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October 2006 Ensign - The Church of Jesus Christ of Latter-day Saints

October 2006 Ensign - The Church of Jesus Christ of Latter-day Saints

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PHOTOGRAPHS BY SHANNA BUTLER, EXCEPT AS NOTED<br />

BY MARILYN FAULKNER<br />

Hope for Jenny depended on the generosity<br />

and support <strong>of</strong> her ward family.<br />

Twenty-four-year-old Jennifer Sabin Sattley looks and<br />

acts like a typical young lady. A faithful <strong>Latter</strong>-<strong>day</strong><br />

Saint and full <strong>of</strong> enthusiasm, she recently graduated<br />

from college with a degree in interior design. On May 26,<br />

<strong>2006</strong>, she married Patrick Sattley in the San Diego California<br />

Temple. Yet Jenny is anything but typical. She is, in fact, the<br />

recipient <strong>of</strong> a double-lung transplant from living donors, and<br />

her story is a chronicle <strong>of</strong> courage, faith, and <strong>Christ</strong>like love.<br />

Jenny is the fourth <strong>of</strong> five children born to Gary and<br />

Valerie Sabin <strong>of</strong> Poway, California. <strong>The</strong>y were high school<br />

acquaintances, but it was after each had completed a fulltime<br />

mission that their life paths merged and they were married.<br />

A daughter, Kimberly, was born, and then a son, Justin.<br />

When Justin was a few months old, Gary and Valerie became<br />

concerned about some unusual symptoms he exhibited.<br />

To their dismay, Justin was diagnosed with cystic fibrosis.<br />

A Frightening Challenge<br />

Cystic fibrosis is a genetic disease affecting approximately<br />

30,000 children and adults in the United States.<br />

Because <strong>of</strong> the damage to the lungs and other organs,<br />

most sufferers do not reach the age <strong>of</strong> 30.<br />

Though devastated by Justin’s diagnosis, the Sabins<br />

devoted themselves to learning all they could. Gary eventually<br />

served as president <strong>of</strong> the Cystic Fibrosis Foundation<br />

and has been responsible for raising millions <strong>of</strong> dollars<br />

toward research. Valerie learned to administer the endless<br />

round <strong>of</strong> treatments that take from two to four hours<br />

each <strong>day</strong>. <strong>The</strong> Sabins had three more children: Spencer,<br />

Jennifer, and Bryan. Spencer was spared the disease, but<br />

both Jennifer and Bryan (now 16 years old with a milder<br />

form <strong>of</strong> the disease) were diagnosed with cystic fibrosis.<br />

<strong>The</strong> Sabins lived in constant expectation <strong>of</strong> a cure that<br />

would save their children. A lung transplant <strong>of</strong>fered a<br />

chance to extend life, but Justin’s already weakened body<br />

succumbed before he was able to undergo the operation.<br />

On April 22, 1998, Justin died at home at the age <strong>of</strong> 19.<br />

A bright, spiritual, positive young man with a sense <strong>of</strong><br />

humor, Justin was serving a mission at the San Diego<br />

California Temple when he died. He was deeply mourned<br />

by family and friends.<br />

Just one year later, Jenny caught a cold that developed<br />

into a dangerous bacterial infection. With deepening<br />

dread, the Sabins watched as Jennifer’s health began to<br />

decline, following the same pattern as her older brother.<br />

<strong>The</strong>re was one bright ray <strong>of</strong> hope on the horizon for<br />

Jenny, a new procedure called a partial lobe transplant,<br />

wherein two living donors each <strong>of</strong>fer part <strong>of</strong> a lung. Lungs<br />

are made up <strong>of</strong> a total <strong>of</strong> five lobes, three on the right side<br />

and two under the heart. Doctors found that one lobe<br />

from a larger, healthy individual can be substituted for the<br />

damaged lung <strong>of</strong> a cystic fibrosis sufferer. Dr. Vaughn<br />

Starnes, who pioneered this surgery at Stanford Medical<br />

Center in northern California, agreed to try the procedure<br />

on Jenny if appropriate donors could be found.<br />

Time Was the Enemy<br />

As Jennifer’s condition grew more critical, she gasped<br />

and coughed continually. On oxygen 24 hours a <strong>day</strong>, she<br />

was literally starving for air. <strong>The</strong> Sabin family underwent<br />

testing to determine who could donate a lobe to Jenny, but<br />

no family members had the needed qualifications. Quietly,<br />

word went out to family and friends that donors were<br />

needed. Within <strong>day</strong>s more than 30 friends and acquaintances,<br />

mostly members <strong>of</strong> the Poway California Stake<br />

where the Sabins have lived for 20 years, volunteered to<br />

be tested. At the hospital the donor coordinators were<br />

shocked at the response.<br />

ENSIGN OCTOBER <strong>2006</strong> 21<br />

ENSIGN OCTOBER <strong>2006</strong> 21

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