Santa Fe New Mexican

Scars of COVID persist for sickest survivors, families

Those who survived stays in the ICU left with ‘human cost of survivorsh­ip,’ doctor says

- By Heather Hollingswo­rth

Freddy Fernandez almost wasn’t here, on his couch in his Missouri home, his baby on his lap, gnawing on the pulse oximeter that he uses to check his oxygen levels after a months-long bout with COVID-19.

Months after being warned her partner might never hold his daughter, Vanessa smiles as the girl works to cut two teeth on the device that Freddy wears like a necklace, a blue ribbon tied around it.

Freddy spent five months hospitaliz­ed a four-hour drive away from the couple’s home in the southwest Missouri town of Carthage on the most intense life support available. The 41-year-old father of six nearly died repeatedly and now he — like so many who survived COVID-19 hospitaliz­ations — has returned home changed.

While more than 1 million died from COVID in the U.S., many more survived ICU stays that have left them with anxiety, PTSD and a host of health issues. Research has shown that intensive therapy starting in the ICU can help, but it was often hard to provide as hospitals teemed with patients.

“There is a human cost for ICU survivorsh­ip,” says Dr. Vinaya Sermadevi, who helped care for Freddy throughout his stay at Mercy Hospital St. Louis. “It is almost like going to war and having the aftermath.”

Freddy’s memories from those long months come in snatches — moments where he regained consciousn­ess, hooked up to machines to breathe for him, clinging to life. Sometimes he asked for his mother, who died of COVID-19 in September 2020.

He missed the birth of his daughter, Mariana, and the first four months of her life. He may never be able to return to his constructi­on job. His other young daughter is terrified he’ll go away again.

As the world moves on and mask mandates fall away, COVID-19 is not gone for them.

“We’re left with dealing with the leftovers of what it caused,” Vanessa says.

Vanessa, 28, was still pregnant with Mariana last summer when the delta variant struck poorly vaccinated southwest Missouri. She was skeptical about the vaccine, but her obstetrici­an reassured her it was safe and she decided to go ahead and get it.

Freddy was warming up to the idea, too. The native of Mexico City, had come to the U.S. around 20 years ago to work constructi­on — cement jobs mostly — and was now a permanent resident. Sometimes he would work from 5 a.m. to 8 p.m., and often at least one day on the weekend.

On the very day in late August that they planned to schedule an appointmen­t to be vaccinated, his throat began to ache. It was COVID-19.

Days later, with Freddy coughing and struggling to breathe, Vanessa rushed him to the emergency room at the local community hospital. Freddy, although worried about his family, recalls thinking that “it’s only a little bit.”

But pneumonia was running through both of his lungs. The next day, he was taken to a larger Springfiel­d hospital that was overflowin­g with patients and placed on a ventilator. That, too, wasn’t enough.

He wound up in St. Louis, nearly 270 miles away from his two young daughters; Vanessa’s 10-year-old son, Miguel, who considers Freddy his father; and three other children with his ex-wife — 10-, 8- and 7-year-old boys.

Freddy was lucky, though. For all the talk of ventilator capacity, what was in shortest supply during the delta surge was something called ECMO, or extracorpo­real membrane oxygenatio­n. It is used when a ventilator isn’t enough, pumping blood out of the body, oxygenatin­g it, and then returning it.

Mercy Hospital St. Louis only had the equipment and staff to care for three ECMO patients at a time. And on Sept. 3, Freddy became one of them.

Survival rates for ECMO patients slipped during the pandemic to around 50 percent, according to a 2021 report by the medical journal The Lancet.

That meant even being on the machine, his chances at surviving were far from guaranteed.

Vanessa delivered Mariana on Oct. 13. Freddy had been in the hospital for 48 days, and he didn’t even know he was the father of a healthy, 6-pound, 11-ounce daughter.

Far away from her fiancé, Vanessa logged into video calls with Freddy’s doctors the same day she brought the newborn home. The news wasn’t good — Freddy was suffering from infections and wasn’t recovering well.

A lung transplant, Sermadevi said, appeared to be his best option, but was a long shot, she warned them.

“I don’t want to give you false hope,” Sermadevi recalls telling the family. “And there is a chance that Mariana might grow up without a father.”

Vanessa, helping the hospital interprete­r translate for Freddy’s family, glanced at the baby snuggled on a bouncy chair by her side. She was wearing the same hand knitted yellow and white sweater and booties that the couple’s oldest daughter, now 4-year-old Melanii, had also worn home from the hospital.

She wanted to keep fighting.

So when the baby was just a week old, Vanessa began making the weekly drive from Carthage to St. Louis, where she stayed in a hotel from Mondays through Fridays. Freddy’s sister joined her, and her parents watched the children. It meant giving up the early months with the newborn.

“I have to split myself into two,” Vanessa remembers deciding. “I knew she needed me, but he also needed me. And so I knew that if I was there with him, there is a chance for him to come home and then we would all be able to be home with her. So I had to take that risk.”

When Freddy’s family came, it made all the difference.

His room was transforme­d, photos of his family thumbtacke­d to the ceiling. Freddy’s family held his hand when he had respirator­y distress, talking him through it. He needed less sedation and pain medication because, she says, “they were that for him.”

With his lungs slowly improving, soon Freddy was up and trying to walk. Three people helped as he took his first steps on legs that were so numb just a few weeks earlier that he asked a cousin whether he still had them. The staff was overjoyed — a manager pulled out pompoms, and there were streamers. Lung transplant talk was tabled. By Feb. 9, he was heading home, 167 days after he first arrived at the hospital in his hometown.

Freddy relied on a walker and a wheelchair at first. He couldn’t sit or eat on his own.

But now the wheelchair is abandoned on the home’s back steps. He walks around the entire block, pulling a portable oxygen canister behind him on a dolly. He’s on the cusp of being able to carry his oxygen around in a backpack, which would give him more freedom.

The family spends hours outside in the late afternoon and evening, Freddy watching the children jump on the trampoline. His German Shepard sticks by his side.

Vanessa is returning to work, life returning “back to normal a little bit.”

They want to wait until Freddy gets better to get married.

Yet they don’t know how much better he will get — or how quickly.

Such is the story of so many, who are alive yet forever changed, says Sermadevi, who has followed his progress from afar. Some of the nurses even became Facebook friends with Vanessa.

“It’s sad and happy at the same time,” she acknowledg­es. “And that’s very hard to reconcile.”

 ?? CHARLIE RIEDEL/ASSOCIATED PRESS ?? Freddy Fernandez sits with his fiancée, Vanessa Cruz, and their 8-month-old daughter, Mariana Fernandez, last month in their home in Carthage, Mo.
CHARLIE RIEDEL/ASSOCIATED PRESS Freddy Fernandez sits with his fiancée, Vanessa Cruz, and their 8-month-old daughter, Mariana Fernandez, last month in their home in Carthage, Mo.

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