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Tag: kidney donation

  • Her little sister needed a kidney. The donation let them both live their dreams

    Her little sister needed a kidney. The donation let them both live their dreams

    As children, sisters Amaris and Dominique Elston were inseparable. Their parents remember the two of them sharing everything and always having each others’ backs, no matter the situation. 

    That bond didn’t change as they grew older, and when an 18-year-old Dominique was diagnosed with focal segmental
    glomerulosclerosis, a chronic kidney disease that soon led to kidney failure, Amaris was again ready to help her sister.

    “I told Amaris ‘Dominique is in kidney failure. Her kidney function was at 19%, and she’s going to need a kidney transplant eventually,’” Denise Elston, their mother, said. “Thirty seconds later, Amaris said, ‘Can I give her one?’” 

    Amaris (back) and Dominique (front) Elston as children. 

    The Elston family


    Amaris, then interviewing for medical schools, knew her family had a history of kidney disease, so she wasn’t sure she’d be able to donate. Dominique didn’t want her sister to put her life on hold but as her condition deteriorated and her kidney function dropped to just 5%, despite dialysis treatments, Amaris knew she had to do something. Without telling Dominique, she got tested and learned she was a match. 

    “She’s my little sister,” Amaris said. “As a big sister, it’s natural to want to jump in and save her from everything that life has to offer, even failing kidneys. I knew this was the best option that she had at getting back on track with life and doing all the things she wanted to do. It was never really a question.” 

    Avoiding years on a waiting list 

    About 140,000 people are on the waiting list for a kidney transplant in the United States, according to Dr. Kelly Birdwell, medical director of kidney transplantation at Vanderbilt University Medical Center, who was not involved in the Elston sisters’ care.

    The average American waits about five years for a kidney donation through the waiting list. Black Americans are also disproportionately represented on the waiting list, Birdwell said. Black people are more likely to have Type B blood, which has fewer compatible donors, she said, and there is also “an excess risk of kidney disease in the African American population.” 

    In 2019, more than 14,000 Black kidney transplant candidates were moved up on the national waitlist after it was found a widely-used test was overestimating how well Black people’s kidneys were functioning, making them seem healthier than they were and extending the amount of time they waited. 


    Thousands of Black kidney transplant candidates moved up on waitlist after testing bias found

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    Amaris said all of those factors were on her mind when she decided she wanted to donate to her sister. In 2023, 21,765 kidney transplants were completed, with 6,294 of those organs coming from living donors. About 60% of living donors are related to the recipient, Birdwell said. 

    To donate a kidney, interested family members do a round of initial testing that confirms the donor is compatible with the recipient. That’s followed by a longer evaluation, Birdwell explained, to make sure the donation won’t put the potential donor at risk. The evaluation includes bloodwork and imaging to confirm the potential donor is in good health. Once those stages are successfully completed, it’s just a matter of scheduling the surgery. 

    For the Elstons, that meant waiting until Amaris finished her first semester of medical school at the University of Alabama at Birmingham. In December 2018, the sisters were again side-by-side, waiting for their operations at the University of Vanderbilt’s Transplant Center. Amaris’ operation was first. Birdwell estimates that a donor surgery is about two hours, while a recipient’s surgery, scheduled for later in the day, is about three hours. 

    When Amaris and Dominique reunited after their operations, the eldest of the two could already see a change in her baby sister. 

    “I remember laying in the bed and being in a lot [of] pain, and Dominique walking down the hallways like ‘No big deal,’ and in that moment, it solidified that I knew I had made the right decision,” Amaris said. “She looked like a whole new person, in less than 24 hours. She was just bopping in my room, sitting in my chair. It was worth it.” 

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    Dominique (left) and Amaris (right) after transplant. 

    The Elston family


    Working together to save lives 

    Amaris gave her younger sister more than a kidney. She also gave Dominique the chance to follow her sister into the field of medicine. 

    Amaris graduated from UAB’s Heersink School of Medicine in 2022. Just two years later, Dominique graduated from the UAB School of Nursing with her bachelor’s degree in nursing. Amaris cheered her on from the audience. 

    “After going through what we went through, it was kind of like a calling for me to go into (nursing),” Dominique said. “It wasn’t really something I had to think about. I felt like it was something that was meant for me.” 

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    Dominique (left) and Amaris (right) at Dominique’s graduation ceremony from UAB. 

    The Elston family/UAB


    Now, both sisters are working in the neurology field. Amaris is a neurology resident at the Medical University of South Carolina, and Dominique is a neurology intensive care unit nurse at UAB. The two are the first members of their family to enter the medical field. Though the sisters are now separated by more than more than 400 miles, their bond is stronger than ever. 

    “It’s been fun having somebody that is with you through everything, because if you want to talk about the bad parts, the good parts, you can,” Amaris said. “It feels good to know that there’s somebody right beside you that can understand how you feel and what you’re going through. We’ve been each other’s best friends amid some of our darkest moments, so this is just another journey that we’re on together.”  

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  • State trooper Kristie Sue Hathaway has saved lives on and off the job. She’s donated two organs to strangers.

    State trooper Kristie Sue Hathaway has saved lives on and off the job. She’s donated two organs to strangers.

    Minnesota State Trooper Kristie Sue Hathaway earned a commendation in 2012 for saving a life on the job, but it’s not the only lifesaving move she has made.

    In 2021, Hathaway stepped forward to donate a kidney. In May, she made a second donation, this time giving away a piece of her liver.

    Both donations were non-directed, meaning the organs went to total strangers. Hathaway told CBS News that she learned about the process of non-directed live organ donation when a friend fell ill. She wanted to donate an organ then, but was the wrong blood type. Still, the situation stirred something in her, and she decided to “look into what goes into donating a kidney.” 

    “Once I did some digging, I learned that … you don’t need to know the person. And I was like, ‘I’ll do that. I’m healthy, and if I ever came across someone that needed one, I’d give them a kidney, so why not?’” Hathaway, 40, told CBS News. “I just felt like I needed to do it.”

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    Kristie Sue Hathaway walking from the ICU after her liver donation.

    Steve Hilyar


    What is live organ donation? 

    Live organ donations account for thousands of organ transplants each year, according to the United Network for Organ Sharing, the nonprofit that manages the United States’ organ transplant system, though most donations come from deceased people. 

    The kidney is the most commonly transplanted organ from a living donor, followed by the liver, according to the network’s website. Most other organs can’t be transplanted from live donors because of their role in the human body, said Mayo Clinic transplant surgeon Dr. Timucin Tanner, who was involved in Hathaway’s donations. 

    In “rare cases, a uterus or segments of other organs” may be transplanted, according to the network.

    Potential donors are screened for mental and physical health, and for compatibility with the recipient of an organ. In kidney donations, one of a person’s two kidneys is transplanted from the living donor to the recipient. In a liver transplant, a section of the liver is transplanted from the recipient into the donor. In the donor, another part of the organ regenerates to compensate for the loss, and in the recipient, the transplanted piece grows to nearly full-size.

    More than 101,000 people in the United States are awaiting a kidney donation, the National Kidney Foundation says online, but just about 17,000 receive one each year. About 12 people die a day waiting for a transplant, according to the foundation. When it comes to the liver, about 14,000 people nationwide are waiting for a liver transplant, according to the American Liver Foundation

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    Kristie Sue Hathaway after her kidney donation.

    Steve Hilyar


    People can spend years on waiting lists. 

    “There are a lot of people at any given time who don’t have access to livers or kidneys,” said Tanner said. “We just don’t have enough deceased donor organs in this country, so living donation is a great thing.” 

    Tanner said that beyond the initial operation and recovery period, living donors do not experience “long-term consequences” from giving away an organ. The Zweig Family Center for Living Donation at Mount Sinai Hospital recommends that a living liver donor not drink alcohol for the first six months after donation, and advises against becoming pregnant until at least a year later. Living donors receive follow-up check-ups annually for five years, according to the center. The National Kidney Foundation recommends a living kidney donor wait at least a year to become pregnant.

    Six months after her liver donation, Hathaway said she is already back to her normal routine of running about 20 miles a week, and recently returned to work at her post of more than 12 years. Tanner said he has seen patients run marathons shortly after recovering from a donation. 

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    Kristie Sue Hathaway after recovering from her kidney donation. 

    Steve Hilyar


    “There are some misconceptions about living donation,” said Tanner. “People sometimes think they’re not able to be active or have a normal life afterwards. Those are all misconceptions. None of those are true.” 

    Tanner said that Hathaway cannot make any more live organ donations, but the state trooper told CBS News that she is still working to make a difference and help those around her. She’s registered as a bone marrow donor, and she regularly donates blood. She’s also trying to educate others about live organ donation. 

    Celebrating the “ripple effect”

    Hathaway said that both times she donated, she has signed a release allowing the recipient to contact her. She has not heard from the person who received a piece of her liver, but the recipient of her kidney, a 29-year-old veteran, sent a “very small note,” followed by a longer letter from his mother. 

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    Kristie Sue Hathaway after her liver donation.

    Steve Hilyar


    Part of what spurred Hathaway’s decision to be a live organ donor is what she calls the “ripple effect” that occurs when someone receives a necessary, often life-saving organ transplant. In the case of the man who received her kidney, he had run out of dialysis access points and would no longer be able to treat a chronic condition without a new organ. Since the donation, he has returned to work and no longer needs dialysis, Hathaway said. 

    “You actually have made a measurable difference, and not just for the person getting it. It’s their whole family,” said Hathaway. “They might have kids. They might have grandkids. You can’t really put a price on somebody getting a few extra Christmases or a few extra birthdays or getting to attend a wedding that they wouldn’t have otherwise been able to attend.” 

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  • Domino Donation: A Kidney to Save Two Lives Instead of One

    Domino Donation: A Kidney to Save Two Lives Instead of One

    Oct. 18, 2022 On a warm summer day in June, Amy Nadel sat in a waiting room at Johns Hopkins as one of her children was coming out of the operating room and another was preparing go in. And in a similar room in another part of the hospital, another family was sitting through the same thing. They were linked not by coincidence, but by one life-saving thing they were about to trade: kidneys.

    Nadel’s son Jonah Berke had just had one of his kidneys removed, where it was rushed across the hospital in a sterile cooler to be transplanted into an anonymous recipient. At the same time, her daughter Rachael Moskowitz was ready to receive a kidney that had just come from an anonymous donor somewhere else in the hospital. You’d be forgiven for thinking this sort of thing only happens in a Grey’s Anatomy episode. But this dramatic process, called kidney paired donation (KPD), is one of the ways people may receive kidney transplants.

    Nadel’s kids were one pair in this sort of donation. Jonah had decided to donate to benefit his sister Rachael, after she had gone through years of complicated health battles. After untold doctors’ appointments, numerous surgeries, and countless hours worrying for Rachael’s well-being, the whole family arrived at Hopkins with hope and a fully loaded Netflix queue, ready for a new chance at life. 

    Nadel looks back on that tense day with pride. She says everyone thinks their kids are special, but she can’t help but think, “My kids started from below zero, and look where they are.”

    As odd as it may sound, their family was lucky Rachael got her kidney and someone else did too. But kidney paired donations are far from the norm. Most people in kidney failure wait an average of 4 years before they get the call that a donor organ is available. Nearly 5,000 people die each year waiting on that list. But if more people were willing to sign up for KPD, that waiting time may shrink, says David Klassen, MD, the chief medical officer at the United Network for Organ Sharing.

    The first successful kidney transplant took place in 1954, using a live donor’s twin brother. For a while, that was the standard route for donating the organ, as society felt squeamish about using organs from deceased donors. Eventually, around the mid-1960s, new guidelines about brain death from Harvard Medical school allowed donations from the deceased to become commonplace.

    Living donation is also an option, whereby one person donates one of their healthy kidneys (as it’s possible to live a healthy life with just one functioning kidney) to another person. A recently removed kidney can last for an estimated 36 hours outside of the body, if stored and transported correctly, which has allowed for some living kidney donations to happen across state lines.

    After the transplant, the person who received the kidney must be on a type of medication that stops their immune system from attacking the new organ. This is called immunosuppression, and most immunosuppressant drugs come with unpleasant side effects. People who get transplants are particularly susceptible to infections and cancer, among other diseases, since their immune system can’t fight at the level it normally would. But if the drugs work properly and the organ does not get rejected by the body, a donated kidney will usually last about 15 to 20 years.

    For decades, direct living and deceased donation were the only options for people seeking a kidney transplant. But in 1991, doctors in South Korea performed the first known kidney paired donation. They were ahead of the curve, establishing a government-run KPD program within the decade. The United States caught up in 2000, completing the country’s first KPD at Rhode Island Hospital. But the use of this new protocol was neither universal nor speedy. By 2005, there were only 26 KPDs per year in the U.S., according to data from the Organ Procurement and Transplantation Network. 

    The slow uptake was owing to a few issues. First, not many people knew about the option, says Susan Rees, a registered nurse and the chief operating officer for the Alliance for Paired Kidney Donation. So, when someone found out they weren’t a match for the person they intended to be a live donor for, the story ended there. Second, it took a while to standardize the data set. Rees calls KPDs a “team sport,” with the need to establish a matching database, and the requirement for multiple entities across different cities and states to work together to compile and compare their data. The alliance was one of the first nonprofits to compile this data, beginning in their home state of Ohio.

    The third reason the uptake of KPD was slow was legal concerns about the process, says Klassen. Transporting organs across state lines for purposes other than direct donation wasn’t protected by the law at first. This was thought to deter organ traffickers. But in 2007, Congress passed the Charlie Norwood Act, which assured the legality of paired donation in specific medical circumstances.

    So today, KPDs have increased, but they’re still not common. Since 1998, there have been slightly over 10,000 kidney paired donations in the U.S., which is a little over 5% of the total 173,000 living donations. The other 95% of living donors were direct match donations. These are the typical donations you hear about, between siblings, friends, or parents and children.

    Rachael is by no means the typical person you’d expect to need a kidney transplant. At 36 years old, she’s a young mom and a full-time first-grade teacher. But she has a complicated medical history, including a glycogen storage disorder, a history of blood transfusions, a former liver transplant, a premature pregnancy, and long-term use of immunosuppressants. Each of those may have scarred her kidneys over time, leading to renal failure, Rachael was told by her nephrologist.

    That failure meant Rachael had to begin dialysis in April of 2020. Not only had the world shut down due to the pandemic, meaning Rachael had to adapt to online teaching, but she was also caring for her 1-year-old daughter. Even with the support of her husband and family, it was exhausting balancing multiple long dialysis appointments each week with normal life. She quickly opted to switch to peritoneal dialysis, which allowed her to get the procedure at home each night instead.

    Though this was an improvement, she says it wasn’t much of a way to live. The logistics were difficult, she had very low energy, and it was getting in the way of her spending valuable time with her daughter. So, though she’s grateful for the machine that kept her alive, “it was like I missed out on life for 2 years,” she says of that time.

    This is consistent with what providers see too. Dialysis is a treatment, but it’s not a replacement for a functioning kidney, Rees says. Even after the procedure, there’s only a brief window of relief. Rees says that the next day, the patients are exhausted. And because of the logistical difficulties and fatigue, she’s even seen people lose their jobs and go through financial crises. 

    While she was going through dialysis, and on a waiting list for a kidney, many people in Rachael’s life signed up to see if they were a match. One by one, they discovered no one was. There are many reasons someone may not be a match for organ donations. But there are a few things that make a person develop more pan reactive antibodies, which make it harder to match them. These include prior blood transfusions, pregnancy, and previous transplant. Rachael had had all three, making her what Rees calls a highly sensitized patient.

    Even with all those compounding issues, what would’ve taken Rachael untold years was solved in mere months, when Jonah volunteered to enter the KPD donor pool. Here’s how that pool works.

    Think of those memory matching games you used to play as a kid. The database serves as the memory storage, the proxy for you. All the cards start flipped over, with unknown donor profiles.

    You start with one card, person 1 (in this case, Rachael) who needs a kidney. Person 1 is a pink circle. You then flip over a second card, person 2 (in this case, Jonah) who is willing to donate a kidney. But person 2 is a purple triangle.

    No match. So, we pull another card. Person 3 turns out to be another person who needs a kidney. They’re a purple triangle, a match for Jonah. And when we flip the accompanying card, we find person 4, a pink circle, a willing donor matched to Rachael. Hurray, matching pairs!

    Because of the database, person 1 can get a kidney from person 4 and person 3 can get a kidney from person 2. This chain can continue on and on, depending on how many people match. There have been chains up to 10 pairs long. 

    This may sound like a big logistical nightmare. You may be thinking, what about organ donation from deceased people? And of course, registering to be an organ donor is an important piece of this puzzle. 

    Both Klassen and Rees and the Berke/Nadel family urge people to sign up to be an organ donor. But only about 2% of people who are registered donors will end up being able to donate their organs, Klassen says. To be a valid option, someone must die while on life support in the hospital. Otherwise, they are pretty much only able to donate tissue. That leaves us at the starting point set out earlier. A person in kidney failure has an average of 4  years waiting time, and each year, that person has a 15%-20% chance of dying while waiting, Rees explains.

    But adding in KPD makes the situation less dire. That is, if there is the database to support it and enough people are willing to sign up. At this point, there are separate databases for people to take part in KPD across the country and the world. The United Network for Organ Sharing and the Alliance for Paired Kidney Donation have some of the bigger aggregates, but they are far from having all the data. Rees says standardization would help.

    The more people in the database, the more possibilities there are for people to match. Though some people may be uncomfortable not directly donating to the person they intended to, Rees says the people she’s observed feel pleased anyway.

    In Jonah’s case of wanting to donate to his sister, this served as only a minor bump in the road. 

    “Well really, it’s like saving two lives with your kidney, not just one,” he says.

    For Rachael, everything has changed since the donation; even her skin tone, requiring her to  buy a new color of foundation. She realizes now how bad she felt each day while on dialysis. But above all, she’s grateful for the sacrifices Jonah and the anonymous donor made, and she’s grateful to be able to rejoin the living world.

    And as for Jonah, life has returned to normal. His recovery was speedy, and he’s back doing the job he loves with his typical cheerful attitude. He’s doing so well, in fact, that if he could go under the knife again, he said he would. He would do anything for his sister. “If I could donate my other kidney, I would do it. I wouldn’t even think about it. You know, if I could donate my heart, I would give my heart up.”

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