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Tag: Cleveland Clinic

  • Iowa community rallies to bring Halloween early for boy with rare cancer

    KCCI EIGHT NEWS AT TEN. THIS IS AN EXAMPLE OF IOWA. AWESOME. A BONDURANT NEIGHBORHOOD CAME TOGETHER TO HELP A THREE YEAR OLD WITH CANCER CELEBRATE HALLOWEEN. A BIT EARLY. YOU’RE GOING TO SEE THE LITTLE MAN RIGHT THERE. AND LOOK AT THAT SMILE ON HIS FACE. KCCI ABIGAIL CURTIN SPOKE WITH HIS PARENTS TO LEARN HOW ALL THE SUPPORT IS HELPING HIM THROUGH TREATMENT. GRIFFIN CELLARS IS KNOWN AS A GIGGLE MONSTER. AT LEAST THAT’S WHAT HIS PARENTS, ASHLEY AND KENNY CELLARS, CALL HIM. BUT SINCE BEING DIAGNOSED WITH STAGE FOUR, PINEOBLASTOMA, A RARE FORM OF BRAIN CANCER EARLIER THIS YEAR, IT’S BEEN HARD TO KEEP A SMILE ON HIS FACE. THE HIGH DOSE CHEMO IS HARD. VERY HARD ON THE BODY. YOU KNOW, YOU THEIR KIDS GET CHEMICAL BURNS INSIDE OR OUTSIDE THEIR BODY. HE’S GOT BURNS IN HIS THROAT. HE DOESN’T EAT. HE’S LOST A LOT OF WEIGHT. PUKING ALL THE TIME. NORMALLY, THEY SAY THEY TAKE HIM TRICK OR TREATING FOR HIS FAVORITE HOLIDAY TO BOOST HIS SPIRITS. BUT BEING SO SICK MEANS PARTICIPATING ON HALLOWEEN WASN’T REALLY A POSSIBILITY FOR GRIFFIN. SO HIS PARENTS TOOK TO SOCIAL MEDIA WITH A PLAN IN THEIR NEIGHBORHOOD FACEBOOK PAGE. THEY ASKED SOME OF THEIR NEIGHBORS TO GATHER AND HAND OUT CANDY, ALLOWING GRIFFIN TO GET A TASTE OF HALLOWEEN MAGIC HE NEEDED, AND THEY DELIVERED. DRESSING IN COSTUMES AND HANDING OUT CANDY. WEEKS OUT FROM THE ACTUAL HOLIDAY, ALL THE NEIGHBORS WE SPOKE WITH SAID HELPING OUT WAS AN EASY CHOICE. IT’S GOOD TO BE PART OF THE COMMUNITY AND TAKE CARE OF EACH OTHER, AND THEY ARE ALWAYS THERE FOR US, EVEN ONES FROM THE NEXT NEIGHBORHOOD OVER. NONE OF US KNOW WHEN OUR LAST DAY IS, BUT YOU JUST WANT TO MAKE EVERY DAY FOR HIM A LITTLE BIT MORE SPECIAL. BUT AS YOU CAN SEE FROM THIS PICTURE, GRIFFIN MADE OUT LIKE A BANDIT. BUT HIS PARENTS SAY WHILE THE CANDY IS GREAT, THE BEST PART IS SEEING HIS SPARKLE COME BACK IN. BONDURANT ABIGAIL CURTIN, KCCI EIGHT NEWS. IOWA’S NEWS LEADER. NOW WE’RE THINKING ABOUT YOU AND SENDING HEALING WISHES YOUR WAY. GRIFFIN. A PART OF THE FAMILY’S STRUGGLE IS THE FACT THAT BECAUSE GRIFFIN’S CANCER IS SO RARE, THE TREATMENTS FOR IT ARE INCREDIBLY LIMITED. BUT THAT’S WHY THEY’RE HOPING TO RAISE AWARENESS. TO LEARN MORE ABOUT HOW YOU CAN HELP, CHECK O

    Iowa community rallies to bring Halloween early for boy with rare cancer

    Updated: 10:22 AM PDT Oct 19, 2025

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    Gryffin Sellers is known as a giggle monster. At least, that’s what his parents, Ashley and Kenny Sellers, call him. But since being diagnosed with stage 4 pineoblastoma, a rare form of brain cancer, in April, they say it’s been hard to keep a smile on his face.”High-dose chemo is hard. Very hard on the body,” Ashley said. “The kids get chemical burns inside, outside their body. He’s got burns in his throat, he doesn’t eat, he’s lost a lot of weight puking all the time.”Normally, she says, they’d take him trick-or-treating to help raise his spirits on his favorite holiday. But because he’s so sick and his treatment has taken such a toll on the 3-year-old’s body, his parents put out a plea on social media, asking their Bondurant neighbors to come together and pass out candy weeks before the actual holiday.Dozens of families delivered.”It’s just good to be part of the community and take care of each other,” Jeffery Conroy, the Sellers’ neighbor, said. “They’re always there for us.” Even neighbors several streets over, like Beth Rodas, took part.”None of us know when our last day is, but you just want to make every day for him a little bit more special,” she said.Gryffin’s parents say he made out like a bandit, collecting so much candy that they plan to give some of it to his nurses. But the best part is easily seeing his sparkle come back.”I feel like his spirit is kind of back because now he’s in the mindset of, I got all this candy to eat, so I need to go do treatment and get home so I can eat my candy,” Ashley said. Gryffin still has a few more rounds of high-dose chemo left, but beyond that, Ashley says there isn’t much else doctors can do. Pineoblastoma is so rare that it makes up less than 0.2% of brain tumors diagnosed in the country, according to the Cleveland Clinic. Because it’s so rare, there isn’t much research devoted to it, leaving families like Gryffin’s seeking older treatments. “His treatment plan is from 2003 for a cancer that’s not even his,” Ashley said. “That’s over 20 years old with no new research, no changes, no nothing.” Even harder, the Pediatric Brain Tumor Consortium, which leads many of the early clinical trials used to treat rarer tumors like Gryffin’s, is losing funding next year. That’s why Ashley and Kenny hope to raise awareness about the cancer in the first place: so that families in the future won’t have to rely on imperfect treatments.For more information on Gryffin’s story and to donate to help the family, click here.

    Gryffin Sellers is known as a giggle monster.

    At least, that’s what his parents, Ashley and Kenny Sellers, call him.

    But since being diagnosed with stage 4 pineoblastoma, a rare form of brain cancer, in April, they say it’s been hard to keep a smile on his face.

    “High-dose chemo is hard. Very hard on the body,” Ashley said. “The kids get chemical burns inside, outside their body. He’s got burns in his throat, he doesn’t eat, he’s lost a lot of weight puking all the time.”

    Normally, she says, they’d take him trick-or-treating to help raise his spirits on his favorite holiday. But because he’s so sick and his treatment has taken such a toll on the 3-year-old’s body, his parents put out a plea on social media, asking their Bondurant neighbors to come together and pass out candy weeks before the actual holiday.

    Dozens of families delivered.

    “It’s just good to be part of the community and take care of each other,” Jeffery Conroy, the Sellers’ neighbor, said. “They’re always there for us.”

    Even neighbors several streets over, like Beth Rodas, took part.

    “None of us know when our last day is, but you just want to make every day for him a little bit more special,” she said.

    Gryffin’s parents say he made out like a bandit, collecting so much candy that they plan to give some of it to his nurses.

    But the best part is easily seeing his sparkle come back.

    “I feel like his spirit is kind of back because now he’s in the mindset of, I got all this candy to eat, so I need to go do treatment and get home so I can eat my candy,” Ashley said.

    Gryffin still has a few more rounds of high-dose chemo left, but beyond that, Ashley says there isn’t much else doctors can do.

    Pineoblastoma is so rare that it makes up less than 0.2% of brain tumors diagnosed in the country, according to the Cleveland Clinic. Because it’s so rare, there isn’t much research devoted to it, leaving families like Gryffin’s seeking older treatments.

    “His treatment plan is from 2003 for a cancer that’s not even his,” Ashley said. “That’s over 20 years old with no new research, no changes, no nothing.”

    Even harder, the Pediatric Brain Tumor Consortium, which leads many of the early clinical trials used to treat rarer tumors like Gryffin’s, is losing funding next year.

    That’s why Ashley and Kenny hope to raise awareness about the cancer in the first place: so that families in the future won’t have to rely on imperfect treatments.

    For more information on Gryffin’s story and to donate to help the family, click here.

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  • Woman diagnosed with breast cancer at 27 after almost ignoring warning sign:

    Marissa Coreno was embracing a new life in 2021. She had just moved out of her parents’ house and was spending more time in the gym. She liked her job at a hospital in Ohio. Everything seemed to be going great — until she found a lump in her armpit. 

    Coreno wasn’t particularly concerned at first. She was 27 and had no family history of cancer. But her colleagues thought she shouldn’t ignore it. An ultrasound found “questionable characteristics.” That was followed by a mammogram, then a biopsy. 

    Three days later, Coreno was diagnosed with Stage II breast cancer that had spread to her lymph nodes. She said she felt like her world had been turned upside down. 

    “It was devastating. It took a while to process. I knew it was positive, and I knew I had breast cancer but in my head, it was like ‘No way,’” Coreno said. “You hear about these cases and you see them on TV but it was hard to believe that this was now my life.” 

    Marissa Coreno.

    Marissa Coreno


    An increase in young diagnoses 

    Breast cancer is the leading cause of cancer death in U.S. women aged 20 to 49, and the incidence rate of breast cancer in women under 50 has risen faster than in women over 50, according to the Breast Cancer Research Foundation

    “I’ve been a physician for over 25 years. When I first started practicing, we saw women in their 40s and now we’re seeing the late 20s and early 30s more commonly,” said Dr. Mary Gemignani, the director of the Women’s Early Onset Cancer Program and chief of the Division of Breast Surgery at NYU Langone, who was not involved in Coreno’s care. 

    Still, breast cancer diagnoses in women as young as Coreno are rare. The American Cancer Society estimates that only about 1 in 1,344 women will develop breast cancer in their 20s. Younger patients are unlikely to have regular screenings, Gemignani said, since most women do not receive mammograms until they are 40. Younger women also tend to have “more aggressive” tumors or be diagnosed with rarer disease subtypes, Gemignani said. There is no proven reason for the increase, she said. 

    Gemignani said younger women tend to have unique needs, including fertility concerns, which make it important for them and their doctors to develop a personalized treatment plan. Coreno said she found few research studies that looked at outcomes for her age group but spoke candidly with Dr. Baidehi Maiti, a medical oncologist at the Cleveland Clinic, about her best options. 

    “Being so young and not having a lot of research or studies or proof out there, every option I had along the way, I chose the most,” Coreno said. “I was very protective.” 

    Connection amid “exhausting” chemotherapy 

    Coreno’s treatment started with four months of “exhausting” chemotherapy to stop her cancer from spreading any further. Her mom moved in to help take care of her, while her dad drove her to every appointment. Coreno said she lost her hair and could barely leave the house. 

    “Going from such an active life — I was in my prime, I was working out on the regular, I was so proud of what I had accomplished — to not even having enough energy to get off the couch was hard,” Coreno said. 

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    Marissa Coreno in the hospital.

    Marissa Coreno


    There was one bright spot: One night, Coreno decided to “eat (her) feelings” and ordered Crumbl cookies. She posted a picture of the delivery on Instagram. She received a message about the sweet treat from Anthony, a former classmate. The two struck up a conversation and “just never stopped talking.” 

    “It was so nice to talk to somebody, have somebody listen to me, have a new friend that I could confide in,” Coreno said.

    Eventually, the two went on a date. Coreno dreaded leaving the house and was self-conscious about wearing a wig but enjoyed herself. 

    “He didn’t even mention the wig. We just had a great time,” Coreno said. “It just felt so natural.” 

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    Marissa Coreno in the hospital.

    Marissa Coreno


    After chemotherapy, Coreno underwent a double mastectomy, followed by a reconstruction surgery and 25 days of radiation therapy, Maiti said. Coreno started hormone therapy in March 2022 and will continue it until 2032. She also has regular scans. The treatment stops her body from creating estrogen to limit the chance of the cancer returning. Coreno is currently cancer-free, Maiti said. 

    “She has not let cancer define her life,” Maiti said. “She’s thriving as a breast cancer survivor and living her life to the fullest.” 

    “Life is beautiful” 

    The hormone therapy sent Coreno into menopause at 28. Working out is harder now, she said, and she grapples with hot flashes and has trouble sleeping. It has taken years for her to get used to the new normal. 

    “I thought this would be the easy part,” Coreno, now 31, said. “After treatment was over is when what I went through hit me the most.” 

    Amid the difficult adjustment, her relationship with Anthony turned more serious. They were married in August 2024 and spent their honeymoon in Italy. Over the summer, they celebrated their anniversary in Cancún, Mexico. 

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    Marissa and Anthony Coreno on their wedding day. 

    Arlee Reust/Azkalynn Photography


    Coreno also hopes that sharing her story encourages others to investigate any warning signs they experience. 

    “I just want everyone to realize that it seems like it will never be you, it seems like it’s always going to be someone else, it seems like it’s going to be a person on the TV, but it can happen to you,” Coreno said. “If you feel uncertain about anything, you need to speak up and get checked out. If, for some reason, you don’t get the best news, there is light at the end of the tunnel. It might not seem like it. It might seem like it’s a very long tunnel. But life is beautiful afterwards.” 

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  • Scary moment as Guardians’ David Fry is struck in the face by 99 mph pitch

    Cleveland Guardians hitter David Fry was taken to hospital on Tuesday after being struck in the face by a pitch during his team’s win against the Detroit Tigers.The worrying incident occurred in the sixth inning, when Fry tried to bunt a 99 mph fastball from Detroit’s Tarik Skubal.The ball missed the bat completely and hit Fry straight in the face. The 29-year-old fell to the floor instantly with his hands on his face, before being attended to by medics on the field.Fry, though, was later able to stand up and walk to a cart before being taken to a nearby hospital.“He’s getting tested. He’s stayed conscious the whole time,” Guardians manager Stephen Vogt told reporters after the game Tuesday. “Definitely some injuries there. So I’ll give you an update tomorrow.”Guardians reporter Tim Stebbins said on X that Fry was initially taken to the Lutheran Medical Center before being transferred to the Cleveland Clinic Main Campus for observation which would likely see him stay overnight. The reporting was shared by the Guardians official channel on X.Scary momentLike many others inside the stadium, Detroit’s Skubal looked shaken by the incident, pacing around the field as Fry was receiving treatment.Speaking to reporters after the game, Skubal said watching Fry go down was “really tough.”“I’ve already reached out to him. I’m sure his phone is blowing up. I just want to make sure he’s all right,” he said, per Associated Press.“Obviously, he seemed like he was OK coming off the field and hopefully it stays that way. I know sometimes with those things that can change. So hopefully he’s all right.“I look forward to hopefully at some point tonight or (Wednesday) morning getting a text from him and making sure he’s all good because there’s things that are bigger than the game and the health of him is more important than a baseball game.”Skubal, who is the reigning AL Cy Young Award winner, struggled to regain composure after the incident, making a string of mistakes.After the game restarted, he threw a wild pitch to Fry’s replacement George Valera, before making another blunder when trying to throw the ball to first between his legs. He then was called for a balk in the sixth inning as the Guardians got back into the game.The Guardians eventually went on to win 5-2.

    Cleveland Guardians hitter David Fry was taken to hospital on Tuesday after being struck in the face by a pitch during his team’s win against the Detroit Tigers.

    The worrying incident occurred in the sixth inning, when Fry tried to bunt a 99 mph fastball from Detroit’s Tarik Skubal.

    The ball missed the bat completely and hit Fry straight in the face. The 29-year-old fell to the floor instantly with his hands on his face, before being attended to by medics on the field.

    Fry, though, was later able to stand up and walk to a cart before being taken to a nearby hospital.

    “He’s getting tested. He’s stayed conscious the whole time,” Guardians manager Stephen Vogt told reporters after the game Tuesday. “Definitely some injuries there. So I’ll give you an update tomorrow.”

    Guardians reporter Tim Stebbins said on X that Fry was initially taken to the Lutheran Medical Center before being transferred to the Cleveland Clinic Main Campus for observation which would likely see him stay overnight. The reporting was shared by the Guardians official channel on X.

    Scary moment

    Like many others inside the stadium, Detroit’s Skubal looked shaken by the incident, pacing around the field as Fry was receiving treatment.

    Speaking to reporters after the game, Skubal said watching Fry go down was “really tough.”

    “I’ve already reached out to him. I’m sure his phone is blowing up. I just want to make sure he’s all right,” he said, per Associated Press.

    “Obviously, he seemed like he was OK coming off the field and hopefully it stays that way. I know sometimes with those things that can change. So hopefully he’s all right.

    “I look forward to hopefully at some point tonight or (Wednesday) morning getting a text from him and making sure he’s all good because there’s things that are bigger than the game and the health of him is more important than a baseball game.”

    Skubal, who is the reigning AL Cy Young Award winner, struggled to regain composure after the incident, making a string of mistakes.

    After the game restarted, he threw a wild pitch to Fry’s replacement George Valera, before making another blunder when trying to throw the ball to first between his legs. He then was called for a balk in the sixth inning as the Guardians got back into the game.

    The Guardians eventually went on to win 5-2.

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  • A restaurant owner wasn’t regaining function after a stroke. New technology changed everything.

    Restaurateur Tommy Fello was driving from his Ohio establishment to his house on Christmas Eve when he started veering off the road. Fello, then 71, had been awake since 4 a.m. local time preparing a holiday buffet for his family. He chalked the disturbance up to a flat tire. Driving slowly and relying on the vehicle’s autocorrect feature, he was able to complete his journey home safely.

    But when Fello stepped out of the truck, he couldn’t get his balance. 

    “I finally realized it wasn’t the truck that was veering. It was me that was veering,” Fello said. He went indoors and talked to his wife and daughter, who said he looked unwell. About five minutes later, they called 911. Paramedics took him to an area hospital, where he lost all movement in his left arm and leg. 

    “They were literally just like appendages on me. I could not feel them and could not do anything,” Fello said. 

    A clot-busting drug reversed the stroke, but the numbness on the left side of his body, including his face, remained. He struggled to swallow, eat or drink. Physical and occupational therapy produced only minor improvements. 

    Tommy Fello walks during a rehabilitative therapy session before his surgery.

    Thomas Fello


    Dr. Sharon Covey, Fello’s occupational therapist and the founder of the Center for Stroke and Hand Recovery, Inc., told CBS News that his arm was essentially stuck in a bent position with his fingers curled when he met her in January 2024. The position and tension in the limb caused Fello constant pain. Working in his restaurant was out of the question.  

    “It was very scary. You take for granted so many of the things you do, and even the common, simplest things become like a chore,” Fello said. “We mark all these small victories … Being able to lift up your arm or pick up a cup is a gigantic accomplishment. Those little accomplishments are gigantic to a stroke victim. They encouraged me to keep going on. But there was always a thought in the back of my mind: ‘Is this as good as it’s going to get?’” 

    A “first-of-its-kind technology”  

    One day, another recovering stroke patient suggested Fello look into an implant called the Vivistim System. The FDA-approved implant, developed by the medical device company MicroTransponder Inc., uses vagus nerve stimulation during rehabilitation to improve hand and arm function for stroke victims. The vagus nerves are the body’s longest cranial nerve, with one on each side of the body, according to the Cleveland Clinic. They regulate the body’s involuntary functions. 

    The Vivistim Therapy system involves a physical or occupational therapist sending wireless signals to the device. That signal delivers a brief, gentle pulse to the vagus nerve while the stroke patient performs rehabilitative tasks. The stroke patient also does at-home exercises. 

    Dr. Erez Nossek, a neurosurgeon and director of the cranial bypass program at NYU Langone, told CBS News that the vagus nerve stimulation can enhance the brain’s ability to rewire itself, known as neuroplasticity. That increased neuroplasticity can result in “greater and faster improvements in motor function for stroke survivors,” Nossek said in emailed remarks. 

    vivistim-paired-vns-system-implant-diagram-callout-labels.png

    An illustration from MicroTransponder, Inc. shows the positioning of the Vivistim System device.

    MicroTransponder, Inc.


    “There is no other FDA-approved technology proven to boost neuroplasticity for stroke survivors, creating new connections in the brain, which is theirs to keep, even after the device is no longer in use,” Nossek said. “This is (a) first-of-its-kind technology that is redefining what is possible for this patient population.” 

    A 108-person trial published in The Lancet in 2021 found that the device generated two to three times greater improvement in hand and arm function for stroke survivors when compared with just rehab. Stroke patients who have limited hand and arm function six months or more after their stroke and are considered to have “moderate to severe deficits” qualify for the device, the company said in a fact sheet.

    Implant aids in recovery

    Fello turned to the Cleveland Clinic, where he met cerebrovascular neurosurgeon Dr. Mark Bain. He studies stroke recovery, especially in the cases of patients like Fello, whose rehab progress has plateaued months after the stroke. Bain determined that Fello was a candidate for the Vivistim System. Fello became the first Cleveland Clinic patient to receive the implant on April 29, 2025. 

    “It didn’t really scare me to try and do it. I was anxious to see how it worked,” Fello said. 

    The device was placed during an hour-long procedure. The vagus nerve sits just below the carotid artery, so Bain and his surgical team made a small incision to place the leads of the implant and hid the scar in a fold of Fello’s neck. The key-fob sized implant was placed under Fello’s clavicle. Bain said the procedure itself is low-risk, with “less than 1% chance of any complications.” Two weeks after the surgery, the device was turned on and Fello returned to his rehabilitative work with Covey. 

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    Tommy Fello and Dr. Sharon Covey during a therapy session.

    Cleveland Clinic


    Covey said Fello has made huge progress since the device was implanted four months ago. She said he has no pain or tension in the limb, and is beginning to practice using his left arm to carry items. The task is difficult, she said, but isn’t “something he could have done before.” Fello, now 72, said he’s been thrilled by the progress he’s made in a short time.

    “I’m very, very happy to do it, very proud to do it, and I’m glad I did it,” he said. 

    “The sky’s the limit”

    About 800,000 people in the United States experience an ischemic stroke each year, Bain said. Vivistim and other new technologies may offer hope to the patients like Fello who struggle to recover with just rehabilitation, Bain said. 

    “I think over the next probably five to 10 years, what you’re going to see is an explosion of procedures, devices and things in rehab that will help people, once they’ve had strokes, to get their lives back,” Bain said. “In the future, I think the sky’s the limit for what we can expect for stroke recovery.” 

    At the time of his conversation with CBS News, Bain had given seven other stroke patients a Vivistim implant. Covey said at her practice, there are eight patients with the implant receiving the paired therapy course. MicroTransponder Inc. declined to say how many patients have received the implant, but shared a map that shows dozens of surgeons and rehabilitation therapists that provide the therapy. 

    “I think this is the newest, most effective strategy for people getting their affected limbs back,” Covey said. “This is the first real technique that has been available, at least in the last 20 years, for stroke rehab. The theories that we use as practitioners to increase somebody’s use of their affected arm are 50 to 75 years old. So this is a new technology that’s really going to turn the stroke recovery world upside down.” 

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  • Local doctors seeing rise in child pneumonia

    Local doctors seeing rise in child pneumonia

    CLEVELAND (WJW) — Doctors at the Cleveland Clinic are reporting an increase in the number of school age children suffering from pneumonia.

    “The main symptoms we’re seeing are fevers, which have been lasting seven to 10 days, a lot of cough, shortness of breath, chest pain — those are the usual signs and symptoms of pneumonia in children,” said Dr. Camille Sabella, who is director of the Clinic’s Center for Pediatric Infectious Diseases.

    Researchers at the U.S. Centers for Disease Control and Prevention are also reporting a nationwide spike in cases of children suffering from so-called “walking pneumonia.”

    “It’s caused by a mycoplasma type of bacteria. Usually, we call it walking pneumonia because it’s not usually that severe and the kids are out there, carrying out their daily life without a whole lot of distress, but we have been seeing a little more severe cases recently,” said Sabella.

    The exact reason for the surge is not totally clear, but Sabella pointed out that the increase coincides with children being back in school.

    “There are many more viruses and bacteria spread amongst them much more easily and we are coming out of the pandemic where some of these viruses and bacteria hadn’t been seen by the children in quite a while and this may be their first re-exposure to some of these,” he said.

    Doctors said the good news is that most of the young patients with pneumonia are responding well to treatment. In some cases, that includes antibiotics, but in other, more severe cases, they require hospitalization.

    The message from doctors to parents, if their child becomes ill, is to be vigilant but not to panic.

    “The most important thing is to make sure that they get seen, they get evaluated by their primary care physician and then followed up closely to be sure that they completely recover,” said Sabella.

    Doctors also recommend that parents take a common-sense approach to limit the spread of the illness.

    “Most causes of pneumonia can be contagious, especially the viruses, and we usually recommend that anybody having acute symptoms, especially fever and a productive cough, should probably stay home until they are better,” said Sabella.

    Jack Shea

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  • Cleveland Clinic to pay $7.6M to settle fraud case

    Cleveland Clinic to pay $7.6M to settle fraud case

    [In the player above, watch previous FOX 8 News coverage on Cleveland Clinic being named among the nation’s best hospitals.]

    CLEVELAND (WJW) — The Cleveland Clinic Foundation has agreed to pay $7.6 million to settle allegations that it lied on federal grant applications.

    Federal prosecutors brought violations of the False Claims Act against the hospital system, alleging it claimed in research grant applications submitted to the National Institutes of Health that its researcher hadn’t received any other financial support — when in fact he had.

    In 2020, federal authorities accused that researcher of wire fraud for the $3.6 million grant, as well as sharing his U.S.-funded research with the Chinese government.

    NIH applicants are required to disclose any other outside research funding. That helps the institutes determine whether the applicant has time to complete the research, whether they can remain objective in their research and if they have multiple sources of funding for the same project, according to a Friday news release from Rebecca Lutzko, U.S. attorney for Ohio’s Northern District federal court.

    In addition, foundation employees were accused of improperly sharing passwords for the institutes’ online grant reporting platform, according to the release. Some of the false submissions came from employees who were “inappropriately given access” to that platform, prosecutors said.

    “Each year, NIH awards federal grants to support research to improve public health, but those funds are limited and the grant process is competitive. Every entity or person who seeks such grant money must strictly play by the rules,” Lutzko is quoted in the release. “As stewards of taxpayer dollars, our office takes seriously its responsibility of ensuring that grant recipients fully and accurately report all required information to NIH so that it may properly award its limited funds to deserving institutions.

    “Today’s settlement illustrates the importance of being truthful at every stage of the grants process.”

    In addition to the settlement, NIH is imposing a special condition for the hospital’s future NIH submissions. Starting Oct. 1, a “high-level” foundation employee must personally attest to the “truth, completeness and accuracy” of anything submitted to the NIH for one year, according to the release.

    In response, the foundation said Friday though it did not agree with the allegations, it settled the case without any admission of guilt “to avoid costly and time-consuming litigation.”

    The allegations center around a former Clinic researcher fired in 2020 for committing “multiple violations of the hospital’s policies over many years,” reads the statement. The foundation claims the man concealed research funding he had obtained through academic positions he held in China — positions which also were not disclosed to the foundation.

    The statement claims the foundation at the time did not know the researcher’s NIH submissions contained false information. The local NIH investigation mirrored others happening at “hundreds of research institutions across the United States” at that time, according to the statement.

    Throughout the federal investigation, the U.S. Attorney’s office assured that the Cleveland Clinic was not its target, according to the foundation’s statement.

    “We were surprised that the U.S. Attorney’s office chose to pursue this matter knowing that Cleveland Clinic worked with NIH and the U.S. Attorney’s office on this issue,” reads the foundation’s Friday statement. “We continue to work cooperatively with NIH to strengthen our research processes and remain a good steward of the federal research funds entrusted to our organization. Every day our researchers are advancing lifesaving and enhancing treatments with the help of those funds.”

    Federal prosecutors ultimately dismissed the case against that researcher in 2021 “for undisclosed reasons,” reads the foundation’s statement.

    The institutes are part of the U.S. Department of Health and Human Services, whose inspectors investigated the case alongside the FBI and the Northern Ohio U.S. attorney’s office, according to the release.

    “The accuracy of information reported in applications and other documentation related to federal grants is critical to ensuring that these limited funds are utilized in the most efficient and effective manner and that the integrity of the application process is upheld,” Special Agent in Charge Mario Pinto, of HHS’ Office of the Inspector General, is quoted in the release.

    Potential fraud, waste, abuse or mismanagement of HHS programs can be reported to the Inspector General’s Office online or by calling its hotline at 1-800-447-8477.

    Justin Dennis

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  • Wayne Dawson shares thanks after ‘health challenges’

    Wayne Dawson shares thanks after ‘health challenges’

    *The above video shows Wayne Dawson recently operating a ‘rover’ at NASA*

    CLEVELAND (WJW) — Cleveland’s Own, Fox 8’s Wayne Dawson, is sending his “heartfelt thank you,” as he recovers from surgery due to “health challenges,” the NE Ohio legendary journalist said Sunday.

    Wayne posted to his Instagram page that, “Last Thursday I underwent a very long but successful 9-hour surgery at the Cleveland Clinic but God was in the operating room guiding the hands of those working on his child,” Dawson wrote along side a photo of many get well cards and flowers that have been sent to him.

    Dawson added, “I’ll explain more about what I’m dealing with at a later date when I am back on the air at Fox 8 but know that I love you all and I miss you very much. See you soon. Wayne.”

    You can read Wayne’s thank you post by clicking here.

    For more on Wayne Dawson’s groundbreaking career and how much he helps others in our community you can also click here.

    Get well soon Wayne and looking forward to seeing you back on the air with the entire team from Fox 8 News in the Morning.

    Paul Kiska

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  • Beating the odds: NE Ohio couple fights cancer together

    Beating the odds: NE Ohio couple fights cancer together

    FREMONT, Ohio (WJW) — Tough times have been a shadow that has loomed in the lives of Jon and Julie Stawowy of Freemont for more than five years.

    But if you ask them, “This is the happiest I’ve been in my life right now and I think you feel the same way. We’re blessed. We have these things we’re overcoming, but were blessed” Jon Stawowy said.

    Cancer has been a part of the family’s life for the past six years. It started when his wife, Julie, was diagnosed with breast cancer in 2017. After a year of chemotherapy and surgeries, she began to get her life back.

    It was just at about that time a difficult-to-diagnose lump was found in Jon’s throat.

    “That’s when they figured out that it was peripheral T-cell lymphoma,” Jon said.

    For the next several months, Jon underwent aggressive chemotherapy and Julie and their two children were at his side for everything.

    “I went through the typical things of chemo. Lost my hair, lost weight” Jon said.

    “I do feel it was my blessing to have cancer,” Julie said. “Once he had lymphoma, I told him I was thankful to have it because now I know the fear, the anxiety, and all the stuff that he was dealing with. I understood that” 

    That love and understanding went a long way in Jon’s treatment, but cancer wasn’t done with the family yet.

    “I went 13 months. Thirteen months I was in remission and I actually went to the doctor to get my port taken out because we were all done with the cancer and they gave me one more and that PET scan came back positive for something,” Jon said.

    With the cancer back, Jon’s only option was a stem cell transplant. He underwent that treatment and was very weak, but he was recovering.

    But then, one day he went to the Cleveland Clinic for some tests because of a persistent cough

    “I went in to have the bronchial scope done and I had a reaction and crashed and wound up in the ICU and woke up three days later,” Jon said.

    That reaction was a result of Graft vs Host disease. GVHD is when the body begins to reject transplanted tissue or cells.

    “Every organ in your body can be affected by this, and in his case, it was the lungs and that could lead to a dangerous and life-threatening situation. I think by the time he got to bronchoscopy his lung function was very low,” Cleveland Clinic Oncologist Doctor Deepa Jagadeesh said.

    At that point, Jon is now on a ventilator, his body is rejecting the stem cells and his prognosis is not good. Doctors didn’t think that Jon would make it through the night.

    “You think you have some grand epiphany during that moment. You’re probably not going to make it to morning and you got to say goodbye to your family. I just wanted to see my family. I wasn’t going to make any great speeches. I just wanted to hold my family and be with my wife and my kids and wake up the next morning,”  Jon said. “I decided I didn’t want to go to sleep that night because I might not wake up. I wasn’t supposed to wake up. In the morning my wife came in and had crawled into the chair she would sit in and I said, ‘I’m not going anywhere yet.’”

    That long night and Jon’s overwhelming drive to live was a turning point for him and his treatment. His doctors worked out a new course to follow.

    “We had a trial opening up at that time looking at this drug, Rextrenaleb, for chronic lung GVHD. We talked to him about it and he was willing to try. He went on that trial and has been on that drug since then and doing well.” Dr. Jagadeesh said.

    After weeks in the ICU, Jon had to fight some more to get his strength back.

    After many months, the man who wasn’t supposed to make it through the night has now been around for more than two years longer.

    He now works as an editor for a website that helps educate transplant patients so they can navigate what’s in store.

    Jon said Julie and his family’s love and the care from so many others is why he’s still here.

    “We’re going to keep going we’re going to keep fighting and keep trying. Thank God for Dr. Jagadesh and thank God for Theresa, the girl whom I never met in person gave me those stem cells. She didn’t know who I was and she gave me this life” Jon said.

    But, the story’s not over.

    Julie’s cancer has returned, but all that love and care will have to continue to flow.

    “John and I are back on the path of coming back to Cleveland Clinic to try to become healthy,” Julie said.

    To find out more about Jon and Julie’s story and more about GVHD, click here.

    Roosevelt Leftwich

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  • Weekly Recap | Cleveland Clinic Health Stories Available for Broadcast and Web

    Weekly Recap | Cleveland Clinic Health Stories Available for Broadcast and Web

    BYLINE: Weekly Recap | Cleveland Clinic Health Stories Available for Broadcast and Web

    Weekly Recap of Health Stories from Cleveland Clinic:

    The stories below are available for broadcast and digital use. They include scripts, web copy, soundbites and b-roll.

    Download password is CLEclinic1921.

    Click here to view other recent CCNS stories available.

    Cleveland Clinic

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  • Cleveland Clinic Researchers Develop New Model for Prioritizing Lung Transplant Candidates

    Cleveland Clinic Researchers Develop New Model for Prioritizing Lung Transplant Candidates

    Newswise — CLEVELAND: A team from Cleveland Clinic has developed a new model for prioritizing patients waiting for a lung transplant, aimed at improving outcomes and reducing deaths among those in need of donor lungs. The new method offers an improved strategy for organ allocation by taking into account how the time a patient has spent on the waiting list could impact the severity of their disease and the urgency of their need for a transplant.

    The results of a study looking at this new method were published today in The American Journal of Respiratory and Critical Care Medicine.

    Currently, lung transplant candidates are ranked by a scoring equation called the Composite Allocation Score (CAS). Candidates are assigned a number based on factors including how stable they are while waiting, chances of survival after receiving a new organ, and how easily they can be matched for available organs. Those with the highest scores are given priority and offered donor lungs first. However, the scores are based on tests given twice a year at transplant centers. That means that unless a patient’s health suddenly and drastically changes, their score will remain the same for at least six months.

    “The problem with this method is that the scoring equations fail to consider how a patient’s health status changes as they spend more time on the list,” said Maryam Valapour, M.D., M.P.P., director of Lung Transplant Outcomes at Cleveland Clinic. “The longer a patient lives with a severe lung disease, the more their risk of developing severe complications increases. This is something clinicians observe every day – that our patients’ risk of developing complications changes over time. Therefore, some patients’ scores may not reflect how urgently they need a transplant.”

    To determine how the amount of time on the waitlist affects clinical outcomes, the team of researchers analyzed data from 12,000 American adults listed for lung transplant between 2015 to 2020. The study showed that for many patients, their risk of death prior to transplant increased as they spent longer times waiting for donor lungs.

    When the team looked at patients who died on the waiting list, they found that many had not been given enough priority in the CAS. To more accurately score the candidates, the team developed a more dynamic method called the multistate composite model that accounted for the type of lung disease and time on the waiting list. When they recalculated the original scores with their new equation, it consistently marked those patients as high priority. However, for patients who originally received low-priority scores and remained stable over time, using the new method did not change their scores. 

    “The approaches we present in our paper are capable of identifying whose trajectory is more stable on the waiting list versus those whose trajectory is worsening between six-month clinical updates. The estimates in our model more closely align with observed trends in individual U.S. lung transplant patients,” says Jarrod Dalton, Ph.D., director of Lerner Research Institute’s Center for Populations and Health Research, who is first author of the paper. “This approach may allow us to more accurately prioritize time-sensitive lung transplant candidates and decrease waitlist mortality for patients with end-stage lung disease.”

    This study was done with the support of the National Institutes of Health.

    “This research advances us towards development of a more comprehensive prediction model for risk of mortality among lung transplant candidates that could help guide decisions about patients who are in greater need for lung transplant and increase their odds for survival,” said James P. Kiley, Ph.D., director of the Division of Lung Diseases at the National Heart, Lung, and Blood Institute (NHLBI).

    In 2022, there were over 3,000 candidates added to the lung transplant waitlist with over 2,600 lung transplants performed, according to UNOS. While the numbers of donors and transplants are improving, there is still a shortage of available organs in the United States.

    Research reported in this publication was supported by the National Institutes of Health under Award Number R01HL153175. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute of Health.

     

    About Cleveland Clinic 

    Cleveland Clinic is a nonprofit multispecialty academic medical center that integrates clinical and hospital care with research and education. Located in Cleveland, Ohio, it was founded in 1921 by four renowned physicians with a vision of providing outstanding patient care based upon the principles of cooperation, compassion and innovation. Cleveland Clinic has pioneered many medical breakthroughs, including coronary artery bypass surgery and the first face transplant in the United States. Cleveland Clinic is consistently recognized in the U.S. and throughout the world for its expertise and care. Among Cleveland Clinic’s 77,000 employees worldwide are more than 5,658 salaried physicians and researchers, and 19,000 registered nurses and advanced practice providers, representing 140 medical specialties and subspecialties. Cleveland Clinic is a 6,699-bed health system that includes a 173-acre main campus near downtown Cleveland, 23 hospitals, more than 275 outpatient facilities, including locations in northeast Ohio; southeast Florida; Las Vegas, Nevada; Toronto, Canada; Abu Dhabi, UAE; and London, England. In 2022, there were 12.8 million outpatient encounters, 303,000 hospital admissions and observations, and 270,000 surgeries and procedures throughout Cleveland Clinic’s health system. Patients came for treatment from every state and 185 countries. Visit us at clevelandclinic.org. Follow us at twitter.com/ClevelandClinic. News and resources available at newsroom.clevelandclinic.org. 

     

    Editor’s Note: Cleveland Clinic News Service is available to provide broadcast-quality interviews and B-roll upon request.

     

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    Cleveland Clinic

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  • Cleveland Clinic-Led Study Suggests More Patients with Community-Acquired Pneumonia Could Be Switched from IV to Oral Antibiotics Earlier

    Cleveland Clinic-Led Study Suggests More Patients with Community-Acquired Pneumonia Could Be Switched from IV to Oral Antibiotics Earlier

    Newswise — Friday, April 21, 2023, CLEVELAND: Findings from a Cleveland Clinic-led study showed for patients with community-acquired pneumonia treated with intravenous (IV) antibiotics, earlier switching to oral antibiotics in clinically stable patients was associated with shorter duration of antibiotics and hospital stay. 

    The results from this retrospective study, led by Abhishek Deshpande, M.D., Ph.D., a staff physician investigator in the Center for Value-Based Care Research and Michael B. Rothberg, M.D., vice chair of research, Cleveland Clinic Community Care, were recently published in Clinical Infectious Diseases

    Current clinical practice guidelines from the American Thoracic Society/Infectious Diseases Society of America recommend switching from IV to oral antibiotics once patients are clinically stable, which is typically after three days of IV therapy. Early switching in stable patients appears safe but data showed it occurred infrequently in patients with community-acquired pneumonia.

    For the study, researchers analyzed data from a national cohort of 378,041 adult patients from 642 hospitals in the U.S. from 2010 to 2015 who were admitted to the hospital with community-acquired pneumonia and initially treated with IV antibiotics. 

    Of this patient group, approximately six percent were switched early from IV antibiotics to oral antibiotics on or before hospital day three, and 30% were switched before discharge. Early switching to oral antibiotics was associated with shorter length of stay and shorter duration of antibiotic treatment and was not associated with worse outcomes. 

    Despite the evidence for safety of early switching in stable patients, the study found most patients received IV therapy throughout their hospital stay. The data highlights the opportunity for hospitals to reduce the burden of antibiotics by encouraging clinicians to follow evidence-based recommendations to switch therapy in clinically stable patients with community-acquired pneumonia.

    “Community-acquired pneumonia is a leading cause of hospitalizations and antibiotic use,” said Dr. Deshpande. “Optimizing the delivery of antibiotics is crucial, as prolonged exposure can lead to increased antibiotic resistance and healthcare-associated infections. Our research suggests many more patients could be switched earlier without compromising outcomes.”

    Over 1 million adults in the United States are hospitalized each year for pneumonia and 50,000 of those die from the disease. The best way to prevent pneumonia is to get vaccinated against bacteria and viruses that commonly cause it.

     

    About Cleveland Clinic

    Cleveland Clinic is a nonprofit multispecialty academic medical center that integrates clinical and hospital care with research and education. Located in Cleveland, Ohio, it was founded in 1921 by four renowned physicians with a vision of providing outstanding patient care based upon the principles of cooperation, compassion and innovation. Cleveland Clinic has pioneered many medical breakthroughs, including coronary artery bypass surgery and the first face transplant in the United States. U.S. News & World Report consistently names Cleveland Clinic as one of the nation’s best hospitals in its annual “America’s Best Hospitals” survey. Among Cleveland Clinic’s 77,000 employees worldwide are more than 5,658 salaried physicians and researchers, and 19,000 registered nurses and advanced practice providers, representing 140 medical specialties and subspecialties. Cleveland Clinic is a 6,665-bed health system that includes a 173-acre main campus near downtown Cleveland, 22 hospitals, more than 275 outpatient facilities, including locations in northeast Ohio; southeast Florida; Las Vegas, Nevada; Toronto, Canada; Abu Dhabi, UAE; and London, England. In 2022, there were 12.8 million outpatient encounters, 303,000 hospital admissions and observations, and 270,000 surgeries and procedures throughout Cleveland Clinic’s health system. Patients came for treatment from every state and 185 countries. Visit us at clevelandclinic.org. Follow us at twitter.com/ClevelandClinic. News and resources available at newsroom.clevelandclinic.org.

     

    Editor’s Note: Cleveland Clinic News Service is available to provide broadcast-quality interviews and B-roll upon request. 

     

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    Cleveland Clinic

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  • ‘It Just Seems Like My Patients Are Sicker’

    ‘It Just Seems Like My Patients Are Sicker’

    The most haunting memory of the pandemic for Laura, a doctor who practices internal medicine in New York, is a patient who never got COVID at all. A middle-aged man diagnosed with Stage 3 colon cancer in 2019, he underwent surgery and a round of successful chemotherapy and was due for regular checkups to make sure the tumor wasn’t growing. Then the pandemic hit, and he decided that going to the hospital wasn’t worth the risk of getting COVID. So he put it off … and put it off. “The next time I saw him, in early 2022, he required hospice care,” Laura told me. He died shortly after. With proper care, Laura said, “he could have stayed alive indefinitely.” (The Atlantic agreed to withhold Laura’s last name, because she isn’t authorized to speak publicly about her patients.)

    Early in the pandemic, when much of the country was in lockdown, forgoing nonemergency health care as Laura’s patient did seemed like the right thing to do. But the health-care delays didn’t just end when America began to reopen in the summer of 2020. Patients were putting off health care through the end of the first pandemic year, when vaccines weren’t yet widely available. And they were still doing so well into 2021, at which point much of the country seemed to be moving on from COVID.

    By this point, the coronavirus has killed more than 1 million Americans and debilitated many more. One estimate shows that life expectancy in the U.S. fell 2.41 years from 2019 to 2021. But the delays in health care over the past two and a half years have allowed ailments to unduly worsen, wearing down people with non-COVID medical problems too. “It just seems like my patients are sicker,” Laura said. Compared with before the pandemic, she is seeing more people further along with AIDS, more people with irreversible heart failure, and more people with end-stage kidney failure. Mental-health issues are more severe, and her patients struggling with addiction have been more likely to relapse.

    Even as Americans are treating the pandemic like an afterthought, a disturbing possibility remains: COVID aside, is the country simply going to be in worse health than before the pandemic? According to health-care workers, administrations, and researchers I talked with from across the country, patients are still dealing with a suite of problems from delaying care during the pandemic, problems that in some cases they will be facing for the rest of their lives. The scope of this damage isn’t yet clear—and likely won’t come into focus for several years—but there are troubling signs of a looming chronic health crisis the country has yet to reckon with. At some point, the emergency phase of COVID will end, but the physical toll of the pandemic may linger in the bodies of Americans for decades to come.


    During those bleak pre-vaccine dark ages, going to the doctor could feel like a disaster in waiting. Many of the country’s hospitals were overwhelmed with COVID patients, and outpatient clinics had closed. As a result, in every week through July 2020, roughly 45 percent of American adults said that over the preceding month, they either put off medical care or didn’t get it at all because of the pandemic. Once they did come in, they were sicker—a trend observed for all sorts of ailments, including childhood diabetes, appendicitis, and cancer. A recent study analyzed the 8.4 million non-COVID Medicare hospitalizations from April 2020 to September 2021 and found not only that hospital admissions plummeted, but also that those admitted to hospitals were up to 20 percent more likely to die—an astonishing effect that lasted through the length of the study.

    Partly, that result came about because only those who were sicker made it to the hospital, James Goodwin, one of the study’s authors and a professor at the University of Texas Medical Branch, in Galveston, told me. It was also partly because overwhelmed hospitals were giving worse care. But Goodwin estimates that “more than half the cause was people delaying medical care early in their illness and therefore being more likely to die. Instead of coming in with a urinary tract infection, they’re already getting septic. I mean, people were having heart attacks and not showing up at the hospital.”

    For some conditions, skipping a checkup or two may not matter all that much in the long run. But for other conditions, every doctor’s visit can count. Take the tens of millions of Americans with vascular issues in their feet and legs due to diabetes or peripheral artery disease. Their problems might lead to, say, ulcers on the foot that can be treated with regular medical care, but delays of even a few months can increase the risk of amputation. When patients came in later in 2020, it was sometimes too late to save the limb. An Ohio trauma center found that the odds of undergoing a diabetes-related amputation in 2020 were almost 11 times higher once the pandemic hit versus earlier in the year.

    Although only a small percentage of Americans lost a limb, the lack of care early in the pandemic helped fuel a dangerous spike in substance-abuse disorders. In a matter of weeks or months, people’s support systems collapsed, and for some, years of work overcoming an addiction unraveled. “My patients took a huge step back, probably more than many of us realize,” Aarti Patel, a physician assistant at a Lower Manhattan community hospital, told me. One of her patients, a man in his late 50s who was five years sober, started drinking again during the pandemic and eventually landed in the hospital for withdrawal. Patients like this man, she said, “would have really difficult, long hospital stays, because they were at really high risk of DTs, alcohol seizures. Some of them even had to go to the ICU because [the withdrawal] was so severe.”

    Later in the year, when doctors’ offices were up and running, “a lot of patients expressed that they didn’t want to go back for care right away,” says Kim Muellers, a graduate student at Pace University who is studying the effects of COVID on medical care in New York City, North Carolina, and Florida. Indeed, through the spring of 2021, the top reason Medicare recipients failed to seek care was they didn’t want to be at a medical facility. Other people were avoiding the doctor because they’d lost their job and health insurance and couldn’t afford the bills.

    The problem, doctors told me, is that all of those missed appointments start to add up. Patients with high blood pressure or blood sugar, for example, may now be less likely to have their conditions under control—which after enough time can lead to all sorts of other ailments. Losing a limb can pose challenges for patients that will last for the rest of their lives. Relapses can put people at a higher risk for lifelong medical complications. Cancer screenings plummeted, and even a few weeks without treatment can increase the chance of dying from the disease. In other words, even short-term delays can cause long-term havoc.

    To make matters worse, the health-care delays fueling a sicker America may not be totally over yet, either. After so many backups, some health-care systems, hobbled by workforce shortages, are scrambling to address the pent-up demand for care that patients can simply no longer put off, according to administrators and doctors from several major health systems, including Cleveland Clinic, the Veterans Health Administration, and Mayo Clinic. Disruptions in the global supply chain are forcing doctors to ration basic supplies, adding to backlogs. Amy Oxentenko, a gastroenterologist at Mayo Clinic in Arizona who helps oversee clinical practice across the entire Mayo system, says that “all of these things are just adding up to a continued delay, and I think we’ll see impacts for years to come.”


    It’s still early, and not everything that providers told me is necessarily showing up in the data. Oddly enough, the CDC’s National Health Interview Survey found that most Americans were able to see a doctor at least once during the first year of the pandemic. And the same survey has not revealed any uptick in most health conditions, including asthma episodes, high blood pressure, and chronic pain—which might be expected if America were getting sicker.

    It’s even conceivable that the disturbing observations of clinicians are a statistical illusion. If for whatever reason only sicker people are now being seen by—or able to access—a doctor, then it can be true both that providers are seeing more seriously ill patients in medical facilities and that the total number of seriously ill people in the community is staying the same. The scope of the damage just isn’t yet clear: Maybe a smaller number of people will be worse off because of delayed cancer care or substance-abuse relapses, or maybe far more people—more than tens of million of Americans—will be dealing with exacerbated issues for the rest of their lives.

    None of this accounts for what COVID itself is doing to Americans, of course. The health-care system is only beginning to grapple with the ways in which a past bout with COVID is a long-term risk for overall health, or the extent to which long COVID can complicate other conditions. The pandemic may feel “over” for lots of Americans, but many who made it through the gantlet of the past two-plus years may end up living sicker, and dying sooner.

    This disturbing prospect is not only poised to further devastate communities; it’s also bad news for health-care workers already exhausted by COVID. Laura, the Manhattan internist who treated the colon-cancer patient, told me it’s disheartening to see so many people showing up at irreversible points in their disease. “As doctors,” she said, “our overall batting average is going down.” Aarti Patel, the physician assistant, put it in blunter terms: “Burnout is probably too simple a term. We’re in severe moral distress.”

    Nothing about this grim fate was inevitable. Laura told me that “going to the doctor mid-pandemic may have posed a small risk in terms of COVID, but not going was risky in terms of letting disease go unchecked. And in retrospect it seems that many people didn’t quite get that.” But there didn’t have to be such a stark trade-off between fighting a pandemic and maintaining health care for other medical conditions.

    Some hospitals—at least the better-resourced ones—figured out how to avoid the worst kind of delays. Mayo Clinic, for example, is one of a number of systems with a sophisticated triage algorithm that prioritizes patients needing acute care. In the spring of 2021, Cleveland Clinic launched a massive outreach blitz to schedule some 86,000 appointments, according to Lisa Yerian, the chief improvement officer. And the Veterans Health Administration provided iPads to thousands of veterans who lacked other means of accessing the internet in the spring of 2020, ensuring a more seamless transition to virtual care, Joe Francis, who directs health-care analytics, told me. Thanks in part to these efforts, Francis said, high-risk patients at the VHA were being seen at pre-pandemic levels a mere six months into the pandemic.

    These health-care systems also suggest a path forward. America may still be able to stave off the worst of the collateral damage by reaching the patients who have fallen through the cracks—and already the data suggest that these patients tend to be disproportionately Black, Hispanic, and low-income. Tragically, it’s too late for some Americans: People who died of cancer can’t come back to life; amputated limbs can’t regrow. Others still have plenty of time. Hypertension that’s currently uncontrolled can be tamped down before causing an early heart attack; drinking that’s gotten out of hand can be corralled before it leads to liver failure in a decade; undetected tumors can be spotted in time for treatment. An uptick in premature death and disability, summed over millions of Americans, could strain the health-care system for years. But it’s still possible to prevent an acute public-health crisis from seeding an even bigger chronic one.

    Tim Requarth

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