Peyton Manning Baby Jersey

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Peyton Manning Baby Jersey

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Peyton Manning; 10 Facts About The Him

Interest will be charged to your account from the date of purchase unless the balance is paid in full within 6 months. Minimum monthly payment required. Subject to loan approval. See paypal loan terms open in a new window or in their adoration for the soon-to-be Hall of Fame quarterback is driven mostly by accomplishments on the field, of course, Adam, a Tennessee Volunteers fan, recalls watching Manning during his college years. ; Sheena jumped on the bandwagon when her beloved Colts drafted him first overall in 1998 – but with the birth of their first son, Mishawaka, the couple got a big perspective and went No. 1 overall. legacy of 18 and appreciation for his work with Ascension Children’s Hospital in St. Vincent Indianapolis.

Seven years ago, the Peyton Manning Children’s Hospital team gave Shramsky’s son the chance of a lifetime.

Clay Alexander Shramsky was born on May 29, 2014 with a rare combination of birth defects known as Cantrell’s pentology. In his case, his organs were growing outside his body, he had a hole in his diaphragm and a cracked sternum.

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“I didn’t hear anyone say it was the end,” Adam recalls. “The probability of a good result is not high, but nobody says it’s over.”

After spending most of the first four weeks on a respirator, the newborn had surgery to repair his intestines and repair a hole in his diaphragm. After about a year, the organs were moved to the right place.

“Without this hospital and the team there, we wouldn’t have Clay,” Sheena said of her son, now a healthy and energetic seven-year-old eager to enter second grade.

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While the focus at this weekend’s NFL Hall of Fame induction ceremony will be on Manning’s exploits on the field, the impact he has had on the Shremsky family and many others through his relationship with Peyton Manning Children’s Hospital.

It’s more than just the name of the hospital, St. John’s Hospital. Vincent-Indiana CEO Jonathan Nalley said, noting that Manning has transitioned into a senior leadership role to make important strategic decisions. He was “intimately involved” in the expansion of the pediatric intensive care unit and, most recently, in the decision to build a new women’s and intensive care tower.

“The Peyton Manning that we know is directly connected to our children’s hospital is a greater leader and advocate to improve children’s lives,” Nalley said. “If people see his amazing performance on the pitch, I can guarantee you it’s 10 times bigger off the pitch.”

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A few months after Clay was born, Adam wrote to Manning, sharing his family’s story and thanking him for the hospital’s support. “Through your generosity and the support of such a wonderful group of professionals, you have helped give our family the most precious gift in the world,” the letter said.

“When a parent is in the ICU, you end up forming a bond with those people (at the hospital), and Peyton is one of them,” Adam said of Manning, who read the letter during a fundraiser at the hospital. “He and that hospital mean everything to us.”

It was a welcome (and unexpected) sound, Adam and Sheena said, a sign that their son’s lungs were at least partially developed. But after a few minutes, Clay ran out of energy and could no longer breathe on his own.

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“They told us we weren’t going to hear him cry because they were going to intubate him right away, so hearing him cry was really nice,” Sheena said. “That’s an encouraging sign.”

Concerns about the pregnancy began when an ultrasound revealed an abnormality in Clay’s abdomen, which was later diagnosed as an omphalocele, a birth defect in the abdominal wall where some of the baby’s organs develop outside the body in a thin, clear sac. At about 27 weeks, Schramskis was sent to Peyton Manning Children’s Hospital, where doctors discovered that Clay’s intestine had slipped into the chest cavity through a hole in the diaphragm and was pressing on the heart.

This particular birth defect (diaphragmatic hernia and omphalocele) is extremely rare on its own, specialists told Clay’s parents, and they never dealt with a baby who had both.

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The absence of chromosomal issues gives some optimism, but the odds are not in Clay’s favor. The diagnosis “washed away our hope,” Adam wrote in his letter to Manning.

“It was a difficult meeting when we got the diagnosis,” Adam said. “We have no choice but to be positive. Sheena is a positive person, so she really wakes me up.”

“(Doctors and staff) would laugh at me after the fact because I was positive, even during that appointment,” Sheena added with a laugh. “I feel like I should be.”

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The outlook was bleak, but Sheena and Adam worked together to keep each other’s spirits up. If one of them “want to go down”, their partner should be positive, and vice versa.

“It was a very difficult situation for them and it was difficult at times,” Sheena said, recalling a time when she fell to the floor crying.

“You feel helpless because you can’t fix it,” she says. “As a mom, you want to be able to do everything for your kids, but & mldr; You can’t put it back together.’

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Adam was in the intensive care unit shortly after Clay was born when he decided to write a letter to the hospital.

He researched Manning’s involvement in the hospital before Clay arrived, and after experiencing the care firsthand, he felt compelled to offer the parents’ perspective on what the hospital meant for them – regardless of the outcome.

“The people at this facility give kids a chance at life,” Adam said. “It’s very powerful and I think it’s important for (Manning) to hear that message.”

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During the weeks in the ICU, Sheena and Adam bond with their son’s doctors, surgeons and nurses, leaning on them for guidance and support.

Her doctors and surgeons made her breathe on her own by surgically repairing a golf ball-sized hole in her diaphragm and repairing her intestines when she was four weeks old. When he was removed from the ventilator two days later, the child not only breathed on his own, but also cried and even started.

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