Becoming Mother

A book and a blog for first-time mothers

Tag: motherhood

Death

August 13, 2022, 4:00 a.m.

I’m running.

My purse knocks against my thighs as I sprint toward the bright red ER sign of the hospital.

It’s okay to go, Mom. It’s okay to go.

My mind flashes to a scene in Contact, where Jodie Foster’s character, Ellie Arroway, is on the verge of being launched into space in an extraterrestrial aircraft. When the spaceship begins shaking as it ignites, through her fear, Ellie continues to utter, I’m okay to go.

Even though she doesn’t know what awaits her on the other side, she continues to say these words.

It’s okay to go, Mom. You don’t have to wait for me, is my prayer.

But I’m still running.

I’m running because none of her children are there.

Because my father died alone, without anyone who loved him to hold his hand.

I’m running because my heart is screaming for just one more moment to be with her before she escapes to places where I cannot follow.

Just one more moment.

Just one more moment.

I’m running because Love compels me.

And I will expend every last ounce of my energy to help someone I love.

The ER sign grows larger in my sight and I am breathless already because I’m so anemic. But I keep running, my heart pounding in my chest, fighting the lightheadedness, my lungs seizing.

And part of me wonders if my heart has known for years that this is how it would all unfold.

If my body was simply following the rhythms of my heart.

And now those early morning runs, my feet pounding the sidewalk at 4:00 a.m., have prepared me for this very moment.

To run to my mother at this very hour, when she needs me the most.

Perhaps my heart has felt this moment approaching for years.

***

(It’s dark.)

I haven’t really slept in days.

(It always seems like it’s dark when these things happen.)

My dreams aren’t dreams right now. They are instant replays of the last three days, holding my mother’s hand, watching her heart rate tick up, up, up as her face loses its color, its tone. Her eyes struggling to remain open.

(Labor and Birth.)

The image had been replaying in my mind for hours and hours.

It’s both too early. And too late.

(Dying and Death.)

***

I burst through the doors to the ER and slow to purposeful walk until I reach a set of double doors. I jiggle them. Locked.

A voice comes on over the intercom.

“Can I help you?”

“I need to get in. My mother is dying.”

A pause.

“Do you need help getting there?”

“No,” I say. Then I repeat the number of the hospital room.

The door unlocks.

And I’m hustling now to the end of the hallway toward the first set of elevators. I need to go to the seventh floor. The buttons read 1, 2, and 3. I press 3, going as high as I can go. I ask for more directions, someone at a nurse’s station, a security guard, a custodian.

Every person stops what they are doing and guides me.

Down this hall, to the left.

What floor? Down that hall, take a second left. You’ll find the elevators to the seventh floor.

What room? Those rooms are in the west wing. Hang a right at the Exit sign.

I’m hurrying down the hallway when I see Doug come out of the room, flagging me down. He hugs me tightly.

“She stabilized again,” he says.

I gaze into the room and see that my mother’s bed has been lowered nearly to the floor. Warren is seated on her left, holding her left hand, the softer, unbroken one.

This room at the top of the hospital is dim, barely lit at all. The brightness and bustle of yesterday’s ICU room proclaimed plans and interventions. Real hospital work. But this room lacks any of that. Instead, it has been emptied, drained of all the light and equipment and interruptions. I wade into its stillness, as if it were a pond, the water barely rippling around my movements as I press forward.

She breathes heavily through her mouth. Says nothing.

There aren’t as many tubes and wires connected to her anymore. Just enough to monitor her heart and oxygen. An IV port for medication. Warren tenderly holds her arm where her last IV was threaded by Maria, an excellent nurse on the fourth floor who took the time to warm my mother’s arm with compresses to thread the IV on the first try into her tiny veins. The tape over the IV still bears the nurse’s initials and the date, MR, 8/11.

The monitor shows her vitals in bright green numbers and letters.

“Her heart rate is 155?” I ask Doug.

He nods.

155 is my heart rate when I’ve been running for 30 minutes.

“She’s been holding at that for hours. Until just before I called you. Her vitals started dropping, but she rebounded.”

He pauses and his voice breaks.

“I think she’s waiting for you.”

I swallow.

I look at her chest rising and falling rapidly, how she is still fighting, even here at this late hour.

We could be here for hours, waiting for her body to surrender.

But I am resolved.

I will bear this moment for her. I will be here for her, no matter how long it takes. No matter how hard this gets.

“Mom, it’s Sharon,” I say. “I’m here.”

She breathes heavily, the cool washcloth still folded over her brow. Her eyes are closed.

I have no plan for this moment. I wasn’t committed to being in the room with her when she passed. I’ve allowed myself to accept whatever fate would have for the end of my mother’s life.

Whatever was bound to happen would unfold just as it should be. And it did not need to involve me.

But here I am.

In this room.

And I know that Death is here.

I feel it thick and still in the air around me. It doesn’t spin around us, like a vortex pulling my mother into some other dimension. It drifts and floats, like dust in the air when the light shines through a window. Only there’s nothing to see. You can only feel it, seeping like thick syrup, settling heavily into your ears, your mouth, your nose. So heavy is Death in this room that simply uttering words takes a concentrated effort, not to mention anything meaningful or heartfelt.

I open my mouth to speak and, at first, I choke, the sob caught in my throat.

I push it down and remember.

I will bear it for her.

“I’m going to play some music for you, okay, Mom?” I say calmly, searching for the live version of Both Sides Now by Joni Mitchell, just recently performed at the Newport Folk Festival less than a month ago. “I’ll start with the one that you said you loved last night. Remember that? I played it for you and you said, ‘I love it.’ It was a little hard to hear you, but I know you said it. Here it is.”

I let the song play without interruption and we all listen to Joni sing to my mother with her haunting, soulful voice. I hold my mother’s right hand, rubbing her knuckles, her fingers. I say nothing.

But now they only block the sun
They rain and they snow on everyone
So many things I would have done
But clouds got in my way

I’ve looked at clouds from both sides now
From up and down and still somehow
It’s cloud illusions I recall
I really don’t know clouds at all

“Both Sides Now” by Joni Mitchell

More tears fall and I wipe them with the back of my hand.

I can tell how loved she is, the ICU nurse on the second floor, Regina, had said as she administered morphine the night before, into the IV that Maria had placed. Two amazing human beings who treated my mother with such compassion.

So many people here with her. You’d be surprised how many people leave this world alone in these rooms.

Have more heart-breaking words ever been said?

The song finishes and soon we are listening to troubles melting like lemon drops, away above the chimney tops, rainbows stretching off into the distance, leading my mother to an unknown land.

I want that so much for her.

Even as my heart cries out for her to stay.

I want for her to wander into a land of rest and peace, where her memories of broken hips and legs and arms and necks, of cancer, of diabetes, of untreatable, chronic pain… Where all these memories become nothing but distant moments in time through which she has persevered. Where she has no need for morphine or demerol or toradol or fentanyl or hydrocodone or any of the other medications that only cut the pain in half.

Tears and more tears. I pull her hand to my wet cheek. Just two days ago, when she could still utter words, I asked her if she was in any pain. She fought to simply whisper the words, “They can never make it pain-free.”

I wish I could have born some of this pain for her.

But I know her better.

She would never have allowed that.

Just as I would never allow my children to bear my pain.

The song finishes again and I look over my shoulder at the heart monitor.

156. 154. 155.

The fog of Death that surrounds us is growing. Why is it getting heavier?

Doug is seated behind me, his head rested against my mid-back, as if literally supporting me so I don’t fall over. Every now and then, I feel him turn to look at the monitors. Warren is gripping my mother’s hand, sometimes pressing it to his face, sometimes lowering to the bed and bending forward over it.

It’s so hard to remain upright. I’m not sure how I could explain to anyone else why, in this moment, simply sitting up and speaking takes unimaginable strength.

But it does.

How many moments has my mother faced that were as heavy as this? What would she do?

And then I know what to play.

The soft notes of the song begin and I’m transported back to those final minutes, laboring with Henry, this song soothing my ears while my screams filled the air and my hips lit on fire. Those last moments just before I hemorrhaged and nearly bled to death on the bed, only minutes after I finally pushed Henry free from me.

“I played this song when I was in labor with Henry,” I say. I pray that she can understand. That she feels my intention. Because I cannot find my words to articulate it in this moment.

What I want to express is that I’ve been here before, in this most sacred of spaces. More sacred than any cathedral or altar. I’ve been here before–But never on this side.

There is a stillness in the air when Life enters this world that I cannot explain to anyone who has not been present for it.

Now, I know that there is also an unexplainable stillness when Life leaves this world.

We all want to bear witness to the beginning of Life. We believe that it is good and holy and pure.

But who wants to bear witness to the end of Life? Even though it is just as sacred?

I will bear it for her, I tell myself.

“Mom,” I hold my voice steady. “I want to tell you that it’s okay to go. You don’t have to stay here for us. We’re all going to be okay.”

I pause and consider what to say next. Doug and Warren are both bent forward, their heads bowed, reverently as I speak, my head lifted, my back straight.

Now, I understand. Why Death is so thick, so heavy.

This room is not empty.

It’s Full.

It’s overflowing with everyone waiting for her.

My father. My mother’s mother. My mother’s father. And on and on. The generations have poured into this room, surrounding her and holding her, just as They held me when I cried out for help in laboring with Henry.

They have returned, these People of my Blood.

My heart almost cannot stand it.

I know what to say now. I close my eyes and I speak without any hesitation.

“And Mom…everyone is here with you. It’s not just me and Warren and Doug. Everyone is here. Anna is here. Nate and Lisa are here. Holly and Corey here. Dominic is here. Felicity and Henry are here.”

The words are spilling forth from me, as if she’s relinquished her sword to me and allowing me to fight this last battle for her.

So I will not stop.

I will do this for her.

I will help her over to the Other Side.

I keep listing all our family, as many as I can remember, all her brothers and sisters, their spouses, their children, her cousins, her friends. My shoulders hurt now, physically ache, simply from the action of sitting upright. I can almost feel my mother transferring her burdens, her cares, her wishes, her regrets, her Love, all to my own shoulders.

Perhaps that’s what Death really is.

A great transfer of all the emotions and cares that one person has carried to those they leave behind.

I will bear it for her.

The hospital door opens, but I don’t look at who it is. Words are still pouring out of my mouth, names, reassurances that we’re going to be okay.

“It’s okay to go, Mom. We will all be okay. You can go. Dad is waiting. Your mom is waiting. Your dad is waiting.”

“It’s okay to go, Mom.”

“It’s okay to go.”

I repeat this over and over, my last reassurance to my mother.

That if she would be courageous enough to press on toward the unknown, I would also be courageous and press on here in her place.

I choose to carry this pain of losing her. For the rest of my life.

Because it will free her.

“You gotta go, Sweetie,” Warren says, his voice as broken as his heart. He clutches her hand to his lips and kisses it, his tears freely falling. “I’ll see you there.”

“Mom,” my voice shakes. “There’s not a single person who loves you who can’t be here for you right now. We are all here and we love you so much.”

Doug taps me, but I keep going.

“But we’re going to be okay, Mom. I promise you. It’s okay to go, Mom. It’s okay to go.”

I say it over and over again.

Doug taps me again, but I keep going.

“And the last thing I’ll say, Mom, before you go…” I take a breath. “I just want to thank you for all the I Love You notes that you’d slip into my sandwiches.”

Warren reaches across the bed, over my mother’s body, and grasps my hand.

“She’s gone, Sharon.”

***

It’s true what they say about how a person changes in that first minute after death. In that first minute after death, I surrender to the wave of grief crashing over me and weep over my mother’s arm and hand until I feel her go cold.

But that coldness is all it takes for me to know wholly and thoroughly that the thing that made my mother who she was–a spirit, a soul, an essence–was not her body. She was not just skin and organs and fluids. She was so much more than this body that is now left, apart from her.

I’m the first to stand up.

It’s surprisingly easy to do.

To get to my feet and walk out of this room, knowing that I’m stepping into the shoes that my mother is leaving behind. She would be the one to say the hardest words to the people who need to know.

I feel it already, the passing on of matriarchy.

I will be the Keeper of Family Memory from now on. The one to memorialize what we’ve lost. The one to keep her memory alive by baking her recipes. The one to be a mother to all of us left behind.

And it starts now. With this walk down the hallway, where I will say the hardest words to say in this moment. I will say it.

At the nurse’s station, a young woman is eating what looks like her lunch, a large bowl of noodles, something that requires her to anchor her head over the bowl to not make a mess. 4:30 a.m. I suppose it is lunch for the night nurses.

She sees me and puts down her spoon.

I point to the room behind me.

“She just passed.”

The nurse’s face goes solemn.

“I’ll let the doctor know right away.”

I shake my head.

“There’s no rush.”

***

Dawn is breaking by the time I arrive back at the hotel.

The sunrise, Saturday, August 13th, Indianapolis, IN

I meet my sister in the lobby of the hotel. She is sitting on a bench, tears already running down her red cheeks. I lean down, hold her by the back of her head, and kiss her forehead. She stands to hug me.

Then, I tell her everything, as much as I have the words for. There is too much that I don’t have words for yet, that I don’t fully understand yet, that I will need time to make sense of, that I will need to find the language for. But I say as much as I can and promise to myself that someday I’ll sit down and commit the sacredness of this morning to human memory, that it may never be lost.

But in this moment, what I say over and over again is this:

“I told her we were all there. And we were. We were.”

A Eulogy for My Mother, Cecilia Tjaden-Rush

When I was 25, I asked Mom if she would teach me how to decorate a cake. She said, “Well, sure.” She showed me how to pile the icing on top and level it out, being careful not to pull crumbs up from the side. I made a lot of mistakes. The icing was too thin in some places. Chunks of cake came loose and  polluted the icing. I pointed to a hole that I had somehow made in the cake. She looked at it and said this:

“Oh, that’s just a good place to put a flower.”

She took a tiny, flat metal flower nail and spun it in her fingers as her hands moved swiftly and without any hesitation, creating a flawless rose. She placed it on top of the hole that I had made.

I cannot think of a better metaphor for Mom’s life. A master of turning the holes into something beautiful.

I want to tell you about who my mom was.

Her name was Cecilia. Born May 9, 1954 in Spencer, Iowa to Cyril and Virginia Bundy. She was the second oldest child, the oldest daughter of seven children. She spent her childhood on family farms in Iowa and Minnesota. When she was in high school, she moved to “the Cities,” a.k.a. Minneapolis/ St. Paul, Minnesota. She attended a Christian university, University of Northwestern, for two years. She met my father, Leland Tjaden in August 1974 at Cross of Glory Baptist Church. They were married here, in the same place that I’m standing right now, on September 6, 1975. From 1977-1984, they had four children, Phillip–who has since become Anna–Nate, Sharon, and  Holly. In 1985, they moved to Dayton, Ohio for my father’s job with Supervalu, a grocery store chain in the 1980s. In 1986, my parents adopted Cecilia’s sister’s child, DeAnna–who has since become Dominic– and they raised him as their own. Yes, two of my mother’s children are transgender. And she recognized and loved them as beautiful creations of God. 

In the summer of 1987, my mother received a phone call while she was decorating cakes for other people’s celebrations–her house was on fire. We lost everything. We were homeless. This event changed our lives. It taught me that the worst tragedies in our lives are almost always the times when we see humanity shine. I witnessed and felt the care of others so many times in this period of our lives. Our church sheltered and fed us until we were back on our feet.

Our family often lived paycheck to paycheck. Our furniture came from Rent-a-Center and we were frequent users of layaway. But we always had enough. We may not have had what our friends had, but we never went without what we needed. My mom could feed a family of 7 on $50 a week in the 1990s. Again, it wasn’t necessarily what we wanted to eat. But we never went hungry. 

In 1997, doctors found a slow-growing cancer in my mom’s small intestine. It was called a carcinoid tumor, a cancer that circulates in the blood and disrupts the endocrine system. My father’s response to the news was devastation and sadness. My mother’s response was level-headedness and optimism. This was just a thing that was true about her now and she would do what she needed to do to treat it. But beyond that, it wasn’t going to rob her of her joy and positivity. She believed deeply that God had plans for her and that those plans were ultimately beneficial to all those she loved–even if those plans included her death at an early age.

She kept that same spirit for the next 24 years. 

I want to tell you some things that my mother loved.

Her Myer-Briggs personality type was ISFJ, like me and my dad. “The Protector” personality. 

She loved musicals. The Sound of Music, Oklahoma, Carousel. Anything Rogers and Hammerstein. She could watch Christmas movies anytime of year.  It’s a Wonderful Life. Literally all of the Hallmark Christmas movies ever made. And Lifetime movies. For music, she loved the Carpenters, Anne Murray, Josh Groban. Almost any Christmas song you can think of–she loved it. 

But then there was her other side that loved action movies like Taken, Westerns, suspense, thrillers, and as Warren calls them, “men-bashing” movies, where the husband is the main villain. There was a period of time when Mom loved a TV series called Snapped, which was about wives who completely lost it on their husbands and ruined their cars or poisoned them or something like that. 

She and Warren enjoyed something they called “Chicago Night,” with TV shows about Chicago PD or Chicago hospitals. Things she could watch over and over included Law and Order: SVU, Heartland, Walker, Texas Ranger, and Little House on the Prairie.  

She was patient. She loved jigsaw puzzles, the more pieces the better. She loved crosswords and word puzzles in Penny Press puzzle books, particularly “Escalators” and “Magic Square Anagram” puzzles. 

She was creative. Her passion and profession was decorating cakes and she truly loved the work. She worked at so many bakeries: Stumps, Cub Foods, the Rolling Pin, Cake Box, Ashley’s Pastry Shop, Kroger, and CJ Farms. She and her dear friend, Judy Smith, even ran their own cake decorating business for a period of time called “Classic Wedding Cakes.” I know she’s my mom, but really, her decorated cakes were among the best I’ve ever seen. She had a real talent for it. I remember taking her into a local bakery and she looked in the case at the cakes. When we left, I asked her what she thought. She just shook her head and said very simply, “Nothing special in there.” That was all she said. 

Her favorite kind of cake was white cake with buttercream icing. If you were going to buy her a donut, she’d ask for a cake donut. Most people knew her for her decorated sugar Christmas cookies, but if she wanted to bake cookies just for herself, she’d make peanut butter cookies. 

Although she was a fantastic baker, she was not known for her cooking. All five of us kids can remember the countless times that we would protest the “hot dish” that my mom had made for us, a concoction of elbow macaroni, ground beef, stewed tomatoes, onion, and sometimes celery? Actually, she put celery in a lot of things that shouldn’t have put celery. Like her chili. I remember my husband, Doug, taking a bite of her chili and a confused expression came over his face. He looked into his bowl and moved his spoon around. “Is there celery in this?” I said, “Yep.” “Who puts celery in chili?” I just shrugged. My mom leaned heavily on cream of mushroom soup and Lipton onion soup mix for seasoning a dish. One thing that it seemed that no one ever agreed with her on was her love of chicken hearts, livers, and gizzards. I remember a stuffing that my mom made. Holly took one bite of it and just said, “Mom… what did you put in this?” And she said, “You can tell?”

Beyond baking, my mom loved to do so many kinds of crafts. She sewed everything from matching Christmas and Easter dresses for her girls to curtains to handbags and even stuffed animals. There was a period in the 90s when she made–with Nate as her assistant–stuffed bunnies out of muslin cloth and dressed them up in little dresses. She quilted and made a lot of quilts for people, including me. She crocheted so many blankets, especially in her last years, when she volunteered to crochet blankets for people in hospice. In the 1980s, she went through a phase when she made barretts, all decked out in lace and beads. 

As a parent, my mom recognized and valued each of her children for their uniqueness. She saw potential in each one of us, even if we disappointed her. She gave second and third and fourth chances. There was no end to the chances she would give. She was proud of whatever we did, as long as we did it to the best of our ability. She was the Keeper of the Peace in our household, the one that kept the ship sailing, even if we didn’t know the direction that we were going as the Sea of Life tossed us this way and that. 

She was the owner of a perfect laugh and a Minnesota accent. And she always granted the most generous interpretation about others, even when she could have extended judgment.

My mom was an eternal optimist.

When I hugged my mom good-bye as I was leaving after my father’s funeral, I said, “I just want you to be happy for the rest of your days.” It was 2014 and the cancer was mostly asleep inside of her, but it was never too far from my mind.

She looked at me and said, “I will be.” So confidently and assuredly. And I knew she meant it. 

I just couldn’t understand how she could be so optimistic, but she absolutely was. She hadn’t met Warren yet. As far as she knew in that moment, she could have been facing a lonely, financially difficult widowhood. 

And yet she believed that the best was yet to come. 

And by God–she was right.

My father was my mother’s first love, the father of her children, and what I say next does not take away from that cherished truth. Warren was her soulmate. Both children of farmers, lovers of the quiet land. They spent 6 incredible years together. He held her hand as she passed and still looked at her with the same adoring eyes that he had for her throughout their marriage. His last words to her were, “You gotta go, Sweetie. I’ll see you there.”

Warren, what a gift you were to my mother. Thank you, from the bottom of our hearts for being in her life. You will be in our lives forever now. You can’t get rid of us! You are my children’s grandfather and we will visit and care for you just as we would my own mother.

On the night before my mother passed, I read a letter to her that intended to read at her funeral. But she deserved to hear it in this life. I’d like to read that letter now.

Mom,

We met on November 24, 1981 at 3:51 in the morning. It was a Tuesday, just two days before Thanksgiving. I don’t remember it, but now that I have two kids of my own, I know that it’s likely that you’ve never forgotten that morning. You told me after Felicity was born that I had been your hardest birth. That surprised me because I was your third child. You didn’t know why it had been that way. But it was. You and Dad had expected that I would be born before he had to leave for his early morning shift at the bakery. But no. At 1:00 a.m., Dad left for work.

And so, while the world slept and my father went to work, you labored alone in those final hours, which I know from experience are the loneliest, most painful, and most detached hours that you can experience in life. No matter how many people surround you, you are still alone in your pain. 

These are hours when you are certain there is no one in the world who is currently suffering as much as you are. They are hours when you bear the entire weight of humanity, pushing, pulling, and pressing you from all sides. There would be no human life if not for the ability for women to bear this pain. 

I repeat: Life depends on the strength and fortitude of women to bear this pain. 

You bore so much pain in your life. You bore it without most people even knowing, a true testament to your roots and upbringing in rural Iowa and Minnesota, where the simple economics of farm life governed. You cannot reap what you don’t sow. You cannot take if you don’t give.

And so when life gave you pregnancies, it also gave you severe hyperemesis gravidarum. When it gave Dad the opportunity to turn his job into a career, it also gave you an extra 800 miles between you and everyone you loved. When it gave you the stress of raising teenagers, it gave you the stress of raising more teenagers. Sorry about that. That was actually completely unfair. 

Mom, you were the oldest girl in a family of seven children. You talked about how difficult it had been to move from farm life to city life in high school. The teasing hurt you. So you turned to your faith. Your faith taught you that even if others didn’t accept you for who you were, you would always be accepted and loved by God. For you, being God’s child gave you the support and comfort that you needed as you grew up in a culture that you didn’t understand. 

Losing Dad was tough, but why does it feel like it hurts more to lose you?

Maybe it’s because it feels like a world without your mother is a world without the greatest compassion and the most acceptance and unconditional love that you have ever known.

For a long time, I didn’t want to be a mom. Moms were so uncool. So passé. So not who I wanted to become. I wanted to be accomplished and talented and maybe someday well-known. I was going to do much, much harder things than being a mom.

What a fool I was. Such foolish, foolish thoughts. So full of pride. How could I ever think that you weren’t exactly the person that I should aspire to become?

How could I ever think that being a good mom was easy?

Being a good mom has turned out to be literally the hardest thing that I will ever do. And I’m finding now, over and over again, the empathy and the perspective that I need to understand just how difficult it must have been for you to raise 5 of us. 

I’m so sorry, Mom.

Mom, it’s because of you that I’m able to keep the whole thing in perspective.

The world will always find another teacher or writer or employee. But your family will never find another you. 

I know that my heart will always call out for you when I’m hurt.

I know that I will always miss your presence, but I know that I’ll miss it the most at Christmastime. Every time I smell those fragrant pine cones, covered in cinnamon and clove, I can almost hear the scratch of the record player starting up Anne Murray’s Christmas Wishes, the notes of Winter Wonderland blending into Silver Bells.

As deep as my sadness is right now, sadness is not what I want this to be about. 

What I want to talk about is my gratitude—all the reasons that I’m thankful you are and will always be my mother. 

Thank you, from the bottom of my soul, for not just being our mother but living your life for us, as if we were your true calling. We never felt like you had something more important to do. 

Thank you for creating a home in which I always felt that there would always be enough—even when that wasn’t guaranteed.

Your optimism and positivity, which eclipsed all of Dad’s worrying.

All the times you were there when we needed you. In all the ways that we needed you. I don’t ever remember you telling us that you could not be there for us, no matter what the problem was.

For your lifelong examples of what it means to love God and live as a cherished creation of God. Through all of the financial and physical hardships, through Dad’s illness and death, you showed us how to feel grief even as you move forward.

Thank you for all the I Love You notes that you’d slip into my sandwiches and that I’d bite into while I was eating at school.

Thank you for the pair of shorts that you sewed for me late into the night when I told you I got laughed at for wearing the same pair of jeans two days in a row in fifth grade. 

Thank you for disregarding the doctors’ original prognosis in 1998 and going ahead and living your life anyway. You showed me why it was important to you to not allow people to only see CANCER when they see you. Even though cancer could consume your body, you would never give it the victory of consuming your spirit. You kept your identity and your wholeness until the end.

Thank you for teaching me that one of the very best things that you can do in this life is to be kind and generous to others—Because you never know when you will be the one that needs to feel that kindness, especially when you feel like you just cannot go on.

Thank you for filling my memory with positivity, laughter, imagination, and creativity. 

Thank you for my freedom, how you basically dropped me off at college and said, “Have fun!” You gave me the space to take ownership and responsibility for my life.  

Thank you for allowing me to feel a broken heart and giving me the space to learn how to keep on living after rejection and loss.

You were pretty amazing with space. Space to allow me to figure out marriage. Space to figure out how to be a mom. Space to feel my way through the pain of miscarriage. You were always there when I needed you, but you were always sensitive to how space could give me agency and ultimately, more resilience.

Life is funny and awful. Because now that I have all the space, what I wouldn’t give to give it all back just to have you back in my life until I’m much, much older. No matter how old you are, you’re never ready to lose your mother.

One of the first thoughts that I had when you told me in August 2019 that the cancer was back was… “Please don’t leave me alone in this world. I don’t know how to I can be okay in this world without knowing you are in it.”

But you have always been preparing me for this, haven’t you? For years, you have been giving me the space to steer my own life. You have been cheering me on from other states as you’ve gone on to live your life. You’ve encouraged me as I’ve developed my own social support network around me through friends and church. In my mind, I know that I will be okay. I know that I will wake up tomorrow, make the coffee, do all the things, and make it to the end of the day.

But my heart doesn’t know that. All my heart wants is to stop losing the people that I love.

When I first asked you why you gave me my name, you said I was named after Song of Solomon 2:1, I am the Rose of Sharon and the Lily of the Valley. This didn’t really mean much to me, especially since I was eight years old. 

But what you wrote in my baby book made more sense. 

You wrote “The Rose of Sharon, the beauty of a desert.”

You saw me as a flower in the desert.

I came into your life at a challenging time. You were a stay-at-home mom to two young boys, aged 4 ½ and 2 years. Dad worked early morning hours at the bakery, often six days a week. We know now that Dad struggled with bipolar depression for years, but at the time, you just thought that he was moody and needed help seeing the positive side of life. And that’s what you were there for—to be his partner. To provide balance. From week to week, money was perpetually tight. I don’t remember, but I’m pretty sure you didn’t complain about any of this, ever. That was your life. He was your husband and we were your children and God was God. And you rejoiced and were glad in it.

You saw me as a flower in the desert.

Desert flowers don’t have deep roots, but they do have extensive roots. They spread out far and wide to gather as much nourishment as possible, to prepare for the lack of rain. I really can’t think of a better metaphor for how I’ve lived most of my life. Drink up as much as you can now because the drought is coming. One way or another, it’s coming.

My roots have never been deep. We are the grandchildren and great-grandchildren of immigrants, uprooted from homes and cultures. Children of rural farmers, isolated for miles on every side. We moved away from all our extended family early in my life. For generations, this was how we lived: stretching out instead of digging down.

There were many seasons in life when you and Dad could not depend on your family because of how far away we lived. So we reached out to the church. And they were our support. They provided structure and guidance. Love and belonging. You showed me how to make a family with those around you. How to help others and how to have the humility to be helped when you needed it. And we often did. We often did.

Thank you for this, Mom. Because now that you and Dad are gone, this is how I will survive. This is how I will bloom and continue to grow in a life where my roots are almost gone. I will reach up and reach out. I will trust that someone will be there because I know the world is full of suffering—and because it is full of suffering, it is also full of empathy. My family that remains. Friends. Always friends. I will reach up and reach out because I need help to face this world without you. 

Dying

Friday, August 12th, 3:30 p.m.

“She’s out of isolation, so you don’t need to bother with a gown or gloves. Whatever it is, it’s not COVID,” the ICU nurse says. I glance at the whiteboard. Nurse: Megan.

Through the window, I see my mother reclined on the hospital bed, her eyes closed, her chest rapidly rising and falling. This labored breathing has been ongoing for days now, her heart rate increasing steadily over the days. 90. 100. 110. 125. 130.

It holds at 140 now.

140 is my heart rate when I’m jogging or doing kickboxing. And there, she lies, reclined on the hospital bed, her body racing as if accelerating toward some unknown destination in the distance. Does she know where she’s going? And when will she arrive?

What’s causing her high heart rate? I had asked the doctor.

It’s the body’s stress response.

To what?

We don’t know.

There would be nothing else to say until more tests were done. More and more tests.

I look at my mother through the door.

She is dying. Surely, they can see that.

Can’t they?

I slide the door of the ICU room open and step inside and rest my eyes on my mother. And the reality of the situation washes over me again, a horrible reminder. Oh, right. It really is as bad as the last time that I was here, just hours ago.

But then, I realize. No.

It’s not as bad as last time.

It’s actually worse.

I want to tell every nurse and doctor and hospital worker, This isn’t what she looks like. She’s really not like this.

In a week, she has transformed from a robust 68-year-old woman into a woman who looks to be in her 80s. Frail.

I place my cup of coffee on the floor beside the chair next to her bed and sit beside her. The welts that have emerged on her face and arms are starting to crust over. The doctors guess that it’s a reaction to antibiotics to treat a UTI, but it’s just a guess.

I slide my hand under hers. It’s not as hot as yesterday, when her fever was 102, but it’s still so warm. Her fingers are swollen. From what? I don’t know. Why is she breathing like this? There are new masses in her lungs, ones that have grown rapidly at some time in the last month, but is that what’s causing her body to run like its out of control?

Her spinal tap is clear. There’s no infection. Her brain is fine. Her heart is fine. Carcinoid cancer is strange. We don’t know everything about it.

“Hi, Mom,” I said, trying to keep my voice steady. “It’s Sharon.”

I open a document on my phone. It’s a letter that I’ve written to her. I was going to read it at her funeral, but she deserves to hear it while she’s alive. My eyes skate over the first line that I’ve written to steel myself to read it, but I can’t see through the blurry curtain of my tears. They drop freely onto my dress.

That looks so nice on you! she had said, not two months ago. Stitch Fix? I’ve never heard of it!

I look around the room for a box of tissues and see nothing. There are never enough tissues in these rooms. I wipe my face with the back of my free hand as I hold my mother’s hand. Then, I pull a used paper towel from the dispenser in her last hospital room and dab at my face again.

I close the app with the letter to my mother and navigate to a song. Something that has comforted me in the past.

See me someday sleeping softly
Flowers draped across my knees
Hear the cries of friends and family
Missing me
Press on

She’s not gone yet, but I miss her already.

I look down at my mother’s hand.

Just two weeks ago, she responded to my touch. One week ago, she could still acknowledge that I was in the room. Yesterday, with effort, she could say a few words–if they were important. I fed her a small piece of strawberry, and with great effort, she chewed it. Now, when she is aware, her communication has reduced to groans and a look from behind glassy eyes.

In this moment, her eyes are closed. I could almost convince myself that she was sleeping, if she weren’t breathing like she were running a race.

My head drops to her hand and I press it to my cheek, where my tears are now sliding over her knuckles and down her wrists. I turn my head and look up the side of her arm, upward at her as she is reclined in the bed and suddenly she seems as large as she was to me when I was a child. Authoritative. Grand. Only now, silent and suffering.

I want to wake her up, shake her out of this nightmare. I want to curl up in her arms. She was not a mother who would say something like, “Everything’s going to be okay, Sweetie.” Instead, she would say something simpler, like, “Hey, now. What’s wrong?”

Her hand is slick underneath my cheeks, my tears still spilling forth. There is Life there, inside of her, as strong as it has ever been. But not for long. Soon, her hand will turn cold and there will be no warming it up with peach tea or coffee with cream. I can still see the steam rising from her mug as she laughed about my ridiculous guesses for unscrambling words in a puzzle book.

The sadness settling over me is so heavy I cannot even hold myself up and soon, I’m collapsed over the rail of the hospital bed. I’m crawling up the side of the bed now, my face and neck pressed against her arm and hand, gazing up at her. I want her to snap out of this. For her breathing to slow. For her to look over at me and say, “I had the weirdest dream.”

But her face is so thin now. Her face has never been this pale, this thin, this drained of life.

I want to go back. To my beginning. When I was the Protected, and she, the Protector. When it was her tears of joy covering me at my birth, not my tears of sorrow covering her just before her death. How short the years were between those two turning points in our universe. I didn’t always take those years for granted. I cherished them more each time she told us the cancer was back. But how many years had the cancer slept–and I lost sight of my gratitude?

Moments with someone you love become so much more precious when you’re threatened with losing them forever. You find yourself making frequent trips to see them. Cherishing every word they say. Not throwing away their cards. Taking more pictures. More videos.

My mind drifts and I think of the woman who wept upon Jesus’s feet and then wiped away her tears with her hair, just before pouring expensive perfume over his feet.

Why was she crying? Jesus and his disciples believed that it was because she was “a sinful woman” and was plagued with regret.

But no one asked her. They just assumed that she was sad about her sinful life.”

But now I wonder if she knew, in the way that I know now, that Death is at the doorstep. I wonder if she felt the same tight tug at her heart when she looked at Jesus, the tightness that I’m feeling now as I gaze at my mother in these final hours, as if she is being pulled into a thick fog while I am anchored here. Unable to follow, even at a distance.

Even though there was a time when we were so connected that the echoes of our heartbeats rippled throughout the same body. My hiccups were her hiccups, and hers were mine.

Wasn’t there a verse in Isaiah (Was it Isaiah?) that said, Death where is thy sting?

I know where it is. It’s here, in this room. I feel it needling me every time a monitor beeps, announcing some new threshold that my mother has fallen too far below or risen too far above.

The nurse, Megan, quietly enters the room and I don’t even try to hide my tears. What’s the point?

“Here,” she says softly, handing me a hospital washcloth. “This is better.”

I nod, unable to even thank her properly. I push the stiff, paper towels into my purse.

She doesn’t say anything.

There is nothing to say.

Life is filled with bitter music
Breeze that whistles like a song
Death gets swept down like an eagle
Snatch us with our shoes still on

Press on

Behind me, I can hear the soft conversations of nurses in the hallway. I can’t hear the content, but the tone tells me that whatever they’re talking about weighs infinitely less than what is happening in this room.

Do they know? Can they tell what’s happening? Is it obvious to them too?

When do we start using that word, dying? Is it too soon? It doesn’t seem too soon.

Instead, it seems too late for someone to be notifying me. Instead, it seems that I was meant to figure this out on my own. It seems that we are in the wrong place here. ICUs are meant for people to get better. Why is she here anyway? Shouldn’t we be in hospice? Why are we pumping high-flow oxygen into her nostrils and administering potassium?

Why did we do a biopsy? Will the results read as clearly as a pregnancy test? Dying or Not Dying? When are the results supposed to come back? After she’s dead? Why are we still testing?

The sobs overwhelm me and I find myself praying not only to God, but also my father. My grandmother. Any ancestors who will hear me.

Please. She needs someone to guide her. She needs help to find her way forward. I cannot stand to watch her suffer like this another day.

I love her too much to allow this to go on.

There is a doctor’s knock at the door. They all knock the same–an interrupting, quick signal that you are next in line. But I cannot even lift myself to acknowledge the sound. If this doctor’s time is money, they’ll need to pay the price for now. And I will come away from this moment knowing that I owe them nothing. I will not shield them from my pain or my grief. They should know the weight of what is happening here, how the gravity of this moment warps time, slows it down, so that every moment is lived painfully and with the greatest effort imaginable.

They should feel it, if even to a small degree, in the way that I’m feeling it now.

My mother is dying.

Whoever is about to sit with me and talk with me already knows that, too.

***

He’s very kind, this doctor in his late 30s. He uses phrases like, “How are you feeling about her condition?” And “Yes, I agree that it’s time to modify her goals.”

When I ask if we can help her pass without suffering, he says, “We absolutely can.”

Then, a new flood of tears arrives as phrases that should be uttered twenty years from now are spoken today.

We can move her to a private, quiet room. Make her comfortable. Give her morphine for pain. Give her anti-anxiety medication.

How long will it take, we ask as a family.

Could be 30 minutes. A few hours. Or days.

More tears.

I’m hoping for a few hours. Time to say what we want to say to her. To pray. To read to her.

But the thought of wandering for days in this Space Between Worlds…

The thought is crushing.

But I know that I will bear it, no matter how long.

I will bear it for her.

***

The night nurse comes, Regina. I believe she is the Holy Spirit, the Great Comforter, incarnate. She can’t be older than 35, but she speaks as someone who has traveled this road of Death many times. She props her hands on her hips like she’s telling us the specials on tonight’s menu.

“I want to be clear about what we’re doing tonight. We’re going to do a terminal wean. We’ll do everything to make her comfortable and relieve her pain.”

It’s not insensitive the way that she says any of this. Instead, it instantly puts me at peace. What we are doing is not unusual or awful. We are only getting out of the way of Death. We are simply fulfilling my mother’s wishes, even though it means that she’s leaving us behind.

We read last minute messages from friends and family who want to say goodbye. We hold the phone up to her ear to allow family who can’t make it to talk to her. My mother says nothing. She cannot talk. All she can do now is groan, and only when absolutely necessary. She breathes heavily through her nose and mouth, which quickly dries out her lips. The tone in her jaw is gone. She cannot keep her mouth closed. Every time Warren carefully applies Chapstick to her lips, tears sting my eyes.

Can she still hear? I wonder. While half of me is glad that we are talking to my mother as if she can still hear us, the other half of me remains skeptical and wonders if this is all a show to make ourselves feel better.

Her brain is fine, the doctors had said.

As I sit on my mom’s left, my daughter, Felicity, walks in, tears slowly careening down her nine-year-old cheeks. She has been pinballing between entering the ICU room and remaining in the hallway.

Anything you want to do is fine, I assured her. Only do what you want to do.

She sits on my lap, facing away from me. She’s too tall for me to hold her like a baby anymore, so I do the next best thing and bear-hug her from behind.

Felicity gazes over at her grandmother and places her hand on top of hers.

My mother groans.

My chest tightens and I swallow.

“She can hear you, baby girl. She knows it’s you.”

Felicity leaves her hand there as her little body shakes in my lap. I know in this moment, my mother hates that she’s making Felicity sad. She hates that she can no longer mask the fact that she’s dying. She wouldn’t want to scare Felicity. She would despise the fact that the only sound she could make to comfort Felicity was a monotone groan. She would encourage Felicity to not let her condition make her sad. She might even tell Felicity what she had said so many times before, “I’m getting better and better every day, Felicity. Don’t worry about me.”

Without warning, Felicity jumps to her feet and moves to the other side of the bed.

“Can I hug her?” she asks.

“Yes. As tightly as you want.”

She leans across the bed and rests upon my mother and pushes out her shaky words.

“I love you, Grandma.”

Warren helps Regina remove my mother’s neck brace, which had been supporting her nearly healed neck after her most recent fall.

They remove the arm brace, which had been keeping her broken right arm in place.

Regina pulls away the tubing that forces high-flow oxygen from my mother’s nostrils.

A lump rises in my throat as a thought occurs to me.

We are removing all her armor now, letting it fall away, leaving her vulnerable. We all understand that she can’t be any more broken than she is now. Nor, are we are protecting her anymore. We’ve wandered off the road to recovery long ago. Now, we’re on a different path, each of us recognizing it at different times, as if we are each acquiring a new language at different speeds. I’ve been able to read the signposts for weeks, but I know that others have only been able to read them for days.

We are handing Mom over to a Thing that we have all feared, no matter what our faith teaches us. No matter how many cheery faces have told us confidently that there’s Heaven waiting for us on the other side, none of us have seen this destination, nor have we traveled there. Perhaps someday I will find comfort in the thought of Heaven. But not today. Because my mother’s path to get there is covered in thorns, ripping at her mercilessly even as she barrels blindly forward.

She will travel this last path alone, exhausting every weapon and tool that she used in this life. She will do this alone, just as she did when she gave birth four times. Just as she did when she fought through unbearable pain when she broke her back in 2007–and all the years of pain that followed. Just as she has fought this cancer for 24 years.

Like every other time before, she would do this last battle all by herself.

No man has ever come close to demonstrating the strength that my mother has.

Not even close.

She is the only person I’ve known who has chosen over and over again to walk into the shadows of Pain and Loss.

And still found the Light inside of it.

And then held that Light up for all to see.

Warrior isn’t the title that she has earned.

She is the Hero.

Maybe that’s why her body is still wielding its sword, slashing at shadows.

We can’t tell her to stop fighting.

But at least we can take away her pain while she fights.

Getting COVID: Two Years into the Pandemic

You know on New Year’s Eve, when we sing “Auld Lang Syne” and imagine that most of our troubles (certainly, not all–let’s not be greedy) are far behind us… And in the back of your mind, you’re kind of already rehearsing tragedy. Preparing what you cannot imagine is coming next.

That’s a good way to describe the feeling that I had on New Year’s Eve this year.

Sure, this year is going to be better. I toast my glass of water (because age has made me incapable of processing alcohol… Like, at all).

I suppose it’s a small feat to have managed to have made it to nearly two years into the pandemic before contracting the virus.

But that all came to an end this past month.

Mark it down: January 2022 will go down in my memory as one of the least enjoyable times of my life.

***

Wednesday, January 5th

After two days of remote work, I drop four-year-old Henry at daycare and drive in to work for an in-person work day. Because now, we have two different kinds of work days: 1) remote and 2) in-person. I park my car and head toward the COVID testing site, which is a free service offered by my university. The line–normally minimal over the last few months–is 30-people deep. Not a good sign. I don’t have symptoms of COVID, but I figure I’ll get tested since we plan to have people over on Saturday, January 8th for breakfast. And this Omicron strain is going around.

While I’m waiting in line–NOT KIDDING–I get a call from the daycare.

Henry has been exposed to someone who tested positive for COVID. He needs to be picked up within the hour. He can return if he tests negative on a COVID test five days from exposure. Or he can quarantine for 10 days.

I hang up and start looking for a COVID test appointment on Sunday, January 9th, but nothing is available in the nearest 50 miles until Monday, January 10th.

As best I can, I try to adopt a neutral attitude about being home with him January 5th-10th. I encourage Doug to stay at work while I stay with Henry. I let Henry paint and use Play-Doh. We use tangrams and crayons, building blocks and Legos. I break out Tablet Time as a last resort. We get through it.

Monday, January 10th

Rapid-test appointment for Henry at a local CVS. We take his backpack and coat because I’m going to drop him off as soon as I get the negative test result.

However, it might be a few hours to process the results because of the backlog.

No problem, I think. I’ll take him to a park even though it’s 15 degrees. He has energy to burn off.

Henry runs from me to different trees in a field, over and over again while I stand there in the cold, refreshing my phone, waiting for the test result to come in.

New Test Result Received.

I clicked on the link.

POSITIVE, it reads in giant red letters, as if to tell me, NO, THIS IS NOT A DRILL.

My first thought? Honestly?

F***. How many more days of quarantine NOW?

I do not think, Oh no! I don’t want to get COVID!

Instead, I think, Sweet Jesus. How many more days of full-time parenting do I need to survive? I am not cut out for this.

Henry has no symptoms. I feel fine. I’ve been around him for five days. I’m vaccinated AND boosted. I decide that we are going to skate past this plague because we are prepared.

I call the daycare with the update.

Well… now that he’s tested positive, he can return 10 days after his positive test result.

SAY WHAT NOW?

So that means… the daycare director shuffles papers on her desk. He can return Friday, January 21st.

10 more days? Seriously? Should I NOT have tested him?

Gone is my positive attitude. I’m going to be home, working, with this energetic preschooler for the next 10 days. Doug cancels his travel to a conference in Las Vegas and says that he will work from home and help. This helps, but my mood is still in the toilet.

I miss My Life.

Tuesday, January 11th

Doug develops a fever. Muscle aches, pains, weakness. He can’t move. It’s up to me now to take care of Henry, work, check on Doug, and keep the household going. Henry still has no symptoms. We wonder if it could be COVID, but we have our doubts. We are vaccinated AND boosted. Probably the flu.

We do not play with tangrams or building blocks. We don’t paint or play with Play-Doh. When Henry isn’t sitting with Doug in the TV room, he takes his tablet and crawls underneath the desk where I work and curls up in his “cave.” Using his finger, he “colors” in pixels of a unicorn with a flowing mane for hours upon hours. It’s now Endless Tablet Time and I have zero Mom guilt.

Every now and then, Henry taps on my leg to let me know that he’s ready for me to tap the last pixel of the picture that he’s working on. Together, we watch as the single tap sets the picture into an animated replay of his coloring. His face lights up and in moments like that, it’s hard to be upset that he is home.

But then, I remember all the times I’ve yelled, Listen to me!

And it all comes rushing back.

Wednesday, January 12th

Doug gets a doctor’s order to get tested for COVID and flu. By the end of the day, I’m wondering if I am feeling rundown from carrying the load of the whole family… or if it is something worse. I go ahead and look to schedule a COVID test. The first one available at a CVS in the nearest 50 miles to my house is Sunday, January 16th.

Thursday, January 13th

I skip my exercise, which if you know me, is kind of a big deal. I don’t do that unless something is really wrong. I’m feeling… off. I don’t know how to describe it. Hazy? Slight fever. Some body aches. But I cope. Doug’s test results are in: Negative for flu and positive for COVID.

Okay, then, I think. Here we go.

Doug is still hurting, so I keep everything going. We send the kids to bed early and I embark on a 13-hour sleep trek that I haven’t treated myself too in… Ever? I cannot remember the last time that I slept longer than 12 hours. Was it before kids? I spent years of my life just trying to get 7.5 hours of solid sleep. Remember all those times, waking up to a screaming baby and trying to figure out what kind of scream it was? My God… How many hours of sleep did we lose?

I fall asleep before I can figure it out.

Friday, January 14th

Doug is feeling better. He is able to work and do household chores. I definitely don’t feel well, but it isn’t enough to keep me from doing the things that I need to do.

Sunday, January 16th

I get tested for COVID.

Monday, January 17th

I’m sick. The kind of sick that makes you want to curl into a ball and forget about the world. It feels like every cell in my body is turned down to 30% energy. For the duration of my illness, fatigue is the biggest symptom that I have. Utter fatigue. Hard-to-climb-the-stairs fatigue. Feeling as tired as I did at the end of a long day while being eight months pregnant. That kind of fatigue.

Tuesday, January 18th – Friday, January 21st

My test results come in at 2:00 a.m. on Tuesday morning and with bleary eyes I see the word that I’m expecting:

POSITIVE.

And all I can think is how NEGATIVE that word feels in my life right now.

POSITIVE?

I’m POSITIVE that this is going push me to the absolute edge.

What happens during these days? I call in sick to work and lie on the couch while Henry watches Encanto, Raya and the Last Dragon, Sword and the Stone, and Robin Hood on an infinite and unpredictable loop. Henry creates The Triangle, the space between my bent knees and the couch, where he shoves his little body so he’s nice and snug while I drift into and out of consciousness to the music of We don’t talk about Bruno… I sleep 13 hours a night. I sweat in my sleep and don’t remember peeling all my clothes off. I develop a brain fog that leaves me feeling completely stupid and helpless.

I MISS MY LIFE. I LONG for Henry to return to daycare so I can finally be left alone to recover. On one day, Felicity complains of a headache at school and the school nurse firmly recommends that we pick her up since she has been exposed to COVID at home.

Sure, I think. Why not have everyone home while I’m trying to get better?

I envy all those people sick with COVID who don’t have to care for children or houses while they are sick. Those people who can walk away from their responsibilities, turn on Netflix, and check out of Reality until they feel better.

But hey, listen, I KNOW.

At least I was employed at a job were I could take sick leave. At this point in the pandemic, that’s not guaranteed anymore. At least I have a partner. At least I have the money to pay for my health care. At least I have a car to pick up contactless groceries for the family. At least I was vaccinated and was able to recover in two weeks. At least I have a house and food.

I know.

***

I was looking back at this blog and thinking of the giant hole that is missing in this chronicle of my life from 2020 to 2022. I have been writing, but not here. Maybe because I don’t know what to say here other than this:

We have been holding on.

For two years, we have been holding on. Waiting for it to get better. And finding over and over again that… Maybe this is it.

We have been navigating…

  • remote learning at home (worst idea ever)
  • remote learning at daycare (a paid version of worst idea ever)
  • mask policies–official and unofficial
  • teleworking policies (1 day per week in person? 2 days? Actually, stay home now. Okay, come back. Actually 2 days per week in person was probably enough. We think?)
  • our own level of risk as a family
  • a revolving door of quarantines (seven–YES, SEVEN–so far)
  • quarantine flowcharts (does the unexposed sibling need to stay home?)
  • the New Social Normal
  • missing our friends
  • missing gatherings

But now I’m really wondering…

What if this is as good as it gets? (At least for the foreseeable future)

“What if this is as good as it gets?” -As Good As It Gets, 1997

Indeed…

What if this is as good as it gets?

***

I have recovered from COVID. The last symptom that I’m still getting over is catching my breath while I’m exercising.

I am grateful for vaccines and modern medicine. I wish more people used them.

In the back of my mind, I’m wondering if/when I’ll contract COVID again. It’s entirely possible. Or perhaps I have gained this “super immunity” that researchers are starting to report.

In looking at pictures from the last two years, I’ve seen my children grow from 3 and 6 years old to 5 and 8 years old. I see them with masks on at the apple orchard, masks hanging from their ears while they are in the car, pulled below Felicity’s chin while we’re touring Chicago. Their childhood will forever by marked by the presence of masks. There’s nothing to be done about that. I don’t hate masks and I don’t love them.

I’m pro whatever-keeps-my-children-in-school-and-daycare. Just tell me what to do AND I WILL DO IT.

I’m simply doing everything I can to move us all forward.

One day at a time.

For the last 700 days.

One day at a time.

2:00 a.m. Writing Life

I typically get up at 4:00 a.m.

Not bragging about that. I know how crazy that is. But, please, do remember that I’m utterly no fun at 7:00 p.m. I am yawning. I am so close to passing out.

Five days a week, Monday-Friday, I get up to exercise before the sun comes up, when I know no one will bother me.

My new addiction is waking up on the weekends to write.

At first, it was the same time frame: 4:00 – 7:00 a.m.

But then… things started to snowball.

I would find myself waking up at 2:00 a.m., 1:00 a.m., and sometimes even midnight, my mind working on overdrive. I would try to go back to sleep, but sometimes, once the train has left the station, it was best just to get on board and let it take me where we needed to go, consequences be damned.

It hasn’t been all bad.

I have written some amazing scenes during this time. I would discover a flaw in my character that would make him more interesting, or a hidden intention in another character that I didn’t originally see.

I have never had a writing experience like this before. There are a few pivotal climactic scenes that I know that I’m working toward, but this series of books is largely being written organically, step by step, following a somewhat planned outline. Still, so much of it seems to be discovered in the moment.

The other thing that makes is super unique is that I feel connected to the story in an almost supernatural way, like the story is fighting to get its way out of me. Like it has been living with me for far too long and wants its own air to breathe, its own space to stretch its wings and fly.

Instead of creating characters that I thought I would like, I’ve let my characters become who they want to be–and I’m finding that its giving them more depth and dimensions than I had planned. Sometimes, my characters irritate me. Sometimes, they downright piss me off. And sometimes, they break my heart with their blindness.

I am thoroughly enjoying this journey of following my characters and seeing where they lead me, even as I know that we are approaching a certain cataclysmic event that will change everything.

It seems ominous–this knowing of the changes that are to come for my characters, anticipating how it will change them and their lives, in devastating ways that will ultimately lead to their greatest growth.

I’m starting to understand how authors can actually grow to love their characters and empathize when they ratchet up the tension and the stakes.

Though it would be so much healthier were I able to do this at a reasonable time of day.

The Line Between Exasperation and Gratitude: (Week 3 and 4 of Pandemic Coping)

…is so very real, is it not?

I feel emotionally dizzy.

I mean, honestly, what bizarre disaster movie are we living in?

From what I recall, even Hollywood couldn’t conceive of the current crisis. In all the apocalyptic movies that I can recall (Deep Impact, Armageddon, 2012, The Day After Tomorrow, Independence Day), the fictionalized president of the United States displayed a measure of calmness and wisdom that the balanced the public frenzy.

We don’t have the opposite of a calm and wise leader.

What we have is actually much worse.

We have a delusional, narcissistic, inattentive compulsive liar. In addition to his irredeemable character flaws, throughout the duration of his time in office, he has managed to drive away all of the last bastions of intelligence and competence from the White House so that he is now solely surrounded by sycophants and butt-kissers that hold onto their jobs by constantly showering him with unearned and exaggerated praise for even the smallest achievement while covering up his most egregious errors, which he makes based on his personal intuition (“That’s my metrics.”) which has always been and will always be directed by his own self-preservation.

Could we ever have imagined that a President would suggest that healthcare workers are either “squandering” or stealing masks? Or who would stand by the statement that the National Stockpile doesn’t belong to the States? Or who would encourage the general public to buy drugs that haven’t been properly vetted for fighting coronavirus? Or who would push conspiracy theories that the media is purposefully overhyping the coronavirus because they want to hurt his chances of re-election?

Just… what?

WHAT ARE YOU TALKING ABOUT?

NOBODY IS THINKING ABOUT THE ELECTION.

At least nobody who’s immediate livelihood is dependent on whether or not they are able to keep their jobs three weeks from now.

Just when you think our President cannot possibly make us feel worse about having him as a leader…

He rises to the challenge.

I just cannot.

This is literally the worst time to have this man in office.

I would take so many other politicians in his place right now.

Mike Pence, whom I despise for his “spiritual” quest to rid the country of birth control and abortion? Yup. Approved.

Mitch McConnell? Put in him.

Lindsey Graham? In this pandemic, I LOVE Lindsey Graham.

Mike DeWine, the governor of my home state of Ohio, whom I didn’t vote for in the last election? I kiss his feet.

I would literally take just about anyone in this entire country who has the ability to apply reason to situations, seek advice from experts, and speak in a calm manner.

My six-year-old is a better choice.

My three-year-old is a better choice.

(Although, admittedly, he’s at his best first thing in the morning or after a nap. Even then… He’d probably be less dangerous to the American people because he would be distracted enough to let others do his job. As long as tiny Oreos are involved.)

***

So that’s the exasperated part of me, lately.

But I want to clarify that it’s not my only mode right now. Because at the height of my exasperation, when I feel that I cannot possibly take another day’s news, my rational brain kicks in and I remember gratitude.

Despite the madness that continues to swirl around my house, we’ve managed to create a zone of (mostly) peace and normalcy within these walls.

It’s different.

It involves more teleconferences, Zoom meetings, and screen time than I’d like to admit.

But it also involves being in the yard and the garden a lot. And taking walks. And having the kids around as we prepare dinner. And reading books together. And listening to audio books as I fold laundry, do dishes, change sheets, and vacuum.

We took our kids to fly kites. They loved it.

It doesn’t leave much time for us (parents) to be alone.

Being a parent during a pandemic without any tangible social support networks turns out to be hard.

It’s hard if you’re still lucky enough to have a job that you’re trying to do while the kids are awake. It’s hard if you’ve just been laid off and are looking for work when all the jobs that are hiring require you to put your health and safety at risk. It’s hard if you have a job–but you’re wondering for how long.

But who am I kidding? It’s hard for just about everyone in different ways.

So, gratitude.

We have jobs.

Getting into the field of e-learning last year turned out to be the absolute best decision I could have made at this point in my life. I recently took on a short-term contract as an independent consultant to advise and collaborate with faculty at a small, private university who are moving their traditional face-to-face summer courses into the online format.

We have a home. We have a yard where the kids can play.

We have food. More than enough food, honestly.

We have education. And friendship. And camaraderie (even if only online right now).

We have love. And laughter. And a sense of humor.

And these days, we **do** have something that we didn’t have two months ago.

Shared purpose.

A reason to look beyond the frustration and stress that we’re experiencing and look for those whom we can help.

For there is always someone who needs more help than you do.

***

And here’s where the emotional dizziness comes in. Because if I think about it long enough, my mind swings back to the realization that…

Wait… I cannot stop at gratitude.

If all I do is focus on what I’m grateful for and not be concerned about how others are suffering, nothing changes.

The cracks in our systems that are opening and swallowing so many people, they will remain.

Just because I have what I need does not, and SHOULD NOT, make me stop noticing and raising issue that the systems that are supposed to support and protect Americans are broken.

It does make me wonder though…

…will Americans finally put their collective foot down?

Will they push for the urgency of providing health care to all Americans?

Not a stop-gap. But real, actual, tangible access to health care that anyone–working, unemployed, full-time, part-time, retired, disabled, even (gasp!) non-citizens–can receive health care at a low cost?

What about sick leave?

What about family leave?

What about universal child care and preschool?

What about humane systems of incarceration?

What about preserving the human rights of anyone who is in this country, not just those who are citizens?

Or will we, once again, be too busy to push for real change?

Will 45% of Americans, as always, follow the President’s advice?

Not me.

Each day’s news, each day’s death toll, each day’s mental and emotional burdens are driving this experience deeper and deeper into my memory. It’s exposing all the flaws of capitalism run amok.

This cuts too deep for me to allow it to be “quickly forgotten.”

Strange and Broken Things (Week 2 of Pandemic Coping)

It’s a strange thing, to be at home in the early afternoon on a Wednesday, walking through the backyard with my kids, flowers blossoming in the bright spring grass. To walk down the street and realize that, Oh, there are kids at that house, too. A dad is pushing his child on a swing, hanging from a tree branch. This dad and I are home in the early afternoon on a Wednesday, playing with our kids.

It’s strange to remind your kids that, Remember, we can’t get too close, okay? Saying, ‘hi’ is okay.

It’s strange to not be thinking about upcoming birthday parties. Or mentally preparing to present at a conference next week. Or coordinating the PTO hospitality lunches for my daughter’s school. Or taking my daughter to first communion classes. I deleted all these events from my Google calendar en masse. Also gone, the reminders: on Wednesdays, pack bathing suit for Felicity, in mid-April, order birthday cake by this day, in the first week of May, deliver Teacher Appreciation lunch.

It’s jarring to see the end of normalcy displayed so clearly in my Google calendar. It’s as if someone I loved had died and I just couldn’t even cope. It has echoes of Grief. But then, when my dad died, I went back to work the next week and the world spun on like nothing had happened. I wanted there to be nothing to do, but there was still everything to do. No one else behaved like there was any reason to change, and so I felt like the odd one.

I also had Choice. I could choose to allow myself to get swept into the rituals and rhythms of Life that no one else had given up and find some reprieve from the pain of my New Reality, however short-lived. It was a quiet suffering that I moved through in my own time. And I made incremental progress toward my acceptance. It was a personal journey and I was in control.

Not this time.

This time, there really is no escape, physical or mental, from this New Reality. I cannot binge-watch Netflix until May. I cannot even do much creative work, like video editing or writing. The kids are home. AND I still need to work. To sit here and write in quiet moments to myself, I get up at 4:00 a.m. and sacrifice a daily workout for the mental clarity that writing gives me.

At a time when I most need a reprieve, there is none to be had.

Being a parent is fun. This is all so fun.

You’d think that with the deletion of all those events and reminders would come a measure of peace and clarity.

Not so.

Instead, my mind is overflowing with news and charts and numbers and questions and predictions and announcements.

I’m constantly thinking about disinfection and washing hands (all. the. time.) and cleaning up the house over and over and over, and getting the kids outside, and Is Felicity reading enough? She should be writing more. Are we doing enough for Henry?, and Relax. You’re doing the best that you can.

My mind doesn’t have much space left to think about anything else other than this Giant Wave that is approaching all of us.

When will it hit Ohio hard? How many people will die? Will someone I love die? Will their body be stored in one of those refrigerated semi-trucks until we can bury them? Was that cold that I had really COVID-19? I had a low fever and a sore throat. Then I felt okay, like nothing happened. Then my lungs were irritated for a couple of days, and that was weird. But no doctor would order a test for me with the few symptoms that I had.

We are all trudging through physical isolation while also being solely responsible for regulating our consumption of the the deluge of news and social media posts that we consume each day about the surging pandemic.

Limit your social media consumption for your mental health, they say.

I don’t want to read about this all of the time, and yet I do. I don’t want to read about another instance of Trump’s feckless leadership and reckless disregard for the consequences of spreading misinformation during a pandemic.

And yet I do. It’s like my mind is begging for another example of,

See! There he goes again, being the biggest jackass the world has even seen! See everyone! He not only sucks at his job, but he’s actively making it worse! See! He doesn’t deserve to lead us one more day! Get rid of him! SOMEHOW!!!

And yet there are still millions of Americans who stand up for this buffoon. It’s not his fault. We can’t put the economy on hold forever. We have to go back to normal. Let’s get back to normal by Easter.

Fools.

And so my mind spins on and on.

A few days ago, I woke up at 2:30 a.m. and just couldn’t go back to sleep. I tried. For an hour, I tried. But once the thoughts started, they rode the steep curve of that red line, riding the most terrifying roller coaster ever, clink-clink-clink, rising exponentially in the coming weeks. Up, up, and up. Who in my life would become part of that line? Who will I lose?

For certainly, we are on a path to becoming a country in which everyone loses someone. We are starting to hear the rhetoric that it’s patriotic to sacrifice ourselves and those we love to a disease that we could have been better prepared to fight had our own destructive president not dismantled the systems that were in place to keep us ahead of the curve.

And to provide our human sacrifices all in the name of preserving the Great American Economy.

It’s too late for the outcome to be much different than that.

It haunts me. That undoubtedly, months from now, after thousands, if not millions of Americans have died, Trump will talk about how much worse it would have been had they not done whatever they had decided to do. Oh, right, sorry. The federal government isn’t responsible. It’s every State for themselves. Hope the States have enough funds to outbid foreign governments for their bulk purchase of medical masks and ventilators. Unless they use flattery to win Trump over. (Which I find even more maddening. Because if governors resort to falsely flattering Trump on the record in order to secure a federal response, now all the Crazy in America will have “evidence” that Trump is doing a good job.)

But in the event that Trump tries to take credit for whatever federal response the government may take, he can always say, More lives could have been lost, and be right. That’s the same argument that we’ve heard after years and years of increasingly horrific mass shootings. Hard to think that the argument will change much.

It haunts me. That Trump will undoubtedly, through tweets and press conferences, rewrite history over and over again so that it looks like he was never wrong. But, hey, at least he can’t use his rallies to rewrite history right now. I revel in the fact that he cannot hold these mass ego-feeding sessions that simply confirm his far-fetched delusions.

Trump will do everything in his power to be seen as the Winner.

But in 2020, it looks like there’s only going to be Losers. Trump included.

And in any case, we don’t need a Winner.

We need a Hero.

(Fauci for President?)

So after an hour of lying in bed, thinking and thinking, I decided to get up and do something for myself.

I did some yoga.

And then I cleaned the kitchen.

***

And then this happened.

After years of erosion along the bank of a creek behind our house, a tree fell over into our backyard. Now it lies against the edge of our backyard, at the end of its life, broken and unable to be properly disposed of as it is not considered an “essential service” at this time.

The morning after it happened, I occupied the kids by having them pick up sticks and put them in a bucket. It was cold that morning and my coffee cup warmed my fingers as I watched my kids poke through the safest parts of the fallen tree.

Looking at its dark branches against the pink of the dawning sky, I remembered a dream that I had about a tree falling over in the backyard, at a time in my life when everything seemed to be turning upside down.

Maybe it’s a coincidence.

I don’t think everything like this has to be a sign.

But I’m not closed to the idea either.

But it’s strange.

And then this happened.

While I was in a conference call, I was twisting my rings on my hands and I noticed that they didn’t feel right.

The setting was just gone.

I didn’t hit it on anything.

It was strange.

(Jewelry repair is also not an “essential service” at this time.)

These things don’t need to mean anything. I can be okay with believing that sometimes stuff like this happens all at the same time.

But it’s strange.

***

The rhythms of our lives are radically different, but we are making it work. I am working from home from the morning to the afternoon and my husband works from afternoon to midnight. There is no one else to help with care-taking. All the social support of friends and church, daycare and after-school care. It’s all gone. The best babysitter now is the TV and a Chrome book, which we use prudently through the week and throw caution to the wind on the weekend.

We are finding the good in being with our kids more. Time that we previously spent simply commuting to work and picking up kids and going to the occasional weeknight event is all now spent at home. We eat dinner together like usual, but our kids now eat with one of us at lunch time. Sometimes, I finish my shift online and find culinary gems like this waiting for me:

(I know. I’m lucky. I married well. I don’t share stuff like this all the time because he’s too good, and no, you can’t have him. I got him first.)

Although it is hard in the immediate moments of taking care of our kids to remember this, it is ultimately good for us to hold our kids close during this time. (Even though 25% of the care-taking still requires the constant vigilance and reminders of No, Hold on, Wait, Put that down!, Where’s your jacket? Away from the road!, No water guns right now, Zip up your jacket, My God! Stay out of the mud!, Too close to the creek!, Stop! No, that’s my coffee, Careful!)

It is good to take them outside to pick up sticks and discover newly blossomed flowers and put on their rainboots to splash in the puddles and watch an earthworm stretch its way across the paving stones for ten minutes and wish him well. Bye-bye worm!

It’s good to give in and read a Five-Minute Paw Patrol story (few girl characters, and they never solve the problems) when I’d totally prefer to read something like the Little Engine that Could (good moral) or even One Fish, Two Fish, Red Fish, Blue Fish (good rhyming schemes).

In all this time with the kids, moments emerge.

There’s the moment when I hear my daughter reading to my son, as the daylight fades from their rooms. They are having a moment together, apart from me. And it doesn’t tear me apart. It makes my heart soar.

There’s the moment as I’m sleeping that I feel my husband’s hand slip into mine and I wake long enough to squeeze it but not long enough for my mind to start spinning again.

There’s the moment when I hear, for the first time, my son say to my daughter, “I love you, Cici.”

Although my places are restricted, time marches on, leaving behind moments in its wake.

Gather ye moments while ye may.

We Are Not Used to This

Both kids are now home.

Both of us are trying to work remotely, tagging each other in as the day allows.

We are creating a New Normal.

We are trying “home schooling” and mandated House Clean-Up times and schedules and nipping bad attitudes in the bud.

We are also just trying to not lose our minds.

I consider it an astounding feat that we have managed to limit TV time to less than 3 hours per day. Winning.

Here’s a real conversation that happened this Tuesday, 3/17.

  • Henry: “Is it Sunday?”
  • Me: “No.”
  • Henry: “Oh, it’s Saturday.”
  • Me: “Nope.”
  • Felicity: “No, Henry, it’s Monday.”
  • Me: “No.”
  • Henry: “No, it’s Saint Patri’s Day!”

Aren’t you jealous?

3/17/2020

***

On Thursday, 3/12, the first wave of anxiety hit me with the announcement of the closure of all K-12 schools in Ohio.

On Sunday, 3/15, we learned that all restaurants would be closing to dine-in customers. The second wave of anxiety hit me. Not because we eat out a lot. Not at all. We actually eat a lot at home.

But it felt like the first sign that soon, very soon, public places were not going to be an option for occupying the kid’s time.

Read: No kid’s museum, no indoor parks, no library, no movies, no all-the-typical-places-where-we-might-take-them-to-stay-sane.

I’m not prone to anxiety. I worry, sure, but anxiety? No, not really.

But the thought of losing my go-to methods of occupying the kids, actually, not even really having a break from home life for 2, 3, or 4 months…

Oh, Sweet, Sweet Jesus.

This is fine meme.
Art credit: KC Green

So after driving to at least four stores to find toilet paper (still haven’t found any. Thanks to friend, Cate, for sharing some rolls), my husband decided that we should order take-out from a local Mexican restaurant, while we still can.

But by the time we got home with the food, he had decided to drop us off with the take-out bags and continue his search for needed supplies, as the thought loomed in our heads: When we will be officially told to shelter-in-place? And are we ready for that?

The kids ate the tacos and beans like champs, happily and hungrily. I stared at my food, cold waves of anxiety rising and washing over me again and again. Feelings that I haven’t had since I had my first baby and my mother returned to her home in Minnesota. That feeling of floating alone in the ocean, holding on to a life preserver, not knowing when the circumstances were going to change. Not knowing if a wave was approaching that I couldn’t see. Not knowing if I had the fortitude to hold on. And then all of the guilt because, let’s face it, I am likely to be just fine. A healthy, 30-something in the suburbs.

Before I knew it, the kids were done with their food, and I was still sitting there, thinking of what I needed to do to get ready for a week with my daughter at home.

They abandoned their plates, leaving the mess behind and disappeared somewhere else in the house.

When I realized they didn’t wash their hands before they had gone upstairs, I yelled at them to do so, but remained there, paralyzed, looking at the take-out bags.

But they washed their hands before dinner. Pretty sure they did. Yeah, they did. Or was it just Henry’s hands?

And then the thoughts started.

You can be asymptomatic for up to 24 days. Wash your hands. Cough into your sleeve. Wash your hands to Happy Birthday. You might not even know you have it. Stay home. Don’t go out. Wash your hands. My hands, but also the kids. All the time. Wash three sets of hands, that’s six hands. Every time you enter and exit a room. The virus can live on surfaces for up to two days. It floats in the air. Someone doesn’t need to cough on you–You can just breathe it in. There aren’t enough ventilators and there may not be enough hospital beds. What about my friend who is pregnant? Is she okay? What about Mom? What if she gets it? Can’t think about that. Can’t let the kids see her until this whole thing is over. What happens when the daycares close?

And then, I started eating. One taco. Two tacos. Three tacos. Chips. Beans. More chips. Salsa. More chips. Beans. The second bag of chips. More salsa. Oreos? What the hell. Sugar felt good. Where’s all the chocolate around here? Maybe some ice cream. Oh, there are cones, too. Hm.

Oh my God, I realized. I’m stress eating.

I haven’t stress-eaten in probably 15 years or more.

When my husband got home, we let the kids play alone upstairs while we processed what was happening around us.

“Sweets, people are getting f***ing crazy out there,” he said, eyes wide. “I saw a guy, two older guys actually, at Sam’s with–I swear to God–nothing but Swiss Miss packets in their cart. Just boxes and boxes of Swiss Miss.”

“Shut up,” I said, relieved at having something to laugh about.

“I’m serious. I’m serious,” he assured me.

It felt good to laugh. (Is there anything more attractive, at this moment, than a partner that can genuinely make you laugh? I think not.) And he was more than happy to oblige, with story after story of Ridiculous Carts in Sam’s Club.

“It’s really hitting me,” he said, “just how many people there are that have literally no idea how to cook. They’re like holding these cans of food and saying things like, ‘Could we make this or this?’ ‘What about this?’ There are people walking the aisles of stores with actual faces of fear and panic. I’ve never seen it like this before.”

And welcome to Life in the Time of COVID-19.

A time when we will choose to either battle our internal demons of the fear of scarcity or succumb to them and war with each other. Over toilet paper and Swiss Miss.

Those end-of-the-world disaster and pandemic movies that massaged our basest instincts to flee or fight, it feels like our brains are feeding on them to fuel our daily behaviors.

We didn’t think we would be here.

Disasters on this scale don’t happen to the U.S., right?

They happen in “third world countries.” They happen in places with less technology and fewer resources. They happen in countries without the same number fighter planes, tanks, and missiles.

Turns out, they happen here, too. We are not so special that we get a pass on this one. Perhaps we shouldn’t have disbanded the National Security Council’s pandemic team in 2018 in the name of reducing big government because “we can get them back if we need them.”

But for some global perspective, let’s remember that Syrians continue to run for their lives as Russian planes swoop in and bomb the living hell out of Idlib. Meanwhile, we are experiencing a very, very, very mild version of the panic and fear that these refugees face every day of their lives.

But we are not used to this.

More specifically, affluent White America is not used to this.

We are not used to restrictions and limitations and “unavailable” and “2 per person” and postponing elective surgeries and schools closing for months and church services moved on-line for safety reasons and March Madness being cancelled. (Okay, honestly, that last one doesn’t bother me at all.)

This is Land of Freedom and Choice and Individualism, baby.

Right?

Not today.

Actually, not for the next 2-4 months.

Now, we’ve got to learn how to be Collectivist, to behave in a way that benefits the common good, to postpone or abandon plans, to cooperate and be kind, to put competition aside so that we can protect lives and ensure that we don’t end up holding the hands of our 60-, 70-, and 80- year old loved ones as they die without proper treatment because of health care rationing.

Think about that.

Toilet paper is the least of our worries.

I’m concerned that there is not enough emphasis on looking out for each other and supporting each other through this difficult time.

That’s what led to my meltdown on Monday night this week, as our son came home from his last day of daycare.

No more daycare. No more support, was how it felt to me.

Now, it’s just the four of us.

No help from grandparents.

Now, we will have to alternate work with care-taking. Now, we will have even fewer quiet moments together without the kids.

Our village of friends, daycare, school, after-school programs, libraries, and church just collapsed into the space of our home.

I wasn’t prepared for this. None of us were.

So that’s where I’m at with coping. How about you?

If you’ve got a story about Ridiculous Pandemic Carts, I could really use a laugh.

Pandemic, Here We Go: Stream of Consciousness # 2

Where to even begin.

For me, it really started on Tuesday, March 10th. There was an emergency meeting of the eLearning division entitled “Pandemic Planning,” which had been set the previous Friday. We were told to expect that very soon all in-person classes would be suspended. As an eLearning division, we would abandon all projects and previous plans and meetings. We would come together as a group to help the university faculty–especially those that have never taught online–be prepared to teach everything online.

Thursday afternoon, 3/12
Deserted hallway at Sinclair.

Yes, it was a bit of a shock. But honestly, I was already on high alert because just a few hours before this meeting, the chair of a department wandered into our media production studio, holding a printed email in her hand, asking me if I would come to a department meeting to help her faculty members understand how to teach online.

I remember the way she looked as she hesitantly held the box of an unopened webcam that we loaned out to her. It was that moment between reluctance and resignation and all the body movements that come with it. She was going to have to be the one to rally her troops.

But none of us were expecting that the end to in-person classes would literally be just hours from that moment.

And then the spotlight swung to the eLearning Division.

***

Ah, eLearning professionals. The unsung heroes of this whole mess.

Here’s how to do a web conference. Here’s how to record it. Here’s how to upload slides into your web conference. Hey, look! You can draw on the slides. Here’s how to do picture-in-picture. Now, you’ll need to publish it, share the link with students, create a document with the list of links. Captions? Here’s how you do that. Should you make all your lectures right now? Why don’t you work on just one week’s worth of content? And keep your videos short. Seriously. Think about what is necessary to say. Remember, they can re-watch the video. IT is working on purchasing more webcams. In meantime, do you have a laptop with a camera?

It’s been fun.

But seriously, it feels good to be able to help others who need help. It is my life’s true calling and I’m happy to do it.

***

In the meantime, we will be fine.

We may run out of toilet paper.

But by God, there will be sausage. And eggs.

***

Kidding aside, yes I’m concerned.

It’s hard not to be in the midst of so much social disruption.

But I know that if I get it or my kids get it, we will likely be okay. It sounds like having it is going to be awful, but hey, our mortality is low.

My prayers go to my mother in her 60s, who is also immunosuppressed right now.

To my stepfather.

To my niece, who lives with Type 1 diabetes.

To 75% of my church congregation, older than 60 years, with whom I typically worship every Sunday.

To all of the grandparents who, now that Ohio K-12 schools are closed and parents need to work, may be watching their grandchildren, some of whom are currently carrying this virus and don’t know it.

To all of the small businesses (and the families that rely on them) that are going to be hurting because everyone is staying home.

Despite the negligence of our current President in treating this public health crisis with the attention and seriousness that it deserves, I’m encouraged, nay comforted, by the leadership of Ohio Governor Mike DeWine. (A REPUBLICAN! Look! It’s possible to do the right thing even when it contradicts what the President says!! LOOK!)

My hope is that leadership at the federal level can also get some legislative pieces in place to protect and aid the most vulnerable. This isn’t time for your lesson in Bootstrapping of whatever other American Resiliency morals you’re trying to teach via withholding vital healthcare services.

And it’s sure as hell not helping to keep on driving the Anti-Immigration narrative by calling COVID-19 a “foreign virus” and adding more countries to the travel bans.

The neat thing about viruses is that they have no nationalities (Did you know?), they don’t need to apply for visas, and they can’t be turned away at the border. And bonus points for them: They’re likely bringing ALL of their family.

And there was no wall that could have been built that would have stopped this from happening.

Birthday Parties: Stream of Consciousness # 1

One thing that I miss about the time before Child # 2 was having a bit of time to write out real-time reflections on parenthood. With one child, I was able to do quite a bit of that because naps existed and there was just one child to take care of.

With two kids, it’s pretty impossible to do much blogging as I once did. At least the kind of blogging that I prefer. The kind where I revise, revise, and revise until it’s just right.

But it’s a new year and it’s time to get realistic about how I use my time. I love to write. I love to share my writing with others. I work. And I also take on far too many creative projects, which I am not willing to give up because they all bring me joy.

So my goal is to change my methods and standards for writing this year.

For this year, I’m going to blog in a more stream-of-consciousness style. Not because I don’t like to revise and make everything just-so.

It’s more out of necessity.

So excuse the typos and love me for my Flaws (of which, I’m sure there are many).

***

So Henry will forever celebrate his birthday on Groundhog Day. Which I think is payment for putting me through 11 additional days of pregnancy past his due date, which, at the time, made me feel like I was living my own personal Groundhog Day again and again.

Three years later, I mostly remember his birthday as being a test of sheer willpower to confront pain and refuse to give up.

And there was lots of screaming.

And too much blood.

And this.

Isn’t it disturbing/befuddling/miraculous that time helps us summarize the most momentous of days in such few words?

***

In any case, we celebrated Henry’s birthday yesterday, and we came out on the other side of it unscathed and only somewhat frazzled.

One of the dads that came asked me while I was getting ready to serve cake and eleven kids were chomping at the bit for sugar how I could “be so calm.”

That was pretty much the best compliment I’d gotten from a stranger in a while. If “calm” is what I’m projecting, seriously, I deserve a medal.

I said, “It’s because I’m not expressing everything in my head.”

Which is so true.

I think that’s what the second/third/nth child does to you–they elevate your threshold of what your expectations are for what you deal with during the day.

What do you do if you go from zero kids to twins? Or triplets?

Yeah, those parents deserve more than medals.

In any case…

Kudos to my husband for cooking the food for the party: a gluten-free, dairy-free pasta bake and broccoli. Sounds gross. It’s really not. But this is what you have to do when your kids have allergies.

And hey, did you know that basically every birthday party has pretty much the same menu that neither of my kids can eat?

Pizza, cake, and ice cream.

Gluten-free, dairy-free cupcake (courtesy of me)

It makes for a lot of texting back and forth with parents who are hosting birthday parties.

The good news is that just about every parent I’ve communicated with is more than happy to secure an alternative.

#inclusiveeating

For whatever reason, we’ve been to about five birthday parties in the last four weeks. ‘Tis the season? I thought kids had birthdays throughout the year, not just in the winter. But okay.

I guess this has been about birthday parties.

Title found.

See you next time.

A birthday cake with Grover and Cookie Monster. It says "Henry" and "3."
Not dairy-free or gluten-free (courtesy of my amazing Mom)
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