In an insecure world of economic thin ice and tragedy seemingly surrounding us, it does my heart good to be able to share a story of joy on Sucarha.com.

     Dahris Clair has made her presence known here in the past with short stories of humor,  Many more of you who follow my suggested links here have read works in “The Infinite Writer” a National e-zine founded by Dahris who still handles the chores of editor-in-chief. Her many other social and writing achievements are listed in the bio at the end of this wonderful report.

     What is compelling to me, is that all of her accomplishments have been achieved  while raising a family of four children, and working a full time job while enduring a special hardship of which you are about  to read. Dahris is one of those rare walking examples of courage, dedication and devotion to others. All things really, both great and small. She is, too, an avid supporter of the North Shore Animal League and various environmental and animal organizations.

“A Long Wait is Over”

 

by

Dahris Clair

 
 

     She was nine when the dreaded diagnosis came:  Diabetes. Already burdened with numerous allergies from infancy, Melissa faced a lifetime of chronic disease and possible complications. We began the learning process of coping as a family, but ultimately it was mother and child who met and shouldered each new challenge.  Her pediatrician struggled with the vagaries of high blood sugars, increasing her insulin dosage only to have her levels plummet.

     Normally a docile, agreeable little girl, Melissa became moody and rebellious.  Dire warnings from her school threatened expulsion if we didn't get the disease under control. When I found petrified peanut butter sandwiches in the back of her closet, I called the American Diabetes Association in desperation. Through them I connected with the only counselor in the South Florida area at the University of Miami Hospital's diabetes unit, and the doctor who would supervise her diabetic care for the next several years.

     Melissa's counselor felt she would benefit by attending the ADA sponsored camp in Ashville, NC.  As a single mother in a new job, the cost was more than I could manage.

     "It's not a problem," her counselor assured me. "You pay what you feel you can afford and the ADA will pay for the rest." So Melissa was off to camp for two weeks, much against her will. She glared at me from the line boarding the plane as if she were being sent to a concentration camp.

     The first letter I received from her gave a glowing report of the camp and their activities, much to my relief. She felt "accepted" and not different, along with learning how to handle her disease.  Each succeeding summer for five years, she went back to camp. My contribution to her costs increased until the fifth year when I was finally able to handle it without assistance from the ADA.

     The many possible complications of the disease began to appear by the time she was twelve, making her life a little more difficult with each onset. She endured test after test and was labeled a brittle diabetic, making her disease more difficult to control. One after another the possible complications became the probable complications as they besieged her little body, all of which she endured mostly with patience. Neuropathy ravaged her nerves, diabetic retinopathy robbed her of her peripheral vision; gastroparesis stalled her digestive process; gynecological problems appeared. What we feared most was renal disease, which launched its attack in her late twenties. When available medical treatment no longer kept it under control and dialysis was her only option, Melissa chose peritoneal dialysisself-administered seven days a week, at night so not to interfere with her job. A bout with peritonitis almost claimed her, but her plucky spirit saw her through.

     Hemo dialysis came next, three days a week. Melissa drove herself to and from her sessions and went to work afterward. We couldn't fathom how she had the energy to work as a server after enduring four hours of dialysis, but she loved her job and was determined to keep it.

     Her tiny veins posed a problem for the fistulas, the joining of a vein and an artery through which dialysis was administered, and the jugular vein was used in the interim waiting for the new site to be ready. A staph infection in her bloodstream carried a morbidity rate of 25%, but once again, our girl beat the odds. Meanwhile, the dialysis itself was causing a problem. She needed a transplant, but so did 89,000 others. Her kidney specialist chose to put her on the list for a kidney/pancreas transplant, which shortened the waiting time appreciably.  On September 25, 2011, the call came. "It's time to go to the hospital."  Nothing short of miraculous, the 20-year-old donor's organs were a perfect match. Melissa came through the surgery in typical survivalist mode. No more finger sticks, insulin injections, or dialysis. A life-saving measure for her and the best birthday present I ever received.

    

***Dahris H. Clair is a multi-published writer whose work has appeared in regional quarterlies, several anthologies, national magazines and online e-zines, such as Yesterday's Magazette. She is the author of the novel, The House on Slocum Road, former editor of The Mainlands 7 News, and freelance columnist for a New Jersey weekly newspaper. She is the founder and senior editor of The Infinite Writer eZine. www.tinyurl.com/InfiniteWriter.

 

     
     

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