Written by: Dave R. My transplant journey began at birth – I just didn’t know it until I was in my 50s. I was born in 1956 with a hole in my heart, and of course, it was undiagnosed because the technology was just not available in the fabulous 50s. The amazing thing is I […]
Power Player – Steve
In 1992, Steve was diagnosed with Primary Sclerosing Cholangitis, a form of liver disease. Fortunately, the disease progressed slowly and Steve’s doctors were able to keep it under control for many years. Nearly ten years later, it had been so long since Steve was first diagnosed that he had forgotten the potential outcome – a […]
Power Player – Kyle
When Kyle was just 20 months old, he was diagnosed with Hypertrophic Cardiomyopathy. Luckily, the impact on his childhood was low. It was not until April 2010 when he collapsed at 5:15 AM one morning. More severe issues came in 2013 when Kyle’s congestive heart failure started. In 2015, he was doing an exercise test. […]
Power Player – Alana
Alana was just 13 years old when she was diagnosed with kidney disease. It took ten years for her to require a kidney transplant, and thankfully, her brother volunteered to be her living donor. The living donation allowed Alana to bypass dialysis, so she was very excited (as well as a little nervous) when she […]
Power Player – Charles
My sister Nancy is seventy. When she was twelve her kidneys began to fail, triggered possibly by an autoimmune response to being stung by a swarm of bees. For the next six years, I watched as medications, needles, blood tests, doctors, hospitals, and finally kidney failure consumed her life. This was the sixties and artificial […]
Power Player – Anne Marie
I was born in Ottawa, Canada with a congenital heart defect. I had 3 heart surgeries as a child, the first one being the day after I was born. Doctors had warned my parents that these surgeries were palliative: problems would eventually start to arise because my heart would start to fail. Although I couldn’t […]
Power Player – Sandra
Sandra was on a family vacation in Mexico, when something happened that would change her life. While playing with her kids in a waterfall, she slipped and scraped her ankles. She had an open wound and entered tainted water. Months later, she began to feel tired. Her drowsiness turned to exhaustion, and Sandra soon went […]
Power Player – Denise
Denise recently celebrated the 20-year anniversary of her transplanted liver. Her donor was 75-year-old, Geraldine Hodges. Her liver is now over 95 years old – and still going strong. Denise found out she would likely need a liver transplant when she was around 18 years old. She was diagnosed with autoimmune liver disease, which ultimately […]
Power Player – Lauren
I am a 28-year-old female who has lived with Cystic Fibrosis her whole life. If you don’t know, Cystic Fibrosis causes thick mucus build-ups in lungs, which become nearly impossible for medicine to cure, thus resulting in a lung transplant. For the last six years, my doctor has causally mentioned lung transplant at various appointments. […]
Power Player – Robert
In 2012, I was working for a landscaping company. I got a couple of hernias and went to a surgeon to have them fixed during our offseason. I had to do regular blood work for the surgery. That is when my doctor called me in and said, sit down. The next few minutes turned my […]
Power Player – Carol
To say that I was an unlikely kidney donor is an understatement. If my high school yearbook had had a “Least Likely to Be a Living Kidney Donor” category, that would have been me. I’ve always been a wimp: I faint at flu shots, IVs, blood tests. And yet, in June 2006, I donated a […]
Power Player – Jill
Written by: Jill Stephenson My greatest gain I count as a loss. As the sister AND mother of organ donors, I can make this statement twice. When I was barely fifteen years old, my eleven-year-old brother J.T. was hit by a car and declared brain dead ten days later. As a family, we were approached […]
Power Player – Ken
Ken was just ten years old when he was diagnosed with kidney disease. His doctors tried to treat the condition for years, but by the time Ken was in college, it was clear he would need a kidney transplant. During his second year of medical school, Ken’s father volunteered to be a live donor and […]
Power Player – Rick
Rick and his wife, Jackie, have always been there for each other. They have been married 36 years and have always taken care of one another. In 2015, Rick gave his wife a Valentine’s Day Gift that will be difficult to top – he became her living kidney donor and saved her life. It all […]
Transplantation: The Science Fiction That Became Mainstream Medicine
Written by: Reg Green To most people — to almost all people — the idea of having someone else’s heart or liver, kidney, lungs or pancreas inside them is too outlandish to think about. But, in fact, all around us there are ordinary men, women, and children who one day have been, or will be, told […]
Power Player – Tatiana Benitez
When I was 5 years old, I was diagnosed with cardiomyopathy, and my only hope of survival was a heart transplant. My case was the first pediatric heart transplant in Paraguay. The surgery was performed by Dr. Jorge Jarolin at the Bautista Medical Center. Today, I celebrate 10 years with my heart transplant. I live […]
American Society of Transplantation Earns GuideStar Platinum Seal
The American Society of Transplantation (AST) announced that is has earned the 2018 Platinum GuideStar Nonprofit Profile Seal of Transparency, the highest level of recognition offered by GuideStar, the world’s largest source of nonprofit information. GuideStar’s Platinum Seal of Transparency recognizes AST’s sharing of detailed quantitative measures of progress and transparency. Less than 5,000 of […]
April is National Donate Life Month
April is Donate Life Month. This month-long celebration of life was first established by Donate Life America in 2003. Below is some essential information to help you celebrate. National Pediatric Transplant Week Brand new this year is the National Pediatric Transplant Week. Celebrated April 23-27, 2018, National Pediatric Transplant Week was created in collaboration with […]
Power Player – Holly
I was the youngest by three minutes. So, I suppose being a twin help me to fight, to give me the will to live from day one. The doctors knew something was wrong. I don’t think we ever did get a satisfying answer as to why I was sick. I ended up being the youngest […]
Power Player – Brooke
March 28th, 2018, marks our one-year Kidneyversary. Last year I was a 38-year-old wife and mother of 2 boys who were 7 and 9, and I decided to be a kidney donor for my brother-in-law. This would be his second kidney transplant. My brother in law, Rob, was diagnosed almost 15 years ago with FSGS. This […]
Power Player – Cynthia
Cynthia Infante is a two-time kidney transplant recipient. She was born in 1972 in Arizona and has lived there ever since. She was first diagnosed with kidney disease at the age of 15 and at the age of 19 she was placed on hemodialysis. While on dialysis, she remembers sitting for three to four hours […]
Law & Order Episode on Organ Donation
On March 14, 2018, an episode of Law & Order SVU aired which featured a story about a child’s organs being recovered without the consent of her parents. While this episode was not based on a true story, the message it portrays is damaging to the public’s trust around organ transplantation and donation. In the […]
Power Player – Anna
I never had any problems growing up and was “normal” for all I knew. I was 21 years old and in my 2nd week of nursing school when I became short of breath for over 3 days. Finally, I went to the ER because of it. That day, I went from being “normal” to finding […]
Power Player – Brigette
Written by: Brigette McKern At the age of four, I was diagnosed with Cystic Fibrosis – a disease that affected my lungs and digestive systems. Even with receiving quality care, my parents were told I would most likely not survive past school age. My parents kept me compliant with treatments, medications, and appointments, and as a […]
Power Player – Matt
My name is Matt Kishbaugh. I will be 35 on January 28, 2018. I live in Pennsylvania. My family and I know what it’s like to deal with kidney disease. I was 13 when I was diagnosed with polycystic kidney disease. Polycystic kidney disease is where a cluster of cysts form inside your kidney. The […]
Power Player – Rachel
Written by: Rachel Adams I donated altruistically to a woman in Pennsylvania. I think I’ll always remember the moment they told me her creatinine levels had gone down to normal. The sun was shining outside my hospital window and my mom and best friend were in the room. I didn’t know how many transplants were […]
February 14th is National Donor Day – Are You An Organ Donor?
For some, February 14th is filled with flowers, balloons, and chocolate hearts. But for those who advocate for organ donation, February 14th is a much bigger day – it’s National Donor Day. National Donor Day was established by the U.S. Department of Health and Human Services, the Saturn Corporation and its United Auto Workers in 1998. […]
Power Player – Paul
Paul is avid about working out and staying healthy. He never misses an opportunity to go to the gym and improve himself. He is also the recipient of two double lung transplants. When Paul was born, he was diagnosed with Cystic Fibrosis. Despite his illness, he played sports and remained active growing up. He believes […]
Power Player – Jennifer
When Jennifer was 14, she was diagnosed with polycystic kidney disease (PKD). Her journey eventually led her to dialysis and to the transplant waiting list. On September 9, 2016, she received a phone call around midnight. Her doctor asked her about dialysis and when she had last eaten. Then, she found out that a kidney […]
Power Player – Jordan
Jordan received a heart transplant as a child. He has been living life to the fullest – with a goal to be the first transplant recipient to visit every country in the world. Written by: Jordan D Marcia Follow him on Instagram and Facebook I was born with a rare, congenital heart defect known as transposition […]
Power Player – Tony
Written by: Tony Alfredo Leon Luna I am from Venezuela. I was diagnosed with myocardiopathy when I was 5 years old. I had my first pacemaker in 2005 and received another one 2011. After the second pacemaker, my heart was growing more and needed more stimulation. Since that the generator ran out faster, I received […]
Power Player – April
After a minor surgery in 2010, April discovered that she had chronic kidney disease. She then found out that she would need a kidney transplant. Unlike many patients with kidney disease, April never went on dialysis. She admits that she was too stubborn to start. Instead, she attempted to line up a living donor, although […]
Power Player – Edith
Edith was living a happy, healthy life when she suddenly became ill and was rushed to the emergency room. She discovered that that one of her lungs had collapsed and she was diagnosed with a lung condition called Lymphangioleiomyomatosis (LAM). She had been living with this condition for several years but was completely unaware. Unfortunately, […]
Power Player – Brandi
In 2014, I was living in Austin, Texas. I loved to exercise and lift weights. I enjoyed watching and playing sports. One day I notice my throat was sore so I went to the doctor. I was diagnosed with strep throat and prescribed antibiotics. After I finished my antibiotics, I noticed it was difficult to […]
Power Player – Miguel
Miguel was living a full life before his heart transplant. He had graduated dental school, started his own practice, and gotten married. In 2012, he began to feel sick. His face started to feel numb, so he went to see his doctor for tests. However, nothing was found in these tests, and he went back […]
Power Player – Stephen
Stephen was born with a very rare kidney disease called Autosomal Recessive Polycystic Kidney Disease (ARPKD) that affects both the kidneys and liver. The disease was discovered during his mother’s 27th week of pregnancy during a routine ultrasound. Doctors gave Stephen a less than 1% chance of living more than a few hours after he […]
Our Medicare policy for kidney transplants is totally irrational
This article was originally published on the Washington Post. By Marcello Tonelli and John Gill Marcello Tonelli is associate vice president of research at the University of Calgary. John Gill is a clinician scientist and professor of medicine at the University of British Columbia and a member of the board of directors for the American Society of Transplantation. They are both […]
Power Player – Riley
By: Riley Tucker My name is Riley Tucker and I am sixteen years old. When I was seven years old I had been diagnosed with strep throat for nine consecutive months. By this time the doctors were starting to think there had to be some underlying cause. My family was recommended to go to Arkansas Children’s […]
Teen Panel – Transplant Patient Summit
We created a “teen panel” at the 2017 Transplant Patient Summit. Find out what it is like to be a teenager and manage an organ transplant. These teens discuss medication routines, friendships, and challenges.
Power Player – Amanda
By: Amanda Washek My name is Amanda and I am alive because of organ donation. At age 23, I was diagnosed with a rare liver disease called Primary Sclerosing Cholangitis, a disease that causes scarring and blockage of the liver’s bile ducts. I went from a seemingly healthy, newlywed, young woman to needing a liver transplant […]
Power Player – Edward
Right before Edward’s 21st birthday, he was not celebrating. Instead, he was finding out that he had end-stage renal disease during a routine checkup. He would later find out that he needed a kidney transplant to survive. Edward had been excelling in school and sports, and now, everything was changing. Initially, his reaction was, “Why […]
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Power Player – Jen
By: Jen White Hi – I’m Jen – @mytransplantlife on Instagram. My Instagram page is educational in nature, as I’m a Registered Nurse with a graduate degree, having worked as a nurse educator, combining my health knowledge with my own kidney disease experience. I was diagnosed with Chronic Kidney Disease in my early 20s, as […]
AST-Endorsed VA Transplant Coverage Act Passes House of Representatives
On November 7, the Veterans Transplant Coverage Act was passed in the House of Representatives. Under this modified act, the Veterans Affairs Department (VA) could pay for a living donation to a veteran by any live donor, including at facilities outside the VA that are part of the Veterans Choice Program. Previously, the VA was […]
Power Player – Maria
By: Maria Margarita Gamboa I am the only child of a single mother. I was born in Caracas, Venezuela (October 12, 1971). I believe in God, love, friendship and good faith. I am in love with LIFE, my family, and friends, ballet, photography, organ donation, music, sailing, and nature. I am crazy about HOPE: […]
Power Player – Larysa
By Larysa Sholom My name is Larysa and I was born in a small town in Eastern Europe. Nine years ago, I graduated from college and was spending my last carefree summer far from home, in hot San Antonio, Texas. Things were normal, nothing you wouldn’t expect in the life of a 21-year-old girl. Until that […]
American Society of Transplantation Announces the First Organ Transplant Research Call-to-Action in the US
Mount Laurel, NJ – October 23, 2017 – Today, the American Society of Transplantation (AST) launches a new fundraising initiative called Power2Save to address the critical need for funding transplant research and to increase public awareness for organ donation. Approximately 50 percent of all transplanted organs will experience failure within five to ten years, typically due […]
Transplant Patient Summit Live Stream
Thanks for watching the live stream! Transplant Patient Summit: Day 1 (part 1) Transplant Patient Summit: Day 1 (part 2) Transplant Patient Summit: Day 2 (part 1) Transplant Patient Summit: Day 2 (part 2) Appearances from Members of Congress: Jaime Herrera Beutler Jerrold Nadler Raul Ruiz Transplant Patient Summit 2017 Program Record your Tribute […]
Power Player – Talitha
By Talitha Juristo On March 4, 2016, after some routine lab work, I got a call from my doctor to go straight to the ER because my hemoglobin was dangerously low and my creatinine was high. Once at the hospital, they quickly realized I was in end-stage renal failure. 30 years of being a Type […]
Power Player – Tawny
By Tawny Blum As a kid, I was very active – shocking I know! I played basketball and softball all the time, that was until the summer before my senior year of high school (1996). I started having GI issues but at that age, who wants to talk about having diarrhea! Eventually, I was diagnosed […]
Selena Gomez Is Working on a Documentary Highlighting Her Health Issues
Last month, singer and actress, Selena Gomez, announced on Instagram that she had received a living kidney donation from actress, Francia Raisa. Now, Selena is gearing up to tell her story through a documentary about her health issues, including her battle with lupus and her kidney transplant. According to an insider, “Since having the transplant, Selena’s […]
Power Player – Alice
By Alice Vogt I am South African and was born with Cystic Fibrosis, a genetic disease affecting the lungs and digestive system. I was diagnosed at age two, and my parents were told that there is about a 20% chance of me reaching the age of 20. However, I had a fairly normal childhood, apart […]
Power Player – Lisa Barker
After living a healthy and happy life, Lisa suddenly discovered she had a condition that only one in a million people develop. Soon after, she was put on the waiting list for an immediate liver transplant. Now, she and her husband are advocates for organ donation and transplant research. By Lisa Barker 2014-the start to […]
AST Statement on America’s Got Talent’s Angelica Hale
On behalf of the American Society of Transplantation (AST), I would like to congratulate Angelica Hale for her success on NBC’s America’s Got Talent. Last night on the show’s finale, Angelica came in second place, but her inspiring transplant story has touched millions. At the age of 5, Angelica lost kidney function after double pneumonia. To keep […]
Kidney Recipient, Angelica Hale, Performs at America’s Got Talent Finale
10-year-old, Angelica Hale, has been stirring up a lot of national attention with her incredible voice and journey with kidney disease. At the age four, she was diagnosed with double pneumonia, which caused both of her kidneys to fail. She was on dialysis for 18 months before she received a transplant from her mother. Angelica […]
Power Player – Melanie
Melanie is just six months old, but she has been through a lot since she was born. When she was two months old, her parents were told that their little girl had been diagnosed with biliary cirrhosis which was causing liver cirrhosis. Unfortunately, the first surgery attempt to help Melanie was unsuccessful and caused her […]
Selena Gomez Receives Kidney Transplant
Selena Gomez just announced on Instagram that she underwent a secret kidney transplant over the summer to help in her fight against Lupus. She posted the news on Instagram early Thursday morning as an explanation on why she had been inactive during the summer. She received the gift of life from longtime friend and actress, Francia […]
Power Player – Bill
Bill considered himself to be a “lucky boy” growing up. He had a great relationship with his father; they played catch and watched baseball games for hours. He grew up in a Catholic household, where he attended church every week and was an altar boy with his brother. However, his perfect childhood came to an […]
Transplantation and Organ Donation Hitting the Big Screen
On September 29, 2017, a transplantation and organ donation focused film entitled “A Question of Faith” will begin playing in theaters. This film features three families who live in the same community and addresses organ, tissue, & eye donation advocacy. The trailer for this movie can be seen here. Sign up for our […]
Power Player – Christine
On October 24th, 1998, at Cedars-Sinai Medical Center, Christine Galan became the first heart and liver transplant recipient in the Western United States. It was a new procedure, but Christine never doubted that it was for the best. Christine was born in Jamaica and moved to San Diego as a child. When she was a […]
UNOS Founder, Gene Pierce, Dies at 87
UNOS founder and original executive director, Gene Pierce, has passed away at the age of 87. Pierce began his transplant career in 1964 as a surgical administrator at the Medical College of Virginia (VCU Health). In 1984, UNOS was founded with Pierce as its executive director. Pierce retired in 1995. The national network had grown […]
Power Player – Rima
Rima has spent most of her life in and out of hospitals due to Cystic Fibrosis. She knew she would eventually need a double lung transplant, but for so long, she was told that she wasn’t sick enough. She was so used to being told it wasn’t time, that when she was finally told that […]
OPTN/UNOS Public Comment
There is currently a lot going on regarding liver allocation. The transplant community is at a crossroads with the OPTN/UNOS Liver and Intestinal Organ Allocation Committee’s recently released public comment proposal on enhancing liver allocation. The new proposal aims to balance equity in access to liver transplants and recognize concerns that are raised regarding the […]
Power Player – Jean
By Jean Mihich One never knows what journey we will undertake in this lifetime. I must say that my journey as a person with kidney disease began in infancy and continues to this day. It has been a series of small steps towards awareness and understanding, which was first started by my parents who had […]
Power Player – Mary
By the time Mary was 12 years old, she had already received her second kidney transplant. After being on peritoneal dialysis for two years at 3-years-old, Mary’s kidneys completely failed by the age of 5. At 5 years old, Mary received her first kidney transplant. Both of Mary’s transplants were from deceased donors, as none […]
Power Player – Rachel
After watching a Katie Couric news segment in 2010, Rachel Bennett Steury made a decision that would change the life of someone she never met. The program was on kidney chains, kidney donation, and organ donation. Rachel never knew that kidney donation was possible while still alive. “I felt like Katie Couric was talking directly […]
Power Player – Nai
A PowerPlayer is anyone who supports the life-saving cause of organ donation and transplantation, from the patients who receive transplants to the donors and their families who make those transplants possible, to those who donate and create fundraisers for research. They serve to remind us that we all have the Power2Save. Our latest, Power Player, Nai Azzi, […]
Power Player – Glenda
When 15-year-old Glenda Daggert was diagnosed with Type I diabetes in the early 1960s, “you hid diabetes.” In spite of her illness, Glenda went on to earn degrees in physical education and instructional technology, then teach for several years. She married Ira Copperman, moved to New York, and joined IBM. After 30 years with the […]
Power Player – Cheryl
A PowerPlayer is anyone who supports the life-saving cause of organ donation and transplantation, from the patients who receive transplants to the donors and their families who make those transplants possible, to the medical professionals who arrange and perform the life-saving miracle of transplantation. They serve to remind us that we all have the Power2Save. […]
Power Player – Tom
Reading can often change our lives or make us think differently. In Tom’s case, reading a blog post from political writer, Virginia Postrel, changed his life and saved another. After reading the blog, he discovered that Postrel planned to donate one of her kidneys to author, Sally Satel. Although Tom did not know anyone who […]
Power Player – Crissi
After overhearing a conversation between her daughter and her daughter’s friend, Crissi made a decision that would change the life of a man she had never met. When her daughter was in high school, Crissi overheard a casual conversation that her daughter was having with a friend. The friend’s father needed a kidney transplant and […]
AST President Featured in USA Today
The President of the American Society of Transplantation (AST), Ron Gill, has been featured in an article published by Media Planet and included in USA Today. The article highlights the challenges that transplant recipients face such as organ rejection, medications, and the long waiting list. In addition, the article touches on the importance of the upcoming […]
Power Player – Lisa Washington
Lisa was born with scarred kidneys. By age 7, she was diagnosed with kidney disease. At 7, Lisa didn’t quite know what that meant, but thankfully, she was able to have a normal childhood. She always knew she would eventually need a kidney transplant, but she continued to live her life, got married, and had […]
Power Player: Lou Ann
There are a number of online pleas for living organ donations for those in need of a kidney transplant. It is a difficult ask for those in need, and it is a significant sacrifice for those who choose to answer. Our latest Power Player, Lou Ann, was surfing the web one day in 2014 when […]
Father’s Day Power Player: Alice
With Father’s Day upon us, most of us who are lucky enough to have our father’s in our lives are finalizing plans, buying gifts, and signing cards. It’s an important day to recognize. Our fathers are part of the reason we were given life. Our latest Power Player, Alice, won’t be able to find the […]
2017 Research Grants
In 2017, the American Society of Transplantation (AST) and the Transplantation and Immunology Research Network (TIRN) facilitated providing $460,000 in research money to investigators in the field of transplantation. TIRN provides both career development grants for young investigators and research funding in specific areas along with outside organizations. AST TIRN/Astellas Clinical Science Faculty Development Research […]
Power Player: Kati
A PowerPlayer is anyone who supports the life-saving cause of organ donation and transplantation, from the patients who receive transplants to the donors and their families who make those transplants possible, to the medical professionals who arrange and perform the life-saving miracle of transplantation. Kati was presented with an opportunity to save someone in her […]
Power Player: Jason Nothdurft
Community service has always inspired Jason Nothdurft. For 66 years, his grandfather served at his local volunteer fire company, followed by his father, who served 25 years, and Jason, who has served five years. His family has been recognized as the first family in New Jersey to have three generations volunteering in the same department […]
22 Years After His Death, Nicholas Green’s Heart Stops Beating
By Reg Green In 1994, The Green family was on vacation in Italy when tragedy struck. Their son, Nicholas, was killed by highway robbers. His parents, Reg and Maggie, decided to donate his organs, which saved the lives of seven people and tripled organ donation in Italy. Today, Reg Green continues to speak out about […]
American Society of Transplantation Welcomes Dr. Ronald Gill as New President
Mount Laurel, NJ – May 11, 2017 – The American Society of Transplantation (AST) announced its recently elected 2017-2018 board members, including its new president, president-elect, and secretary, at the American Transplant Congress (ATC) in Chicago. The AST inducted its new president, Ronald Gill, PhD, during its annual meeting on May 1, 2017. Dr. Gill is […]
How Will the AHCA Law Impact Transplant Patients?
The American Society of Transplantation (AST) recently issued a statement regarding the newly passed American Health Care Act (AHCA). The AST has several concerns about the law, as it is likely that it will result in many transplant patients losing insurance coverage. For more information, read the full release.
Power Players: The Vargas Family
Sarah Vargas, and her husband, Tony, are true Power Players in our eyes. Their daughter, Rosalina, was born with Maple Syrup Urine Disease (MSUD), which was discovered when she was four days old through newborn screening. At just 11 days old, the couple came close to losing their daughter. After that, they vowed to do […]
Lindsey’s Story: One Transplant for Life
At only 14 years old, Lindsey Duquette bravely testified before the FDA about the importance of organ transplant research and organ donation. As a young child, she contracted a rare kidney disease that resulted in hundreds of hospitalizations and the need for a kidney transplant. Luckily, her father was the perfect match. Hear her story […]
Power Player: Frank Greaney
Frank Greaney is happy to be alive, and he credits his survival to his organ transplant. In 1997, Frank Greaney was diagnosed with an autoimmune liver disease, Primary Sclerosing Cholangitis (PSC). PSC is a progressive liver disease for which there is no cure. He was soon listed for a liver transplant in the New England […]
Power Player: Steven Turner
Seven years ago, Steven Turner made a “Good Samaritan” decision – he became a living donor to a stranger. His story is truly heartwarming, as his selfless act kept another family whole. At the time, there was local news coverage about a young family that was facing the nightmare of kidney failure. The couple had […]
Manchester United and England Former Player Receives Kidney Transplant
Former Manchester United and England player, Andrew Cole, has received a kidney transplant. The 45-year-old suffered kidney failure after contracting an airborne virus in 2015. Manchester United released a statement, which indicated that Cole will be taking a break from his club ambassador role during his recovery. On behalf of Cole, the club issued the following statement, […]
April is National Donate Life Month
On March 31, 2017, President Donald J. Trump released a statement proclaiming April as National Donate Life Month. This month was first proclaimed in 2003 by President George W. Bush. This month, Power2Save will be honoring organ donors, recipients, and those who advocate in several ways – including featuring several stories from those who have […]
Power Player: Todd Gambill
We had the opportunity to chat with kidney recipient, Todd Gambill, on the one year anniversary of his kidney transplant. Todd shared his incredible story, although he insists that it is his donor’s story. When Todd was just a year old, he was diagnosed with a Wilm’s Tumor, which is the most common type […]
Transplant Pioneer, Dr. Thomas E. Starzl, Dies at 90
Thousands of lives are saved every year by organ donation and transplantation. The treatment of transplantation has allowed recipients to experience longer lives and has given them a second chance at life. This treatment, however, would not be possible without the researchers and surgeons who perform these acts. Dr. Thomas E. Starzl was known as […]
AST President Interviews on NPR About Kidney Transplants
Earlier this week, the President of the American Society of Transplantation, Anil Chandraker, was interviewed on NPR’s “The Point” about kidney transplants. He was joined by a kidney transplant recipient, Hanu Singh, in a fantastic show that provided an overview of the role of the kidney, kidney transplants, and AST’s Power2Save initiative. There are more people in […]
Charity Navigator Has Awarded Power2Save with 4-Star Rating
Power2Save, which was created by The American Society of Transplantation (AST), has been awarded a 4-star rating from Charity Navigator. Charity Navigator is the largest charity evaluator in America and it’s 4-star rating is its highest rating given to organizations. This rating has been given to AST and Power2Save as a result of its strong financial health […]
21-Year-Old Army Reservist from Colorado Donates Kidney to Stranger
A Boulder woman received a kidney donation from a complete stranger who said it was the right thing to do. Kelsey Crider’s mom, Debbie Crider, said it still gives her goosebumps. Nate Toci was driving by a rotating billboard along Interstate 25 in Monument on his way home from work one day when he saw the sign seeking a kidney donor for Kelsey.
Do You Realize that You’re a Champion in Their Eyes?
Bob Stewart took on a daunting task in 2015. After being tested as a donor for his wife Michelle, he was found to be an incompatible blood type. After many others stepped forward and were either denied or incompatible, Bob knew he had to think outside the box.
2016 Research Grants
In 2016, the AST Transplantation Immunology Research Network (TIRN) facilitated the allocation of over 1.3 million dollars in research funding to investigators in transplantation. In addition to the annual career development grants that AST has awarded for over 20 years, the AST TIRN has aligned with outside organizations to offer research funding in specific areas of study.
Power Player: Isabel Stenzel Byrnes
Despite being born with the incurable genetic lung disease cystic fibrosis (CF), Isabel Stenzel Byrnes and her twin sister, Anabel Stenzel Byrnes, persevered to live rich lives and become advocates for organ donation and transplantation.
PowerPlayer: Rita R. Alloway
Fascinated by the complexity of drug regimens and the value they have for long-term success of organ transplantation, Rita Alloway, PharmD, FCCP, uses her pharmacology background in the transplantation field. “I still consider transplantation a modern-day miracle that is life-altering when it is successful,” says Dr. Alloway.
Power Player: Lindsay Ess
For Lindsay Ess, hands are a gift and something she feels truly blessed to have. She was part of the relatively new hand transplantation surgery (that only about 70 people around the world have received) to improve the quality of her life. Now, she continues to support organ transplantation community to offer this and other […]
Impacting Liver Transplantation
“We have the ability to give the option of life to many people who are exceptionally sick and about to die,” says liver transplant researcher Sergio Duarte, PhD. “That is what I really like about my research — the ability to help and impact so many people.”
Power Player – Jason Kilderry
Jason Kilderry was an avid and passionate competitive runner in high school, but a polycystic kidney disease (PKD) diagnosis his freshman year of college brought an end to his racing days. “The most difficult part of the struggle with PKD was the impact it had on my abilities as an athlete,” says Jason. As the […]
Celebrating Life at the Donor Dash
Members of the American Society of Transplantation (AST) and the American Transplant Congress (ATC) staff participated in the Gift of Life’s 20th Annual Donor Dash on Sunday, April 19, 2015.