Remembering Sen. Harry Reid, Soft-Spoken Man of Consequence

This article is part of TPM Cafe, TPM’s home for opinion and news analysis.

Harry Reid was the most consequential Senate leader since Lyndon Johnson. In large part because of his hard work, 31 million Americans now live longer, healthier, less pain-wracked lives because they have health insurance through the Affordable Care Act. In large part because of Harry Reid’s work on the American Recovery Act, the Great Recession of 2007 to 2009 did not become a second Great Depression. In large part because of Harry Reid, millions of Americans have protection from fraudsters under the Dodd-Frank Wall Street Reform and Consumer Protection Act.

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States Are Hoarding $5.2 Billion In Welfare Funds Even As The Need For Aid Grows

This story first appeared at ProPublica. ProPublica is a Pulitzer Prize-winning investigative newsroom. Sign up for The Big Story newsletter to receive stories like this one in your inbox.

When Congress passed welfare reform in 1996, states were given more autonomy over how they could use federal funding for aid to the poor. They could demand welfare recipients find work before receiving cash assistance. They could also use their federal “block grants” to fund employment and parenting courses or to subsidize childcare.

Twenty-five years later, however, states are using this freedom to do nothing at all with large sums of the money.

According to recently released federal data, states are sitting on $5.2 billion in unspent funds from the federal Temporary Assistance for Needy Families program, or TANF. Nearly $700 million was added to the total during the 2019 and 2020 fiscal years, with Hawaii, Tennessee and Maine hoarding the most cash per person living at or below the federal poverty line.

States have held on to more of this welfare money amid rising poverty. According to the U.S. Census Bureau, 16.1% of children under age 18 lived in poverty in 2020, up from 14.4% the year before. The poverty rate also ticked up for people aged 18 to 64, from 9.4% to 10.4%. As unused TANF dollars have accumulated, applications to the cash assistance program have waned, though it’s not for a lack of need, say experts and people who have applied to the program.

Bonnie Bridgforth experienced the counterintuitive reality of a state, Maine, that is stockpiling more welfare money while using less to help those in need.

Two weeks away from giving birth near the end of 2014, the stay-at-home mom was thrust into the role of sole income provider when her then-husband was convicted and sentenced to jail time for possession of child pornography. Her family of five was left without a regular paycheck.

Bridgforth, then 35, turned to the Maine Department of Health and Human Services, where a caseworker looked past her pregnant belly and told her that to get aid she’d need to meet the state’s requirement that she get a job. After explaining that it would be difficult to find employment with her due date weeks away and four children at home, Bridgforth was approved for $981 a month in cash assistance with the understanding she would start working after she gave birth.

Soon, with two of her children in school and her infant, 2-year-old and 4-year-old in the care of extended family, Bridgforth started working at a gas station. She earned $8 an hour, 50 cents above Maine’s minimum wage at that time, later receiving a 50-cent raise. Bridgforth was also pursuing an associate degree in justice studies and taking a full course load.

Yet less than two years later, DHHS informed Bridgforth that she no longer qualified for assistance, including child care. The notice from the agency said her family did not meet the “deprivation” standard, a TANF requirement that assesses the extent to which children have been deprived of financial support from one or both parents. Bridgforth’s children no longer met the standard because her husband had been released from jail and they were now considered a two-parent household, even though the couple was estranged and he was not living with them. They divorced soon after.

In an email to a DHHS welfare specialist, Bridgforth asked for an explanation. “I think I have whip lash. It is exhausting,” Bridgforth wrote in the Aug. 30, 2016 email.

The specialist replied, “Sorry Bonnie. An eligibility worker was reviewing the case and it appears that a decision was made that deprivation does not exist, I am not an eligibility worker so cannot make this determination.”

Reflecting back on the rejection, Bridgforth told ProPublica, “No one seemed to care that we were living in significant poverty.” During this period, she said, she struggled to buy diapers, gas, clothing and her children’s school books. Her oldest daughter, who was 12, “felt very poor because we couldn’t buy the good shampoo,” Bridgforth recalled.

The same year Bridgforth was kicked off TANF, Maine was sitting on $111 million in unspent welfare dollars. It spent only $45 million on the program that year. The following year — as Bridgforth “fought to keep a roof over my kids’ heads” — the unspent welfare money continued to pile up, reaching $141 million. While its surplus has since declined, Maine continues to have one of the largest per-capita stockpiles of welfare money in the nation, $93 million as of fiscal year 2020. That comes out to $657 per person in poverty.

The unused welfare stash tells a larger story of how the 1996 welfare reform law has failed the poor: It allows states to not distribute cash assistance even when they have the money to do so.

Each year, the federal government awards states a block grant, or lump sum, of funding, with the intention that the money be spent to help poor people meet their basic needs, become employed and start two-parent families. States have discretion in how they can use, or not use, the money and have increasingly used it to fill unrelated budget gaps. Experts say it’s reasonable for states to have some TANF reserves, even as large as their annual block grant, but when they stockpile the money from year to year it’s cause for concern.

Tennessee has $790 million in federal welfare funding sitting around — the largest pool of unspent welfare dollars nationwide — though it has recently promised to spend it. Hawaii has $364 million idling in an account, equivalent to $2,923 per person living in poverty. And Oklahoma has $264 million, nearly double its annual TANF budget of $138 million.

Devin Stone, director of communications for the Tennessee Department of Human Services, said, “Fluctuations in caseload and decreased participation in the state’s TANF program resulted in a surplus of TANF funds accumulating over a period of several years.” In fiscal year 2020, Tennessee reported its lowest-ever TANF caseload, about 17,000, down from 68,100 cases in 2006.

Jackie Farwell, a spokesperson for the Maine DHHS, gave a similar explanation for that state’s unspent TANF funds, saying it was caused by the Maine Legislature limiting lifetime welfare eligibility to five years. As a result, “Maine’s TANF caseload rapidly declined from 13,522 in January of 2012 to 4,320 in January of 2018,” she said. “This reduction in the number of people served by the program in turn led to an increase in Maine’s TANF block grant balance.”

Oklahoma’s Department of Human Services did not respond to a request for comment.

The coronavirus pandemic and accompanying economic travails did not make a dent in states’ TANF reserves. Between June and November 2020, the national poverty rate made its largest jump since the government began tracking it 60 years ago, from 2.4% to 11.7%. Other parts of the federal government’s social safety net increased aid to help some of the 7.8 million Americans who fell into poverty, with stimulus packages and expanded unemployment benefits. TANF, conversely, is helping fewer people.

TANF acceptance rates have steadily declined over the past few years, with some states — Texas, Mississippi, Arkansas and Nebraska — denying about 90% of applicants in fiscal year 2020, according to federal data.

“During the COVID pandemic, when unemployment rates and hunger rates were skyrocketing nationwide, TANF funds were still sitting unused,” said Ashley Burnside, a policy analyst at the Center for Law and Social Policy, a national advocacy organization for low-income Americans. The devastation wrought by the pandemic “is as much of a ‘rainy day’ as states could have had. If funds are still left unused, it makes me question what states are waiting to use this money for.”

Ty Bishop, a spokesperson for the Texas Department of Human Services, which has the nation’s lowest TANF acceptance rate at just 7% of those who apply, said most applicants there “exceed the income and resource limits.” To qualify, a family with two children and one caretaker must have less than $1,000 in assets and a monthly income of less than $188. Those requirements haven’t changed despite the state’s $281 million in unspent TANF funds in fiscal year 2020.

In 1995, Congress debated a precursor to the welfare reform law that ultimately passed the following year. Then-Sen. Carol Moseley Braun, a Democrat from Illinois, predicted some states would choose to not spend the federal dollars instead of distributing them to the poor. She proposed an amendment to prohibit states from carrying over unused welfare funds from year to year.

“If we send the states this money in a block grant, there is nothing to prohibit that state from saying we do not want to have assistance for poor children,” Moseley Braun said. “We are not going to address the issue of job creation. We are not going to train people to go back to work. We are not going to provide the children with any assistance. We are just going to further squeeze the amount of resources devoted to the whole issue of poverty in our state and we are going to take the money we get from the federal government and use that to go from year to year to year to year and not maintain our own effort. I think that would be a real tragedy.”

Moseley Braun’s “race-to-the-bottom amendment” — intended to prevent states from “trying to underbid one another” in assistance to the poor — did not make it into the final bill that President Bill Clinton signed in 1996.

Representatives of the human services departments in Maine, Tennessee and Hawaii said their states are working on plans to spend the welfare funds on new programs that will help families on the brink of poverty find greater financial stability.

Hawaii plans to use its surplus to extend employment services like job coaching and placement for noncustodial parents who have children receiving TANF and to provide diaper assistance to families that are eligible for the program, said Amanda Stevens, a spokesperson for the state. The state is also considering increasing benefits and offering monthly housing assistance, said Stevens.

In Maine, the money will be used to pay for a variety of programs and “system-wide improvements” to better serve the poor, said Farwell, the DHHS spokesperson. These include counting the pursuit of a high school diploma as an approved work activity for receiving benefits; updating the state’s application system so TANF recipients can recertify their eligibility online; and providing “coaches” to help families set goals and access resources.

Tennessee lawmakers passed legislation this year pledging to work with community “partners” to spend down the state’s $790 million in TANF reserves. The law, which went into effect in July, increased monthly cash assistance for a family of three to $387 a month, from $277. It also includes a two-year pilot program to allocate $50 million to community organizations that serve low-income families and to provide additional cash assistance to individuals pursuing educational opportunities.

Despite those efforts, advocates and state welfare caseworkers say, the steep decline in TANF applications nationwide shows the program has already irreparably lost the trust of the poor.

“Many families living below the poverty line are deciding that the benefits TANF provides are not worth the onerous upfront requirements to get on and stay on the program,” said LaDonna Pavetti, a welfare expert at the Center on Budget and Policy Priorities. “Reserves are going up because caseloads are going down.”

If they qualify for TANF, applicants also risk losing any child support they might receive from a noncustodial parent, said Moriah Geer, a caseworker at Maine Equal Justice, a legal aid organization that assisted Bridgforth as she navigated TANF.

“There are so many unknowns and confusing parts about the program,” Geer added. “Families don’t want to go through the indignity of applying to this program again, even if more funds and programs are now being offered. I have many clients who choose poverty over having to go back and beg for cash assistance to be able to feed their families and keep a roof over their heads.”

Sky Arnold, a spokesperson for Tennessee’s Department of Human Services, said there are other explanations for the decline in welfare applications, including that “less families need the money. Our economy has been gangbusters in recent years and this is a sign of it.

“Decreasing applicant numbers speak to our state’s ability to build families who no longer need assistance,” said Arnold, who recently left the agency.

The Center on Budget and Policy Priorities, a progressive think tank that analyzes the impact of federal and state policies, disputes the notion that TANF’s decreasing numbers indicate families no longer need assistance. The organization designed a metric to show how many people living in poverty are actually helped by welfare. According to its “TANF to poverty ratio,” many states, including Tennessee, are largely failing to meet the needs of poor families. In 2019, the state assisted only 18 out of 100 poor families with children, down from 67 when the program began in 1996, according to the analysis.

A report this year found that TANF serves only one in four Maine children living at or below the federal poverty level, and that 84% of families in the state leaving the cash assistance program in 2019 were still living in poverty.

Today, Bridgforth, who completed her associate and bachelor’s degrees while remaining the sole breadwinner for her family (her ex-husband remains incarcerated; Bridgforth remarried in May 2021), works in special education. Her dream is to attend law school.

In September, she provided a written statement to the Maine Legislature about her experience with TANF and suggested how the state could improve the program.

“I made it despite the monthly attempts to kick me off TANF before I was ready,” Bridgeforth wrote in her statement. “I am no different from so many other women who find themselves on welfare.”

Here’s What It’s Like When The Right-Wing Mob Tries To Get Your Book Banned

September 2021: A blonde white woman takes the podium at a school board meeting for Lake Travis Independent School District, west of Austin, Texas. She claims that instead of speaking about a need for a second high school — the subject of the meeting — she had been “sidetracked” by something she read in a young adult novel that’s available in middle schools in the area. She was here to talk about that instead.

The parent, named Kara Bell, begins to read.

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COVID Notes #8 (Special Masks Edition)

This is an uncharacteristic post. But I realize that a lot of people are looking for information like this. So I am sharing what I’ve learned on this topic.

For all the polarization and argument over masking, there’s much less discussion or guidance about what kind of mask you should wear. At the beginning of the pandemic any mask was better than none. High quality masks needed by health care workers and first responders were in short supply. But that hasn’t been the case for a very long time. High filtration masks are widely available at relatively low cost. And you should be wearing one.

Cloth masks are better than nothing. But that should not be your standard. Even if you’ve got it hostage-taking tight around your face it’s still providing much less protection than a real filtration mask. Surgical masks are fine. But a high filtration mask provides a much higher level of protection than those too. You now have the ability to give yourself a high level of protection even if you’re somewhere where others aren’t masking or aren’t masking well.

What’s A Good Mask?

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Jan. 6 Panel Reportedly Planning Dramatic Presentations On Trumpworld’s Big Lie Actions

The Jan. 6 Committee is reportedly set to hold more public hearings in the new year as it works to deliver an interim report on the events surrounding the deadly Capitol insurrection by summer, according to the Washington Post.

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E.O. Wilson’s Lifelong Passion For Ants Helped Him Teach Humans About How To Live Sustainably

This article is part of TPM Cafe, TPM’s home for opinion and news analysis. It first appeared at The Conversation.

E. O. Wilson was an extraordinary scholar in every sense of the word. Back in the 1980s, Milton Stetson, the chair of the biology department at the University of Delaware, told me that a scientist who makes a single seminal contribution to his or her field has been a success. By the time I met Edward O. Wilson in 1982, he had already made at least five such contributions to science.

Wilson, who died Dec. 26, 2021 at the age of 92, discovered the chemical means by which ants communicate. He worked out the importance of habitat size and position within the landscape in sustaining animal populations. And he was the first to understand the evolutionary basis of both animal and human societies.

Each of his seminal contributions fundamentally changed the way scientists approached these disciplines, and explained why E.O. – as he was fondly known – was an academic god for many young scientists like me. This astonishing record of achievement may have been due to his phenomenal ability to piece together new ideas using information garnered from disparate fields of study.

Big insights from small subjects

In 1982 I cautiously sat down next to the great man during a break at a small conference on social insects. He turned, extended his hand and said, “Hi, I’m Ed Wilson. I don’t believe we’ve met.” Then we talked until it was time to get back to business.

Three hours later I approached him again, this time without trepidation because surely now we were the best of friends. He turned, extended his hand, and said “Hi, I’m Ed Wilson. I don’t believe we’ve met.”

Wilson forgetting me, but remaining kind and interested anyway, showed that beneath his many layers of brilliance was a real person and a compassionate one. I was fresh out of graduate school, and doubt that another person at that conference knew less than I — something I’m sure Wilson discovered as soon as I opened my mouth. Yet he didn’t hesitate to extend himself to me, not once but twice.

Thirty-two years later, in 2014, we met again. I had been invited to speak in a ceremony honoring his receipt of the Franklin Institute’s Benjamin Franklin Medal for Earth and Environmental Science. The award honored Wilson’s lifetime achievements in science, but particularly his many efforts to save life on Earth.

My work studying native plants and insects, and how crucial they are to food webs, was inspired by Wilson’s eloquent descriptions of biodiversity and how the myriad interactions among species create the conditions that enable the very existence of such species.

Biologist E.O. Wilson with models of his life’s greatest subject, ants. Rick Friedman/Corbis via Getty Images

I spent the first decades of my career studying the evolution of insect parental care, and Wilson’s early writings provided a number of testable hypotheses that guided that research. But his 1992 book, “The Diversity of Life,” resonated deeply with me and became the basis for an eventual turn in my career path.

Though I am an entomologist, I did not realize that insects were “the little things that run the world” until Wilson explained why this is so in 1987. Like nearly all scientists and nonscientists alike, my understanding of how biodiversity sustains humans was embarrassingly cursory. Fortunately, Wilson opened our eyes.

Throughout his career Wilson flatly rejected the notion held by many scholars that natural history – the study of the natural world through observation rather than experimentation – was unimportant. He proudly labeled himself a naturalist, and communicated the urgent need to study and preserve the natural world. Decades before it was in vogue, he recognized that our refusal to acknowledge the Earth’s limits, coupled with the unsustainability of perpetual economic growth, had set humans well on their way to ecological oblivion.

Wilson understood that humans’ reckless treatment of the ecosystems that support us was not only a recipe for our own demise. It was forcing the biodiversity he so cherished into the sixth mass extinction in Earth’s history, and the first one caused by an animal: us.

Color-coded map of forest losses.
E.O. Wilson long advocated conserving the world’s biodiversity hot spots – zones with high numbers of native species where habitats are most endangered. This image shows deforestation from 1975 to 2013 in one such area, West Africa’s Upper Guinean Forest. USGS

A broad vision for conservation

And so, to his lifelong fascination with ants, E. O. Wilson added a second passion: guiding humanity toward a more sustainable existence. To do that, he knew he had to reach beyond the towers of academia and write for the public, and that one book would not suffice. Learning requires repeated exposure, and that is what Wilson delivered in “The Diversity of Life,” “Biophilia,” “The Future of Life,” “The Creation” and his final plea in 2016, “Half-Earth: Our Planet’s Fight for Life.”

As Wilson aged, desperation and urgency replaced political correctness in his writings. He boldly exposed ecological destruction caused by fundamentalist religions and unrestricted population growth, and challenged the central dogma of conservation biology, demonstrating that conservation could not succeed if restricted to tiny, isolated habitat patches.

In “Half Earth,” he distilled a lifetime of ecological knowledge into one simple tenet: Life as we know it can be sustained only if we preserve functioning ecosystems on at least half of planet Earth.

But is this possible? Nearly half of the planet is used for some form of agriculture, and 7.9 billion people and their vast network of infrastructure occupy the other half.

As I see it, the only way to realize E.O.’s lifelong wish is learn to coexist with nature, in the same place, at the same time. It is essential to bury forever the notion that humans are here and nature is someplace else. Providing a blueprint for this radical cultural transformation has been my goal for the last 20 years, and I am honored that it melds with E.O. Wilson’s dream.

There is no time to waste in this effort. Wilson himself once said, “Conservation is a discipline with a deadline.” Whether humans have the wisdom to meet that deadline remains to be seen.

Doug Tallamy is a professor of entomology at the University of Delaware.

This article is republished from The Conversation under a Creative Commons license. Read the original article.

The Conversation

They Were the Pandemic’s Perfect Victims

This story first appeared at ProPublica. ProPublica is a Pulitzer Prize-winning investigative newsroom. Sign up for The Big Story newsletter to receive stories like this one in your inbox.

By the time Cheryl Cosey learned she had COVID-19, she had gone three days without dialysis — a day and a half more than she usually waited between appointments. She worried how much longer she could wait before going without her life-saving treatments would kill her.

The 58-year-old Cosey was a dialysis technician for years before she herself was diagnosed with end-stage renal disease. After that, she usually took a medical transport van to a dialysis facility three days a week. There, she sat with other patients for hours in the same kind of cushioned chairs where she’d prepped her own patients, connected to machines that drew out their blood, filtered it for toxins, then pumped it back into their fatigued bodies.

Her COVID-19 diagnosis in the pandemic’s first weeks, after she’d been turned away from a dialysis facility because of a fever, meant Cosey was battling two potentially fatal diseases. But even she didn’t know how dangerous the novel coronavirus was to her weakened immune system.

Had she realized the risks, she would have had her daughter Shardae Lovelady move in. Just the two of them in Cosey’s red brick home on Chicago’s West Side, looking out at the world through the sliding glass door in the living room, leaving only for her dialysis.

After Cosey’s positive test in April 2020, Lovelady had to take her mother to a facility that treated patients with suspected or confirmed COVID-19. The facility fit her in for one of its last appointments the next day.

At that point, Cosey had gone more than four days without dialysis.

Four hours later, after Cosey completed her treatment, Lovelady returned to the nearly deserted building to bring her mother home, the sun having long disappeared from the sky. Cosey, dressed in a sweater and a green spring jacket, was disoriented, her breathing sporadic.

Alone with her mother on the sidewalk, Lovelady ran inside to ask workers for help getting Cosey out of her wheelchair and into her car.

“They offered no assistance,” Lovelady said. “They treated her as though she was an infection.”

(A spokesperson for the facility said employees aren’t allowed to help patients once they leave, for safety reasons.)

As Lovelady waited for paramedics to arrive, she grabbed a blanket from her car to wrap around her mother.

“My mother has COVID. I know she has COVID, but I didn’t care,” Lovelady said. “I hugged her and just held on until the ambulance came.”

Then she followed the flashing lights to the hospital.

In the three decades before the pandemic, the number of Americans with end-stage renal disease had more than quadrupled, from about 180,000 in 1990 to about 810,000 in 2019, according to the United States Renal Data System, a national data registry. About 70% of these patients relied on dialysis in 2019; the other 30% received kidney transplants.

The Midwest stood out as the region with the highest rate of patients with the disease, and Illinois had the nation’s third highest prevalence after Washington, D.C., and South Dakota, according to the Centers for Disease Control and Prevention.

A rare bright spot was the downturn in the death rate. Although diagnoses have been going up, death rates for patients who are on dialysis have declined since the early 2000s.

Then COVID-19 struck. Nearly 18,000 more dialysis patients died in 2020 than would have been expected based on previous years. That staggering toll represents an increase of nearly 20% from 2019, when more than 96,000 patients on dialysis died, according to federal data released this month.

The loss led to an unprecedented outcome: The nation’s dialysis population shrank, the first decline since the U.S. began keeping detailed numbers nearly a half century ago.

They were COVID-19’s perfect victims.

“It can’t help but feel like a massive failure when we have such a catastrophic loss of patients,” said Dr. Michael Heung, a clinical professor of nephrology at the University of Michigan. “It speaks to just how bad this pandemic has been and how bad this disease is.”

Before most patients reach advanced kidney failure, they are diagnosed with diabetes, hypertension or a host of other underlying conditions. Their immune systems are severely compromised, meaning they are essentially powerless to survive the most dangerous infections.

Many are old and poor. They also are disproportionately Black, as was Cosey. A 2017 study called end-stage renal disease “one of the starkest examples of racial/ethnic disparities in health.” Those inequities carried through to the pandemic. Dialysis patients who were Black or Latino, according to federal data, suffered higher rates of COVID-19 by every metric: infection, hospitalization, death.

Their deaths went largely unnoticed.

To get their treatments, the majority of dialysis patients in the U.S. must leave the relative safety of their homes and travel to a facility, often with strangers on public or medical transportation. Once at the dialysis center, they typically gather together in a large room for three to four hours.

The fear of contracting the virus was enough to keep many from venturing out for medical care, including those already on dialysis and those set to get the treatment for the first time. Exactly how long patients can go without dialysis depends on a number of factors, but doctors generally begin to worry if they miss two of their thrice-weekly sessions.

Dr. Kirsten Johansen, director of the United States Renal Data System, said the rates of people starting dialysis had been relatively stable until the pandemic. “Then the floor fell out,” she said in an interview.

COVID-19’s collateral damage played out in other ways as well. It meant that people delayed going to the hospital for everything from heart disease to cancer. For dialysis patients, whose life expectancy in some cases is three decades shorter than the general population, the results were calamitous. Hospitalizations of dialysis patients for reasons unrelated to COVID-19 dropped 33% between late March and April of 2020, federal data shows.

Dr. Delphine Tuot, a nephrologist and associate professor at University of California San Francisco and Zuckerberg San Francisco General Hospital and Trauma Center who focuses on vulnerable populations, found herself pleading with some of her patients to come in for their regular dialysis appointments.

One of them was a 60-year-old man whose shortness of breath landed him in the hospital in February. Doctors scheduled dialysis three times a week, and though he was initially resistant, Tuot said, he came around once he realized he would die without it.

Still, he missed appointments. When Tuot followed up, he told her he was afraid to leave the house because he was caring for his wife who had cancer, and he didn’t want to contract COVID and bring it home to her. Soon a cycle began. He skipped treatments, fluid built up in his body and an ambulance rushed him to the hospital because he couldn’t breathe. He got dialysis, was sent home and got back on track.

When cases surged and the delta variant took hold this summer, the cycle restarted — until he skipped dialysis for three weeks in a row, so long that his heart couldn’t recover, according to Tuot. He died last month.

Despite early efforts to mask and isolate patients at dialysis facilities, one study found the rate of COVID-19 hospitalizations of dialysis patients from March to April 2020 was 40 times higher than the general population.

Even with skyrocketing hospitalizations, it took three months after vaccines were approved before federal officials provided vaccinations to dialysis clinics, despite advocacy groups urging that this high-risk population be prioritized.

Although dialysis centers were swift to implement safety protocols in the pandemic’s early days, some facilities didn’t follow their own infection control policies, including washing hands properly, keeping workers home when sick or disinfecting equipment, federal inspection records show.

And home dialysis, which has been shown to be safer for patients during the pandemic, is out of reach for many, especially Black and Latino patients. Nephrologists had pushed for greater access to home dialysis before the pandemic; that need is more apparent now than ever, Tuot said.

“The fact that individuals had to go to a center with other individuals who are equally immunocompromised and had to get to that center, whether that was by public transportation or by van transportation, it’s clearly additional risks,” Tuot said. “Bottom line, they are very vulnerable. They’re very sick.”

The ambulance took Cosey to Chicago’s Rush University Medical Center. Lovelady filled in the staff on her mother’s medical history of end-stage renal disease, high blood pressure and asthma. The next day, Cosey called her daughter from her hospital bed. Lovelady noticed marked improvement from the night before.

“She sounded like herself,” Lovelady said. “We joked around a little bit. I asked her what kind of medicine she was on. She said they started her on dialysis.”

One by one, Lovelady added her sister, cousin and brother to the call. They told Cosey she had scared them, but now that she was doing better, they teased that they needed her to come home to bake her famous cheesecake. Her grandchildren hadn’t stopped asking about her either. They missed movie nights at Cosey’s house, when she made them popcorn and covered the floor with blankets.

Cosey’s boisterous laugh reassured them.

When Lovelady sensed her mother tiring, she told her she’d call her back the next day.

“Go ahead and get some rest,” she said.

While the arrival of the pandemic rocked the health care system as a whole, the effect on dialysis facilities has received little attention.

The Centers for Medicare & Medicaid Services typically monitor the facilities through routine inspections and surprise visits to investigate specific complaints. But federal officials are two years overdue on more than 5,000 inspections at dialysis facilities across the country, Medicare data shows, and three years behind on more than 3,000 of them. Since the start of 2020, the number of inspections to dialysis facilities by government officials fell by more than 30% from the previous two years, ProPublica found. Complaints made up a larger portion of investigations. In 2019, 35% of total visits were in response to complaints. Last year, it jumped to 51%.

A spokesperson for the Centers for Medicare & Medicaid Services said in a statement that the pandemic forced the agency to temporarily suspend or delay inspections for non-urgent complaints and routine inspections to focus on infection control and critical concerns that placed patients in immediate jeopardy. The agency is working with states, which act on behalf of federal officials, to address the resulting backlog, the spokesperson said, but “nearly all state agencies report insufficient resources to complete the required, ongoing federal workload.”

The spokesperson said “the COVID-19 pandemic has presented a unique challenge unlike any other in history and has impacted our routine oversight work,” adding that “complaint investigations remain our first priority to ensure we address the immediate needs of patients receiving care in dialysis facilities.”

Insufficient funding has compounded those challenges. The budget for inspections has “been flatlined” since fiscal year 2015, while the number of dialysis facilities has increased by 21% to nearly 8,000 today, according to the agency. After several years of requesting more money, the centers were approved to receive an increase for fiscal year 2022.

When investigators did inspect dialysis facilities, they found some violations specific to COVID-19 and others that involved general safety lapses, according to federal records from March 2020 to July 2021.

A dialysis patient who started treatment just before the pandemic died after a nurse at a Kentucky facility failed to properly dilute an antibiotic, according to inspection reports. Minutes after the medicine began dripping through an IV, the patient said: “My body is on fire! It’s going through my whole body,” records show.

At a New York facility, another patient died after losing more than 1 1/2 pints of blood when their catheter became disconnected, according to federal records. That same facility underreported its number of deaths in the first 11 months of the pandemic by 16 people.

Federal officials issued their most serious citation to an Indiana facility for refusing to provide dialysis to a patient suspected of having COVID-19. The patient’s previous dialysis had also been cut short because their assisted living facility did not provide them transportation after 9:15 p.m. So they did not receive a complete treatment.

An estimated 5% to 10% of end-stage renal patients live in congregate settings, such as nursing homes or assisted living facilities. The same factors that led to nursing home populations being decimated — age, health, difficulty isolating — applied to those dialysis patients. In the first months of the pandemic, they contracted the virus at a rate more than 17 times higher than those who lived independently, according to one study.

Workers at those facilities weren’t immune either. Oluwayemisi Ogunnubi, 59, worked as a nurse administering dialysis to patients inside a nursing home on Chicago’s South Side. A Nigerian immigrant, she had sent money home to pay for her children’s schooling until she was able to bring them to the U.S. Her smile and supportive nature made her popular among her coworkers, according to an official at Concerto Renal Services, the dialysis company where she worked.

On April 21, 2020, Ogunnubi’s body began to ache, and she was sent home early from work. She was later taken to a hospital, where she tested positive for COVID-19. She died three days later, federal and county records show.

Occupational Safety and Health Administration officials cited Concerto, and levied a penalty of $12,145. The company provided employees who performed dialysis on patients with N95 respirators, but investigators found that Concerto’s written procedures weren’t complete and that the company had failed to provide medical evaluations that ensured employees knew how to use the respirators.

Two other Concerto employees, including one who fell ill the same day as Ogunnubi, contracted COVID-19 at the time but survived. Within two weeks of Ogunnubi’s death, 10 residents at the nursing home died of complications related to COVID-19, according to Cook County Medical Examiner records. Half had kidney failure.

Kyle Stone, Concerto’s executive vice president and general counsel, said the first and only COVID-related death of an employee shook the company. Stone said Concerto “made a difficult choice” to use respirator masks without providing medical evaluations to employees, but it “was clearly the correct choice under the circumstances.”

If Concerto had been required to fulfill every aspect of OSHA requirements for a written policy that early in the pandemic, he said, the company would not have been able to provide the respirator masks, “almost certainly resulting in greater risk of harm and death.”

OSHA’s failure to “see and appreciate” the trying circumstances at the time, Stone said, was “baffling and disappointing.” Concerto eventually settled with OSHA, which downgraded the violation and reduced the penalty to $9,000.

“We are quite proud of our work in 2020 during the eye of the COVID storm,” Stone said.

As devastating as the pandemic has been, many experts say it could have been worse. Dr. Alan Kliger, a clinical professor of medicine at Yale School of Medicine, co-chaired the American Society of Nephrology COVID-19 Response Team that held weekly calls with chief medical officers from 30 or so dialysis companies, including the largest two, DaVita and Fresenius. The facilities, Kliger said, implemented universal masking and patient screenings before the CDC recommended them. They also treated COVID-19 patients in separate shifts or at specifically designated isolation clinics.

“There’s been a tremendous amount of collaboration and sharing of information and uptake of best practices in this group of competitive companies,” Kliger said. “They really rallied together to protect patients.”

Epidemiologist Eric Weinhandl said that there’s another battle on the horizon with the omicron variant spreading rapidly, which he finds especially worrisome given how federal officials failed by not distributing vaccines to dialysis facilities in December 2020.

“It’s heartbreaking because you look at this, and much like nursing home residents, these patients are completely vulnerable. But they still have to go to a dialysis facility three times a week,” Weinhandl said. “Why wouldn’t you prioritize this population?”

The CDC said in a statement that “demand exceeded supply” when vaccines were first authorized and “as supply increased and states adopted CDC’s recommendations, older adults and those with underlying health conditions began being prioritized.”

It wasn’t until March 25 that the Biden administration announced it was partnering with dialysis facilities to send vaccines to patients at the centers.

Now, Weinhandl wonders if dialysis patients will be a priority if the federal government approves a second round of boosters for high-risk patients.

“Is there a plan? Because I think that there should be,” he said. “I think this is getting pretty predictable. Every time COVID surges, you see the dialysis population’s excess mortality surge with it.”

Sometimes the frailty of dialysis patients is no match for COVID-19’s brutality.

Oscar and Donna Perez were the kind of siblings who loved each other without judgment or condition. After Oscar began dialysis in 2018, Donna picked him up from his appointments three nights a week. She cut his toenails when his feet were too swollen for him to reach and massaged them when the pain woke him up at night.

He was her son’s godfather, her best friend who shared his love of music with her — especially the 1960s R&B singer Billy Stewart — and annoyed her in the way only brothers can, swatting her feet off chairs just as she got comfortable and pestering her with questions when she was deep into Instagram.

But Oscar Perez was sick. In addition to his failing kidneys, the 38-year-old Latino father struggled with hypertension, diabetes and congestive heart failure. In early January, doctors performed coronary bypass surgery. He was not yet eligible for the vaccine, but the hospital tested him for COVID-19 when he was admitted. He was negative.

He went home on Jan. 18, the same day as the wake for his uncle, who, his family said, died after he missed too many dialysis appointments. But the next day, Oscar collapsed at home, confused and mumbling in pain, with signs that the coronavirus was flourishing in his lungs. He was rushed back to the hospital. A doctor called to tell Donna Perez that her brother had tested positive and needed to be intubated.

On Jan. 31, doctors called Donna again and told her that her brother’s condition was declining fast. She picked up her parents, another brother and his girlfriend, and headed to the hospital to visit Oscar from outside the glass door of his room. They told doctors to try to resuscitate him if his heart stopped.

That night, after they returned home, Donna Perez’s phone rang one more time. Oscar’s doctor said he probably wasn’t going to make it through the night. This time, they could visit him in his hospital room in PPE.

Seeing her brother up close, swollen and helpless, she leaned in, hugged him, and said, “I can tell you’re tired. You can go.” Donna promised to take care of his daughter.

Her family pushed back and said she had to tell him to be strong.

Donna told them they needed to let Oscar go. He died a few hours later.

“This disaster is one that befalls dialysis patients, with diabetes especially, regularly,” Dr. David Goldfarb, clinical director of the nephrology division at NYU Langone Health in New York City, who reviewed Oscar Perez’s medical records for ProPublica.

“Of course, it’s possible to do better,” he continued. “Given his age, it’s really tragic.”

The advent of technology to filter a patient’s blood revolutionized kidney care in the 1950s, and people lined up to get access to the limited number of machines. In 1960, one hospital created its own admissions panel, later nicknamed the “God committee,” to review cases to decide who would receive the groundbreaking treatment.

Twelve years later, Congress approved legislation that created the Medicare End Stage Renal Disease program, which guaranteed coverage of medical care, including dialysis and kidney transplants. It remains the only disease-specific Medicare entitlement program, credited by some as possibly saving more lives than any other federal government program. Generally, Medicare only covers those over age 65 and the disabled, but this program is available to people of all ages with end-stage renal disease.

Total Medicare-related spending in 2019 on end-stage renal disease patients topped $50 billion. Even with that budget, the agency hasn’t been able to fix persistent health disparities. That year, Black patients were more than four times more likely than their white counterparts to have the disease.

Black patients also progressed from chronic kidney disease to end-stage renal disease three times as often as white patients. Yet they are less likely to start off their dialysis treatments on a waiting list for a transplant — or eventually receive one from a living donor — than white patients.

In a statement, Medicare said it is working to address the disparities and said it is “committed to ensuring the health and safety” of all its dialysis patients.

Another area of concern is home dialysis, which research has shown is cheaper than in-center dialysis and offers similar or better survival rates, enhanced quality of life and greater flexibility. Barriers to home dialysis affect all patients, but the percentages of Black and Hispanic patients receiving home dialysis in 2019 were 10% and 11% respectively, compared with white and Asian patients at 17% each.

The push for closing that gap has gained traction, bolstered by federal data that found COVID-19 hospitalizations rates of patients who underwent home dialysis from late March to June 2020 were between one-quarter and one-third those of patients traveling to dialysis facilities.

“We do have to figure out a way to do better because we’re really, in essence, causing harm, when we’re not able to divert proper resources to patients who most require them,” said Dr. Kirk Campbell, a nephrology professor and vice chair of medicine for diversity, equity and inclusion at the Icahn School of Medicine at Mount Sinai in New York City.

Some patients don’t have the space to store the supplies needed for home dialysis. Others are overwhelmed by the prospect of having to keep the area around the catheter clean to prevent infection. But, Campbell said, that’s where patient education comes in. The most common type of home dialysis, called peritoneal dialysis, often is done at night while the patient is sleeping and does not involve blood flowing outside the body.

While home dialysis isn’t possible for all patients, some doctors are hesitant to recommend it at all, in part because the clinicians lack the training, experience or a certain comfort level with it. That’s especially true, Campbell said, for patients of color and those from disadvantaged backgrounds. There’s often an unconscious bias that those patients won’t be able to handle it, he said.

Campbell and others said it’s critical that clinicians receive additional training in home dialysis. He leads one of the few nephrology fellowship programs in the country where doctors can spend an extra year specializing in home dialysis. The results have been so promising, he said, that they hope to expand.

In July 2019, the Trump administration issued an executive order aimed at revamping kidney care in the United States through the Department of Health and Human Services’ Advancing American Kidney Health initiative. The goals of the initiative were lofty — some say unrealistic — and included having 80% of new end-stage renal disease patients in the U.S. receive in-home dialysis or transplants by 2025. In 1972, the year the Medicare program passed, 40% of patients were on home dialysis. Currently, about 13% of patients are receiving dialysis at home.

Starting January, the Centers for Medicare & Medicaid Services will offer facilities greater reimbursement for improving their home dialysis rates for low-income patients.

Some observers say the change doesn’t go far enough. In September, U.S. Rep. Bobby Rush, an Illinois Democrat, and Rep. Jason Smith, a Republican from Missouri, proposed legislation that would require Medicare to pay for workers to assist patients who need additional help with home dialysis. The measure, which was introduced without much fanfare, also calls for greater patient education around the treatment and a federal study analyzing racial disparities.

Hong Kong, where about three in four patients are on peritoneal dialysis, is a global leader in home treatment. Patients there receive peritoneal dialysis first unless there is a medical reason that would preclude it.

Dr. Isaac Teitelbaum, a nephrologist who has been the medical director of the home dialysis unit at the University of Colorado School of Medicine since 1986, said expanded training for clinicians and incentives for patients, including a reduced co-pay or a tax credit, could encourage more patients to dialyze at home.

“You don’t live just so you can do dialysis. You do dialysis so that you can enjoy life,” he said. “You do dialysis so that you can watch your children and grandchildren grow up and so that you can participate in family events and go on vacations.”

Cheryl Cosey was not offered home dialysis, her family said. Shardae Lovelady said it might have made all the difference for her mother.

Cosey’s health deteriorated quickly after the call from her hospital bed. Doctors transferred Cosey to the intensive care unit, put her on a ventilator and gave her medication to push the oxygen from her lungs into her bloodstream, according to hospital records.

The family braced themselves. Lovelady drove to Minnesota to pick up her sister. She gathered everyone for a big dinner the way her mother used to do.

Lovelady and her sister stayed up late talking, finally dozing off when the house quieted.

When the phone rang at three in the morning, Lovelady recognized the hospital’s 312 area code.

Everything she had done to prepare for that moment suddenly vanished, and she allowed herself to hope.

The call was short. She never even flipped on the bedroom light. She turned to her sister, who was asleep next to her, and nudged her awake.

“Mama gone.”