Scrawny Little Tree

               By Ann Onymous

It seemed only yesterday we were undressing the tree. Taking down the ornaments that our kids had made thru the years now triggered golden memories. Handling them with care because they were so precious to us. Wrapping them in used Christmas paper (a trick my mother taught me…you know "waste not want not!") and storing them until the next time. Every year we buy a tree or a bush that we can plant in our once barren yard. Pretty soon we’re either going to be forced to buy the lot next door for the trees or start another tradition! This year was going to be something "off the wall." I hadn’t decided what just yet. I think maybe one of those funny looking shrubs. I don’t know what they’re called, but they look like sticks with big balls of four-leaf clovers on top of them. I never could remember names and now it was even worse.

Time was passing so fast. Fifty-five! This year I’ll be 55!!! How did this happen? How did I get here? I’ll think about that tomorrow…for now it’s the season to be jolly!

Back to the tree…what should we get this year? I pulled my housecoat around me to shut out the wind. Burr, as pretty as it was out here on the deck, it was pure torture sitting in the cold. All of a sudden, I thought of the tree we got a couple of years ago. Little did I know that only five months later I would be disabled!

I remember that poor little tree. It was pretty on one side but the other side looked like someone used it for a whipping post. For some reason, I wanted that tree. Hubby wasn’t thrilled, but he could see what it meant to me so he didn’t put up a fight. He figured we could hide the bad side. We took it home and I babied it. Hubby’s part in decorating the tree was putting the lights on and then the rest was my chore. You know, I’ll never understand why men get that particular job. But all the men I’ve ever known, put the lights on the tree and turn the rest over to the "woman of the house" and the kids too when they’re little.

The lights were placed carefully on the limbs, shining brightly. Well, really they were strung around and around the tree in no particular order looking like the tree had already tipped over a couple of times or been the cats object of affection. Until recently, I always had to come along behind hubby and fix the lights! I laugh about that now, but I sure didn’t then.

I remember, thinking that the tree looked so weak and fragile but still stood tall and proud. I took my time decorating that tree. In the gaping hole right in the front, I placed the "Baby Jesus House" as my kids used to call it, on a bed of angel hair. I recall standing back, assessing the quality of my labors. I had done the best I could for that disabled little scrawny tree. It made me sad to look at it and think about how I had been feeling lately. Though I was far from scrawny and being disabled was the furthest thing from my mind, I identified with that tree. It too, once was full of life and was pleasing to look at.

It just so happened that this was the first Christmas without my Momma. She had died eight months earlier of cancer. Now, my Momma is a whole different story that I’ll tell someday, but you can understand how sad I was that year. And just to make matters worse, my son and his family were not coming home for Christmas. I was at the point of wanting to sleep till the spring thaw.

As I recall, my daughter, who is of my spirit but not my mind necessarily and who I love more than life itself, was going thru some growing phases of her own. In other words, she really didn’t want to be around me that much. I had a way of always picking out the faults in her that I detested in myself and that didn’t make for a good relationship for a few years. We were on the mend, but still had a hump or two to get over. One thing we had had in common was denying that I had Parkinson’s. We had been successful at that for many years. I had finally accepted it and was dealing with it but she wasn’t ready. To be honest, that aggravated the heck out of me. It was my disease, what right did she have to deny it.

So you can see, we were a bit "testy" that Christmas. Yes, all of the ingredients for a horrible season of glee were there. I remember when I woke up Christmas Eve morning, I wanted to cover my head and hide. But my vanity wouldn’t let me admit defeat…I was the strong one. The one who always had a smile on her face. The one people thought was maybe even a bit of a snob when it came to socializing. I preferred them to think that rather than know I couldn’t afford to go to movies with them and such. But that day, there were no smiles…the strength had faded into a façade with a gaping hole in front that once held a warm heart full of love.

Christmas Eve had always been my side of the family’s time to swap gifts. This year we were meeting at my sister’s house instead of Momma’s. None of us could bear going there as we had all of our lives. We all managed to get thru it without a tear for Dad’s sake. He could never handle our tears let alone his own.

My daughter went home with us and spent the night. She hadn’t done that in several years. Hubby and I always left the tree lights on Christmas Eve and that year was no exception. The daughter hadn’t been over since we had put the tree up so she hadn’t seen it. At the time, I didn’t even think about that. She and I went in the house first and as soon as she saw the tree she sort of gasped. I thought she’d forgotten something…stepped on something…or somethin…you know what I mean. Maybe even seen a ghost! She just looked at that scrawny little tree with the gaping hole that I had so cleverly hid and said "Oh Momma, that’s awesome!" And I looked at her, wondering what the heck she was talking about when I noticed she was crying. I asked her what was wrong and she said, "look at that." The house was still dark with only the tree lights shining. I looked at the tree and for the first time I saw it was beautiful. The darkness hid the scrawniness and the lights hit the limbs with just the right effect. But the most beautiful part of the entire tree was the gaping hole. The "Baby Jesus House" was the center of attention. The lights had a halo effect and when I looked at the tree, my eyes automatically went to that battered and broken space that I had so cleverly tried to hide. The gaping hole that now was filled with a symbol of love and hope.

My girl is now one of my very best friends. Shortly after that Christmas, she sat me down and asked me to tell her everything Parkinson’s was doing to me. Somehow we had gotten over the hump. Now there was a bond that would never be broken…a bond of love and hope.

Good grief, how did I get on that subject? I gotta decide what I want for a Christmas tree this year. This year, I’m not the only one with an ailment. This year, September 11, left many gaping holes. Reckon I could find a scrawny little tree?

  Write to Ann Onymous

 

 

All Our Days Belong to the Lord
(A Parkinson's Prayer)

Please give to me good length of days
in which to do your will.
Some days for singing songs of praise,
some days to just be still.

Lord, grant me courage to go on
and willing hands to serve.
Be patient with my anxious thoughts
and fill my heart with love.

When trouble comes upon me
and life's an uphill climb;
Help me surrender to your love
and feel your hand in mine.

For there's no doubt I need you,
without you I am lost.
Help me to lay my burdens
upon your rugged cross.

And when at last I see you,
and look into your face,
I'll life my hands up to the one
who saved me by His grace.

By: Pauline J. Neck


    

QUIET PROTEST

a story by Barbara Custer

My name is Elaine Peterson. I’ve just celebrated my seventy-fifth birthday at the Sunset Nursing Center. The doctors put me here because I have emphysema. When I’m well, I enjoy walking through its rose gardens. At the moment, though, I feel the muscles in my chest tightening, cutting off my air and making me sound as if I’d been running for days. My breath comes out in short pants. They tell me that anxiety causes this, but I think they’re wrong.

The wheezing started after my afternoon walk. It was chilly outside, and cold weather aggravates my symptoms. On bad days, I feel as something were smothering me. My breathing gets worse at night. At home, I keep my mini-nebulizer and inhalers nearby in case I would have a spell; but here, I must ring for the nurse. Right now, she’s sitting at the desk, which faces my room. I pray that she hurries with my medicine. Last time my breathing got this bad, my son Robert rushed me to the hospital, and I wound up on a respirator.

Robert promised to visit tomorrow so he can show me pictures from his recent trip to Africa. I always feel better after we talk. But I still have to get through tonight, and no one has answered my call. Maybe I can sleep sitting up. It’s getting harder to breathe.

I think about going home this spring. By then, I will have finished my rehabilitation. Robert’s arranging for a home health aide to stay with me. Maybe I can plant a rose garden of my own. I also want to grow tomatoes, peppers, and other vegetables. Robert plans to take me to Florida for a week. We travel every year, and I never let emphysema stop me. He rents a wheelchair for me if I get short of breath.

But now, I’d better stop thinking. Getting excited uses my oxygen stores.

The nurse hasn’t moved from her desk. She appears to be asleep. I want to sleep too, but I need a treatment badly. I lean forward, propping my elbows on the table, hoping this will help me to get air. My breathing just becomes worse. I’m tired, and my chest is starting to ache. I try getting up and calling for help, but my poverty of breath makes shouting and movement impossible. Tears come to my eyes and I let them flow. Sometimes crying loosens my secretions and helps me breathe easier.

If only I had my medicines at the bedside. Then I could take the treatment myself without bothering anyone. The nebulizer treatments give relief within minutes. According to the nurse manager, Sunset Nursing Center doesn’t allow residents to have medicines at the bedside.

One aide often tells me that extra treatments won’t help and that I should quit bothering the staff. They’ve got a crowded floor and no time to cater to my whims. I don’t understand it. The nurse finally answers my call. She gives me Xanax, a drug to relieve my anxiety. Xanax makes me sleepy, but it doesn’t help me to breathe. She tells me not to worry, that I’m not going to die.

Early the next morning, while the radio drones on about government cutbacks in health care, I see the lights fading, and I prove her wrong.

THE END

 

 

     

pwnkle.com