
Mount Vernon teen undergoes bone marrow transplant, starting long road to recovery
Jun. 11—MOUNT VERNON, S.D. — While many teenagers are spending their summer break working part-time jobs or relaxing at the pool, 15-year-old Josie Trebil of Mount Vernon is beginning a summer of recovery.
She is undergoing a bone marrow transplant Thursday at Minnesota Masonic Children's Hospital to treat severe aplastic anemia, a rare but serious blood disorder.
The procedure marks the start of what doctors refer to as "Day Zero," the beginning of a 100-day recovery process during which Trebil will remain in Minneapolis under close medical supervision. The transplant is considered the most effective treatment for severe aplastic anemia, which occurs when the bone marrow stops producing enough new blood cells. The condition increases the risk of fatigue, infection, and uncontrolled bleeding.
Trebil's medical journey began in April 2023 during a family vacation.
"She developed what looked like a rash," said her mother, Tera Tramp. "We saw our doctor as soon as we got home. Her blood levels were all low — dangerously low."
The family was sent to Sanford Children's Hospital in Sioux Falls, where leukemia was initially suspected but later ruled out. Further tests pointed to aplastic anemia. Over the next several months, Trebil received multiple blood and platelet transfusions and was placed on the bone marrow transplant list. Her condition briefly improved at the end of 2023, and she was removed from the list. However, after a hospital stay in January 2025 due to influenza A, her blood counts declined again, and a February biopsy confirmed a re-diagnosis of severe aplastic anemia.
"All her numbers began to tank and we were back at square one," Tramp said.
From January through June, Trebil has had more than 18 transfusions. She's had five bone marrow biopsies since April 2023. She has missed significant time at school, including parts of three academic years, and has had to sit out of the sports she typically plays — volleyball, basketball, and softball.
Because Trebil does not have siblings — who are typically first checked for a match — her doctors turned to the National Marrow Donor Program. In early May, a matching international donor was identified in Israel. The donor's marrow was collected overseas and flown to Minneapolis for Thursday's transplant.
"She just wants to be a normal teenager again," Tramp said. "We're grateful a match was found."
Trebil was admitted to the hospital on June 2 to begin intensive chemotherapy and radiation, which prepares her body to receive the donor's marrow. There will be a mandatory residence within 30 minutes of the hospital for at least 100 days post-transplant to monitor for complications.
"They compare transplant to being a newborn baby. She will come out with absolutely no immune system," Tramp said. "At about two weeks post transplant, her marrow will begin to produce white blood cells again. This is a long process and she will be very susceptible to sickness and there is always a risk of rejection."
After returning home, most of Trebil's follow-up care will take place at Sanford Children's Hospital in Sioux Falls. Her recovery is expected to take about six months, which makes her return to school uncertain due to the timing and the precautions still needed during flu and cold season.
"The problem with that is then we are in prime cold and flu season. And she will be without all of her immunizations," Tramp said.
One year after the transplant, Trebil will need to begin receiving all of her childhood immunizations again.
The impact on her daily life has been significant.
"Not being able to play softball this spring or volleyball in the fall is very hard for me," Trebil said.
Trebil has also been involved with Helping with Horsepower, a therapeutic riding program where she previously volunteered but is now also missing out on because the risks are too great.
"She's an avid horse lover," Tramp said. "My rough and tough cowgirl has been told she can't be rough — but they can't take the tough away."
One recent highlight: attending prom this spring, a rare moment of normalcy.
Support from both Mount Vernon and her previous hometown of Crofton, Nebraska has been steady. Fundraisers have included a euchre tournament, raffles, auctions, and a recent cornhole event. An account for donations has been set up at First Interstate Bank where Tramp works, and Main Street Treasures in Crofton will hold a benefit shopping day on June 18.
"The support we've received has been overwhelming," Tramp said. "It's really helped us get through this."
Tramp hopes Trebil's story encourages others to consider donating blood, platelets, or joining the bone marrow registry.
"When there's a shortage, it affects real people," she said. "We've waited at transfusions for blood to arrive from out of state. That's the reality."
While the road ahead includes precautions and adjustments, the transplant brings Trebil closer to resuming daily life — school, sports, and time with friends — on her own terms.
"I am ready for this to be over and for life to get back to normal," Trebil said.

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12-06-2025
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Mount Vernon teen undergoes bone marrow transplant, starting long road to recovery
Jun. 11—MOUNT VERNON, S.D. — While many teenagers are spending their summer break working part-time jobs or relaxing at the pool, 15-year-old Josie Trebil of Mount Vernon is beginning a summer of recovery. She is undergoing a bone marrow transplant Thursday at Minnesota Masonic Children's Hospital to treat severe aplastic anemia, a rare but serious blood disorder. The procedure marks the start of what doctors refer to as "Day Zero," the beginning of a 100-day recovery process during which Trebil will remain in Minneapolis under close medical supervision. The transplant is considered the most effective treatment for severe aplastic anemia, which occurs when the bone marrow stops producing enough new blood cells. The condition increases the risk of fatigue, infection, and uncontrolled bleeding. Trebil's medical journey began in April 2023 during a family vacation. "She developed what looked like a rash," said her mother, Tera Tramp. "We saw our doctor as soon as we got home. Her blood levels were all low — dangerously low." The family was sent to Sanford Children's Hospital in Sioux Falls, where leukemia was initially suspected but later ruled out. Further tests pointed to aplastic anemia. Over the next several months, Trebil received multiple blood and platelet transfusions and was placed on the bone marrow transplant list. Her condition briefly improved at the end of 2023, and she was removed from the list. However, after a hospital stay in January 2025 due to influenza A, her blood counts declined again, and a February biopsy confirmed a re-diagnosis of severe aplastic anemia. "All her numbers began to tank and we were back at square one," Tramp said. From January through June, Trebil has had more than 18 transfusions. She's had five bone marrow biopsies since April 2023. She has missed significant time at school, including parts of three academic years, and has had to sit out of the sports she typically plays — volleyball, basketball, and softball. Because Trebil does not have siblings — who are typically first checked for a match — her doctors turned to the National Marrow Donor Program. In early May, a matching international donor was identified in Israel. The donor's marrow was collected overseas and flown to Minneapolis for Thursday's transplant. "She just wants to be a normal teenager again," Tramp said. "We're grateful a match was found." Trebil was admitted to the hospital on June 2 to begin intensive chemotherapy and radiation, which prepares her body to receive the donor's marrow. There will be a mandatory residence within 30 minutes of the hospital for at least 100 days post-transplant to monitor for complications. "They compare transplant to being a newborn baby. She will come out with absolutely no immune system," Tramp said. "At about two weeks post transplant, her marrow will begin to produce white blood cells again. This is a long process and she will be very susceptible to sickness and there is always a risk of rejection." After returning home, most of Trebil's follow-up care will take place at Sanford Children's Hospital in Sioux Falls. Her recovery is expected to take about six months, which makes her return to school uncertain due to the timing and the precautions still needed during flu and cold season. "The problem with that is then we are in prime cold and flu season. And she will be without all of her immunizations," Tramp said. One year after the transplant, Trebil will need to begin receiving all of her childhood immunizations again. The impact on her daily life has been significant. "Not being able to play softball this spring or volleyball in the fall is very hard for me," Trebil said. Trebil has also been involved with Helping with Horsepower, a therapeutic riding program where she previously volunteered but is now also missing out on because the risks are too great. "She's an avid horse lover," Tramp said. "My rough and tough cowgirl has been told she can't be rough — but they can't take the tough away." One recent highlight: attending prom this spring, a rare moment of normalcy. Support from both Mount Vernon and her previous hometown of Crofton, Nebraska has been steady. Fundraisers have included a euchre tournament, raffles, auctions, and a recent cornhole event. An account for donations has been set up at First Interstate Bank where Tramp works, and Main Street Treasures in Crofton will hold a benefit shopping day on June 18. "The support we've received has been overwhelming," Tramp said. "It's really helped us get through this." Tramp hopes Trebil's story encourages others to consider donating blood, platelets, or joining the bone marrow registry. "When there's a shortage, it affects real people," she said. "We've waited at transfusions for blood to arrive from out of state. That's the reality." While the road ahead includes precautions and adjustments, the transplant brings Trebil closer to resuming daily life — school, sports, and time with friends — on her own terms. "I am ready for this to be over and for life to get back to normal," Trebil said.
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Lackawanna County residents rally for 20-year-old cancer patient
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Yahoo
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Ohio State quarterback Will Howard helps bring attention to bone-marrow needs
If an onlooker standing outside the Ohio Union on March 27 asked what the long line snaking around the building was for, anyone in the line would have probably had the right answer: Will Howard. But there's more to the story. Two months before Ohio State's star quarterback spent that Thursday afternoon posing for photos and signing autographs, he was sent a message by 21-year-old Charlotte "Charley" Bauer. On Jan. 29, Bauer wrote the following note from the hospital to Ohio State's star quarterback, thanking him for his advocacy for the National Marrow Donor Program (NMDP). 'My name is Charley Bauer, and I am a nursing student at Ohio State. This past year, I've been battling high-risk acute myeloid leukemia at Nationwide Children's Hospital. Recently, someone sent me a video of you raising awareness for the NMDP registry, and I love that you are advocating for donors to join! I received my stem cell transplant last September, and I have been in remission ever since. I'm still not fully recovered from the transplant, but I'm working really hard to get there," the message read. 'I don't think students fully grasp how crucial a stem cell transplant is to patients in need. I wouldn't be here today without mine, and I carry that knowledge with me every day. Diving into the actual impact students can make if they say 'yes' to being a donor could inspire more people to get swabbed. If you ever want to collaborate on something — now or in the future — I'd love to help share my experience.' The message, provided by the NMDP, never made it to Howard while Bauer was still alive. The Ohio State nursing student succumbed to her fight to acute myeloid leukemia (AML) on Feb. 16. In a quote provided via the NMDP, Charley's mother, Alyssa, noted the importance of joining the stem cell registry to provide those who are battling the same journey the chance to survive. "Our family is extremely grateful for each individual who joins the NMDP stem cell registry. Although Charley was unable to secure her perfect 10 out of 10 match, she would be honored to know that her story has helped grow the registry for others in need," she said. "From the moment she was diagnosed, Charley was determined to survive AML and the transplant. She fought her battles with everything she had. Through it all, she remained positive, optimistic and connected with her nurses, doctors and patients on the oncology floor of Nationwide Children's Hospital. "Her final words were 'It will be OK,' and 'I can do hard things.' The world is certainly missing out on having Charley here with us. She was destined to do great things not only as a future nurse, but as a kind and compassionate human. She leaves behind a legacy of courage, hope and above all else, pure love.' Just a month after Bauer's death, the NMDP, in partnership with Ohio State's Be The Match Club, held a drive in her memory. Howard joined the event, as did other student athletes and a fleet of Buckeye Paws therapy dogs — including dogs Bo, Norman, Shiloh and Indy — as Bauer was a dog lover whose special joy was the Butterfly Paws team at Nationwide. To remember Bauer's legacy and encourage students and faculty to sign up for the bone marrow registry, the celebration reminded the community of her core message through treatment: "I can do hard things." Attending the registry drive as a friend to both Bauer and Howard, 10-year-old Katelyn Weirich floated around the crowd with her parents, Tara and Jeff. Looking out at the long line of people patiently waiting to meet with Howard, Tara Weirich said she was "super happy" for what it meant for the NMDP registry. "Katelyn and Charley were friends. We were both praying for each other for a long time. Her mom and I are friends now," Weirich said. "If she (Charley) would have had a 10 out of 10 match, then it could have saved her life. There were three people in the whole world that had a 10 out of 10 for her and weren't able to donate at the time, so we need more people in the registry so there can be a greater number than three in the entire world." Ohio State's Be The Match Club president Shreaya Madireddy said she started the chapter to diversify and grow the NMDP bone marrow registry. "Matching is based on your HLA (human leukocyte antigen) type, which is based on your background. Since OSU has so many students with so many different backgrounds, we thought this would be the perfect place to start a club," Madireddy said. "Right now, we're honoring Charley." Howard said he has been involved with the NMDP — formerly called Be The Match — for several years, inspired by his mother, Maureen, who worked as an occupational therapist at the Children's Hospital of Philadelphia. The 23-year-old quarterback, originally from Pennsylvania, started a drive at Kansas State University, but he wasn't able to participate last year due to the quick turnaround while moving his college football career to Ohio State. "It's such an easy process to swap somebody's mouth and get them on the registry. There could be somebody out there that could be the match for one of these kids that has these blood cancers, or one of these adults, and need a bone marrow or stem cell transplant," Howard said. "I try to encourage as many people as I can to get on and help save a life because I've seen that three or four people that I've gotten on the registry have saved lives now, and it's crazy." Noting the March 27 drive had already surpassed its goal as of an hour before its scheduled end time, Howard said he was happy to be able to participate this year. "It's way more important than anything I do on the field. I love what I do on the field, but, I mean, this is what it's really about," he said. Sophia Veneziano is a Columbus Dispatch reporter supported by the Center for HumanKindness at The Columbus Foundation. She may be reached at sveneziano@ The Dispatch retains full editorial independence for all content. This article originally appeared on The Columbus Dispatch: Will Howard, National Marrow Donor Program host OSU registry event