Suffering

Last month, I started writing posts from prompts in the Writing Down the Bones Card Deck by Natalie Goldberg, and I’m continuing this month so that I can experience the entire deck of prompts.Today’s post asks us to consider all the ways people suffer.

I’m not in a mindset to write as much about suffering since I’ve seen my father’s suffering through illness and death so recently – and it has left some raw wounds not yet healed – but I am in a mindset of certainty that once the suffering is over, there is great reward and comfort in the arms of a loving Heavenly Father. I can imagine the desserts at the buffet are pretty tasty, too, and calorie-free, but I have appealed to the Lord to please ban Dad from the dessert table until we get his house and storage rooms cleaned out. I have a secret hope that there is a big screen TV in Heaven and he’s having to sit in a time-out chair and watch us clean it all out while all the other angels up there are swooning over the cakes and pies. We asked Dad so many times to please let us help him clean up and get some affairs sorted out, but we were always met with his insistence that he had it under control. And his attitude.

His definition of ‘under control’ and ours were on opposite ends of the spectrum. Nothing was under control. Most things in his house, health, mind, and world were, in fact, spinning out of control. This, too, I’m convinced, was all a part of his suffering in not being able to admit he could no longer function – – and having too much pride to accept the help he so desperately needed.

I’m convinced: we are all suffering. If we were to all sit in a circle and generate ideas about the order of the worst kinds of suffering, we might could gnaw all the meat off the bone with our stories.

And then, there is Romans 8:18: For I consider that the sufferings of this present time are not worth comparing with the glory that is to be revealed to us. And herein lies a Haiku to remind us of this truth:

all the suffering

cannot compare to the joy

of Heaven’s blessings

Amen.

Taking a Walk

This month, I’m writing posts from prompts in the Writing Down the Bones Card Deck by Natalie Goldberg, shared with me by my friend Barb Edler of Iowa. Today’s prompt gets us outside. We are to take a walk – just a slow walk, one step at a time……and then to return and begin with “What I Didn’t See….”

Vertigo

elevator drop

days are quicker to live out

than tilt-a-whirl days

What I didn’t see was anything standing still. It’s been a week. My slow, one-step-at-a-time walk happened from the conference room at Griffin RESA back to my car after a resurgence of Vertigo I thought was over – after making it only a half hour into the workshop session happening from 8:30-3:30. I left, dizzy and nauseated, at 9:00.

Vertigo had me in a spinning head lock that wouldn’t turn loose.

After years of living with its intrusion into my life with no announcement that it plans to pay a visit, I’ve often been asked to describe what it is like to suffer from this condition that medical professionals still find mysterious and undefinitive still in 2025. It sounds so cliche to reply, “It’s different for everyone, and no two bouts are really the same.” Because that same thing could be said of the flu or a stomachache or a sinus infection.

But let me try to describe what I mean about Vertigo and the way it happens to me. most commonly. Come along on this walk, of sorts, with me.

My frequency of Vertigo attacks started increasing from about two full blown episodes a year to maybe 4 ripply ones and a couple of full blown ones. The full blown ones always, always start at the beginning of the day. I wake up, but when my eyes open, I feel like I’m falling down a circular tunnel, kind of like how Alice in Wonderland must have felt when she fell in that hole, but there’s no wondering about this. It’s for real, and it will pull the rug right out from under your feet.

On these days, I can’t walk straight, so I feel my way to the bathroom and back to bed. I always pray that because I know these days will come, that when they do I’m home and not having to get up and be out of a hotel room by 10:00 or travel on a plane or by car or be somewhere that would be expensive to miss – like a conference or appointment of some sort. On these full blown days that I describe as Elevator Drop days, there is no functioning. I can only either lie down or sit up, depending on the nausea, close my eyes or leave them wide open, depending on the dizziness, and turn the temperature down.

I had my first attack when I was 12 years old, and I remember it clearly. I didn’t know what had happened. My bedspreads on my twin beds were 1970s bright bold sunshine yellow, bright Caribbean blue, and bright lime green. There were dots and designs all over them, and I had a small wicker nightstand between them with a lamp, an 8-track tape player, and a selection of 8-track tapes, most notably Donny Osmond singing Puppy Love. My rug was a shag green and blue, and I had just gone to tell my mother that I wasn’t feeling well one morning when I was returning to bed and suddenly it felt like someone had cut the cable in an elevator and the whole room started going up, up, up, up, up and I was falling down, down, down, down and could not stop. I fell to the floor between my beds and pulled myself back up. For the rest of the day, I could not open my eyes without feeling sick and endlessly plummeting.

As the years passed, I remember the same thing happening to both my parents. Dad had Vertigo days, and Mom had migraine days. Dad would lie on the couch for two or three days on end, and Mom would go into the bedroom and pull the heavy curtains shut to block out all light, lie flat on her back with a wet cloth over her head, and threaten to choke anyone who made any noise. I seemed to fall more into the camp of Vertigo, even though later I learned in my vestibular therapy sessions that vertigo is often referred to as a vestibular migraine. Apparently, there are crystals in the ear that form and break up, and when this happens it causes the fluid in the ears to tell the body that it’s dizzy. I do the Epley Maneuver, and when I do, it sounds like small aquarium pebbles gritting together when I turn my neck, and it makes me feel even sicker than before the maneuver. That’s the double-edged sword in all of this — that the attempts of things like eye exercises to stave off the vertigo often make it worse before making it better. The medicine to treat it basically knocks a person out, so going anywhere or trying to work is out of the question either way.

The tilt-a-whirl days are different. These can come on in the middle of the day, and I noticed the first time that ever happened to me, I was standing in the Chamber of Commerce window on the town square in downtown Zebulon, Georgia arranging canvases for National Poetry Month in April. The sun was bright, the heat was grueling, and I climbed a ladder a few rungs up and stepped into the display window to move the easels around. When I looked down, the world had tilted as I stood mere feet higher than the sidewalk and felt like I was on a high dive with a fast merry-go-round attached to it above a concrete pool with no water in it. I did not yet know that tilt-a-whirl days do not always end like elevator drop days once a full night of sleep has been had. Tilt-a-whirl days can stick around for a couple of days beyond the initial half day.

I get up the next morning and see that often times, things seem like there is a flame under them, the way it looks when a candle has rising heat and things move and ripple back and forth in that heat. I call these Jello Jiggles. These happen when you’re looking at a door frame or an object in a room and suddenly it looks like someone thumps it and it’s Jello. Only instead of moving like Jello, it’s much faster, like one of those spring doorstops that dogs run into and scare themselves half to death with the surprise noise they make.

I can at least function a little on tilt-a-whirl days , and sometimes I even get comfortable for a few minutes – – but inevitably I will find myself in a space where there is not enough air flow or it feels too hot or I turn my head a certain way and BAM! It’s back again. And then I have to get home from wherever I am. I take deep breaths for air to try to calm the nausea – – in through my nose, out through my mouth in a slow motion like blowing through a straw.

I wait until the wave of nausea and dizziness passes, and then I make my way to the car. I turn on the air conditioner full-blast on the coldest setting and take about 25 of those deep breaths. In. Out. In. Out. Slowly. But I do not tilt my head back as my mother would often do, closing her eyes to shut out the light. I keep my nose pointed straight forward and avoid any sudden movements. I take out my Vertigo essential oil and put a few drops on a Kleenex, wave the Kleenex like the queen waving a handkerchief to dry the oil, and place it over my nose and take a few deep breaths. This doesn’t fix the dizziness, but it sure works wonders for the nausea.

When things have stopped most of their moving around, I grip the passenger seat next to me with my left hand as I steer with my right. It doesn’t really make the world stand still, but it tricks my mind into believing that the road and sidewalks and mailboxes are not actually a swinging bridge – – that I can drive on it and won’t go plunging. And if that does not work, I wait longer and try again. And if I feel it coming back on again as I drive, I pull over. I know how to turn on the flashers and wait it out, even if there is not a great place to pull over. I also know to keep my bottle of Meclizine handy so that if a cop comes up, I can explain that I am just trying to get home to take my vertigo medicine and am waiting for the ground to stand still. Because there is no way I would pass a sobriety test walking a straight line with vertigo.

What I now know after complaining that they came to cut all our trees down when it was time to harvest the timber on our Loblolly farm is that there is a silver lining – the sky – which was hard to see at vast expanse when the trees blocked it. Nothing moves up there when there are no clouds clouding the way. When I get in the driveway, I can put my window down and, without tilting my head too far back, raise my eyes to the blue skies. There’s nothing there to tilt or fall – – and it tricks me into believing that I’m grounded. Sunglasses keep the brightness at bay so I can have the blank canvas of sky all to myself, where everything is still.

My left eye feels pressure behind it, on the outside section closest to my ear. It feels like someone is tightening a screw in there, and sometimes I feel tiny prickles on my orbital bone just a finger’s length from my ear. I hold my 3 middle fingers on my left hand up in front of the air conditioner as if I’m doing a Scout’s Honor gesture and then press them on the orbital bone under my eye. Immediately, this brings relief to the pressure even though it doesn’t last long. Sometimes, it feels like my ears are wanting to fold down as my sense of hearing performs an involuntary strain to keep noise out. Those are moments that I understand why my mother wanted to choke us for making noise.

All I can do is wait out the day as unproductively as ever clock watching can be. I can listen better than I can look at anything, so reading and writing is most often out of the question. Watching a movie can make it worse, as I’m looking into a lighted screen but hoping to keep the room dark. An audiobook is a good option for these days. I can’t look at the corner of a room – – a fixed point on a flat wall is a good friend. Sometimes I can lie down. Sometimes that makes it worse, so I have to sit up. Sometimes I can recline. Sometimes that makes it all worse too. Each time is different. Vertigo is different for everyone, and no two bouts are the same.

Now. About that walk and what I didn’t see. It is never about the physical things that are missing or present. It’s always about what’s around the next curve – or what isn’t. In so many ways, the not knowing is what makes it all doable – the small steps of this moment and the next without having to see the entire road map that may hold relief or may hold worsening. For today, I see the blue sky and not the wobbling horizon.

It’s easier that way, the not seeing.

How I Learned to Drive

This month, I’m writing posts from prompts in the Writing Down the Bones Card Deck by Natalie Goldberg, shared with me by my friend Barb Edler of Iowa. Today’s post inspires us to write about how we learned to drive.

In a Volkswagen

I learned how to drive in a

red Squareback stick shift

I still remember those days vividly – especially the day I pulled out in front of a car coming around a curve to make a left-hand turn at the last minute, thinking I had time. I don’t know how I avoided a collision, but I am convinced it was the other driver’s reaction time that kept us from wrecking. My mother was on the passenger side, and I remember the look of sheer fear on her face. She screamed, and the other driver laid on the horn.

This is what comes to mind when I think of the patience of my mother. She didn’t take my license away or put me on restriction – she quietly reminded me of the consequences of decisions that are made too quickly without enough forethought. Unintended consequences often have impacts on others that can’t always be undone.

Some lessons are never forgotten, and some words come rippling back right through the years.

Last night at our County Commissioners’ meeting, in a count of 4 to 1, our Commissioners did something no other Board has ever done in Georgia history. In a “hold my beer” move by one Commissioner who confused courage with a lack of sense, he made a motion to reject the school board’s millage rate proposal. The consequences for this are now that our county Tax Commissioner will not be able to collect taxes until the millage rate is submitted. The deadline is September 1. Today is August 27. I fear for the ripple effect that may close our library doors or other county departments; this impacts far more people than school leaders who are charged with making the best decisions for their schools and taxpayers worried about pennies on the dollar in their own pockets.

The one vote against this act of senselessness was my husband, I’m proud to say. As one who rarely comments or gets involved in politics on any level, I applaud his standing up for what is right in the face of overwhelming opposition. He voted for what was right.

It’s comforting to know that there are drivers who, unlike me in my learning days, do not put others in jeopardy. I rest fully in the confidence of his ability to lead and to drive. I pray for the ones who do not know what they do not know and do not count the costs.

Saying Goodbye

In Dad’s final days, we recorded some audio clips that will keep him close to us and help us process this consuming grief we are feeling. My brother and I spent countless hours by his side as he reluctantly shifted his weight from this world to Heaven to be with our mother again, a lot like a kid being dropped off for summer camp who wants to go but keeps coming back for one more reassuring hug before being able to go pick a bunk. His words here are powerful reminders to do things while we still can.

There are lessons on this side in the moment of hearing Dad’s recorded words spoken, but there are the realities of this on the other side, once a person has left this world, in seeing so many things that did not get finished. We see it in the unfinished projects, the bookmarks, the tasks, the notes, and the paperwork. My brother stood in the shed last weekend and held up an ornate wooden spindle: for the stair rail we were going to refinish back in the 1980s, he explained. It struck me in a visual way when I walked in his kitchen and saw the Lazy Susan still on the counter, covered in shot glasses that were filled with his medicine doses. That’s how he organized his medicines for the week. I gave it a spin and watched it whirl, then slow, then stop.

Then, I discarded each pill and stacked the glasses in the box I was packing to be donated, wondering where each would land beyond its purpose here in the grand scheme of their own lives as medicine cups before I moved on to the next counter and the cabinet after that and the shelves after that.

How quickly a life shuts down and the physical space once occupied becomes a hollow cavity. A dumpster. A donation box. An estate sale. A few memorable pieces tucked into the folds of our own homes as reminders that what matters truly are the memories – – not the stuff.

no one leaves this world

feeling like they’re finished with

all that needs doing

End Zone Ball

In Dad’s final days, he was full of metaphors about life experiences and advice. Here, he shares what to do when we fumble the ball, after referencing the iconic high school yearbook photograph of him in the end zone, midair, arms up, eyes focused, reaching for the football.

The Plays You Fumble

you can’t catch every

pass but it doesn’t matter

the next play matters

when you drop one, you

get another chance

The Good Housekeeping Seal of Approval

This month, I’m sharing stories I captured on audio in the final days of Dad’s life. There were funny moments, serious moments, sad moments – – all of them with levity and meaning. In today’s audio below, listen for the phrase “the Good Housekeeping Seal of Approval.” Translation: someone passed every level of acceptance and had made it to the inner circle of the Haynes family. While every family has its way of declaring their acceptance of a new member of the fold, this was Dad’s – – and, of course, we as his children had to get through the tests of our own spouses’ families’ gate keeping systems, too.

At our family dinner following the graveside burial, all in attendance were invited to share stories. My husband, eyes brimming with tears as they often do when something hits deep, stood and shared the story of the day he’d “done the old-fashioned thing and asked Felix if he could marry his daughter.” He described the scene: there they were, standing at the top of the dock along the Sapelo River, Spanish Moss gently blowing in the limbs of the Live Oaks, where Briar had expected it to be just him and Felix.

Only it wasn’t.

Felix was “the easy one to get by,” he shared. Miriam……..not so much. But there he was, face to face Felix AND with Miriam and all her intuition, when Dad looked over at Mom and saw that Briar got a passing score – so Dad gave Briar his blessing with two conditions: 1) “get your arms around the kids;” and 2) “encourage Kim to finish her doctoral program.” Briar had just received the Good Housekeeping Seal of Approval.

He was in! And 17 years into our marriage, Briar has done both of the things my father asked of him – the kids love him, and I finished my doctoral program, ten months after Mom died of complications from Parkinson’s Disease. Even though she wasn’t physically present to see these things happen, somehow I know she knew. She knows everything, still.

Fast forward to June 2025. In the hospital room with Felix were Ken and Jennifer and I. Somewhere between Heaven and Earth, Mom stepped from behind the veil to join Dad and deliver a message to Ken and Jennifer through Dad’s words.

Did Jennifer get the Haynes family’s Good Housekeeping Seal of Approval?

She got The Grand Slam Good Housekeeping Seal of Approval!

Listen above for

the Good Housekeeping Seal of

Approval: She’s in!

Bottom of the ninth,

bases loaded with Felix,

Miriam, and Kim,

and Ken hits a Grand

Slam homerun with his choice of

a winning soul mate!

Telling Stories to Pass the Time and Touch the Future

Today is Slice of Life Tuesday, and we’re writing to a prompt shared by Jenna Komarin: “The only thing that makes life possible is permanent, intolerable uncertainty; not knowing what comes next.” — Ursula K. Le Guin

That quote aptly describes the past six weeks, from the time my father took a steep nosedive the last week of May after finishing chemotherapy treatments and died of complications from Pulmonary Fibrosis on Friday, June 13. Even though there was a known certainty in the dense fog of uncertainty, the glimmer of hope in the uncertainty is what kept us all going.

Throughout the month of July, I’ll be using Dad’s stories I captured in the final weeks of his life to share poems about things that were on his mind – and I’m using the actual words from recorded audio, preserving the wording the way he spun it. I’m grateful to my friend Janette Bradley for sharing the idea to record these conversations to play again whenever I need to hear his voice.

When my brother Ken and I were there with Dad as he was rapidly deteriorating, we asked him to tell stories of family and his younger days to pass the time and keep his (and our) mind off the endless waiting and dreadful reality as things kept taking turn after turn like some sputtering single-plane engine spinning wildly out of control before the crash. It took some effort through broken breaths and the din of the oxygen machine that reminded me so much of a noisy generator, but he managed to share priceless treasures full of nuggets of wisdom from a life well lived with rich descriptions of family and friends from long ago.

In one story, he spoke an unintended haiku about his mother out of thin air. He told us, “Your grandmother said, ‘we dig our graves with our teeth,’ and she was not wrong.” I counted the syllables and captured the wisdom that he was sharing with his children ~ wisdom that his grandchildren and great grandchildren will appreciate in the coming years as they continue to remember Dad. Even when – – no, especially when – – life feels so uncertain.

Media Clip: Dad Telling About His Mother’s Sayings

Dad’s Thin Air Haiku

your grandmother said

we dig our graves with our teeth

and she was not wrong

Note: My grandmother’s quote is attributed to Thomas Moffett, a physician from the 1600s, and later to Thomas Edison, who often gets credited as the originator.

Special thanks to Two Writing Teachers at Slice of Life

Thursday the 12th: Leading up to Friday the 13th

The last person to see our father alive who knew him was Nick Doster.

My brother Ken and I had been trying to keep vigil next to Dad’s bedside so that he didn’t die alone in a room, but the hospice nurse urged us to go take showers and grab an hour or so of sleep when we’d become too exhausted. Some patients look for those moments to die alone, preferring not to have loved ones near in their final moments, she’d assured us. We knew the time was close, too, because just that afternoon Dad had begun the conversations with the others not of this world, but with whom he was having undeterminable conversations and for whom he was reaching.

Nick Doster and Dad had traveled to Wrigley Field in Chicago to see the Cubs play several years back, and shared a deep love of all things sports. So it was no surprise that when Nick showed up in the remaining hours of Dad’s life with a red Georgia Bulldogs hat, Dad found strength for an appreciative smile.

Imagine our bittersweet sadness when the call came at 4 a.m. that Dad had passed. We felt the grief of the loss and the joy of the release of all pain and suffering from this earthly realm into the Heaven he preached about all his life. Now. Imagine us walking into that Hospice room to spend time prior to the funeral home coming for the body.

Take all the time you need, the hospice nurse offered.

Imagine us opening that wide door one last time and looking at the bed, only to see a bright yellow blanket embroidered with Psalm 119:76 in black stitching on one corner covering Dad’s body – the sunshine of Heaven. And imagine a face at total peace, no wires or tubes protruding, no oxygen machine droning, the red hat still on his head against the stark white of the pillow.

My brother and I agreed – – he wears the hat to Heaven. We know it will be the perfect complement to his black doctoral robe with the velvet on the sleeves and the red piping. Above all, we know it will bring smiles to those who will come for visitation to see that Dad, ever the champion of going as far as one can go with education and cheering as strong as one can cheer for the Georgia Bulldogs, can still cause a stirring of hearts.

Imagine the grief

Imagine the laughter

Imagine the joy

Friday the 13th For Real

This is a time of reorienting after the loss of my father on Friday, June 13. He was diagnosed with pulmonary fibrosis four years ago, and with both prostate and colon cancers in the past year. He began to suffer from SVTs, a heart arrhythmia that mimics a heart attack, because of the cardiopulmonary functions working in tandem with lack of oxygen from the lungs to the heart. In other words, the lungs weakened too much to support the heart, and with the chemo cocktail on his frailty, he didn’t have anything to fight with as he reflected on his choice.

These past three weeks have been a blur, since things took a steep nose dive the Tuesday after Memorial Day. He was transported by ambulance to the hospital, on to a rehab center, back to the hospital, back to the rehab center, and back to the hospital and then a hospice facility. He never returned home, his beloved dog Kona left there to wonder what happened to him. Within hours of his first ambulance ride, one of his many dog park friends came to get Kona and will keep her as her own, assuring both Dad and us that as long as she has Kona, she will have a part of Dad; we’ve arranged for Kona to see his body at the funeral home so that she understands he did not abandon her by choice. The blanket provided by hospice covering Dad during his ride to the funeral home was not laundered at my brother’s and my request – – this will be a gift for Kona. We hope it holds Dad’s scent for her forever.

These weeks have been filled with frustration, sorrow, laughter, denial, peace, acceptance, silence, noise, unforgettable moments, and hundreds of friends and family reaching out from across the miles to get the daily update and express their condolences. His grandchildren and great grandchildren who had traveled from as far away as Nevada to say goodbye arrived in intervals on Friday, just a few hours too late – – but we know Dad left on his own terms, and we believe he did so to keep their memories of him as they knew him in healthier days. Sunday was our first Father’s Day without our patriarch.

And now, our father – pastor, friend, brother, and legend – has reunited with our mother in heaven. We celebrate them and know they are at peace, and we lay him to rest on Saturday in Christ Church Cemetery on St. Simons Island right next to her, where she has been waiting since December 2015. So many stories have been lived and shared over these past few weeks, and there will be so many more as we navigate the days ahead – – stories and events that Dad continually referred to as the serendipitous steering currents of the spirit. His service will be live streamed on St. Simons Island First Baptist Church Youtube channel at 1:00 Saturday, June 21 for any of his friends who are reading and would like to attend virtually.

serendipitous

steering currents, Dad reminds,

are of the spirit

We anticipate and welcome these moments, and we’re on the lookout for every sign and every miracle that we know will be divinely channeled our way from Heaven.

Goodbye, Dad. Until we meet again.

Say Yes to Oui

I find inspiration in the lids of the yogurt I eat. I buy this brand not just because it’s delicious, but for the messages and the pure glass containers that will root new plant life for me to share with friends. Here is a poem inspired by Say Oui to Time Off!

Say Yes

we said yes because

what we know about us

is that we like a big window

and gray and white

and newness and matching

towels and linens

not odd assortments

and light,

plenty of light

and good music speakers

front, back, and outside

for good 70s tunes

and fifteen trips to France but

not going there

instead, staying close to home

but still away, oui?

and time off

to enjoy it