Millions of Americans can’t shake coronavirus
As COVID-19 swept across the country early last year, the primary concern was for the dying. So far, the pandemic has cost at least 656,000 American lives.
But there are others – as many as 12 million and counting – who took months and months to recover, or are still struggling. These “long-haulers” suffer from what’s called Post-Acute Sequelae of SARS-CoV-2 infection, better known simply as long COVID.
Edwin “Avi” Luna was a suit salesman in the Brooklyn borough of New York City when he came down with COVID-19 early in the pandemic. He loved joking around with his children and was passionate about kicking around a soccer ball in his spare time.
Now, Luna, 33, is a double-lung transplant recipient, slowly regaining his strength. His humor is back, but he struggles to climb the steep stairs to the apartment he shares with his parents, wife and two kids.
During nearly 11 months in the hospital, including all of summer 2020 in a
coma, he lost more than 40% of his body weight. “I went from an Oompa-Loompa to a stick figure,” he said. Luna makes light of his several near-death experiences but cries, too, when telling his tale.
Ronald Rushing Sr., 46, thought he had a cold when he came down with a sore throat, cough and a headache July 27, 2020. A grocery store manager living in Southern Pines, North Carolina, Rushing’s district manager sent him home to get better.
More than a year later, he’s still not. Pain shoots through his head from the moment he opens his eyes in the morning until he closes them at night.
Working his old job remains out of the question. Though his company extended his employment so he still has health insurance, he was replaced as store manager. The father of six doesn’t blame his bosses, but without that job he questions his identity and selfworth.
“On a daily basis, I feel alone and I feel like no one cares,” said Rushing, who hopes telling his story will help others feel less isolated and restore his sense of purpose. “It’s become the majority of my life, because I’ve lost everything else.”
With the delta variant raging and the U.S. enduring its fourth coronavirus surge, the USA TODAY Network spoke this summer with dozens of experts and patients to understand the consequences of long-haul COVID-19.
Over the next five days, we will share stories of families desperate to regain what they’ve lost and scientists doing everything they can to help.
Many of the people we talked with help run or participate in long-haul clinics, which have popped up in nearly every state, designed to address the wide range of symptoms that commonly include fatigue, brain fog and breathlessness.
Others are trying to unravel the economic impacts of COVID-19, to figure out how to spend the $1.15 billion Congress allocated last December to address long COVID.
Still more are delving into different aspects of the medical condition, providing insights that will lead to new information and eventually lessen its burden. Studies are published every week revealing aspects of the lingering disease and potential ways to treat it.
Dozens of patient support groups have sprung up, including Survivor Corps, with 150,000 members, and the covidCAREgroup, with more than 45,000. The Facebook group BIPOC Women Long COVID-19 Support Group focuses on women of color, another with a self-explanatory name is the PatientLed Research Collaborative.
And then there are the patients. They struggle with a huge range of problems, compounded by the emotional drain of not getting better. Some can’t even prove they had COVID-19 because testing was unavailable or hard to get when they were infected. In other cases, they are told, it’s all in their head.
They’re all waiting for help and for a better understanding of just what is making them so miserable.
“I do very much understand the feeling where your body is feeling a bit out of control and none of the doctors know why,” said Dr. Stuart Katz, principle investigator of NYU Langone’s Clinical Science Core, which has been tasked by the federal government with leading the long COVID-19 research activities of clinical sites around the country.
Katz, a cardiologist, had symptoms for months after his own infection in December. “Obviously it’s very, very disturbing,” he said.
Particularly early on, some doctors questioned whether long-haul symptoms were anything more than just anxiety after being ill. But in part because so many caregivers like Katz felt the symptoms themselves, most now are convinced.
“I’m sure that these (symptoms) are real and I’m sure we will someday understand them, but it sure is confusing right now,” said Dr. Julie Gerberding, a former director of the Centers for Disease Control and Prevention, who knows several people suffering from long-haul COVID.
Viral illnesses have long been known to occasionally trigger prolonged symptoms, but the scale of those with longhaul symptoms is unprecedented, she said, as are the range of problems and the devastation of lives.
“This clearly is different and exaggerated and more pronounced and more frequent than anything I’ve ever seen before,” said Gerberding, now executive vice president and chief patient officer at Merck & Co. “We will be able to understand this. It’s just not happening fast enough to be helpful to the people who are currently afflicted.”
The good news is most people will recover eventually, said Dr. Ravindra Ganesh, medical director of the post-COVID clinic at the Mayo Clinic in Rochester, Minnesota.
In the meantime, said Dr. Steven Flanagan, a specialist in rehabilitation medicine at NYU Langone Health in New York, “anybody who’s had COVID, regardless of your race, whatever your socioeconomic status is, you need help.”
Not even the same person
The medical system didn’t do much for middle school English teacher Chimére Smith,39, of Baltimore, as she fought COVID-19 and then sought help for the unrelenting brain fog and pain that followed.
People of color, whose communities were hardest hit by COVID-19, often face additional challenges as they try to recover. Smith, who is Black, said she was turned away repeatedly when she tried to get help for her initial infection, which began March 22, 2020.
Short of breath, feverish, unable to pass waste and losing her vision, she says she watched white people across the emergency room hallway treated as if they were positive for COVID-19, while her symptoms were dismissed as merely acid reflux and dry eye.
“This is all in your head,” she said she was told. “It made me sicker. I was humiliated. I was ashamed.”
It took until this summer, 15 months after her infection, for a doctor to finally note in Smith’s medical record that she was presumed to have had COVID-19.
Like Smith, many people of color had a harder time getting diagnosed with the virus than white people, particularly early in the pandemic. It can be harder for them to access care for long-haul symptoms, said Dr. Amy Kontorovich, a genetic cardiologist at the Icahn School of Medicine at Mount Sinai in New York.
“I don’t think there are any groups that are genetically predisposed,” she said. “But I wouldn’t dismiss the possibility that we’re not seeing even representation of people who are affected in more marginalized communities because of issues like access.”
Latino communities were devastated by COVID-19 infections, so they are likely to represent a high number of longhaulers as well. “It is the Latino community
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that is projected to carry the biggest burden,” said Noreen Sugrue, director of research for the nonprofit Latino Policy Forum.
“We’re losing, I hate to say a generation, but certainly a significant number,” added Sylvia Puente, the forum’s president and CEO. More than 1 in 11 Latinos in her home state of Illinois has had COVID-19, and the death rate has been higher in her community.
Many are now unable to return to the two or three jobs they used to hold, either because of their own symptoms or because the virus unraveled their safety net – a grandmother who can no longer care for her grandchildren, for instance.
The Latino Policy Forum is leading an investigation into the long-term social and economic consequences of COVID-19 in the Latino community, Sugrue said. “A lot of people have started picking up on this.”
It’s important to create dedicated studies, because people of color may have distinct issues, said Marina Del Rios, an emergency room doctor and associate professor at the University of Illinois Chicago.
The signs of heart attack were missed for years in women because most heart attack studies were in men. Del Rios worries the same thing will happen to minority populations if research into long-haulers focuses mainly on those who seek care.
Abigail Echo-Hawk, executive vice president at the Seattle Indian Health Board, said she’s “deeply concerned” by the lack of data on long-haul COVID-19 in the Native American and Alaska Native populations, who are 31⁄2 more likely to be diagnosed with COVID-19 than non-Hispanic whites.
“Anecdotally, I am hearing story after story after story that is related to longhaul COVID, yet I am seeing no meaningful efforts to include American Indians and Alaska Natives in research studies,” said Echo-Hawk, also director of the Urban Indian Health Institute. “Since western research began, we’ve been under-represented within clinical trial research studies and we’re seeing that happen again.”
It’s also hard to track these populations in electronic medical records, because many fail to collect appropriate racial information, she said, which means there will be fewer resources for her community going forward. “What