Seasons of Caregiving

It’s been over 25 years since my mother first showed signs of Alzheimer’s. I helped care for her for 14 years and many days were long and hard. After she died, a part of me thought I was done with caregiving; I had served my time. But, of course, that’s not how life works. I was, however, given a reprieve.

This summer I was reminded of what caregiving looks and feels like as I faced a series of family health issues – each one requiring something different from me.

My husband after his first kidney stone procedure.

The first one happened at the end of our week at Lake George, when my husband was suddenly struck with the pain of a kidney stone. His exuberant personality shifted into a hardly recognizable grimness that spread across his face. Before I knew it, he was throwing up repeatedly, and we were on our way to the emergency room. When someone you love is in pain, the only true relief comes when the pain eases. There’s no time to think about yourself; it’s hard to even remember to breathe.

The second health scare was even more traumatic. I received a phone message saying that my brother had been in a serious car accident. He survived, but his sternum was broken, his kneecap had been shattered, and they were checking him for other injuries. He was in the hospital, and I was his closest of kin. Time suddenly stopped, or maybe it went reeling backwards. This was a brother I grew up with and adored. Scenes of us playing with Matchbox cars, riding bikes to the park, swimming inside the shark nets in Panama flashed through my mind. As a teenager he totaled his car. I remembered how my mother said she cried when she saw his crumpled car because she didn’t believe he could have survived. But he did. Back then. And now again.

My brother compared his leg wrap (right) to Apollo 11 (left).

This summer, I spent time at the hospital, whispering in the ante room before his surgery, foIlowing my brother’s own meandering memories about the moon landing. Fifty years ago, we sat side by side on the cool tile of our Florida room watching black and white footage that became history.  I composed poems in my head about astronauts and rocket ships and snippets of our conversation. But inside the thrum beat of my heart repeated: “Please live. Just live.”

I didn’t want to be a caregiver again. I felt like I had PTSD and was being plunged headlong back into a tunnel I couldn’t escape. My mind flashed over all the responsibilities I had – not just mine, but my brother’s. I couldn’t do it. I couldn’t take care of him – his needs were too great – and be present in my own life.  Yet, how could I not.

Sunny, before her illness.

My third caregiving role snuck up on me with a gentle nudge from Sunny, our golden retriever. Granted, my focus had been elsewhere, yet her gradual loss of energy registered. She was a dog who spun in circles at breakfast, raced up and down our driveway, barked at every delivery van, accompanied me to the barn each morning and took long walks with her tail lifted high. Over a period of a couple of days, Sunny seemed to age – she moved slower and the light seemed to dim in her eyes. My first thoughts were “the heat” or that she’d dug something up on the farm and eaten it. But when she struggled to climb the single step into our mudroom, I knew it was time to go to the vet.

With a possible diagnosis of an infectious disease and two bottles of medication, I started out the week hopeful. We could fix this. Sunny had always been strong and energetic with an unquenchable spirit (much like my husband). But one of the lessons I’ve been learning this summer is that healing takes time. And each day brings its own unique set of circumstances.

Ruby and Foxie coming in to eat.

Caring for the horses on our property reminds me that we can’t rush time. Foxie and Ruby need to be fed every day, and they receive allergy medication twice a day to keep them from rubbing themselves raw. Every morning and every evening I walk down to the barn and call them in. I scrub out their water buckets, apply ointment on the slow-healing wound on Foxie’s belly, give the horses a scratch on their necks and look into their friendly, dark eyes. This predictable schedule is grounding.

My husband will have a second procedure to finally remove his kidney stone next week, my brother has transitioned from the hospital to rehab to home, Sunny makes her daily trek to the barn with me while I watch her for signs of new life.

Despite my anxieties about caregiving, I’m grateful for these days that remind me to appreciate each moment.


Endings and Beginnings

Endings and beginnings. This month I seem to be in the midst of both of these passages. Everywhere I turn, it seems there’s another ending — a change, a loss, a time to say goodbye. But lest I get too caught up in grieving the passing of a season, I can’t help but see the seeds of new beginnings all around me as well. Read the rest of this entry »


Grandson of Secretariat: Champion of my Heart

Each year as the Kentucky Derby rolls around, I get a lump in my throat thinking of my horse Crimson Express. He was the horse that carried me through the years when my mother descended into Alzheimer’s, and I experienced a series of miscarriages.

Crimson was the horse I leaned on, literally, as the weight of grief pulled me down. Read the rest of this entry »


World Alzheimer’s Day and the Gifts of September

This time of year has always been special to me. Typically in the Carolinas, on the first day of fall the summer heat begins to ease and we get a hint of the cooler weather that is to come.

World Alzheimer’s Day and my birthday happen to fall side by side, which somehow seems appropriate.

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After the Eclipse

The evening after the eclipse, Sunny and I take a walk. The sky is mostly clear, except for a few dramatic clouds hovering behind the tree line. The horses are grazing as usual, their coats covered in fine sweat that is just beginning to evaporate as the heat and humidity slowly lift. It is 8 o’clock, four hours after the sun and moon finished their dance through the sky.

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August Sky: Preparing for the Eclipse

Three days before the eclipse and the sky is on fire. Not in the west, like it normally is when the sun is going down, but in the east. What does it mean?

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Alzheimer’s Support, Part II: A Window Into Caregiving

Spending time with my sweet mom while I was yearning to have a child.

As someone who has lived through a parent’s Alzheimer’s, I have deep appreciation for AlzAuthors and the compassion of its authors. I traveled a lonely path, caring for my mother whose memory began slipping when I was in my early 30s and trying to become a mother myself. Mom’s slow dance with Alzheimer’s lasted for 14 years.

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As June Gives Way to July — Pausing to Give Thanks

Is it really July already? For some reason, I thought June would continue on for a while longer. It was jam packed with so many special events and days. As usual, I need to take a moment to slow down and process all that has happened. From a family trip to the beach to my 35th college reunion where I had the opportunity to gather with classmates and hear astronaut Tom Marshburn talk about space as I shared about the experience of writing my book to the week of the summer solstice when so many people affected by Alzheimer’s joined together for #TheLongestDay campaign.

 

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Podcast: Straight from the Horse’s Mouth

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In last week’s post, I talked about how the process of marketing Motherhood: Lost and Found has added new layers to my story. Each time I prepare for a presentation, sit down to write a press release or have an interview about my memoir, I have the opportunity to look at my relationships anew.

I treasure this time spent in contemplation about my mother and the depth of her influence on my life.  While Alzheimer’s shifted the course of our relationship in unexpected, painful and challenging ways, it also taught me to slow down, release expectations and open myself to the gifts within each moment.

My perspective has changed, of course, with my mother gone. It is much easier to see that while the care taking and the grieving seemed endless at the time, it was but for a season. I am reminded that all of us lead lives that are a series of seasons, seasons that in the conglomerate make up who we are, seasons that lead to our final act.

I have transitioned from a childless woman in her early 30s to a mother in her mid 50s who has laid her own parents to rest. Time has evaporated. The reason I continue to share the story about my mother’s Alzheimer’s and my own infertility is to provide a message for those who have suddenly become stranded on their own island of grief. My hope is to reach out a hand, to let my readers know they are not alone.

I hope you find meaning in this podcast. Thanks for reading and listening!

Click here to listen to the podcast.

To order a copy of Motherhood: Lost and Found, click here.


The Resonance of November: Part II

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November 17th is the anniversary of my mother’s death. This year, with the recent release of my eBook, and “A Conversation about Alzheimer’s and Dementia” at Main Street Books scheduled for this same day, the date feels even more loaded than usual.

I find myself reliving my mother’s last days. Nine years ago, we had a drought similar to the one we are having now. I remember my husband and I walking the path at Jetton Park and seeing the stretches of red clay populated with dark tree trunks and boulders that were usually underwater.

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As we traversed my mother’s last weeks and days, it felt like we were walking on the moon. Normal life had receded like a distant planet as caregiving took over my days. I felt like an alien in my own skin. This week, as my husband and I return to Jetton Park, we’re seeing the same strange landscapes that are usually covered by water.

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Nine years ago I waited for the fall colors to blossom and fade. I kept thinking that the leaves would be gone by the time my mother died. But they hung on, flashing a kaleidoscope of gold and crimson, russet, ginger and auburn. I drove by one particular tree on my way to the nursing home, and each day it got brighter until the day of her death it was like a burning flame.

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As the years have passed by, my mother’s voice seems to grow stronger. Not a nagging voice of a mother encouraging a child to do the right thing. But the loving essence of her, the joy she took in reading and writing, her delight in nature, her natural sense of nurturing, her keen desire to continue learning and her depth of connection to her family. All of this and more surrounds me as I move through my days.

I could not be more grateful that she was my mother. Perhaps I need to say this aloud, to write it over and over because I didn’t fully appreciate who she was when she was alive.  The thought makes my eyes fill with tears. I wish I had done more for her. And yet, I know she understood and gave me grace. Even when I was a self-centered teenager. She never expected me to fulfill her. I pray that I can share the same kind of unconditional love with my daughter.

So I celebrate my mother this November. Who she was and how she seasoned my life so tenderly with her love.

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Me and Mom