21 November, 2014

Reflection on Thanksgiving

                                                                        dee winter 2013

A Thanksgiving Hymn: Pray to God

In times of doubt,
In times of joy,
In times of darkness,                           Pray to God
In times of hope,
In times of loss,
In times of understanding,
In times of despair,                               Pray to God
In times of love,   
In times of anger,
In times of jubilation,
In times of regret,                                  Pray to God
In times of insight,                                   
In times of fatigue,
In times of certainty,
In times of anger,
In times of thanksgiving,                        Pray to God           

As the moon rises,
As the moon sets,
As the sun rises,
As the sun sets,                                        Pray to God


     

04 July, 2013

Gladness




Hold fast, Holy Time,
who determines all things,
Halt the mighty river of life’s
triumphs and stings.
Grant us a moment, a respite, a pause
Give us reprieve from the pain and the loss.
Pierce us with gladness
O Holy Time,
We are nothing without thee, 
We're forever thine.


dee    7.4.13

02 April, 2013

A PRICE TO PAY





The revision:                                       A PRICE TO PAY

When I first conceived of the Token Theory, it was because I felt like I was giving too much of myself simply to perform the tasks of daily living; it could be a challenge to get dressed for an evening out or to take a morning walk or to go for a Sunday morning drive with my husband. I found myself done in by the simplest things. Everything felt like it took a toll on me physically; an inescapable fact of my life seemed to be that there was a significant cost to whatever I did. I imagined what it would be like to use money to buy the freedom to do what I chose. That idea morphed into the thought that I should have a stash of tokens to pay my way forward. The notion of having a tangible way to quantify the costs of participating in life made sense to me. During some long, sleepless, nights I refined the concept. In a surprising way, it gave me more of a sense of control over a process I could not directly manage myself.
Some of us have chronic health issues that tax our accumulated wealth of physical energy supplies.  We tap into our stores in order to function.  Eventually, our reserves run low. At that point, those of us who are physically compromised in some way, become acutely aware that we need to budget our remaining energy and conserve our resources. The breakthrough came when I started to think in concrete terms.  It seemed sensible to assign tokens as a way to quantify the cost of functioning when dealing with physical challenges. I pictured an energy bank where I keep my tokens. Sleep, rest, exercise, a healthy diet and stress-coping techniques are all methods I can use to earn new tokens to spend on activities of daily living. I can spend them (be active) or save them (rest). Typically, I keep a supply of tokens on hand.  I usually spend my tokens until they run out. At times, I may even run a negative balance of tokens.  

  In my fantasy world, I can use some of my savings or borrow from the next day's allowance.  If I exhaust those resources, I pay for what I do with an increase in pain. I discovered a core truth; Everything costs something. This is true for us alI. It  just happens to be a whole lot more apparent for me. To tell the truth, I do not think this is fair, nor do I think this is reasonable. But it happens to be a condition of my life at this time. It is. When I use my tokens, it is an act of deliberate choice. I have come to think of this mindful awareness of each moment as an unexpected gift of living with a disability. 
    I have had to learn how to maintain a deliberate awareness of how I script each day. I strive to  use my tokens in a way that is both meaningful and satisfying to me. The Token Theory is a powerful way to set intention and keep me present in the moment. With the high price I pay for each thing I do, I feel compelled to make every moment count.

Wrapped in a favorite, but badly worn silk robe, I recently seated myself on a small teak bench in my bathroom. I used my thumb to turn on the blow-dryer with one hand while using a small -bristled brush in my right. I thought, “Let the dance of the blow-dryer begin.” Some time ago, I would stand to blow dry my hair. I liked to watch my reflection in the mirror over the sink, but eventually, I would grow too tired to stand for the fifteen minutes it took to dry my hair. I did what we humans do, I adapted. Being seated helped the fatigue, but my shoulder became problematic -- it often dislocates if I lift it higher than perpendicular to the floor. It took some creative maneuvers to figure out how to dry my hair without lifting my right arm, but I prevailed. Using a new, seated-blow-drying technique, I learned to dry my hair from underneath or upside down. I have come to think of blow-drying as an Olympic Sport. Then, the unexpected happened.  I could no longer hold the blow-drier in my left hand; it was too heavy and I could't push the buttons.  We humans survive because we acclimate to change. Now,  I allow my hair to air-dry. Only for special occasions do I engage in the blow-drier-hustle.  Continuing with my morning routine, my makeup is next. I smooth on lotion with SPF30, draw a few lines, puff a brush or two, follow with a stroke of lip gloss and TADAH , beauty incarnate.....sort of. On difficult days, it is all I can do to get dressed in bra and panties. My heart starts racing, my hands begin shaking and I am too dizzy to walk.  This is called POTS or Positional Orthostatic Tachycardia Syndrome. Basically, one's heart rate increases with changes in position. I lived with it for a good forty years before I knew there was a name for it!  Turning away from the mirror, I pulled my robe more tightly over my long, thin frame. I made the bed, gathered up towels and laundry, started a load of wash, emptied the dishwasher, then, with an eye on the clock, eased myself back onto the bed. My hands, wrists, right shoulder, hips, spine, knees, ankles throbbed. I was exhausted. I thought, “ Why does it cost me so much just to get going in the day? “ As I lay there, I played with that idea.   This was the moment of inception of the Token Theory.  What if I started the day with a bucket of tokens. Every action or task completed would cost one or more tokens. I began assigning values to the chores and activities of everyday life. My token list is mine, and mine alone. What might be an easy-breezy one token for me, might cost someone else three. The point, the very nugget of this idea was that I had to learn to mange my tokens better. I was not distributing them in a way that was best for me. I calculated what it cost me each day to make it to bedtime. The quantity of tokens I have each day is determined by how well I sleep, whether I have taken good care of myself the day before, how I have managed stress in my life. I recognized that these were my tokens and it was up to me what I wanted to do with them. In my mind, I am lithe, nimble and ready-to-leap-tall-buildings in-a-single-bound. My body, however,  rebels. Over and over,  I am disappointed. 
I have repeatedly, clearly to the detriment of my health, tried to ignore the tolls I incur when I determinedly set out to do the things I enjoy: weeding, taking an extended ride, going for a mile walk, hanging a painting, typing without a break.  There was a time that I was fully convinced that I could cheat --
"To hell with the consequences, I will do what I want to." 
Well, this kind of mind-over-matter-I-believe-I-can-do-it mentality didn’t work out so well for me.  I make the critical mistake of believing that I can forge through, practice mind over matter, institute a no pain, no gain attitude. With a reliability as certain as each new sunrise, when I employ these strategies, I pay dearly for trying to beat the system. Inevitably, I am injured or set back in a significant way. ( Why can’t I cut down this tree myself? Why shouldn’t I take a three-hour bus ride?)  I have the Emergency Room discharge papers to prove this. There are people who do not understand these parameters because they do not have to observe such limitations themselves.  They want to reject the notion that I am actually impeded in my aspirations. They comment that I look so "normal." The underlying text is that I am lazy or not giving it my all. Someone who is not hindered by physical limitations cannot appreciate what it is like to desperately want to resume what was once a "normal" life.  Out the door for a quick 5K before breakfast, then a mad rush to get my three kids off to school.  At that juncture in my life, I could no more have imagined that I would have to pause to calculate what slip-on shoes I could manage to get on my feet than my friends can understand how my token theory reigns my life today. 

The bottom line? There is a premium I must pay in order to move forward with anything in the physical realm. It is exactly for that reason that I have turned so much of my attention to the emotional, psychological and spiritual realms for fulfillment. I have learned to work hard to read, to write and to travel world wide on the web.
 Mentally assigning values to the daily activities of life has given me a framework that helps manage my days. The idea that there is a cost --in tokens-- to everything I do and that I choose how to spend my tokens has given me more of a sense of control over my life.
Sometimes, I borrow against tomorrow’s tokens but there is a high price to pay for that luxury. What lies just off-stage is the looming threat that a respiratory infection or a fall or some untoward event will knock my knees out from under me and my bucket will sit upside down for weeks.
A full bucket of tokens is a profound luxury that goes unappreciated until it is gone. Most people my age start their days with seemingly infinite stamina and possibilities. They make their plans without careful consideration of the ramifications that their activities will have on their well-being budget. I do not waste my time being jealous of them. I only wish they could fully appreciate what an amazing gift that it is to be free from counting tokens. Father Time ticks for the disabled at the same rate as for everyone else. The difference is, our health leads us to constantly, consciously, choose how we want to spend our reserves. We keep one eye on the running clock as it races through the minutes and the hours,

I am not the only one! I read an essay by Christine Misrandino called “The Spoon Theory.”1. When Christine’s best friend asked Christine to tell her really, truly, what it was like to live with a chronic, debilitating illness, Christine read the sincerity in her friend's face as she cast about for the words to describe it. She and her friend were seated in a diner where they often shared stories and meals and life (as in Seinfield or Sex in the City). page3image1000
Christine gathered up all the spoons she could find from her table and the tables surrounding her. Christine handed over this bouquet of spoons to her friend and said, “Here, hold this, you have Lupus.” Christine explained to her friend that one of the biggest differences between being sick and being healthy is that when you are healthy, you do not pause to consider the consequences of every single choice you make. Christine asked her friend to list off the tasks of her day, including all the “basics.” Her friend started with “getting ready for work.” Right away, Christine chastised her. ”’No! You don’t just get up. You have to crack open your eyes, and then realize you are late. You didn’t sleep well the night before. You have to crawl out of bed, and then you have to make your self something to eat before you can do anything else, because if you don’t, you can’t take your medicine, and if you don’t take your medicine you might not be able to function. " Having said that, Christine took away a spoon.
As I read Christine’s account, I compared our versions of our Pay As You Go Lives.  What struck me most was that basically, we agreed. In essence,  our attitude and self-care dictates what we start with in the bank, our disability determines what things cost. As individuals, we have to choose how we want to spend our tokens.
In her essay, Christine talked about how challenging it is to slow down and to make choices about what is most vital. She wanted her friend to understand her sense of frustration that she can’t do the hundreds of little things that come easily to most people. Instead, she must constantly weigh how she wants to spend her spoons. With a pithy courage I could admire and to which I aspire, Christine disclosed one of her secrets, “I have learned to live life with an extra spoon in my pocket, in reserve. You need to always be prepared.” Unsaid, but understood, is that the good stuff that life tosses our way might be just around the corner. And it pays to be prepared!  Whatever the cost.
page4image1016


I had a brainstorm. I thought it might be worthwhile to pull some of my favorite posts from my blog, A New Dawn, and polish them up. Perhaps, in my late night yearnings, I posit, a small bound book of them? It can be embarrassing to open the door to my literary past-life.  I confess; my work is flawed. It is uncomfortable to look back at my earlier work and see mistakes. True, in my diligent drive to produce an essay per day for 365 days, some of the finer points were lost. What a relief that  punctuation, grammar,  and facts, for the most part, were correct. However, in hindsight, it is ever too easy to find mistakes.  Of course, I am the kind of person who enjoys finding mistakes. There is a small clan of people who share my editorial leanings.  We are the ones who will while away wasted minutes spent waiting by editing restaurant menus and telephone books. Having embarked on this particular journey, I must set ego aside and bravely, pick up a red pen and edit.  One of the first essays I want to revisit appeared in A New Dawn  on March 8, 2012. Even as I wrote The Spoon Theory meets The Token Theory, I sensed that I would want to return to it for an intimate session of revision and editing.

The original:
http://dawnings-anewdawn.blogspot.com/2012/03/spoon-theory-meets-token-theory.html#.UVtDQ79NFaE


1.
*http://www.butyoudontlooksick.com/articles/written-by-christine/the-spoon- theory-written-by-christine-miserandino/ 

06 December, 2012

No Regrets Living


In her article, Regrets of the Dying, Bronnie Ware, a palliative nurse, reported asking her patients their regrets as they faced their last days.  She cited the five regrets that were most commonly expressed. 

1.  I wish I’d had the courage to live a life true to myself, not the life others expected of me 
2.  I wish I didn’t work so hard. (Every terminal male patient she had nursed expressed this view.) 
3. I wish I’d had the courage to express my feelings.
4.  I wish I had stayed in touch with my friends.  
5.  I wish that I had let myself be happier.
This article struck a particular chord with me.  When I was seventeen, I started to work with the Visiting Nurse’s of Martha’s Vineyard.  They had a new program they were starting and offered me the opportunity to work with them as a nurse’s aid; it was called Hospice of Martha’s Vineyard.  We had weekly sessions to discuss Death and Dying. We read Elizabeth Kubler Ross, author of On Death and Dying. What was most important was that the small group of us were part of a new focus dedicated to caring for the patients and families of those who had been identified as having terminal illnesses.  If life has chapters, that chapter of my life was one of the most formative.  I spent the summer of 1976 through the Spring of 1980 working with dying people.  The first three months were the hardest.  I had five patients.  I lost five patients.  I was the one who stayed by their beds when things got messy, when they were scared, when no one else would feed them or listen to their fears.  I was willing to ask, “Are you afraid?”  “Is there anything I can do to make you more comfortable?” Sometimes, patients answered with mechanical adjustments like plumping a pillow, bringing a book, baking a cake. However, when they were feeling low or angry, I found that they simply wanted me to be there.  I worried about being paid to sit, but one of my early patients, Nettie Allen, told me that she was paying me and I would do what she wanted me to do.  Some days, I canned fruit or weeded her garden under her direction. Some days, I sat next to her on a bench and we listened to bird calls.  Her feisty spirit waned, but her lessons did not. I learned a lot about dying over those years. I observed that people die as differently as they live.  Some fight hard, but go quietly, others seem to have given up, yet linger.  Some people talk about the past and their mistakes, others focus of leaving things in order for their families. There is an intimacy borne of death. The questions that may have gone unspoken without the impending sense of leave-taking may be asked openly.  The one I asked every patient was, “Would you have done anything differently?”  It was that question that prompted me to label the kind of life I hoped to lead as No Regrets Living.  The biggest takeaway that those years working for hospice -- first on Martha’s Vineyard, then later, in western Massachusetts -- gave me was a belief that each of us should strive to live in a way that we do not harbor regrets. I asked myself, “What if we lived life large?  Took a risk to do exactly what we wanted to do with our lives?” I wondered if regrets could be nothing more than an acknowledgement of our mistakes.  Are they an inevitable result of life?  After all, part of life is failing. The more important part is getting up again. Did my patients have regrets because they were misinformed, too afraid to choose the path they desired or because they simply did not get back up when they failed?  No matter how regrets are defined, these patients were unanimous in their message to try to live as close as I could to a No-Regrets Life.  This imperative has been a compass rose for me.  Faced with life’s hardest decisions, I still pause to ask myself, “What would I do if I knew tomorrow was my last day? Would I regret this choice?” This strategy has stood the test of time.
Bronnie Ware did a commendable job summarizing the five regrets most often expressed by people who were dying.  If only we could heed the message contained there in, we might be better equipped to live a No-Regrets Life.  For now, maybe I will just print the five regrets on card stock and hand them out to everyone I meet. If one person, just one, changes the direction of his or her life because of the sage advice of moribund patients, the strategy would be worthwhile. We will all have earned a spot on the stage to sing alongside Frank Sinatra...  “Regrets? I’ve had a few, but then again, too few to mention.”
Bonnie Ware’s essay may be found at  http://www.inspirationandchai.com/Regrets-of-the-Dying.html

18 July, 2012

On the Island




dee~ July 2012
On the Island
On the Island,
Water holds history
haunting lore of pasts
hopeful tales of tomorrows,
--Please, excuse me, make way,
c o m i n g  t h r o u g h
with urgent scents, sounds and sights of 
today.
Soak in the sun, drink in the rain, breathe in the beauty.
The Island is for all of us,
is all for us.

12 July, 2012

Chestnut Mountain Viewed


                               
written 10/2010
   
Years ago, the cover of a newsstand magazine caught my attention.  Headlined in the August edition was the 1996 Better Homes and Gardens Home of the Year.  Ever since then, I have kept that magazine preserved in a manila envelope covered with large bold words in red ink; SAVE, SAVE, SAVE.  The plans in that magazine changed my life.
Back in August, 1996, my husband, three children, two cats and one bird were pushing out the boundaries of our 2200sq. foot restored farmhouse.  We were at a cross-road; we needed to expand our living quarters, build or purchase a new home.  The plans in Better Homes and Gardens captivated our attention and claimed out hearts.  I mailed a check for the architectural plans and we allowed our dreams to blossom.  We searched six months for an appropriate lot that would meet our budget and construction requirements.  Our efforts were not fruitful.  Reluctantly, we shelved our desire to build the 1996 Better Homes and Gardens Home of the Year.  We put our one hundred year old home on stilts, dug a full basement, constructed a solid foundation and added a family room and a library.  We loved the property we rebuilt.  We had a comfortable home, an in-ground pool and over an acre of land for privacy. And yet…
From a box, under our bed, in an envelope labeled SAVE, SAVE, SAVE, our future whispered to us.  By tacit, unspoken agreement, we kept a six-year vigil for the hillside property that might accommodate our house.  My husband stumbled upon it in a casual conversation with an insurance client.  The property on Chestnut Mountain had proven difficult to develop and the client wanted to sell it.  
Together, my husband and I hiked up the remnants of a logging road that disappeared into an overgrown tangle of thicket.  After climbing 400 feet up Chestnut Mountain, we took to trails left by deer and other fauna of western Massachusetts.  My husband gained purchase of the view by shimmying up a tree.  I climbed on until I reached a rock-roped ridge with a stream of water trickling down it.  My heart beat loud and fast, whether from exhilaration or exertion, I was not concerned.  I had a strong, sure sense of coming home.  Unfolding below us was the wide, expansive vista of the rolling hills and mountains that lend the geographic identity to this region.  The Connecticut River Valley coursed through it, threading its way south toward Springfield, toward the sea.  
The land transaction was readily accomplished.  What followed was anything but easy.  We endured a two-year legal wrangle with the local Zoning Board who were invested in flexing their muscles on our project.  Less committed dreamers may have abandoned their dreams, but we had a secret inspiration.  We had a magazine with a full photo-shoot of our dream house as it would rise from the end of a 1200 -foot long mountainous driveway.   
We moved into Chestnut Mountain View in December, 2005.  Today, numerous projects are still underway, including:  landscaping, constructing the wrap-around deck, finishing the first floor space.  Time, energy and resources have been at a premium.  These factors in no way diminish our deep sense of gratitude that we live on ten acres in a home that can only be described as a hallowed place: we live perched between earth and sky in a spacious and light-filled home once featured in Better Homes and Gardens.

Letting Go



from October, 2011
I stood in a ten by eleven foot room this afternoon wailing.  I hadn’t seen it coming.  These sobs from deep in my belly rolled up and out.  My nose ran and my eyes rained tears.  Loss seemed to have multiplied in black body bags.  I was surrounded by five contractor size garbage bags of my father’s life.  For three hours, I pulled items from his closet, from his desk from one of his four brief cases, from his bookcase, from his stereo cabinet and from boxes stored under his desk.  I salvaged more than I intended.  Four boxes of records dating back to the late 1800’s.  A suit, a shirt, two ties, for the day he might require them.  A collection of tape recordings made over the past 25 years.  Several touching notes and letters written to my sister and me for such day that I was doing such a heart-breaking task.  My father’s relocation to the Holyoke Soldier’s Home will provide him a new start on life.  He left behind the detritus for my sister and I to sort out.  The visceral pain of touching the pieces of his life that he treasured most were what was most difficult.  My great-grandmother’s sepia photograph wrapped in a velvet sack laid alongside money from the mid to late 1800’s. It was hard to ponder what brought these items together.  The batteries and pens and stationery and the stamps on letters never mailed were inventoried and sorted.  
My brother-in-law and I had spent hours and hours over the weekend right here in the exact same spot.  We had removed close to a ton of clutter and cast aways from the house already.  I tried to steel l myself to it.  I tried to apply my very exceptional skill to sort and organize like and unlike items (learned from playing hundreds of games of solitude, I am convinced) without the emotional burden of being present  - while I toss an entire refrigerator filled with half-eaten food.  It is not easy.  Loss always seems to declare itself as I finger a book, turn over a photograph, gather up items for the Thrift Shop.  Letting go, no matter who, no matter how, no matter when, is simply never easy.

13 May, 2012

Teaching Principles of Motherhood


Whatever we teach our children, we teach ourselves.
Teaching Principles
molly lemeris and dawn elise evans
1986
Acceptance-
To teach our children to practice tolerance of others and self-acceptance.
Commitment-
To teach our children the importance of self-discipline.
Faith-
To teach our children that there is a greater force that guides them and to trust in the unseen.
Freedom-
To teach our children that liberty means freedom for all.
Generosity-
To teach our children that to give is to receive; that giving comes from the heart.
Gentleness-
To teach our children to look for, and appreciate life’s many miracles. Use tenderness regularly.
Joy-
To teach our children to celebrate life whenever possible.
Light-
To teach our children that light is possible because of darkness.  Live in light.
Love-
To teach our children that love is given unconditionally and that love drives out fear.
Patience-
To teach our children to relinquish making demands on others and of life.  Focus on intention instead.
Peace
To reach our children that peace is found first in the heart.
Truth-
To teach our children that truth is paramount.  “Be still and listen to the truth.”
                              This quote is from A Course in Miracles

04 February, 2012

Hope Springs Maternal


Somewhere in my files of abandoned essays is an essay entitled, Hope Springs Maternal.  I started writing the piece about fifteen or twenty years ago when my children were irrepressibly curious and impossibly busy.  I was acutely aware of my failings as a mother.  I  regretted my short, critical words, my lack of patience, the missed moments of connecting with my children.  I mourned my ineptitude as a mother and held on to the notion that tomorrow, tomorrow, I would be a better mother. A particular incident still stands in sharp relief in my memory.  My four-year old daughter called me into the kitchen.  Her three-year old sister was napping and her brother had not been born.  I was the harried mother of two.  Hannah came into the kitchen with pure joy on her face.  She had something else on her face as well. From check to check she had drawn a red slash of lipstick that covered her lips and an 1/2 an inch all around them.
 “Oh my, what did you do?”  I cried.  In her hand was my broken Estee Lauder lipstick.   Her look of proud joy and thrilled excitement deflated into misery with my harsh words. 
“I wanted to be like you, Mommy!”  I felt dreadful for having hurt her.  Hannah’s eyes welled with tears that she fought to keep back.  Mine did, too.  Immediately, I regretted that I had been thoughtless.  There were so many ways I might have handled the situation in a positive, teaching manner. Instead, in that moment, I crushed her spirit. Truly, I tried to recover and from there, I think I handled things well.  However, as I laid in bed that night, I ruminated.  I distinctly remember the feeling of deep regret.  I promised myself that tomorrow I would do a better job, tomorrow, I would be a better mother.  Remorse is a heavy load.  I discovered that remorse and regret smother hope.
I pause to reflect on this today, the anniversary of the most difficult year of my life.  It is worth noting that against all odds I have survived whole and in tact.  Upon hearing the list of hardships my family has endured over the past 365 days, one long-lost friend remarked that Job has nothing on us.  The same friend offered to drive me to my next doctor’s appointment as some form of meager recompense for not helping more she said. I grasped her outreached hand. 
It is these kinds of generous acts of kindness from others that have illuminated my path and given me hope through the darkness.  Hope.  In the recipe of life, hope shares equal measure with love.  They are, to my mind, inexorably tangled.  Against all odds, hope has wheedled its way into a life that had been nearly crushed by sorrow, fear and pain.  
The descent into despair is not sudden.   I imagine the slippery sides of a cavernous hole disappearing into the ground.  There are handholds of persistent weeds, small outcroppings of rock, and convenient ledges to grasp as the descent begins.  It is a manageable climb with a bright blue sky still stretched above like a taut blanket.  There may be voices calling down echoing and not-quite audible in their encouragement.  At some point, the plunge no longer seems a good idea, but there is no reversing the motion down, down, down. The walls become slick, wet; there are short, terrifying moments of free-fall until an abrupt and unexpected arrest on no more than a toe hold of rock.  Whispered prayer and quiet determination prove no match against gravity for long.  A head over heel tumble through black space suspends thought and feeling.  It ends in a painful HUMPH as the lungs are forced to release their air.  The body lies broken and still while the mind seeks its bearings.  No rays of light touch the walls of this dark prison.  Perhaps there are some muffled sounds from above, but they are hard to too hard to discern above the lupdup, lupdup of the heart’s relentless urge to beat.   
If I were an Edgar Allen Poe aficionado, the story might end here, with a nod to The Tell Tale Heart. Poe wrote, “It is impossible to say how first the idea entered my brain; but once conceived, it haunted me day and night.” Lying at the bottom of this grave-like pit with only a beating heart for company, one’s thoughts drift hauntingly in dangerous directions. 
However, a single brilliant ray of light can penetrate the deepest darkness.  Emily Dickinson brought us this thought, 
Hope is the thing with feathers
That perches on the soul
And sings the tunes without the words
And never stops at all.  
Hope is what fills the body with light and lifts the weight of sorrow before it can crush the spirit.  
As a junior in high school. I read Dantes’s Inferno.  So much of its symbolism and meaning escaped me simply because the landscape of my life had not yet been populated with that kind of sorrow and strife.  Henry Wadsworth Longfellow translated Dante’s work with a colorful and rich prose and descriptive imagery.  In the early 1300‘s, Dante succeeded in describing his own view of darkness that was no different than Longfellow’s in the 1800’s or our perspective today:  
He wrote, 
Midway upon the journey of our life
I found myself within a forest dark,
For the straightforward pathway had been lost.
Thirty-eight chapters later, Dante reached the end of his journey through the nine circles of hell.  He ascended on Easter saying,
Hence we came forth to rebehold the stars.  
From the fiery gates of hell, a place that represents infinite despair, Dante emerged above ground to witness the shimmering light of distant stars and the promise of hope..  
William Styron made note of this optimistic message –often lost in the telling of Dante’s Inferno – in his book about depression called Visible Darkness.   Stryon’s volume is a small one, easy to hold open in one hand.  The generous chairs at Barnes and Noble provided me with a comfortable resting place to read it, cover-to-cover in one sitting.  Like any great writer, William Styron changed my view of the world with that book.  Not only did I better understand the demons with which he had wrestled for so long, I better understood myself.  
I was never diagnosed with depression, but I felt more than a passing acquaintance with the subject of depression as Styron described it.  Perhaps, unwittingly, I have been wrestling with some demons of my own.  What I did know after reading Styron was that from the time that man has walked upright, he has been seeking light. What I did know was that anything that fosters one’s belief that tomorrow might be better than today is what instills hope among the downhearted.
Whether it’s a penlight, a flashlight or the blinding light of day, when light penetrates the cavernous pit in which the forlorn are entombed, a seed of hope is born.
Hope Springs Maternal
by
Dawn Elise Evans

Hope is never a leap.  It’s a small series of little movements that hardly qualify as steps.  
Hopes comes unbidden but unceasingly. 
Hope is irresistible and seductive. 
Hope looks like sunshine or a ray of light, a smile, an hour in the garden.  
Hope is a friend’s call and offer to visit.  
Hope is shaped and molded by memories of the past. 
Hope, like love, when accepted and encouraged, can lift and sustain us.
Hope comes dressed as the promise of a tomorrow.
Hope trumps despair. 

14 October, 2011

The Spirit Giveth Life and Other Incredulous Tales of Life


Since last spring, I have optimistically anticipated attending my 35th high school class reunion at the Wheeler School.  Wheeler figured too large in my life story not to go back and see the girls, now women, who populate my memories and shaped my life.
The class of ’76 was not untouched by tragedy.  In my junior year, I was assigned the role of “Big Sister” to an incoming freshman.  I remember her as exceptionally quiet and unexpressive girl.  Standing against a wall, she would disappear.  She wore a cloak of invisibility.  She seemed to disappear among us.  Her aunt, Miss Rowe, taught at Wheeler, so I checked in with her to see if I was doing something wrong. She assured me it was not me, her niece was having a hard time adjusting to some big changes in her life.  When I came back to school after Thanksgiving break, Miss Rowe took me aside before morning assembly.  I listened numbly as she told me my that “little sister” had committed suicide. Rumors were bruited about school later that day, that week, about how she did it.  I removed myself from all discussions. I remember feeling stunned, almost shell-shocked.  Today, counseling would have been provided for any of us whose lives had intersected with her’s.  At that time, we were on our own to figure it out.   I found myself asking what I could have done differently. Suicide always leaves the survivors wondering. 
Kris Kersch was an eighth grade Wheeler student who did not make it to freshmen year.  I did not know her, but I admired the story of her valiant fight against leukemia.  Early one September morning, the entire student body assembled in the courtyard to plant a tree in her memory.  The song, “I Can See Clearly Now,” which forever has her face attached, was part of the service.  Another rather public tragedy was the loss of Jeanie Goulder’s good friend, Billy Boots.  It seemed obscene that he was killed by a n automobile while he was jogging. Deaths and grave illnesses touched many of the families of our classmates.  We students resolutely carried on.  However, these untimely losses delivered an indelible lesson; life is capricious and we are all at risk.  There would be times when a group of us would be studying and I would look around the table and wonder which of us might not make it to middle-age. Even now, I am tempted to whisper, I don’t want the powers to be to hear me, I don’t want to tempt fate.  To my knowledge, the Class of ’76 has lost three classmates   -- Jane Sheridan, Amy Kalberer Sullivan and Lisa Aronson Wyland.  Each death leaves a hole in the fabric that binds us.  Lately,  I find myself  flipping to the page of obituaries in the Now and Then at Wheeler Magazine to see if any more of our contingent have joined the departed. 
In a state borne of ignorance and youth, I never considered there were fates other than death that can profoundly alter a life. In 1976, I am not sure I even considered disability as a circumstance that had any real bearing on any of us.   Neither the literature I read, nor the life I enjoyed, predisposed me to consider that disability could unhinge one of us or alter our paths.  Furthermore, I would never have had the imagination to believe it would be me.  Nor could I have imagined how often I would come back to the Wheeler principle that “”the Spirit Giveth Life.”  When your body does not always cooperate, your must rely on something more.  I have derived strength from those words repeatedly over recent years.  This summer,  I turned in both of my hips for models built of titanium and porcelain hoping to improve pain and functionality.   Afterward, I spent six weeks in Spaulding Rehabilitation Hospital in Boston doing hours of physical therapy and occupational therapy daily.  My post-surgical days were part providence, part torture. I learned that the road to better is steeply inclined and the terrain is rugged.  However, it is not without surprises.
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    At Spaulding Hospital, the fabric curtain walls that separate patient from patient in two-bed rooms afford little privacy.  I was listening (despite politely putting on my Bose sound-canceling headphones) to the hospital intake drill as my third roommate in a month was being admitted.   Her name was June.  Or Judy.  A man hovered nearby… a spouse?   My new roommate lived outside of Boston.  I didn’t hear her birthday, nor did I dare guess her age.  A former roommate was 93, but looked not a day over 85.  I gleaned that June/Judy had hip surgery after a particularly nasty fall at her summer home in New Hampshire.  I was able to block out much of the remainder of the interviews.   However, one word, above all others, yanked my attention back to the mysterious, and, as yet, unseen woman on the other side of the curtain.  She had uttered the word, “Wheeler.”
I confess to clicking the power button on the headphones to “off” for this part of the conversation.
Judy, as I had learned was her name, described having boarded at Wheeler for high school in the sixties.  Her mother placed her in an all-girl boarding school after the premature death of her father.  This solitary piece of information reshaped my impression of my roommate instantly.  Right or wrong, I felt drawn to her immediately; she walked the halls of Wheeler, had dined on Wheeler soups, watched the musicals, been to the Farm and shared a life that I, too, had lived.  That piece of knowledge unlocked something.  I felt a kinship I had not felt when all we shared was osteoporosis and unhappy hips.
Having Judy for a roommate was like being hospitalized with a close friend.  Her wisdom, humor and intelligence were a source of solace to me --  and the stuff on which our friendship blossomed.  I could talk to Judy about how hard Madam Erlenmeyer pushed me and she understood.   We speculated that when Madam was teaching Judy to conjugate etre, she probably was in her fifties.  To think, she had seemed like an elegant old woman.  How years can change one’s perspective.  Judy and I reflected on the fundamental values that, day-by-day, were inculcated into our thinking.  She was there during the heyday of the Women’s Revolution. I was there after Elizabeth Curley Brown had made her mark on our society.  Nevertheless, we were branded Wheeler girls.  A label we would never freely exchange. 
As I recuperated last summer, I had an inordinate amount of time to reflect upon how I define myself.  Three years ago, I was diagnosed with a congenital collagen disorder.  I have struggled with its symptoms for my entire life.  Only recently have we had a label for it.  Unfortunately, age accelerates the effect that the syndrome has on me.  Slowly, in bite-sized increment, it has disabled me. My diagnosis came about as a result of my daughter receiving a diagnosis. When the geneticist and cardiologist cast about for the gene donor that brought about her disorder, it was a little like spin-the-bottle.  The bottle stopped.... pointing at me.  A lifetime riddled with illness, injury and miscarriages suddenly snapped into focus, I had Ehler’s-Danlos Syndrome.
Ehler’s-Danlos Syndrome (EDS) comes about as a result of a collagen disorder.  Collagen is the ‘glue” that holds the body together; it is distributed all through the body.  The symptoms may be mild to severe. There are six sub-categories. I was diagnosed with Type III, Hypermobile.  In the 1 out of 5000 people with EDS, their collagen is flawed leaving it too flexible and stretchy to work properly.  This translates to ligaments that don’t do their work and in muscles that do not sustain mass.   Skin may be stretchy, often there are gastrointestinal problems, as well.  As a group, we bleed easily, become cold easily, and have a high tolerance for pain.  For me, it means my joints are easily unhinged--  my knees dislocated, my spine broke and my vertebrae are deteriorating, my hips wore out and I am hobbled by pain.  It affects my heart because the collagen that makes up the aortic root stretches over time. Both my daughter and I have changes in our hearts that are typical in patients with this disorder.  Fortunately, I have the class of EDS that generally does not result in sudden, cardiac events.  All of which brings me back to my Wheeler days.  In my youth, I never considered there would be those among us whose paths would be altered by anything less than death.  Imagine my surprise and my lack of grace in accepting the news that I had a disorder that I unwittingly passed on to my child.  Imagine my overwhelming sense of gratitude that I would have a child who accepts the cards that life has dealt her and goes about the business of living as fully as possible.
My days spent with Judy at Spaulding helped bring to mind one of the most important pieces of my Wheeler education.  When I was younger, I believed Wheeler, as an all-girl school,  was responsible for imbuing me with a sense of self-esteem.  I have, in ensuing years, discovered Wheeler helped contribute to more than my self-esteem.  Some kind of transformation was gradually wrought over my years at Wheeler.  It was the resilience of spirit under any condition or circumstance.  It was precisely because of the losses we observed at Wheeler that I was christened to life’s hardships.  When I was faced with my own trials, I grew stronger.  Over a summer when I felt untethered and alone, I found that my Wheeler connections were a lifeline.  Thirty-five years after graduating, I had friends from Wheeler willing to help me weather life’s storms.  Ellen Pinkos was a regular correspondent, advocate and friend.  Jan Fierman Weiner reentered my life as a loyal friend, ever a comedienne.  And, of course, the universe delivered up my new Wheeeler friend, Judy.  
I will not be at my 35th reunion. At this juncture of time, I can’t travel comfortably. However,  Skypping brings me face to face with friends.   I spend inordinate hours on my computer traveling unfettered by my body.  I write my blog.  I write magazine articles, continue to look for an agent for my literary novel (here’s the plug; I accept all leads and track down all suggestions to get me an agent and my book published) and I manage my family life from bed.
I am constantly bumping up against what I desire to accomplish with what my body allows me to do.  However, my fingers and my Mac give me an open-ended ticket to travel.  My spirit remains indomitable.  And, as Wheeler taught me, “The Spirit Giveth Life.”
My blog may be found at http://dawnings-anewdawn.blogspot.com/
For more information about Ehler’s-Danlos Syndrome go to www.ednf.org.