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Ethical Quicksad

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Submitted By maxahunter
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Just down the hallway, in Room 356, Curtis Kelly’s body lay covered to the chest by a white blanket, his torso rising and falling with the help of a ventilator. A neurologist at Fairview Southdale Hospital had declared him brain-dead nearly six hours earlier. Checklist in hand, Mr. LeMay, a family support coordinator with LifeSource, the organ procurement organization in Minnesota, counted off the body parts that might restore the health of long-suffering patients. Because there was no record that Mr. Kelly, 46, had registered as a donor, he asked Mr. Kelly’s 18-year-old son, Kelli Brown, to approve each request for these “anatomical gifts.” They hoped to take the heart, the kidneys, the liver and lungs, Mr. LeMay explained softly, as well as the intestines, pancreas, blood vessels and skin. Bone might be removed from the pelvis and leg, he said, but undertakers could insert prosthetics to make the body look natural for a viewing at the funeral. Mr. Brown, wearing gray sweats and a ball cap, sat listening with his hands clasped in front of his mouth. “I just want him to look nice,” the son whispered. Across the globe, Chrissy Girdharry did not get the lung and liver transplants she needed to survive. “She was ill from the day she was born,” recalled her mother, Vicky Girdharry, just days after a memorial service for her daughter, who died last month at age 29. “She was born Feb. 14, and she came about three months early and was born with CMV hepatitis.” When it comes to resolving disparities in organ donation in the United States, the discourse is a mundane discussion of need but emerging proposals for payment for living organ donors suggest that truth might be stranger than fiction.

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