/OT clinic launch a brand new offering (Thursday Night Live) for teens with connective tissue disorders and their parents. This is what warrior moms do. We are not just fighting for our own children to have the most whole life possible but also for the ones to come after us. Will you please pray for my friend and her family today?

Even Giants Fall
By Cindee Snider Re

(This post was written about five years ago when Sam was 15 and about 2 years into diagnosis. Kyle was 17. The boys are now 22 (Kyle) and 20 (Sam). You may remember Sam shared his story here earlier. You will want to go back and read it if you missed it or are a new reader here.)

It was late Tuesday afternoon. My son Sam and I were driving home from Children’s Hospital. Traffic was heavy and although the radio was on, I wasn’t listening. Sam was. “It’s true, you know,” he said.

“What’s true?”

“That ‘you never know what you’ve got till it’s gone,’” he answered as the song’s chorus replayed in the background. “I never understood that before, never appreciated waking up and feeling good or being able to do whatever I wanted when I got out of bed. I just took it for granted, figuring it’d always be that way.”

Tears welled in my eyes as I struggled to find words to answer my son. In February, he’d been diagnosed with Eosinophilic Gastroenteritis, an auto-immune disease affecting his GI tract. He’d lost 22 pounds in ten weeks and spent time in the new acute care wing of Children’s Hospital. Sam’s illness had caught us off guard. He’d been a physically strong, able, active teen who regularly ate us out of house and home, and suddenly, overnight, he wasn’t eating at all and rarely left the house, rarely left the recliner.

Tuesday afternoon, four months into treatment, we were heading home from more appointments. “I’d give almost anything to go back to before I got sick and really appreciate what I had,” Sam continued.

His words sliced through my soul. “Oh Lord,” I prayed, “why does my son have to go through this? He’s only fifteen, such a hard age to be different, sick, unable to eat his favorite foods or go out to eat, and he never, ever complains. He just gets quiet and tries so hard to focus on something, anything besides the pain. This is hard, Lord!” I silently cried out. “And I don’t know if I’m strong enough to help him through this.”

My oldest son, struggling with similar emotions and rocked by the changes in his brother and their relationship, poured his heart out in song.

This is a song of my greatest friend,
The one whom I love and would die to defend,
Whose honor and loyalty have no compare,
A soldier in a battle, too much to bear.

(Chorus)
I thought that you were unbreakable
That my faith was firm and unshakable,
But now I find that I was wrong.
There’s only one Being who’s that strong.

I can’t stand that you’re in pain,
And I don’t have the power to take it away.
It’s just too much for me to take,
That even a giant like you could break.

(Repeat Chorus)

So hold on, Sam, this storm will pass.
Just hold on, Sam, this pain won’t last.
Hold on. Hold on. Hold on.
God’s got you in His Hands.

I feel like I’m dying on the inside,
And I’d rather run than face a lie, cause
When it comes to compassion, I’m hit or miss
But you stand and say that we’ll get through this.

And He’s watching, watching out for you,
Just have faith, and we’ll make it through
Together.

“Father, there are no answers, just questions and emotions and a family holding on in faith, knowing You’ll see us through, and that we’ll make it there together, hand-in-Hand, standing strong in You! Amen.”

Cindee

About Cindee in her own words:

I’m wife of 23 years to an amazing husband and mom of five creatives — Kyle, 22, Sam, 20, Sarah, 18, Anna, 17, Megan, 14. We’ve homeschooled for 16 years — kindergarden through high school. Quite an adventure! Our oldest graduated from college (with honors!) in May. Our home is often filled with teens/early 20s I’d claim as my own in a heartbeat. I love words, photography, nature, hiking, cotton, denim, and tea. And I crave quiet. Four of our five (and me) have Ehlers-Danlos, a genetic connective tissue disorder, through which I’m learning the deeper the valley, the greater the joy. I live in hope, grateful for grace.

Cindee’s blog can be found at http://www.breathedeeply.org

SHARE YOUR STORY. If you are walking a Gauntlet or are close to someone who is and would like to contribute to our Thursday community please email me at mkayesnyder@gmail.com, and I will send you the instructions for submitting. Share with anyone you know who might like to join our Gauntlet Story Feast. (Please use the hash tag #GauntletStoryFeast when sharing so we can find and follow one another.) Our Hope remains.

Photography by Cindee Snider Re. Used with permission.

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Dear God, Please Take My Hand. A Prayer Gift. A Healing Prayer

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Prayer Beads
“Of all spiritual disciplines prayer is the most central because it ushers us into perpetual communion with the Father.”–Richard J Foster

I have always loved holding on to something physical when I pray. I have a collection of special rocks, some painted or engraved with words, several are special gifts from friends, a cross made from olive wood gifted to me last fall from a woman I just met who is now a dear kindred sister, and a delicately embroidered handkerchief that was Dan’s grandmother’s. These objects have no power or influence over the prayers, but they keep my focus on praying.

Yesterday I received a package in the mail from a friend I met at The High Calling retreat last November. I’ve written about her before and even shared her newest book with you. She knows about physical suffering and understands the struggle to keep your mind and heart on prayer when pain overwhelms you. The gift was beautiful smooth pink prayer beads with a silver cross attached. They come from Prayerworks Studio. They are not a rosary, but Protestant (Anglican) beads. I know I will use them as I do my other objects, something to hold while I lift my heart, but they also have specific meaning as a “Full Circle Prayer.” It is described like this:

This devotion is intended to take us through a complete path to God, one that puts a “new and right spirit” within all of us: praise, confession, intercession, and thanksgiving.

Cross: In the name of the Father, Son and Holy Spirit, Amen.
Invitatory Bead: Create in me a clean heart, O God, and put a new and right spirit within me. (Psalm 51:10)
1st Cruciform Bead: I praise you, Lord, for . . .
1st set of Week Beads: use each bead to praise God for His wondrous acts of grace.2nd Cruciform Bead: I ask, Lord, for forgiveness for . . .
2nd set of Week Beads: use each bead to confess your sins before God.
3rd Cruciform Bead: I pray, Lord, for . . .
3rd set of Week Beads: use each bead to list prayer concerns for yourself or others.
4th Cruciform Bead: I thank you, Lord, for . . .
4th set of Week Beads: use each bead to recall something for which you are thankful.
Invitatory Bead: recite The Lord’s Prayer
Cross: In the name of your Son, Jesus Christ, Amen.

Sometimes I pray like I’m a child. This is the easiest. I’m just talking to my Father. Other times I pray properly, like I’m being graded for getting all the “right” things in when I approach the throne. There are prayers when I groan and no words will come at all. This is when I believe the Holy Spirit is carrying my pleas and Christ Himself is praying for me. I spent much of last year studying prayer. I now own a shelf full of books on the subject. I’m most grateful for the wisdom from Richard J. Foster’s Prayer: Finding the Heart’s True Home. Richard writes,

“I discovered that regular patterns of devotion form a kind of skeletal structure upon which I can build the muscle and tissue of unceasing prayer.”

I realized that much of my “pray without ceasing” life was throwing out little thoughts towards Him throughout the day and calling it prayer. After reading Richard’s book I began set times during the day to pray. I haven’t always been a knee praying person, but I knew if I was to follow the discipline of a pattern of prayer I would need a place, and it might need to be a little uncomfortable. This is when I bought my prayer bench.

Prayer Bench

The past few months I have struggled the most I think I ever have to find words. I kneel at the bench with my heart broken open, and I cry. It is during these times I am grateful for the prayers of other saints lifted up and also recorded. I read them out loud. I repeat them. I thank God they found the words for me. The following prayer is one I took to the hospital with me for my surgery, and I have prayed it over and over again since.

Dear God, please take my hand and help
me walk through this fire.
Don’t let me slip away, please hold me
in your power.
Help me see the light and to hold on
tight, to have faith.
Help me to learn what it is you want
me to learn.
Help me retain my dignity and help me
to accept what I can’t change.
Guide me … sit in my heart.
Don’t allow despair to swallow me.
Please God, show me a road out of here.
Help me find the strength to cope …
and to grow.
Help me regain my health … please God.
Carry me if I can no longer manage to
stand,
and set me under the shade of your tree
so I can heal.
Please show me the path to peace, and
mend my heart.
God, I am powerless in this valley of pain,
please lift me up and always let me know
your presence.
Please be in my heart and take my
shaking hand.
Amen

A Prayer By Sherry Larsen

Is there a written prayer you cherish? Do you find discipline aids or hinders your prayer life? I’d love to know what God has taught you about praying.

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Sweet Tea and Jesus

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Sweet tea

I have been quiet here. I continue to write elsewhere like I breathe. The fire of suffering the past months has been wild. Just when I think it might be under control there is a flick of a cigarette. The wind blows the sparks over my dry bones, and once again I am choking in the smoke of loss. Deep pain, my own and that of those I love, fans the flames. My pride keeps me from putting my whole heart here. I fear if you truly saw my charred fleshy wounds you would want to turn away. I’m finaly beginning the hard work of sifting through ashes. I’ve been through too many fires to doubt there is beauty here somewhere. I’ll find it. I will. Until then my God and my friends sit in my lament and let me cry.

I am continually amazed at the reflections of my life through blogging. The following post is from a year ago to the day, August 10th, 2014.

Today was the last Saturday of our summer. From the second I woke up I held on to moments like golden strands of fine thread needing to be tied off carefully so the tapestry won’t unravel. I am not sure if I ever fully believed God might give me a day like this . . . or a week . . . or a month . . . or three months, but I fought like He might, and He did.

I have been in recovery. I am a person who lost part of my brain and my soul. I have been relearning the simple things in life most people take for granted. I am in many ways like a child. If you spend time with me I will probably exclaim out loud about a hundred things you think are ordinary. I may have seen them or heard them, smelled them, tasted them or felt them before, but it has been years since anything did not pass through the brutal filter of chronic pain.

Dan and my girls are getting to know me again.

Delaney told me today I was funny. She only ever saw this mom in old home movies. I was the crazy one drinking a bloody mary for breakfast while dancing around the living room doing Elaine Benes impressions and belly laughing. I still believed life was good. She will tell me “Thank you” in an “I can’t believe you were able to do this for me way” for normal mom stuff like making her a peanut butter and jelly sandwich. It takes me off guard until I remember she has been making her own lunch and Danica’s lunch for too long. She turned around from the yard and said to me tonight, “I’m so proud of you mom. You’ve been through so much and still you provide.” I asked her, “What do I provide?” Her answer, “Kindness and love.” A tear falls, and I think . . . maybe she is going to be okay after all. Maybe I haven’t hurt her too much. Maybe she sees the big picture at almost twelve years old. Only the gift of the summer we’ve had could give this kind of clarity.

I see flashes of pure joy on my husband’s face when his old Monki shows up. I’ll do something simple for him like a wife might do for her husband. Maybe it’s just asking him if he needs a drink or a bowl of cereal, but I know symbolically it takes the tiniest bit of the incredible load he has carried for so long off him. It starts to tip the balance back to give and take instead of him always giving and me always taking,

For Danica it is different because our relationship was built on pain, mine or hers, and she doesn’t remember me any other way. She is thrilled to have a mommy planning playdates or going shopping with her, but she is not tenuous like Dan and Laney are. For Danica the fact her mom is out of bed is just her life today, not something she’s terrified we might lose. Still, her bedtime prayers have changed. Every night for as long as I can remember she would end with her little plea to a big God, “Please make mommy better.” I would cringe wondering how messed up a child’s faith could get if the answer never came. Slowly this summer she has moved on to pray about other things and for other people, letting me slip off the list. I love knowing her tender heart is getting a break from worrying about her mama.

During my plasmapheresis and IVIG treatments I made a list of things I really wanted to do this summer if I was well. Some of them were simple like taking the girls putt putting yesterday. Others were bigger like attending an outdoor concert, a major league baseball game and a trip to the beach, all activities that brought me true enjoyment before I became so ill. We never got to the bigger things because of money, but in some ways I think it was for the best because we learned how to live and love in this sacred space of home and everyday life again.

I also set out to lose steroid weight and become thinner over these summer months. This hasn’t happened, because I’m hungry for the first time in years, and I want to eat. I’ve realized the part of my brain that forgot how to enjoy anything is loving food again and drink and the community it invites too. I’m letting myself remember these right now. I’m showing myself grace. This body has been through hell. It’s okay to look in the mirror and respect the wonder of flesh and blood surviving all I have no matter what the scale says.

This evening our family was hanging out on our deck. We had just finished my “famous” corn dip. The sun was setting behind the trees. Over the Rhine was crooning “Favorite Time of Night” from our playlist. The girls and Twixie were playing badminton and soccer. I got that thick feeling in my throat as the cicadas sang. I felt my anxiety about all we are facing financially begin to sprout in my mind and try to rob me of the perfect night. I felt my fear about the evil in the world and the sadness for the suffering and brokenhearted. Why are we allowed to be here like this when so much of humanity is wailing tonight? Why does my heart ache over my own medical debt when people are starving and dying? How do I balance the goodness of God with all these things?

I have always been too serious. Life has always been a struggle between the highs and lows. I feel everything too deeply. I think about you and you and you, and I pray for you too. I wonder how you are today. I’ll write you a note to let you know. I’ll buy you a gift when I see something that makes me think of you even when I can’t afford it. If I just met you I want to cut through anything casual and hear your story. I want to know what you read and the music you listen to. I want to know what makes you laugh and what makes you cry. I know for sure God is real, and I’ll give the reason for the Hope in me. I know for sure life is hard and love is real, and we have to keep believing no matter what. All this is exhausting. Most don’t have the stomach for it and need to numb themselves or dumb it down as a coping mechanism. I get this. I do. I’ve tried to change. I’ve tried to medicate away the very thing I am learning is most likely a gift not a curse.

In this age of trying to capture our feeling in a facebook post or a tweet, I try to imagine telling some kind of narrative in just a few words. It’s not natural for me. Most of the time I just can’t do it, and I run to write for real in places no one reads. Instagram is a little easier. After all a picture is worth a thousand words, right? Sometimes I run to grab my camera and capture the way the light is falling or the girls are playing. I’m grasping to simplify what has always been so complicated for as long as I can remember. I don’t often succeed. On the rare occasion it happens it is usually just a few words strung together, hanging out there like a mantra for my soul. My OCD brain holds onto them, and I chant in my head like a child rocking to sooth away the day and finally sleep.

Today it came in a pillow that showed up in the mail.

SWEET TEA AND JESUS.

This I know.

I feel my symptoms returning slowly. I have quietly let the people who need to know begin to monitor how far we let this go before I get help again. I’m terrified, because I was released from a kind of prison, and I need to be free like this no matter what. No matter what the cost. No matter what the toll is on the people around me. No matter how many more scars. I can’t go back where I was. I knew another round might be needed. I remember asking, “How long will this last?” The answer was, “We don’t know. Maybe three months, maybe six . . .” I scribbled this in my little notebook I kept in the hospital those worst twelve days.

SWEET TEA AND JESUS. SWEET TEA AND JESUS. SWEET TEA AND JESUS.

This I know.

. . . It’s Sunday morning now. No church for us. Dan and the girls have taken a month off, and I am not sure when I can go back. I’m not sure why, but it has been good. We slept in until almost nine. All of us. We had coffee and breakfast and played Scrabble. I am so tired from my twitching body and racing mind. Symptoms. Our family will work on thank yous today. Gratitude for a family who gave us Christmas in July. It was amazing. Gratitude for a used laptop that showed up on our back deck when mine died. Someone who knows my world is still small and the keyboard and screen are the place I sort things out and reach out and am touched by you too. Gratitude for a friend who tells me this. “I don’t believe God brought you this far and provided all you need to walk away from the help you might still need to fight for your life.” She’s right. I ask, “Do we have everything we need today?” Once step in front of the other. Be faithful. Do the next thing. Love harder. Celebrate the gifts. Give the rest to Him.

SWEET TEA AND JESUS.

This I know.

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Do you See? Gauntlet Story Feast

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*“Our whole business, then, brethren, in this life is to heal this eye of the heart whereby God may be seen.”–St Augustine

DSC_0156

I wrote the following post December 2, 2011, having just returned home from my first neurosurgery. I’m now snuggled under the same quilt in my own light filled home recovering from my seventh neurosurgery. I am so filled with suffering I can scarcely breathe. It is not the physical hurt. I’m convinced I could win a pain endurance trophy in a suffering Olympics. I am only slightly bothered by intense post surgical pain, because I can mentally understand it. Compared to the headaches before this latest fusion and the insane burning of my hands and feet, both of which resolved instantly with the pressure removed from my spinal cord, I know this is the good kind of ache. This is skin and flesh binding to one another over additional scaffolding in my delicate spine. The suffering I face now is in my mind and my heart.

I believe I see clearer than ever, but those who have necessarily walked this Gauntlet with me seem to have cloudier vision and lost more perspective each time we’ve done this. Maybe they are just tired. My oldest daughter, Delaney, came to the foot of my bed yesterday. We were talking about upcoming school shopping and in the honesty we’ve always shared she said, “This is just hard. You are grumpy, and I know it is because you are hurting, but every summer is like this.” I am wrecked. The truth is I have one of those “on this day” apps for Facebook, and I realize how many years we have been in continuous crisis, leading up towards it or recovering from it. Dan and I had a fight last night. We don’t fight. Ever. Truly. I sometimes want to give him an out. He has to want that. All I wanted was a hug. He said I was too “brittle.” I know he wonders if he will ever have his wife back. We both know he is not cut from the cloth that cares for someone sick long term and certainly not disabled. He cannot advocate. He can barely sit in a hospital room. I don’t think his love for me is tied to this. I think it’s just too much to ask of him. I know that’s a real thing. You’re a fool if you think it’s not. My dad reminded me recently one of the most painful things I know to be true. “Most men would have left.” It is only my little Danica whose empathy seems to know no bounds. Although she cannot remember fully her own surgeries or even the months of being held in a brace which kept others from real touch she finds me and clings to me in the awkward way you must when your mommy is wearing an Aspen collar all day and night.

I see like the blind man who Jesus took outside the city and spit on earth and covered his eyes with clay and healed him. When I read this oh so old post I almost laugh at the beginning of that miracle in my life. Surely it was not only meant for me. The suffering I feel today comes from my vision being almost crystal clear and less myopic every day, and the paralyzing fear those close to me are seeing less and less. As I wade through my usual post surgery self pity I push to begin going back to work. I am finishing my book. I edit based on these new stories I’ve gathered and the added perspective they bring. I realize more than ever this book is for those of us who drag our chairs around in a circle each week and say, “Hello, My name is Monica, I have,” and we state the laundry list of conditions that are not us but that make up our bodies and have become the threads that hold together our lives. We share the things even those who love us most and try the hardest can only make out through a mist.

Nora Gallagher was presenting at a writing conference in Washington DC the weekend our family left for the beach. I desperately wanted to attend. I took her book Moonlight Sonata at the Mayo Clinic to read on our trip. I suggest anyone beginning or walking through a journey in the world of illness and medicine and sorting out their faith in the darkness and sometimes blinding light the long walk brings to read this honest and beautiful narrative. In her last chapter she writes:

Following Jesus was meant to be an ongoing movement, not a creed, not a wall of set in stone words. A place where practices, like prayer, like meditation, were taught, where stories and memories, largely about vulnerability and suffering were collected and shared. The body’s pain and suffering were meant to be a part of this whole: I don’t think Jesus had in mind a place where you had to tolerate the empty predictability of a service and stand upright at the coffee hour if you had been diagnosed with lymphoma or sarcoidosis or lung cancer. He was, at the heart of his ministry, a healer.

And the stories of his followers were meant to be taken seriously to become part of the ongoing larger Story. A river of stories, joining the sea. The living stories of a faith’s followers are what keep it alive.

I have more regard for how each of us finds a way, the man in scrubs playing the Moonlight Sonata at the Mayo Clinic, the girl in the wheelchair, the boy with no hair running in the wind, each of us feeling our way in the dark. “The infinite value of one human being,” a friend said, “isn’t that what it’s all about?”

This land of illness, behind the wall, is much larger than I thought, and through its lens, the world we all live in, what we call the natural world, becomes more precious. I said I would give quite a lot to have my own body back, but yesterday I saw the evening light falling on the old oak trees in our park, their bark like the skin of elephants. This world is so beautiful, and not only can I still see it, I no longer pass through it quite the same way I did before. I, at least sometimes, am in it, in its beauty, in its enchantment, in its divine life…”

I want healing in so many ways, but more than any physical restoration I want the kind of heart healing that causes me to see Him clearly. This is my work. This is my calling. This gives me purpose in my suffering this afternoon.

Do You See?
By Monica Kaye Snyder
Written December 2, 2011

I’m sitting here in bed propped on many pillows and covered with my favorite “story” quilt from home. I’m looking at the sun glistening off the peaceful lake right outside the floor to ceiling doors and windows to the left of where I rest. I watch the dancing rays on the simple colors and patterns of the soft rug covering the hardwood floor. Classic and simple furnishings comfort me and are a present wrapped in the way beautiful space has always been a gift to me. There are pictures of people I do not know smiling at me. They have a summer life here, and because they are part of this big household of faith they opened their home to me to heal. I have wanted this. I have prayed for this. I have desperately needed this time and place more than I ever could have imagined. I see.

If you have been reading this blog from the beginning you know my theology has often brought me to ask many questions to a God I believed in and trusted but still held at bay when it came to His providence and how it worked in tandem with my sin. I especially questioned Him when it came to the suffering of Danica and my family. He recently brought me to this passage from John 9:1-3.

“As he walked along, he saw a man blind from birth. His disciples asked him, ‘Rabbi, who sinned, this man or his parents, that he was born blind?’ Jesus answered, ‘Neither this man nor his parents sinned; he was born blind so that God’s works might be revealed in him.'”

Four years ago Danica was born through months of intense physical suffering and great loss on many levels. The verse I would cling to was from Job 42:5, “I have heard of You by the hearing of the ear; but now my eye sees You.”

I have literally a hundred amazing stories to tell about my trip to Maryland and surgery and healing. They all speak directly of a God who is always in the details and thrives in showing His Grace through people. The morning of my surgery my sweet sister-in-law Amy took me to the hospital to get registered and get my PICC line placed. I did not feel so much nervousness as I did really dreading the process that leads up to actually being wheeled into the room and getting to the real business of surgery. If you’ve been through many surgeries you know that everyone comes in and meets you and chats about certain history and reminds you of the risks and complications that could arise and then has you sign a bunch of forms. There were two people during this process who blew me away. First I had to go over and register and show my identification and insurance card, etc. When anyone finds out you are a patient of Dr. Henderson it seems there is a special kind of reverence and care surrounding all the dealings moving forward. This sweet woman saw a countenance on my face that she instantly recognized as being a “believer.” She said, “I am already praising God with you for what will happen in that operating room today and during your healing.” I see.

When Dr. Henderson came in to speak with us he had his classic blue blazer on and held my hand tightly as he prayed over Dan and I. He asked for God’s guidance of each movement of his hands and each decision he would make during the surgery and then he asked specifically for my healing so I would further be able to glorify God by doing His will in His kingdom.

Stop. Read it over again. This man who would cut open my head and neck and painstakingly move around in my brain stem and spinal cord had just prayed the desire of my heart. All I have longed for is to be doing God’s will and giving Him glory. I know these heavy burdens are not given lightly. With them come great responsibility to bear them into something beautiful and eternal. This is why Dr. Henderson does this work. I cannot be healed and go back into a life anything like what it once was. I’ve SEEN and have to tell about it.

When I came out of surgery and began to get my bearings in the recovery room all I could say over and over was, “I CAN SEE.” The black floaters I had suffered from for years, particularly in my right eye, but most severely the last months as the pressure in my head had worsened were completely gone. As I type this now I have no obstruction of my vision at all. Although I am in considerable pain from the rib harvesting and my large head and neck incision I do not have the paralyzing vice grip in the back of my head. I do have quite a bit of nerve “damage” from the screws put in my upper skull to hold it in place during surgery. I have felt like my head is numb. I know many of these post surgery pains will take patient healing and rest to make it a true success.

I am praying that all the faith being made sight will unfold in your life and mine so the power of God can and will be seen in us.

About Monica Kaye:

Monica Kaye Snyder is a voracious reader. She is a blogger, a writer and maybe even an author. She continues a long journey of chronic illness and daily physical suffering. Some of her diagnoses include Chiari malformation, Ehlers-Danlos Syndrome, Tethered Spinal Cord, Craniocervical Instability, Postural Tachycardia Syndrome, Intracranial Hypertension, Mast Cell Activation Disorder and most recently PANS/PANDAS. She’s seen real miracles happen and holds on to Christ’s Hope as an anchor for her soul while living in great pain. She is wife to Dan and mother to Delaney Jayne and Danica Jean. She knows for sure if she does nothing else well in her life, this will matter and be enough.

MonicaBW

SHARE YOUR STORY. If you are walking a Gauntlet or are close to someone who is and would like to contribute to our Thursday community please email me at mkayesnyder@gmail.com, and I will send you the instructions for submitting. Share with anyone you know who might like to join our Gauntlet Story Feast. (Please use the hash tag #GauntletStoryFeast when sharing so we can find and follow one another.) Our Hope remains.

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I Said Yes. Gauntlet Story Feast. In Memory Of

by

Morgan

This post is late.

It is not written by a warrior but in memory of one.

I will never forget the first time I saw her striking beauty in the waiting room of Diagnostic Imaging in Lanham, Maryland. She was there with her equally lovely mother. She was wearing a classic tulip skirt and finely knit cardigan. She was tall and willowy with the most translucent skin, piercing eyes and perfect pixie cut. I waited for a long time. They were waiting too. I was finally called back. I had a brutal IV attempt for contrast, a painful CT scan and was sent out to wait some more for the tech to look at my images. I must have twitched during one of the pictures, because he let me know we needed to go back in to redo a few. I was crying. My arm was quickly turning all shades of purple. I saw these same colors in multiple bruises on the young girl’s long legs. They were the only outward sign there might be anything wrong with her at all. I glanced at her face. She was crying too. Our eyes met. We recognized the messy DNA in one another in an instant. We didn’t speak that day or introduce ourselves. Caught up in our own unfolding suffering we did not use an ounce of energy to form relationship or step into one another’s worlds. We did not need to. They were already overlapping in the venn diagram way the hearts and lives of each of us with these rare disorders are connected.

Much later, when I understood I needed ongoing plasmapheresis for my chronic autoimmune disorder, my dear friend Pam connected us online. I realized I “knew” her already.

Morgan Amanda Fritzlen.

Just as long as I have breath
I must answer yes to life
Though with pain I made my way
Still with hope I meet each day
If they ask what I did well
Tell them I said yes to life.
Just as long as vision lasts
I must answer yes to truth
In my dream and in my dark
Always that elusive spark
If they ask what I did well
Tell them I said yes to truth.
Just as long as my heart beats
I must answer yes to love
Disappointment pierced me through
Still I kept on loving you.
If they ask what I did best
Tell them I said yes to love.–Alicia S. Carpenter

SHARE YOUR STORY. If you are walking a Gauntlet or are close to someone who is and would like to contribute to our Thursday community please email me at mkayesnyder@gmail.com, and I will send you the instructions for submitting. Share with anyone you know who might like to join our Gauntlet Story Feast. (Please use the hash tag #GauntletStoryFeast when sharing so we can find and follow one another.) Our Hope remains.

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Recapture My Heart

by

DSC_0055

I wish your care was always easy, predictable, safe—
a cool drink
a soft pillow—
but you are too wise,
too loving,
too committed to your work of
transforming grace.
So your gracious care comes to me
in uncomfortable forms:
the redeeming care of
disappointment,
the unexpected
trial,
suffering, loss,
These things don’t tell me you’re
cold-hearted,
absent,
uninvolved.
No, each is a sign of
zealous grace,
redeeming love.
I struggle to grasp how much you
care,
so I struggle to rest in that
care.
You care enough to give me what I
need,
not what I want.
You care enough to break my bones
in order
to recapture my heart.

By Paul David Tripp

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She Will Pollute The Shadows. Gauntlet Story Feast. Our Stories Of Strength giveaway

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“The world is rated R, and no one is checking IDs. Do not try to make it G by imagining the shadows away. Do not try to hide your children from the world forever, but do not try to pretend there is no danger. Train them. Give them sharp eyes and bellies full of laughter. Make them dangerous. Make them yeast, and when they’ve grown, they will pollute the shadows.”― N.D. Wilson, Notes from the Tilt-A-Whirl: Wide-Eyed Wonder in God’s Spoken World

Laity1

I have written privately to my girls since they were in my womb in journals I will gift them someday. Dan too keeps a journal to them. We have amazing little rituals like writing notes to one another, especially if we are mad, sad or sorry. We have a treasure box where we keep them all. I know there are so many things we share that busy “soccer moms” might never get to with their kids. We snuggle a lot. We read and talk about what we read. We collage our visions and hopes and prayers for the seasons in our lives. We pray. Since writing “Gauntlet With a Gift” I have had this fresh perspective on the gifts that are wrapped in ugly packages like chronic illness and pain. I do believe our slow life, early bedtimes and lots of talking and listening to one another has shaped us. The compassion I see growing in both my girls for me in my suffering is forming their character.

Through all our hard we’ve tried to teach our girls these simple things. THE SHADOWS ARE REAL. Just because you know Jesus doesn’t make the sun shine all the time. THERE IS DANGER. Keep your eyes open. Laugh. You, be more dangerous. You, grow up bigger than the bad. You, shine brighter than the dark. YOU WILL POLLUTE THE SHADOWS, MY CHILDREN.

Delaney wrote the following as a paper for school. Because of the length and the necessary scientific references some parts are edited out. If you are interested in her full study you are welcome to contact me. I love she chose this topic to explore. I appreciate her honesty and conclusions about the juxtaposition of light and dark in a very difficult life for a child and adolescent to navigate. I grew from viewing our world through her eyes, and I hope you do as well.

Bringing Good Out Of Bad
By Delaney Jayne

In 2009, I was eight years old and found out that my little sister, Danica, had Chiari malformation. She was two when she had her first brain decompression. She was three years old and had to have a second brain surgery and rare spinal fusion. For a year and a half she was in a neck and brace and a wheelchair. Many long trips to Cincinnati Children’s Hospital for check ups left me at my grandparent’s house or with friends every time my parents and Danica were away. I learned to be independent early on because even when my mom was pregnant with Danica she had to be hospitalized in Maryland for three months, and I came to live in Ohio with my grandpa and grandma. I began kindergarten at Lake Center Christian School when I was only four years old.

Research suggests that when one family member’s health is challenged or unpredictable the whole family is affected. And while all children rely on their parents to help them feel safe and secure, parents in families with health concerns may be too preoccupied or overwhelmed to provide this attention. Other important family research states that some lingering negative effects on well siblings growing up with an ill sibling or parent may appear in late adolescence and early adulthood. Specifically, the later negative effect it has on their social functioning, including their ability to be comfortable and trusting in social relationships becomes a critical issue as a child matures. The results of the study also suggests that parent’s ability to manage the needs of their well children is crucial to their children’s resilience. If parents focus the majority of their attentions on the ill child at the expense of the well child, a higher probability exists that the well sibling would be susceptible to behavioral and emotional problems in late adolescence.

After Danica’s second surgery my mom quit her job to take care of Danica, and she was getting sicker herself. This, and many medical bills, led us to lose our home and live in my grandparent’s finished basement. Even though I had my own room, and we had our own bathroom, and a small kitchenette, it was a place to stay and not our home. My grandparents had just built their home one year before we moved in. It was brand new, but just like every basement there were bugs, very little sunlight and mold. My room didn’t have a window at all. This is when my mom started to feel even worse. She had several rough surgeries for endometriosis that had been growing all over her insides, but I think the stress of everything she did for Danica and the living environment made her feel the worst she ever had. She went to a doctor in Maryland and found out she had Chiari and EDS too. Her neck was always in pain and some days she couldn’t lift her head or even get out of bed. My life changed drastically when Danica had her first brain surgery and hasn’t been the same since. Really, it began back when mom got pregnant with Danica in 2007.

An issue of The Journal of Child and Family Studies published in 2012 states that when children grow up with a parent who has a chronic medical condition they are at risk for adjustment difficulties. Illness or disability in the family can have many effects, negative and positive. Differences in behavior, academic outcomes and psychosocial outcomes may occur. Many benefits can come as well, like becoming more responsible, being a kind and loving person, and valuing life.

Children in families with disability or chronic illness usually face real life concerns at an earlier age than most. This was definitely true for me. I feel like I had to grow up quickly because I had more responsibility for my own self care, school work, and around the house than most kids my age, One of the biggest ways my life is different than my friends is how much we are at home. My mom is in bed a lot and never knows how she will feel, so we cannot plan ahead, and I rarely get to have anyone to my house. She is allergic to all kinds of smells, so she has trouble coming to events at school and cannot go to church. She can be feeling okay one day and suddenly be very sick.

The American Academy of Pediatrics published a study that highlighted the positive opportunities of growing up in a home with a chronically ill sibling and parent. It can provide opportunities for the family to bond closely and develop resilience. For our family this is definitely true. No one understands how hard the past eight years have been for us. We appreciate small things and good days others might take for granted. I also have an understanding of pain that helps me be empathetic to others hurting. I know what it is like to lose material things and be aware of what really matters. I appreciate my mom and how hard she fights to keep moving. This has taught me to never give up. Even though we don’t do a lot of normal things, we have more time to just be together instead of running from activity to activity. For me, my grandparents really helped take care of Danica and I while my parents were away for medical reasons, and often times people provided meals on days where my mom was too sick to cook. I know what it is like to be loved by many other people.

Going through all this has been really hard for everyone in the family, and as I get older and grow up I will always remember everything that has happened to me through the years. It may make me feel sad or depressed, but I know many benefits have come out of it all. I have become more mature and responsible with my chores, taking care of Danica as well as my mom and much more. Most kids my age get together with their friends all the time, but I never have anyone over to my house except my friend Lauren. She has been my best friend since kindergarten and has stuck by my side since then. She has encouraged me through everything my family has been through.

My life has been full of sadness, and it has been hard to get through it all. There are times I wish my family was different, but I also know God is using the bad and the good to make me into who I am supposed to be. I have learned that family is very important when you are in a situation like this. God has also been a big part of it all. He has healed my sister and encouraged my mom mom through all her surgeries and treatments and trying to make it through day by day.

It’s true negative things can develop from growing up with a family member who has a chronic medical condition but many benefits can come as well.

About Delaney Jayne:

Delaney Jayne is twelve years old and entering the eighth grade in the fall. At four years old I let her leave me in the hospital in Maryland and come here to Ohio with my parents to begin kindergarten. She has always been fiercely independent. She sees the world through color, pattern and texture. She collects vintage cameras, lockets and art books. She loves Jesus, Audrey Hepburn and Harry Potter. She is friendly with all but has one or two close friends. She guards her heart. She dreams of traveling to Europe and having her own life far away from here. I hold her loosely.

Laney Trees

I am donating the highly anticipated book Our Stories of Strength: Living with Elhers-Danlos Syndrome as this week’s giveaway. Mysti Reutlinger and Kendra Neilsen Myles have beautifully woven together an inspirational collection of stories, filled with devastation, heartbreak, triumph, and strength as written by those affected by different types of Ehlers-Danlos Syndrome. Our community’s dear geneticist, Dr. Clair Francomano writes the foreword.

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WHEN DID YOU FIRST HEAR THE WORDS EHLERS-DANLOS SYNDROME? WHEN DID YOU FIRST SUSPECT YOU OR SOMEONE CLOSE TO YOU MIGHT HAVE THIS CONNECTIVE TISSUE DISORDER? Enter for a chance to win a copy of this amazing book by leaving a response here in the comments section of this blog post. Share this story somewhere on social media with the links below using the hashtag #GauntletStoryFeast. Each share will be an additional entry to win the book. The winner will be randomly chosen next Wednesday, June 17th after midnight and announced with next week’s Gauntlet Story. Don’t worry! If you don’t win, you may also click through the above link and purchase the print or Kindle version on Amazon. Please join the Our Stories of Strength online community here.

SHARE YOUR STORY. If you are walking a Gauntlet or are close to someone who is and would like to contribute to our Thursday community please email me at mkayesnyder@gmail.com, and I will send you the instructions for submitting. Share with anyone you know who might like to join our Gauntlet Story Feast. (Please use the hash tag #GauntletStoryFeast when sharing so we can find and follow one another.) Our Hope remains.

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An Inspiration. A Hero. Broken. Gauntlet Story Feast

by

Broken

This week’s Gauntlet Story Feast writer, Sarrah, holds a very special place in my heart. I met her through a local friend who shares an EDS diagnosis and the same neurosurgeon. She attended high school with Sarrah, and they reconnected online while she was in Boston getting her master’s degree. This friend opened her home so Sarrah could have needed surgeries in Maryland and recover here. Sarrah’s bravery to leave her dream job and seek treatment blew me away. Her courage to take her recovery at face value, move by herself to Texas and jump back into her career inspires me even more. This piece shows the achingly honest truth about the brokenness we suffer.

An inspiration. A hero. Broken
By Sarrah Hannon

An inspiration. A hero.

I’ve been called these things many times by family and friends. They have observed the events of my life and the hurdles I’ve overcome. And because all they see is the outward appearance I’ve adopted of humor, self-assurance and smiles, they tell me this is who I am.

My story is not heroic. It is not inspiring. If I am supposed to be an example of how to live when you’re dealt a difficult life you can’t control, I worry for others like me.

“You’re just being modest,” you say. No, I’m just being honest.

What people cannot see is the every single day struggle. I’m not talking about the physical struggle. The physical struggle is impossibly difficult but you develop ways of managing it. And while the pain is unbearable and takes over your life, it is sadly not the most paralyzing obstacle. No, I’m talking about the mental and emotional struggle. The one that you think you have handled at the start of every day until you realize that you’re just lying to yourself. You end up having the same arguments in your head repeatedly, no matter how many times you’ve had them before. And yet each time you come to the same conclusion after arguing both sides of the story; your life has changed, you have changed. That realization feels like a fresh wound every single time.

Just a few years ago I would wake up each morning the minute my alarm sounded. I would bounce out of bed instantaneously and be ready for work in no time. I performed my job with the greatest of energy, producing more work than 4 people in half the time. My mind was moving a million miles a minute while I assessed and analyzed each facet of my job. After work I was going to classes, getting my masters degree. Pushing my mind even further. I loved it. I was invincible. “A force of nature,” as my dad used to call me in high school. My type A personality and OCD served me so very well. My energy was poured into applying my extensive knowledge or, outside of work, pushing my young body to new limits. I handled all of my adult responsibilities with ease; money, taxes, appointments, vacations, cleaning, etc…I had aches, pains, injuries and even serious surgeries, but they didn’t stop me. My spirit was stronger than my body.

Not anymore.

I’m a shell of that person. It takes me a solid twenty minutes after my second alarm goes off to just convince myself to drag my body out of bed every morning; not just because of the pain but because I no longer have that thirst for the day. My type A personality and OCD are now a mortal enemy to me. I struggle to keep up with my adult responsibilities because of the anxiety that grows inside of me. My mind still runs a million miles a minute, but it is filled with worries instead of analyses. I get anxious every time I receive mail from a hospital or doctor, to the point where I simply do not check my mailbox. I get anxious calling doctors to make new appointments, and that anxiety completely freezes me when I actually have to attend the appointment. Cleaning seems like a daunting task, not because it will take me time to do it, but because I know that it will lead to hours upon hours of rest afterwards to recover.

I am constantly running the figures in my head to determine just how much energy I can spend. Arguing with myself about the things I really would like to do versus what my body should actually be handling. I convince myself that my pain is justified, and this is not big scary go to the ER pain. Minutes later I’m in a puddle of tears, because I have also convinced myself I’m being a baby. Suck it up, Sarrah, you’re not that sick. Minutes after that I’m reassuring myself its okay to feel this way. I AM sick.

They tell you that your faulty collagen will cause your bones to be less dense, tendons and ligaments to stretch, digestive tissue to shred, and anything else that uses collagen as glue to fall apart. This breaking happens over time, all at once, and most of the time more than once. They give you surgeries and medicine to temporarily patch these things up. Each break comes with a barrage of doctors who know what to do or can at least come up with a plan.

What they don’t tell you is that it will also break your spirit. And only you can find a way to put those pieces back together. Only you can figure out how to navigate the inner turmoil of re-defining yourself. No doctors can help. There is no plan. Every time your fragile spirit shatters you’re forced to pick up the pieces and define yourself yet again. But how many times can you do this? How many different labels and definitions can you give yourself? How many different people can you try to be?

An inspiration. A hero.

These are labels.
The sign I wear today says

Broken.

About Sarrah:

Sarrah is a 28 year old forensic toxicologist. She has three degrees, in chemistry, forensic chemistry and a masters in forensic science. Sarrah is a self proclaimed gypsy girl, growing up in Ohio, then living in West Virginia, Boston and now Texas. She is living with Ehlers Danlos and a host of other conditions. Recently she had three spinal surgeries. In her free time she’s a fervent pit bull rescuer and advocate. Her boy Orfie is her savior.

Sarrah

If you are walking a Gauntlet or are close to someone who is and would like to contribute to our Thursday community please email me at mkayesnyder@gmail.com, and I will send you the instructions for submitting. Share with anyone you know who might like to join our Gauntlet Story Feast. (Please use the hash tag #GauntletStoryFeast when sharing so we can find and follow one another.) Our Hope remains.

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A Quote. A Poem. A Song. On Hope

by

HOPErock

“The difference between shallow happiness and a deep, sustaining joy is sorrow. Happiness lives where sorrow is not. When sorrow arrives, happiness dies. It can’t stand pain. Joy, on the other hand, rises from sorrow and therefore can withstand all grief. Joy, by the grace of God, is the transfiguration of suffering into endurance, and of endurance into character, and of character into hope–and the hope that has become our joy does not (as happiness must for those who depend up on it) disappoint us.” ― Walter Wangerin Jr., Reliving the Passion: Meditations on the Suffering, Death, and the Resurrection of Jesus as Recorded in Mark

I wanted to write today, but my head hurts so badly I cannot form complete sentences. I need to take some pills and crawl into bed. Dan will leave work early to help with the girls. I do it rarely, but we both know when it hits like this I have to clock out.

On the way to my cool, dark room I got on my knees at my prayer bench. I couldn’t even muster a guttural plea. Not even a “Dear God, Please.” Nothing. Numbness. I held my favorite heavy gray stone in my shaking hands. It is engraved with my life word. HOPE. I thought of a song I’ve claimed as “mine” for eight long years. How do the lyrics go? I came back to my computer to find my folder on hope. It’s a digital scrapbook of anything I’ve ever read, watched or listened to on the subject. Next to the download of Natalie Grant and Christa Well’s song, “Our Hope Endures,” the above quote is saved in a text file. I listened to the song. I read the words, and I wrote this. It is only the second poem I’ve written since my early twenties. I’m going to lie down and soak my pillow now.

Pain.
I call him Sorrow,
Because there are no new words.
I’m crying out,
“How long, Oh Lord?”
Does He hear?

Happiness.
I miscarried her early on.
I don’t visit the grave.
I won’t miss someone I don’t know, but
She didn’t deserve to die.
Should I believe this?

Joy.
Born of suffering.
Endurance was the doula’s name.
Her mother was Hope.
I held her wet with vernix.
Would I clip the cord?

Grace.
The place we live together now.
Adoption is true religion.
Character is the swaddling cloth.
Suffering is transfigured.
Could this ever disappoint?

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