Telling the Truth

connecting the dots of my life

Tag: Childhood

The Air I Breathed | Part 1 of 3

It took more than beatings and Good Girl Rules to groom me to be a victim.  It also took small, calculated and uncalculated, direct and indirect intrusions on my body, my spirit, my mind and my emotions.  I call it the air I breathed.

Beatings have a distinct advantage over the air I breathe. Read the rest of this entry »

aging southern belle

IMG_4953

aging southern belle
matriarch of the river
beckons me homeward

* * * * *

Summer 2009
the day of my father’s memorial service
three cars full of family members drive out to the old house
at the end of the road Read the rest of this entry »

Eulogy for Sister #3

Houston, Texas – 17 February  2006

Diane directed that my remarks today be “personal, with no preachy tones.”  As I thought about what to say, I came up with only one topic that guarantees I’m being personal—that I’m not avoiding the subject Diane knows none of us can avoid when we talk about her.

Remembering Diane’s Body

Diane had a human body—loved by God
A female body:
—The body of God’s beloved daughter child
—Known to Jesus Christ as a sister for whom he died
—A female temple of God’s Holy Spirit on this earth

A one-of-a-kind body:
—Created and sustained by God
—Loved and nurtured by God’s ministering servants here on earth:
——Her husband, two sons and one daughter
——Her large, extended biological family
——Her church family
——Her nursing family
——Even the family collection of dogs

Diane’s life was shaped by bodily infirmity.
—She would hate that I just used that word!

Diane refused to think, act or behave as a person identified by an “infirmity.”
Yet the truth is simple:
—Diane’s life was shaped by loss in her left arm due to polio.

From a parental point of view, Diane’s weak arm was cause for protective measures.

From Diane’s point if view it was cause for excelling in whatever she supposedly couldn’t or shouldn’t do.

Not only would she do all these things,
She would do most of them better than any of us, things like
—Riding a bike, swimming and playing basketball
—Sewing dresses and suits
——not hankies and curtains, but fancy dresses, and suits with tailored blazers
—Then there was photography, not with small, lightweight equipment,
——b
ut with the best possible equipment and attachments she could afford and lug around!

Diane developed an uncanny knack for figuring out how to carry out activities like these without compromising quality or expertise in the slightest.

She also developed an uncanny knack for taking advantage of our parents’ desire to protect her.

Only as an adult did she confess that her habit of disappearing from the house to do yard work (and not housework) was not motivated chiefly by her pure desire to help Daddy.  Rather, she knew neither Daddy nor Mother would send or call her back inside the house for the latest instruction or practice in vacuuming, dishwashing, dish-drying, table setting, ironing or putting clothes away.

To us, Diane’s body was both normal and different—though it all felt pretty normal most of the time.  Certainly not life-threatening.

Then each of us, her three sisters, got a telephone call from Diane in January 1996.
Diane had ALS.  She was direct and clear:
—There is no cure.
—The disease is terminal.
—I’m going to need help.  Lots of help.

Diane’s left arm shaped her as a child, as a young person and as an adult.
Now Diane’s entire body began shaping her and her family,
beginning most painfully with her husband, two sons and daughter,
and reaching out to all of us gathered here today.

For the last 10 years I’ve flown down to Houston about 4 times a year to visit Diane.  But not just to visit her.  I’ve come to witness a journey—Diane’s very personal journey with ALS.  A journey that relentlessly put Diane’s physical body at the center of attention.

As young girls we weren’t encouraged to pay much attention to our bodies. 
Bodies were a necessary but usually uncomfortable necessity—especially female bodies.  Now, with ALS, Diane was consumed by what was and was not happening in her body.

She suffered losses beyond comprehension—most in fairly rapid succession over a period of years, starting with physical losses such as mobility, ability to care for her own personal needs, eating and swallowing, ability to speak on her own, and breathing. 

She also suffered loss of her position here at the church:
—Loss of her dream of being ordained
—Loss of work and personal relationships as her body more and more seemed to intrude as a difficulty or a problem to be solved
—Loss of time for herself or her family and friends, as personal care began gobbling up hours out of each day
—Loss of privacy:  total and absolute, with only one exception—the thoughts in her mind, which included her life with God
—Loss of little things such as swatting at a mosquito feasting on her neck (as she put it); scratching where it itches; singing in church; being in the middle of the action and making wisecracks

More painfully, she suffered loss of other things such as giving her children a hug, or embracing her husband face to face.  As a female she suffered what most women dread—loss of control over personal presentation of herself:  hairstyle, makeup, body language.  She became the subject of stares and quickly averted eyes.

Diane’s body seemed to be calling the shots.

True to who she already was, however, Diane kept showing up—fully with and in her body marked more and more by ALS.  It was as though she were saying

  • I’m still here—in my body
  • I’m still Diane—in this body
  • I am not whatever you think a terminally ill person should be
  • I am not predictable
  • I am not a saint
  • I’m still Diane!
  • I’m still here and I’m still fully engaged in living–living with ALS
  • I will be who I am—angry, frustrated, filled with anxiety, filled with human longings and everyday needs; direct and clear without being mean
  • I’m dying
  • We need to talk
  • Now

As always, nothing was too sacred for a good healthy laugh.  Especially about her body with its unpredictable body parts, behaviors and small crises:  facial movements, biting her own lip, laughing uncontrollably, head falling over from time to time, drooling from time to time.

Diane continued to be who she already was:
—Determined to speak for herself in her own words, not yours or mine
—Determined to be heard and heeded

She was still directive—now in ways that boggled the mind:
—To-do and Do-not-do lists for family, nurses, friends and strangers
—Rules for how Mom is to be driven in her new van and who gets to say when the rules are being broken (Mom, of course).
—She was still a masterful strategic planner—only now she had to figure out how to get you to do what she could no longer do, but somehow knew must be done.

As always, Diane wasn’t about to fade into the woodwork.  She kept showing up in the flesh—in her ALS-shaped flesh:  at church, in shopping malls, at weddings for her daughter and one of her sons, and even—one month ago, believe it or not, to inspect her daughter, son-in-law and granddaughter’s new home.

Diane remained insistent that she be given choices, and that her choice was the final choice:
—Clothes and accessories for church
—Medical options
—What to keep and what to discard from the kitchen cupboards
—Which movie to watch
—And how this service today would be shaped,
——including the names of all active male pallbearers
——and the names of all 25 honorary female pallbearers!

Diane made her concrete mark in, with and through her concrete, ALS-shaped body.
To deny she was among us in the flesh would be to deny her existence.

To some extent, each of us gathered here to honor and grieve her passing has been a witness.  So many of you are so full of memories.  I can’t speak for you and I won’t get preachy, but I will be confessional:

  • I’m listening, God, for what my relationship to Diane means for the rest of my life in this world you love so much.  Amen.

Eulogy delivered 17 February 2006, © Elouise Renich Fraser, 17 February 2006
Blog post © Elouise Renich Fraser, 15 April 2014

Survival Rules for Good Girls | Part 2 of 2

When I read through my list of survival rules, my heart sinks. By age 7 or 8 I’ve found a way to do what Daddy wants me to do by explaining it to myself my way.  For all my supposed independent thinking and determination to be my own person with my own will and my own voice, I failed. Or did I? Read the rest of this entry »

Survival Rules for Good Girls | Part 1 of 2

By the time I’m 7 or 8 years old, I have a daunting list of survival rules.  Later they backfire in every part of my life.  In the meantime, they have the virtue of seeming to get me through.  Here they are, Read the rest of this entry »

nest in clover bank

nest in clover bank
sleepy summer afternoon
salty river smell

* * * * *

I’m 8 or 9 years old—
a budding writer looking for somewhere to write
and something to write about. Read the rest of this entry »

Down to the River to Pray

“O sinners let’s go down, Down in the river to pray. ”  The lyrics of this haunting song echo in my head when I think about my life on the river.*  An eerie juxtaposition of natural beauty and heavy-laden humanity. Read the rest of this entry »

Sexual Healing at Age 7?

Until the last two weeks, this question never crossed my mind. Now I can’t leave it alone. If the answer is Yes, how can that be? As noted in Unpacking My Suitcase, I’m not yet sexually aware. But I’m carrying an unwelcome load of something in my female body and spirit. Read the rest of this entry »

Unpacking My Suitcase

Moving from California to the Deep South marked the end of my early childhood.  Though I wasn’t yet sexually aware, I was already carrying a heavy load in my 7-year-old female body and spirit.  Because we didn’t have room in the car for extra luggage, I left behind more than I wanted to.  I also brought things I didn’t want or need.  Here’s what I’ve unpacked from my suitcase as of today.  I have no doubt there’s more. Read the rest of this entry »

moss-laden oaks loom

moss-laden oaks, magenta azaleas

moss-laden oaks loom
magenta azaleas blaze
deep south path through woods 

* * *

Late summer, 1950

It’s past midnight
I’m asleep with Sisters #2 and #3
Are we almost there?

Mother’s tired voice wakes me up
Nothing but darkness outside
and cobwebby stuff hanging from tree limbs

A log-cabin tavern fades into view
Neon beer ads flicker on parked cars, old trucks
Daddy reluctantly stops for directions

He goes into the tavern.
Are we lost?
No. We just aren’t there yet.

Daddy drives slowly
No street lights no signs
The old road is dark, narrow, mysterious

Mossy oaks loom overhead reflecting
weak rays of yellow light from car headlights
Weary shacks line the road

Unexpectedly we pass grand fenced-in wooded lots with driveways to nowhere
Then modest houses and a few larger houses
The road ends abruptly.

Daddy stops, gets out, peers at the giant mailbox
He turns into the driveway
We’re there.

Deep South
moss-laden oaks, no blazing azaleas
Just heavy humid air, wealth next door to poverty, fiercely guarded secrets

© Elouise Renich Fraser, 10 March 2014
Google image – Springtime in Savannah, Georgia