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Cav kid fights his own battle Sgt. Bailey Kramer

Antonio Laguna (bottom), son of Sgt. Frank Laguna, a small arms/artillery repairer assigned to Company B of the 115th “Muleskinner” Brigade Support Battalion, 1st “Ironhorse” Brigade Combat Team, 1st Cavalry Division was diagnosed with the rare and terminal disease rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation. Upon learning of the severity of his son’s illness, Frank said teary-eyed, “We lost it. What are we suppose to do. They just gave him a death sentence.” Although his condition is serious, people he meets describe him as a fun-loving and energetic child. (U.S. Army photo by Sgt. Bailey Kramer, 1st BCT, 1st Cavalry Division Public Affairs)

FORT HOOD, Texas – To a Soldier, the Fort Hood water tower with a big “A” at the top might represent the First Army Division West, but to one chubby-cheeked young boy, it is the headquarters of Captain America.

This chubby-cheeked young boy is Antonio Laguna, also known to his family and friends as Supertonio, the 7-year-old son of Sgt. Frank Laguna, a small arms/artillery repairer assigned to Company B, 115th “Muleskinner” Brigade Support Battalion, 1st “Ironhorse” Brigade Combat Team, 1st Cavalry Division, and he lives a normal life despite his illness.

At the early age of 6, this superhero was diagnosed with the rare and terminal disease of rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation.

Candace Laguna, Antonio’s mom, said ROHHAD affects everything the body is supposed to do naturally like weight management, eye focus, bowel movements, breathing, temperature regulation, and even psychological behaviors.

“It’s like a computer,” Candace explained. “Even though it is supposed to run automatically it glitches and doesn’t always do that, it’s dangerous.”

Antonio’s parents knew something wasn’t right when Antonio was just a toddler.

Antonio gained 40 pounds in two months when he was 2, spiking worry in his mother.

The Lagunas took Antonio to see multiple specialists, who kept insisting it was his exercise and diet plan, but his parents knew that wasn’t the case.

“He is engaged in sports,” Frank said. “He eats fish and vegetables … no 3-year-old has ever had a more perfect diet.”

So, they kept trying.

While seeing an asthma specialist, the doctor noticed Antonio was hyperventilating.

When his records were rushed to a pulmonologist at the Brooke Army Medical Center in San Antonio, he was finally diagnosed with ROHHAD.

Even though there is no cure for Antonio’s condition, Candace believes that finding an answer saved her son.

Since ROHHAD affects the body’s ability to remind the body to breath, the doctor got Antonio a bilevel positive airway pressure (BiPAP) breathing machine to help him breathe when he is sleeping.
Although the Laguna’s were grateful they finally knew what the issue was, they were devastated by the results. Frank was at work when his wife called saying she was coming to pick him up. Antonio had a terminal disease.

“We lost it. What are we suppose to do,” Frank said, teary-eyed. “They just gave him a death sentence.”

After learning the few options ROHHAD patients have, Antonio’s parents spent night and day searching for doctors across the country who could give him even a little hope. After many disheartening phone calls to specialists, they received a hopeful message from Johns Hopkins Hospital.

They had an experimental chemotherapy treatment they wanted to test. Wanting to give their son the best chance for a normal life, the Lagunas packed up and traveled to Baltimore.

“They told us before we left they wouldn’t know if the treatment worked until he outlived us,” Candace said. “So I told them, ‘OK, I will just wait around for that.’”

While in Baltimore, the Lagunas found a support group with children who also suffer from ROHHAD. Within their first year in the group, the Laguna family saw three children lost. The children were between the ages of 5 and 9, the normal lifespan of a child with this condition.

While undergoing chemotherapy, Antonio was granted the opportunity of a lifetime, the wish of his choice.

Antonio’s wish: an orchard and greenhouse, where he could raise fresh fruits and vegetables to sell and raise money to plant more trees.

“It’s also fresh,” Antonio said. “I like fresh.”

Since being diagnosed, Supertonio hasn’t let the diagnosis get him down, and his parents have done what they can to support a normal life. He goes to school, takes care of his garden and chickens, and has chores.

“We are mean parents,” Candace said. “We make him do chores.”

In only meeting Antonio a few times, Command Sgt. Maj. Russell Salter, the Muleskinner’s senior noncommissioned officer, said that despite everything he has endured, Antonio is still an energetic, fun-loving young man.

“(He is) excited about life,” Salter added about the young superhero. “Let me tell you, Antonio cares about other people.”

The Laguna family has done everything they can for their son and are thankful for every minute they get with him.

“A lot of people think they have so much to complain about, and so much isn’t good enough or enough,” Candace said. “Be thankful. Stop complaining.”


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Public Domain Mark
This work, Cav kid fights his own battle, by SGT Bailey Kramer, identified by DVIDS, is free of known copyright restrictions under U.S. copyright law.

Date Taken:04.08.2014

Date Posted:04.16.2014 18:04

Location:FORT HOOD, TX, USGlobe

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