Parents have 3 of their children die in 3 days. Years of suffering - and months of struggling with the decision to end it - had brought them here: To a bright white living room where three of their children lay side by side by side, waiting to die. Les and Celeste Chappell loved the children, of course, and the thought of letting them go was excruciating, but holding on was just as painful. The children - Christopher, 2. Elizabeth, 1. 9; and James, 1. Life support was only prolonging the inevitable. So one Thursday in July, at their home in Springville, Utah, their parents braced themselves for what would become a long weekend of death.

Three hospital beds were set up in the living room with the cathedral ceilings and high- reaching windows that let in the streaming sun. The three children were made comfortable with morphine and lorazepam, a sedative used to control seizures, and their parents started to pray. Then they stopped the tube- feedings and watched their children, one by one, silently slip away. The obituary was a single notice, cataloging all three deaths. Surrounded by family, Christopher Lamont Chappell, age 2.

Sunday July 1. 6, 2. He was born December 1. Then: “Elizabeth Anne Chappell, age 1.

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Friday July 1. 4, 2. She was born June 2.

Then: “James William Chappell, age 1. Saturday July 1. 5, 2. He was born October 2. Christopher, Elizabeth, and James were born to Lester and Celeste Chappell of Springville,” it read. Each had for many years courageously fought a degenerative neurological condition, juvenile Batten disease.” It was an unusual obituary - three siblings, three deaths, three days - that raised questions among those who knew nothing of the family’s circumstances.

But the local authorities had no reason to look into it; they knew it to be an incomprehensible tragedy for a family with a genetic curse - but nothing more. A 2. 01. 0 family photo. Watch The Pickup Artist Season 1 Episode 1. Front left: Jennifer, Samuel, James, Elizabeth and Christopher Chappell. Back left: Jeffrey, Emma, Les, Celeste, Sarah, Matthew and Larissa Chappell. Courtesy of the Chappell family Courtesy of the Chappell family Death had come quicker than Les and Celeste expected. The hospice team had told them that the three children might hold on for days or even weeks - which the parents were not sure they could endure.

But not long after noon that Friday - only hours after the tube- feedings stopped - Celeste watched Elizabeth take her last breath. Afterward, Elizabeth’s parents and sentient siblings sat around her body for hours, sharing favorite memories about a girl who once played with princesses, but also loved to be outdoors. Her father pulled out the Book of Mormon and read about the paradise where they believed she had gone. When the mortuary eventually came to take her body away, Les and Celeste followed the gurney outside. Then they went back in, to wait once again. There had been 1.

Chappell children in all, but Elizabeth was now gone, and two of her brothers were dying. And Les and Celeste’s youngest boy, 1. Watch House Mojoboxoffice on this page.

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Samuel, also had the fatal disease. Surrounded by family, the parents prayed quietly and constantly - pleading for strength, comfort and peace, and holding tightly to their belief that they would all be reunited one day in heaven. By Saturday morning, James, who had struggled the most with juvenile Batten disease, had also died. His mother sat with him as he took his last breath, then the family remembered a baseball- lover so devout that even after he had gone blind, he begged his father to toss the ball and tell him when to swing. Again, the mortuary came to retrieve the body.

Again, Les and Celeste followed the gurney out to watch their son being taken away. Again, they returned to their living room, where Christopher was diminishing rapidly. The couple stayed up late that night, clinging to their son’s bedside, desperately trying to stay awake. They were physically and emotionally exhausted. But how can I sleep when my babies are dying?” Celeste thought. As the parents woke up early Sunday morning, Christopher, too, was fading.

He’s gone!” his mother said, watching intently as the color drained from his face. Family members shared stories about a boy who had loved toy cars and trains. Again, the mortuary came - and again, Les and Celeste watched as another one of their children was carried away. It had been unbelievably difficult, but it was done.

Elizabeth, James and Christopher Chappell in July, days before their deaths. Courtesy of the Chappell family Courtesy of the Chappell family Les and Celeste began seriously discussing the disease that would fracture their family during a date night, in late 2. After dinner, the couple pulled over in front of a sporting goods store in Schaumburg, Ill., a Chicago suburb, to talk about three of their children. Christopher, Elizabeth and James had been having issues with their eyesight, and Elizabeth and Christopher were now starting to have seizures, too. Something was obviously and terribly wrong.

The Chappells had taken the children to see specialists, and had heard for the first time about Batten disease. It is the most common among several rare autosomal recessive disorders, and for those who are diagnosed with it, it is also a death sentence: It often kills its victims by the time they are in their late teens or 2. When Les finally began to research the disease, the symptoms seemed eerily familiar: Batten disease typically presents with vision problems and seizures in children between the ages of 5 and 1. National Institute of Neurological Disorders and Stroke. Christopher had struggled to see since he was 3. He started standing too close the TV to watch cartoons and there was also hesitation in his movements, most evident when he tried to run to keep up with his siblings. Early on, Elizabeth had lost the ability to see colors: When she was 6, her mother told her to pick up a crayon from the bathroom floor - but the young girl couldn’t identify what color it was.

Then came the seizures. So that night, Les finally said it out loud - that he thought the children had the disease. Celeste, too, had been researching the disease on her own, and she knew he was probably right. They both understood what that meant - dementia could descend on the children, erasing their memories and thrusting them into episodes of anger and tears.

They could lose the strength to run, then to walk, then to crawl. Their sentences could become repetitive and incomplete, until they were left with no words at all. Then they could lose the ability to swallow, which would leave the parents with an agonizing choice: Tube- feed their children, or let them die. Elizabeth was genetically tested for Batten disease about a month later, and the results confirmed the couple’s fears. Doctors then diagnosed Christopher and James by their symptoms alone. The genetic condition is rare, affecting just two to four out of every 1. United States; but it is not unusual for Batten disease to strike multiple children within the same family.

Such was the genetic misfortune of Les and Celeste: They had already been visited by juvenile Batten disease three times - and there would be a fourth. Samuel, back left, with Christopher, James and Elizabeth Chappell in October 2.

Courtesy of the Chappell family Courtesy of the Chappell family Celeste was pregnant with a son, Samuel, who would also be diagnosed with the deadly condition. The devastating diagnoses robbed the Chappells of the dreams they held for their terminally ill children. Christopher - smart and curious, always asking questions - should have grown up to be a doctor, his mother always believed. Elizabeth was perhaps destined to be a gymnast, and James a ballplayer. Instead, Les and Celeste watched them decline, grieving each loss as it came - seeing, walking, taking, eating, and then living.