August is Month of Miracles! Here at RE/MAX INTEGRA, Midwest, we will feature miracle children from across our region throughout the month. The stories we share represent thousands of children whose lives have been impacted by our local CMN Hospitals and contributions from RE/MAX associates.
This week, Maria Gomez & Isidro Arcos tells us how Gillette Children’s Specialty Healthcare has impacted their son, Mateo’s, life – and help him live with hope, love, and cerebral palsy.
This is my son Mateo. He was born with a brain injury, and as he grew developed cerebral palsy, epilepsy, and was treated for infantile spasms. Mateo has faced challenges in his young life, but he is so much more than his illness, or what comes back on his test results. He’s a fighter, but he’s also a happy, goofy, loving child. Mateo is a miracle. Mateo is our miracle. He brings so much joy to our lives, and hopefully some to yours as well.
As he ambles down a long hospital hallway, smiling with every step and practically daring you to do the same, it can be pretty easy to forget that none of this was supposed to happen. Mateo Arcos was never supposed to walk.
When Mateo was born, he was diagnosed as having a severe case of hypoxic-ischemic encephalopathy (HIE), a brain injury caused by deprivation of oxygen and blood flow to the brain. “Mateo was very ill, says Beverly Wical, MD, pediatric neurologist at Gillette Children’s Specialty Healthcare. “In severe brain injuries like this, we must work very quickly to prevent further injury. We now have techniques that can limit damage and improve outcomes in babies like Mateo.”
For Mateo, this required therapeutic hypothermia, a process by which his body was cooled down to 92.3 degrees, and kept there for the next 72 hours. The treatment slows the metabolic rate of the body, and has been shown to protect the brain from some of the aftershocks and cell death that can occur following an acute injury from lack of oxygen and blood flow. His care team also screened for seizures with bedside brain wave testing, as early treatment of seizures is very important. Mateo’s testing was severely abnormal, and many electrical seizures were occurring.
After three days had passed, Mateo’s brain activity had improved. But as Wical looked over his tests, signs for optimism were scarce.
“Mateo’s MRI showed changes that suggested both hemispheres of his brain had been damaged significantly, and his EEG indicated a strong likelihood that he would have seizures in the future,” says Wical. “Mateo’s mother asked me if I ever saw miracles happen. I said that while I see small miracles happen every day, with how things looked, it was quite possible that Mateo would have severe cerebral palsy. He might never be able to walk, talk, or be able to learn in a significant way. Mateo’s family received news that is among the worst a family can get.”
3-6 Months: The Complications of Cerebral Palsy
The complicated nature of cerebral palsy stems from the fact that it isn’t one condition. Really, it’s a group of conditions that are the result of brain damage or atypical brain development that happens around the time of birth or early in life.
“Cerebral palsy isn’t a progressive condition, in the sense that the brain injury that causes it is an isolated event,” Wical notes. “That said, the repercussions of that event and the symptoms it causes may not be seen in the first few weeks of life, and more typically present in the first several months. It is very difficult to ‘wait and see’ when it comes to your child’s future.”
However, when it came to Mateo, the first milestone in his evaluation revealed surprisingly good information. When Wical saw Mateo at his 3-month checkup, she thought his mother’s request for a miracle had been approved.
“In terms of his movement and how he was behaving socially, he was right where you would expect a healthy 3-month-old to be,” says Wical. “But at 6 months, we could see that things were starting to change. Mateo began to show signs of abnormal muscle tone consistent with cerebral palsy, and some developmental delays began to emerge. We also monitored his seizure medication, and were pleased he was not having any seizure problems.”
Such developments are not uncommon for patients who experience a brain injury around the time of birth, which is why close monitoring during these key stages of development is so important. Mateo continued on medication to control his seizures, and began working with therapists at Gillette to aid with his movement, feeding and speech.
9 Months: “Where’d he learn that?”
Around 9 months of age, Mateo’s parents noticed that he began to exhibit a strange new behavior. Periodically, he would bob his head to the side, and his eyes would roll back and become distant. At first they thought it was a new mannerism he had picked up somewhere.
Two days later, the events became more frequent. Wical quickly arranged for Mateo to come to Gillette. When the events rose to more than 100 times within the span of 15 minutes, his family brought him in immediately. There they would learn that Mateo had infantile spasms (IS), a rare seizure disorder.
“Only 2,500 children are diagnosed with IS in the United States every year, but among our patient population it’s certainly something we see more often,” says Wical. “These movements initially seem harmless, but they are actually small seizures that can be subtle enough for parents to miss. Early treatment of the condition is key, so Mateo’s parents recognizing his symptoms early played a major role in ensuring that he didn’t regress, and lose the developmental progress he had made.”
Mateo was treated with adrenocorticotropic hormone (ACTH), a steroid therapy that that requires very careful monitoring for potentially serious side effects. He had multiple EEG tests to monitor his progress. Mateo responded well to the treatment, and the spasms disappeared. He stayed on track with his development—gaining new skills day after day.
Today, Tomorrow and Forever
Mateo is now 2 years old. He does have cerebral palsy, and some difficulty in speech and development. Yet, he is walking, talking, laughing, and learning new things. He is working hard in his therapies, and blossoming in ways never expected in the dark days of his acute injury. He has also beaten one of the worst seizure problems of early childhood.
“Working with children like Mateo, and his dedicated family, is what makes my work worthwhile,” notes Wical. “He has exceeded every possible expectation we had for him when he was born—and I’m so happy to see how bright his future now looks.”
While there are many days yet to come, and challenges still lie ahead for Mateo, he and his family—and his team at Gillette—will be there to meet them together.
This story was originally written and posted by Gillette Children’s Specialty Healthcare.