Smokescreen

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Our waters are surrounded by a smokescreen.

For weeks and days our waters on the Puget Sound are shrouded by a smoky fog, the result of fires burning out of control to the north of us in Canada and the south of us in Oregon.

Just now I hear a ship’s foghorn bellowing a warning of its approach.

For in these waters we cannot see what is ahead of us, but must move forward.

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Last week my sister and I sat together at the table with a social worker from hospice.

Our mother had been admitted two weeks ago, and we meet to talk about mom’s situation.

We have just discussed our mother’s end of life plan over a form we must fill out that checks off which measures we will take or not take to extend her life.

CPR. No.

Feeding tube. No.

Ventilator. No.

Antibiotics…….this is a grey area difficult to define.  Will we administer antibiotics to prolong life?  Or for comfort measures only.

For now, we check the box….to prolong life.

She was admitted to hospice after being diagnosed with aspiration pneumonia. Her breathing was labored and shallow. She was weak, and tired. Yet a smile still lights up her face when we walk into the room.

Her pneumonia cleared up after a round of antibiotics. But with her swallowing reflex diminishing, she is at risk of aspirating again.

Over the phone in a twenty minute conversation, the hospice doctor patiently walked through the steps of the hospice decision with me after doing an assessment on my mother.

“When we come to this stage in the Alzheimer’s disease, we need to prepare ourselves that it is not the Alzheimer’s that will kill her, but another ailment. An infection such as pneumonia can be the cause of her demise. At some point we must assess, are we prolonging the inevitable at the cost of the quality of her life? This is a point for you and your family to decide.”

We review the living will she filled out ten years ago, before this Alzheimer’s fog arrested her brain.

At that time she stated, “I wish no extensive measures to prolong my life, as long as quality of life is not compromised.”

How do we measure the quality of a life?  Who helps us decide that?

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There was one point out on the water on my paddleboard this morning I become suddenly afraid, gripped by fear of the darkness below me.

The view that at first was calming and beautiful out on the still, clear water, drew me slowly over the dark and ominous, deeper cold waters of the Puget Sound.

Fear drove me to push myself closer to shore. Paddling over shallower waters I could see the beauty of the bulbous kelp’s long ribbons floating below, tiny red crabs holding on for a free ride. The pouf of a grand Lion’s Mane jellyfish appeared underneath. I watch the pulse of its feathery red tendrils.

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(Photo by Dan Hershmanhttps://www.flickr.com/)

From above an osprey plunges into the cold waters, clenching life from the sea into its talons to take life into the air, towards the sky.

Below the surface life abounds, just beyond the eye’s first glimpse. 

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I step into my mother’s room for just a few moments, on the way to meet my husband for our 36th anniversary dinner.  He has walked this path of caregiving with me for one-fourth of our married life. He first met my mother when he was 17 years old, my high school sweetheart. He was been first hand witness to my mother’s decline.

Today when I walk into her room her eyes light up with recognition.

I sit next to her wheelchair, kiss her cheek, and hold her hand.  Her sweet smile shows me this is enough, to be next to her, rubbing the folds of her soft hand in mine, though the rest of her mind is lost in the darkness of Alzheimer’s. I read to her a story I wrote about her, one called “Messy Edges”, a story that shares how she has taught me to see beauty in difficult places through her disease, Alzheimer’s. She continues to hold my hand as I read to her out loud.

For many years she read to me at my bedside, aloud. She was the one who taught me to love words. She was the one who taught many others to love words and stories in her role as a third grade teacher.

Her words are few now. Yet her smile expresses all that is unsaid.

Today she is able to listen intently at the words I have written, my first in print. I end the story. I tighten my grip on her hand. 

“Mom, you always told me I was a writer,” I tell her.

She looks up at me and smiles, her angelic smile from heaven.

She nods.

“You are.”

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To read a copy of the essay, “Messy Edges” and many other beautiful essays on the grace of aging, follow the link to The Wonder Years, 40 Women over 40 on  Faith, Beauty and Strength , an anthology edited by Leslie Leyland Fields

https://www.amazon.com/Wonder-Years-Women-Beauty-Strength/dp/0825445221

https://alzauthors.com/2018/08/29/meet-vina-mogg-alzheimers-blogger-at-seaglasslife-com/

I am an AlzAuthor

A tribute to my father……

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I am grateful to share my father’s and my family’s story as a guest blogger on granndparentslink.com

I am even more grateful for the legacy my parents have left to our family and our children.

Please join the link https://www.grandparentslink.com/experts-corner/a-fathers-day-tribute/

Dreamer….one man’s legacy…one family’s purpose…

IMG_2860Today my father would have been 98 years old.

At his bedside in 1998, twenty years ago, he quietly revealed to my older sister his story of approaching the Golden Gate Bridge on the deck of a ship, she barely old enough to stand at his side as they passed under the monument that signified his entry into America.

“We will have a good life here,” he whispered into her ear.

He was a silent man, of very few words. We three sisters had never heard this story, his last spoken before his last breath 24 hours later in the US Army hospital where I was born.

His entry into the port of San Francisco was gained through his service as a Philippine Scout in World War II, and his survival after escaping from the Bataan Death March. After his escape, he journeyed 60 miles by foot, emaciated with malaria back to his home in the province. Slowly he recovered in a nipa hut, his home, until the liberation in 1945, when he jumped onto the US Army trucks rolling past on the road back to Manila to join the US forces and Mac Arthur in Leyte.

From America he would send stipends to his mother in the province. She proudly had a gate made to the entrance of her home that said, “Sgt. Jesus C. Bermudez, US Army.”

My father was the gatekeeper for others to come to this country, the one who would open the doors decades later as a sponsor for his brother and his family, my mother’s sisters and their families, to pursue the good life that my father dreamed of as he passed under the Golden Gate Bridge: A house. A car. An education.

Over years, decades of waiting for papers, affidavits, job opportunities, these dreams materialized not only for my father but for generations to follow.

Our children set foot on the the shores of our Philippine homeland, the land of my father, for the first time last Christmas. The children and grandchildren and nephews and nieces of my father, their Lolo (grandfather), gathered on the on the island of Boracay to serve on a medical and dental mission to the Ati people, an indigenous tribe in the Philippines.

These first and second generation Filipino Americans of my father are living the American dream he longed for: homes in Malibu, Newport Beach, Seattle, Orlando. Cars he dreamed of: Porsches, Ferraris, Mercedes Benz. Educations to be proud of: USC, Virginia Tech, Texas A&M, Baylor, Ohio State. Careers to make him proud: doctors, dentists, accountants, software engineers, NFL producers.

On the dirt roads of my parents homeland, fifty of us—brothers, sisters, cousins, second cousins, nephews, nieces — gathered under a makeshift shelter and thatched grass huts of a remote village to bring medical and dental care to a people who had been outcast and isolated for the darkness of their skin.

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We called it the Kamay Project: Kamay means hand in Tagalog, the Filipino language. Our families were joining hands and resources to help the Ati people. We saw 230 patients that day, giving basic medical and dental care, distributing medicines we had collected, sharing bible stories and balloons with the children, and the biggest draw, playing basketball with the kids.

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Shoulder to shoulder,
Hand to hand
Hands extending to extract a tooth, to take a blood pressure reading, to lift a child up on a shoulder, to pass a basketball up for a shot.
Hands extending over generations, language, economics.
Hands reaching out to give out reading glasses, medicines, toys, balloons.

 

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The recipients were not the only ones receiving a gift.

The ones handing out received smiles and hugs
reciprocally greater in exchange.

Kamay is also the word that describes the Filipino tradition of eating by hand. Food is spread out on the table on banana leaves. The great granddaughter of my father’s mother, a rising Filipino chef just honored at the James Beard house in NYC, prepared a traditional meal of fresh dried fish, shrimp, pancit, and rice.

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As our family worked together side by side, elbow to elbow to present the food, arranging it artfully atop banana leaves on rickety wooden tables, my cousin, one of the dentists, grabbed my hand. Earlier that day he had extracted and examined teeth for over one hundred patients.
He grinned at me from ear to ear, the way I first remember his smile when he was eight years old and just had arrived from the Philippines. He had the same bright, hopeful look in his eyes as the children gathering all around us. At their age, his mom and his three siblings lived with us for nine months preparing for a new life in America.

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“You know we all would not be here it was not for your mom and dad,” he said, nodding towards the tables where our siblings, my cousins, our children, and spouses stood shoulder to shoulder side by side presenting the New Years Eve dinner for the villagers.

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We hugged.
We cried.

Drops of rain pattered on the tin roof of the shelter. Wind blew water through glassless windows. A storm was brewing just off the island. But nothing would dampen that evening of smiles and laughter and feasting and dancing and music as generations and lifestyles and bloodlines merged, a night of celebration.

Today, we honor and celebrate you dad, for it was your hand that opened the gateway for us to give.

In six weeks you will receive your gift, the highest honor paid by this country you love:  the Congressional Gold Medal.

You and your comrades will receive a bronze copy of the Congressional Gold Medal recently awarded to Filipino and American soldiers of the Bataan Death March.  You will be recognized for your sacrifice for the atrocities you endured to defend this country and the American Flag.

The flag that was draped around your casket and handed to your widow during a 21 gun salute.

The flag that you cheered for with your cancer ridden lungs, shouting “USA! USA!” during your last Winter Olympics in 1998.  We watched them as a family from the shores of Hawaii, the closest we could get your homeland.  You were too weak to go to the Philippines one more time.

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Decades later, we have returned.

 

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For more information on the Kamay Project, an ongoing outreach to the children and families of the Ati village in Boracay, Philippines, please go to kamayproject.org

 

 

Ina: Generations of Mothers


She raised a generation of daughters. And they in turn are raising another generation of daughters and sons.

The concentric circle extends even father outward, as she was the “Tita”, the aunt to an extended generation of daughters, her nieces, whom she raised as her own and even more significantly, brought them here to the United States. She continues to be the matriarch and mother figure for decades of lifetimes beyond their own, to their children’ children, even as she lies in her hospital bed, the place where her nieces and sister gather around her now. 

The strength of my mother’s love reaches past borders and generation, touching lives even as she lies still, her left side paralyzed, her heart still as full and loving now, smile filling her entire face.

During this gathering of my cousins and aunt we shared a weekend of tears, hugs, laughter, and our favorite Filipino food, Kare Kare (oxtail soup), my aunt’s specialty. When my mother was admitted to hospice several weeks ago I had asked them to come to see her. Her Alzheimers was taking its toll on her memory and she was losing weight rapidly.

“Please come see my mother,” I asked them.

And they did. They travelled from the other coast to be here.  My mother’s only surviving sister of nine siblings, at 87, came to be at her side. My cousins, two the daughters of this sister, and one, the daughter of my mother’s younger beloved sister who passed away two Mother’s Day ago, with Alzheimer’s.

Together we leafed through old black and white photographs. Since they were raised in the Philippines and I was born here, my cousins knew so many details of the family’s life that I did not. Our bedside visit became a story telling session of our family’s past.

We pick up a photo of our grandmother. She is dressed in her best Filipino embroidered gown, a “terno”. Her waistlength grey hair is wrapped in her signature bun on top of her head. On the back of the photo in her very best writing, she writes this:

 Dear Bing and Jessie

 This picture was taken in inside the house with my appliances.

 Your loving mother,

 Filomena C. Bermudez




My cousin Carina explains to me that our grandmother was the queen of the province where she lived in the remote farmland of the Philippines. She was the only one with electricity, with appliances- an electric fan, a refrigerator, a radio, a television. Carina remembers the neighbors peeking into the window of the concrete block house, the biggest one on the street, to get a glimpse of the television working, a novelty back in the 1970’s.

My father would send his mother money to purchase these appliances from his meager salary as a food service worker at the Veteran’s Hospital. He was a veteran himself, 24 years in the US Army, a retired sergeant who had risked his life as Philippine Scout to escape from the Bataan Death March in World War II. My father, an enlisted man who fought on the front lines of the Korean War, would be so proud to know that Carinas’ sons now serve as officers in the US Army and Air Force, one as a major and one as a lieutenant as well as other cousin’s son, one who bears his name, Bermudez, a major in the Army.

These sons of Carina were taught by my mother how to read. They had just come to this country, and I remember my mother, a former third grade teacher, sitting on the couch reading our favorite children’s books, Where the Wild things Are and Curious George to these sons who are now officers serving our country.
Carina leans over the bed to my mother. She whispers, “Thank you, Tita Bing, thank you for teaching my sons to read. Thank you for all you have done for us to have a good life in this country.”


Carina’s sister, Marlene, turns to me. “I don’t like seeing your mom like this,” she cries. “She is the strong one, she is the one who did everything for us. She is the one who would make our favorite food and we would all eat at her house. Her house was the gathering place for us.”

Her mother sits quietly by mom’s beside.  There are no words between them, only a smile and grasping of hands

 
We pick up a photo of our mother’s mother. Veiled and stoic, hosting the same eyes and my mother, she is receiving an award from their priest at their parish.  I know this now because my cousin reads out loud the back of the photograph written in Tagalog in my grandmother’s handwriting.  At the end of the paragraph she signs in script, “Ina”.  


“What does that mean?” I ask Carina.

“Mother.”

Yesterday, the day we celebrate mothers, the great granddaughter of these grandmothers who lived in provinces in a country  10,000 miles away hosted a Mother’s Day Filipino Brunch in honor of these mothers.  She prepared food native to our country in a city, Seattle, known for its foodies. Her heritage menu  was promoted in a local magazine as one of the Nine Best Mother’s Day 2017 Brunches in Seattle.
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As the circle of mothers and daughters extend further out so does the gathering around the table, not only including family, extending to guests.  The tradition of welcoming and gathering with food and laughter ripples out  through the generations.


The center of this outward circle is not forgotten

My cousin Grace leans over to say good bye with tears and words of gratefulness for all my mother has done. 

“Thank you Tita, for bringing my family here, for taking care of us, for giving us the chance fo a new life here.  We love you Tita Bing.”

The cousins gather around her to sing a song, a Filipino love song that was the favorite of my mother and father.  Although the names of my cousins are barely recalled, the words of this beloved song are not forgotten.

“Dahil Sayo”.

Dahil sa’yo (Because of you) Nais kong mabuhay (I want to live)

Dahil sa’yo (Because of you) Hanggan mamatay (for the rest of my life)

Dahil sa’yo (Because of you) Ako’y lumigaya (I’ve become happy)

Ang lahat sa buhay ko’y (Everything in my life is)

Dahil sa’yo (Because of you)

​​

Measured by the moon.

The moon hangs like an orb, suspended in the sky. Weightless. Floating. Full.

As if it does not carry the weight of measuring time and days as it brightens the dark sky on its descent into a new day.

This day it drops into is my birthday. Another measure of time, in years. A span of 365 risings and falling of the moon, marking 56 times today.

But the one who gave birth to me that day 56 years ago does not remember.

For her time is still, only measured in present. No before or after moments. Only now.

At times it is a gift, this only present moments. There is no sorrow about the past. No worries about the future. Alzheimer’s has taken away time consciousness. Perhaps it is not thievery. Perhaps it is freedom.

Time is suspended as I sit beside her bedside now, stroking the soft, thin folds of her hand in mine. I move for her this hand and arm, the one she cannot move, rendered still from a stroke months ago. She moves the other gracefully to the beat of an old Filipino song, O Ilaw:

Oh light, in the dark night

You’re like a star in the sky

Oh light in the quiet night 

Your picture, dear, makes one hurt. 


O Ilaw, sa gabing madilim

Wag is mo’y bitiun sa langit.

O, tanglaw, sa gabing tahimik

Larawan mo, Neneng,  nagbigay pasakit.
I read the translation to this song we have listened repeatedly over the past months.  Today it strikes me how true these words are.  How is hurts to see her bedridden, to see her bones so frail, her arm still, her head and neck so weak.  But her smile and the light behind her pale eyes still shine so brightly, the way they always have.

Those eyes close now, yet her hand continues to move to the beat of the music

Her voice is barely a whisper as her mouth forms the words.

Only months ago we would sing this together aloud as I took her for a walk outside, to take her out to feel the sun on her skin and see the flowers she loves bloom.  Those days now are few as her lack of mobility makes it difficult to put her in the wheelchair.

She no longer marks the days. Yesterday I told her, “Tomorrow is my birthday.”
She raised  her eyebrows with a familiar smile.
“Oh it is? I did not remember,” she says. “What month is it?”
“January,” I tell her.
“January,” she repeats.

“Do you know the day?” I ask.
She shakes her head no
“My birthday is January 13,” I tell her.
“Oh,” she mouths quietly, then whispers, “What do you want for your birthday?”
“A new dress,” I tell her.
She smiles. “Ok.You get one.”
“Ok, I do you want to go shopping with me?” We used to spend hours shopping together.
She shakes her head no.
She whispers again, “What do you want?”
I think of the time we spent only months ago, when I could push her outside and we could sing her favorite song together,

I tell her, “I want you to sing, sing really loud mommy, so I can hear you.”

Together we sing in Tagalog words that have become familiar these past months, translated:

Awake and arise from slumber, from your sleep so deep. Open your window and look out to me, so that you may understand my true lament

I read the translation to this song, this day before my birthday. This day I have scheduled hospice to come to do an evaluation of mom’s condition. Her strength has declined markedly since her stroke last August. My lament over her condition has rendered me sleepless and worried.

This day before I start a new year, I need to know. I need someone to help me measure the amount of my mom’s decline, need to know where she was at in her stages of Alzheimer’s. And the hospice coordinator comes to the door shortly after we finish our song.

“Hello,” she greets my mother, “How are you. Who are you? Can you tell me your name?”

“Bing,” she answers with a smile.

“I want to know if she has a awareness of who she is,” the coordinator had told me earlier in a brief interview.
“What do you mean,” I asked.

“Does she have a sense of who she is,” she answered. “Can she answer the question, ‘Who are you?'”
On this  birthday of mine I ask myself, Do I have a sense of who I am? Can I answer this question: “Who are you?”

In the past years it has been entangled between caregiver and mother.And lately I have fallen exhausted into both. But that is not the woman my mother raised me to be.

She would want me to answer that question, as she still can: “Who are you”

Me separate from my mother, from my children

Me the one who is shaped by caring for others but not defined by it

Me, searching for to be fully the one I was created to be

The day my mother brought me into this world 56 years ago
If the measure of our days here on earth is to have a sense of self, let me be the one my mother led by example for me to be.

Loving others, caring for their needs, listening, laughing alongside.

As she has for years

And has she does now

In each moment

Suspended still in the air

Like the moon, full.

Going Home

 

 

 

The sun climbs over my roof this morning, and under it my children are home.
Even the cat had been waiting expectantly for their return.

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Home, a place to let down your guard, a place of rest, much needed after a season of change.

Just the other day my youngest, a freshman in college, called.

“Hi sweetie,” I answer, “how are you?”

It is the 14th week of her freshman year. She has been away from home for over three months now.

“Hi.” She has that voice, the one that I have, the one where everything is ok but it is not.

“I’ve been trying to call you.”

“I’m sorry sweetie, we’ve been out.”

We’d been away on an empty nest retreat to Pebble Beach for her dad to play in a golf tournament. His life’s work, golf. And I am grateful his life’s work brings us to this place of crashing waters that shift to cerulean to grey with the winds and the sun. He can play the game he loves and I can walk these shores I love where the rocks jut out of the seas and the sandpipers nip at the shores and dogs run unabashedly into the surf in complete freedom.

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For the first time in months I felt that same freedom as I walk and reflect on the things I love and the ones I love and the salt air fills my lungs and the skies shift from grey to lavender to orange early in the morning and the surf sounds calls me to walk and think and pray along its edges during this season of shift and change of all things familiar.

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This was a gift of a week alone, in this new season of being alone.
A gift of a week before the kids come home.
A gift to reflect and pause and be thankful.

Lauren whispers into the phone,

“I just want to be home.”

“Only two more days,” I tell her.

“I just want to be home now,” she tells me.

Her voice breaks. I ask her to face time so I can see her face to face. She says no mom I don’t want you to see my face right now.

And I hear the sobs in her voice.

I want to fix it. What do you want I ask.
I want you to pick me up and take me to dinner with you and dad.
All of me wants to find a flight right now that will take me to where she is thousands of miles away to pick her up for dinner.

She’s alone tonight. All her friends are gone, a lot of them home already.

My little girl just wants to go home.

Depending on whose voice, that statement means different things at different times.

It used to frustrate me at times when my mom, in her Alzheimer’s state of mind, used to say, “I want to go home.” She had a place under our very roof, and I used to wonder “what else can we do for her?” until my caregiving counselor explained to me that when she asks to go home, she is looking for her place of safety and refuge.

Later she used to say, I want to go home, and playing along with her, I would ask, where is home?

She would smile, and point her finger up to heaven.

Yesterday during our visit at the place that is now her home, we sang songs from the sound of music, her favorite. We both laughed out loud when we sang together “so long, farewell” and in her raspy voice, weakened by a recent stroke, she sang out “Goodbye, Goodbye!” so loud it startled even herself!

 

 

When I kissed her on the forehead to say good bye, she asked me, “Where are you going? Where is your home? I don’t remember.”

Tomorrow I will try to find a good place for her to sit at home comfortably at the table in her wheelchair.

Tomorrow we will gather all together.  At home.

imageAround extended tables will be our children and our friends who have gathered around the Thanksgiving table with us over the past 20+ years, friends who at that time were far away from home and were making a new one.

And for the first time my son will gather around the table with his new wife and her parents, as the circle extends out concentrically of starting a home.

 

Managing Storage…coping with Life’s system overload

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It was ignored for a very long time. Months, maybe a year. The little white icon that pops up on the IPad screen: Your storage is full. Manage in Settings. Like many other things in life, I kept ignoring it, thinking it would go away or I would deal with it later.

Then came the day when I tried to open up a new page to write a new document, and ARGHHHHH! It would not open. Worse yet, I could not retrieve any of the older documents I had written. All those words, all those pages! Panic set in. I knew they were in the cloud somewhere, but I had no idea how to get them out of there. With none of my kids around to coach me through this (they would laugh at me anyway) I caved in to the only thing I could do. Call Apple Support.

The voice of a very nice young man got on the line. I prefaced the rest of the conversation with this statement: Explain everything to me as if you were talking to your mom.

I could picture the grin on his face as he chuckled. And step by step, he patiently coached me on how to manage my storage so I could have more room to update my settings so I could have room to load my previous documents and make room for more. After all my anxious questions, “Where is the ICloud? Where do these items go? What happens if I delete this?” he said to me, “You’re doing great! You got this!”

“Don’t worry, he told me, your items are still there and you will have access to them. You just have to manage where you place them. ”

Ha! I think to myself. That’s the story of my life.

From his desk at Apple Support he doesn’t see the piles of items in the spare room or the boxes in the garage or the bins of photos that need to be sorted in the upstairs closet. Managing items is an ongoing problem of mine, my nemesis for years. Those closest to me also try to coach me through longterm fault. For my birthday a few weeks ago my dear friend gave me the book, The Life Changing Magic of Tidying Up after she saw me browsing through it in the bookstore. One of the statements author Marie Kondo makes is this: To truly cherish the things that are important to you must first discard those that have outlived their purpose.

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This is true for my IPad. To make room for more I must take time to delete some of the photos that are taking 8.2 GB on my 12GB device.

This is true for my closet. To be able to neatly put away the piles of laundry on the living room couch I must discard some of those tops stuffed in my drawers I haven’t worn for years.

This is true for those long term anxieties that have been stuffed down in my soul. Worries about when am I ever going to get this stuff in my house organized. Worries about my grown children’s future. Fears and apprehension about their goals, and mine, being achieved. Fears and anxieties over personal traits I need to work on.

All this stuff drains energy from me. Wastes too much space in my mind and in my day. Keeps me from being who I fully want to be.

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Last night the signal that blares to me that I must learn to manage my own personal settings is mirrored in front of me.

Mirrored in my own daughter.

In the angst of anticipating the 6pm announcement of a college acceptance, a myriad of emotions and tears come spilling out of unseen places…..will or will she not get in, my classes are too hard, I can’t study for all these AP classes, I keep trying and trying and I can’t get where I want to be….

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My heart breaks that my daughter is caught in this swirl of expectations and achievement and information overload. I had no clue how much tension she was storing underneath the surface until she broke. Her system was full. She had reached maximum capacity.

I had not noticed the signals that she was on overload.  That she was feeling so much pressure to keep up schoolwork and grades. And so quietly, calmly, even though my heart was breaking, I did what Apple Support did for me that morning: coach my sweet daughter to look through her days and examine what we could delete from her busy life.

What was necessary and what was extra.

What was too much.

What to do if she was feeling anxious and fearful.

Most of all, what she needed to focus on to keep space free in her mind to relax and breathe.

“Mom,” my daughter told me later, “when we were fixing our phones last week the tech told me that when a IPhone starts reaching its maximum capacity, it starts acting strange. Not functioning correctly. I guess that’s what was happening to me.”

iPhones and IPads come in different capacities:  12 GB, the 32GB and the 64GB. It has nothing to do with their efficiency, it’s merely how they are designed.

All are designed differently. Each has different gifts and capacities. And in this crazy world of achievement and information and overload that we all get into I need to observe the messages silently put out that the expectations can be too much. In my children’s world.  And in my own.

In those places where we gain more space by deleting the extra, we need to replace the busyness with places of rest. Places to shut down and restore. Places to recharge in quietness.

For the benefit of freeing up the clutter of our minds, our souls, our days is that we gain space.

And when we gain space, we are more available to receive what is around us.

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