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Kolata - Mercies in Disguise

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The author and publisher have provided this e-book to you for your personal use only. You may not make this e-book publicly available in any way. Copyright infringement is against the law. If you believe the copy of this e-book you are reading infringes on the authors copyright, please notify the publisher at: us.macmillanusa.com/piracy.

To Amanda and the Baxley family

The two most important days in your life are the day you are born and the day you find out why.

MARK TWAIN

What if trials of this life

The rain, the storms, the hardest nights

Are your mercies in disguise?

Blessings, BY LAURA STORY

The two people Amanda Baxley loves the most begged her not to be testedat least not now. Please, her mother pleaded. Your dad is so sick. We are hurting so much already. Her boyfriend implored her not to invite news that could cast such a long and dark shadow over their future. You dont know what it will do to you, he warned.

But she had always been so stubborn, so sure of what she wanted, so able to push past trepidation. And she was driven by the impossible expectations of what this day would bring; she had to know her future in order to control it. If she had the mutated genea forecast of a horrifying and fatal illness, one without treatment or cure, passed down in her family from generation to generationshe vowed it would stop with her.

So today, with her mother and boyfriend beside her for support, Amanda sits across from her therapista man she first saw when she was in college, when her troubles with her boyfriend seemed overwhelming. Now, at twenty-six years old, she is facing a dilemma that seems to reach beyond her young adulthood, into the ageless realm of the surreal. Which life will it be? The one in which the years stretch outward boundlessly or the one where the future twists into a discernible, ghastly shape? Amanda glances around the room. The office is as it ever was: cozy with a fireplace across from a love seat and a couple of chairs. She has been here many times before, but now it is another world.

A gamine with huge brown eyes and short, glossy brown hair, Amanda vibrates with energy. And though she isnt able to bring it to bear at this particular moment, she is an optimist, always reaching instinctively for promise. Shes a hugger and a weeper, someone who does not hide her emotions. Today, she is still glowing from a recent trip to Africa, where she was able to forget herself a little while helping people who had so much less than she. At times, she was even able to forget this day, persuade herself it was not coming, this moment that will inextricably change her life.

Amandas fate resides in the result of a blood test. It will reveal whether she possesses a single mutated gene, one that has contorted the fates of so many of her family members. The results are with a doctor in California, whod ordered the test. In a few minutes the phone will ring and that doctor, on the other side of the country, will open the envelope and tell her, over speakerphone, the fateful news.

* * *

If your family carried a mutated gene that foretold a brutal illness and you were offered the chance to find out if youd inherited it, would you do it? Would you walk toward the problem, bravely accepting whatever answer might come your way? Or would you turn away, hoping to protect yourself from knowing too much?

Testing would allow you to prepare; it would permit you to plan your life accordingly, tying up loose ends and making adjustments for your truncated future. It would be practical. Perhaps it would feel the only responsible thing to do: to tell your partner or spouse that he or she will be bound to this illness, as you are. It might keep you from passing your fate on to unborn children. On the other hand, divining this illness could rob you of the limited number of carefree years left to youyears that could be spent pursuing a life youd once taken for granted. Perhaps choosing not to know would allow you to retain a certain innocence, hopefully preserving a part of the person you were before being faced with such a dilemma. Were you to choose to live in ignorance, though, you might remain peripherally alert to the first signs of fatality: a slackening grip or a spasm in a muscle. But then, we all know the rough outlinethere is the certitude of death for everyoneso why take on the weight of learning the specifics? What would you do with this information, knowing there is nothing you can do to stop the illness?

* * *

This is the story of an almost archetypal family in a small town in South Carolina faced with a medical mystery they were determined to solve.

The Baxley family is a proud and determined clan, including among them respected doctors, dignified in their approach. They are a family that works hard to maintain a close-knit bond. Though they experienced the usual abrasionsteenage rebellions, angst over career choices, personality clashesoverall, life was good.

Until, without warning, they were thrust into a harrowing medical dilemma. One by one, various members of the family were struck with an inscrutable disease, made more perplexing by the fact that it changed form slightly with each new person who got it. Often it started with a dizzy feeling or a bit of confusion. This progressed to shaky hands that could not hold a pen and moved on to lurching movements of the body. The disease ultimately rendered its victims unable to talk or to swallow without choking. And it always ended in death.

Doctors, even specialists at leading medical centers, were perplexed. The disease mimicked some of the physical symptoms of Parkinsons and some of the neurological symptoms of Alzheimersand yet this illness exists entirely in its own sphere.

* * *

For a brief and intertwining period of history, the scientific world and the Baxley family found themselves on parallel missions to unlock the mystery of this illness.

The scientific quest began with diseases like none the researchers had ever seen before. Their very nature seemed to violate the laws of biology. This class of disease was infectious but could also be inherited through mutated genes. But the principal hypothesis for why this would be truesubstantiated in studies and experimentswas fiercely rejected by many prominent researchers. Gradually, however, the pieces fell into place and that once crazy-sounding hypothesis, involving distorted proteins and gene mutations that can produce them, gained credence. The revelations were so groundbreaking that two Nobel Prizesseparated by nearly thirty yearswere awarded to the lead researchers. And though the Baxleys had not yet discovered it, their family was carrying one of those mutated genes.

As these two tales convergedscientific and familialthey brought to light a fatal gene mutation and a blood test that could reveal who had it. Now the Baxleys could know who in the family had inherited this curseand who would be spared.

This is a story of a family that took matters into its own hands when the medical world abandoned them. It is a story of how science presented the Baxley family members with a responsibility theyd never asked for or anticipatedbut that each took on in their own daring way. And it is a story of how a horrific disease taught a family forbearance and the ability to find hope even as the daunting circumstances threatened to extinguish it. This is a story of disrupting destiny.

* * *

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