Archive for the ‘Uncategorized’ Category

Kidney donor’s gift pays off at graduation

Monday, July 19th, 2010

By news-press.com • July 19, 2010

Almost five years ago The News-Press editorial cartoonist, Doug MacGregor, donated a kidney to his high school friend, John Bielefeldt.

John, 53, has a polycystic kidney disease, a genetic, incurable disease that created cysts that covered his kidneys. The News-Press wrote about their reunion and successful surgery in Jacksonville in September 2005.

One of the many reasons Doug donated his kidney was so John could live to see his oldest son graduate from high school.

That wish came true a few weeks ago.

Eric Bielefeldt, 18, graduated with honors from Creekside High School in Jacksonville, and John and Doug applauded for him side by side.

“It was a proud moment,” Doug said. “One of the greatest days for parents is to see their kid graduate.”

Doug plans to attend the high school graduation of the two younger Bielefeldt children.

John was thrilled to have Doug share the day with his family.

“He’s a great guy with huge heart,” John said. “We’ve gotten closer with this bond. It’s humbling and I am very grateful.”

John said his health continues to improve. And Doug has had no medical problems since donating his kidney.

“I would encourage anyone to consider an organ transplant, specifically a kidney,” Doug said. “It was worth every moment.”

Kidney donation chain reaches Grand Rapids

Tuesday, May 11th, 2010

Jessica Puchala

GRAND RAPIDS, Mich. (WZZM)- There’s proof in Grand Rapids today that one person’s generosity can affect many lives. It all started with an anonymous kidney donor in the Southern part of the United States who started a chain reaction.

From that one anonymous donor four people were able to get a kidney donation. That donor started a chain that reached from an unknown southern state to South Carolina, to Sacramento, California to Grand Rapids, Michigan.

One of those recipients is Sam Karadsheh. Here’s where it gets confusing. Sam’s sister Suhad wanted to give him her kidney, but she wasn’t a match and no other match could be found. As a result, Saint Mary’s Hospital’s Donor Coordinator signed Sam up on a donor exchange list. From there they were able to connect with the woman in Sacramento who donated her kidney to Sam. Now Sam’s sister is donating her kidney to a man in Rockford.

Suhad Shatara says, “I’m happy everything’s go good and I can’t wait to do mine actually. I ask the doctor today hey take a break go have cup of coffee and come to me because I want it done.”

From there the Rockford man’s wife will donate her kidney once she finds a match. So you can see why it is called the Paired Donor Exchange. It creates a chain that Missi Ostapowicz with Saint Mary’s Kidney Donor Program says not only saves a life but creates a bond.

Ostapowicz says, “It’s a special kind of donor I believe that comes forward and says I’m willing to go out of state and heal in an unfamiliar area, people I don’t know at a hospital, they are willing to do that for their loved one I think says something extra special.”

There’s no telling how long this chain could go. The longest one was 26 lives. It doesn’t cost the donor anything to donate their kidney.

April is organ donation month.

Altruistic Organ Donors Give To Perfect Strangers

Tuesday, March 30th, 2010

By Kenny Goldberg

March 18, 2010

Most live kidney donors give to a close family member. But each year, a small number of people give a kidney to someone they don’t even know.

At San Diego’s Sharp Memorial Hospital, Kay Wolff sits in a private room filled with orchids and roses.

She’s not here because she’s sick. Wolff is 72 years old, and in excellent health.

She’s recovering from surgery to remove one of her kidneys. A few days ago, Wolff donated it to a complete stranger.

“It’s a little extreme to give an organ,” Wolff admits, “but I felt extremely motivated to do it. I just felt this is a way to leave a legacy, and to really help someone in an important way.”

It took her years to decide this was the best gift she could give.

“Some people give money, and some people give their time,” Wolff points out, “but I thought this is something that I thought was significant and important, and I think it’s a time to think about donating an organ.”

None of her family needed a kidney. Wolff had tried to donate to some friends who had kidney disease. But she was never a good match. So she decided to donate to a perfect stranger.

That lucky person is Zeny Pruna. She’s been on kidney dialysis for the past six years.

Pruna came out of the transplant surgery with flying colors.

“When I wake up, they say that the kidney is working already,” Pruna recalls. “That’s a miracle for me, also. I’m very thankful.”

Altruistic organ donors are extremely rare. There are only about 100 in the U.S. each year.

Like other people who want to donate an organ while they’re still alive, altruistic donors go through a battery of medical tests. Then there’s another level of scrutiny.

Cathy Chappell is a social worker with Sharp’s kidney transplant team. She puts potential altruistic donors through an extensive interview.

“We’re looking at someone to make sure they aren’t looking for notoriety, they don’t want a lot of publicity about this,” says Chappell. “Anybody who wants to have some kind of unusual relationship with the recipient, we’re not interested in that. We really want someone who just wants to be, you know, a caring humanitarian.”

Chappell says they’re looking for a fully informed, stable person whose life won’t be adversely affected by the donation.

And she says Kay Wolff made the cut.

“I’ve been with the transplant center for five years, and in that period of time, we’ve had numerous people come to us wanting to donate altruistically,” Chappell says. “This is the first one who’s passed our screening.”

There are 17,000 kidney transplants performed each year in the U.S. Doctors say it’s a relatively safe operation. But there are risks.

Dr. Robert Steiner is the director of transplant nephrology at UCSD Medical Center. He says potential altruistic donors need to be fully informed.

“If you’re going to give a kidney,” says Dr. Steiner, “You need to know you have, depending on how old you are and your other circumstances, anywhere from let’s say one percent up to six percent risk of going on dialysis some day, and that time would be shortened if you gave a kidney. But you also need to know that you could give the gift and it is possible that a person could leave the hospital with the kidney not working at all.”

Steiner says even if it is working, it may not last.

At 15 years, about half of those who receive a live kidney are back on dialysis, and about 4 percent of transplanted kidneys fail after one year.

Still, Kay Wolff is glad she stepped forward. And she’d like to do more. But she’s not sure how she can top this.

“I don’t know, but I’ve been thinking about bone marrow,” says Wolff, “And I understand that that’s a piece of cake after a kidney.”

About 1,500 San Diegans are still waiting for a kidney. With an average wait time of three to five years, some of them will die before they make it to the top of the list.

B.C. transplant patient finds kidney online

Tuesday, March 30th, 2010

CTV News Video
Michele Brunoro on kidney donoR

By: ctvbc.ca

Date: Thursday Mar. 25, 2010 11:09 AM PT

Dave Wilson has been on a kidney transplant waitlist for four years. Now he’s recovering from a successful transplant, thanks to a donor he found after placing an ad online.

His wife Lois placed an ad on Craigslist out of desperation when she realized she wasn’t a match.

“I’m willing to donate my kidney to someone else out there who needs it, if they have a partner who’s willing to donate their kidney for my husband,” Lois told CTV News.

Publicity surrounding the ad finally helped Dave find a donor. Of 30 people who came forward, a complete stranger ended up being a perfect match.

What’s he getting out of it?

“The satisfaction,” Lois said. “He said, ‘I can donate it because I have two.’”

For Dave, this means a chance at freedom from the four hours each day, three days a week, that he spends hooked up to a kidney dialysis machine.

The Wilsons say no money was ever exchanged, and Lois didn’t have to give up her kidney in a trade.

But the donation is still highly controversial.

Dr. Paul Keown, Director of Immunology at Vancouver General Hospital, says cases like this might be problematic for the kidney donor system.

“It creates competition between patients on the list when we have multiple personal appeals for organs, and it really undermines the whole structure of the waiting list,” he said.

Anita Ho of the UBC Centre for Applied Ethics said placing an ad raises ethical questions, too.

“When we’re talking about putting up a private ad, there’s very little checks and balances happening in the private realm, so some people might worry that now kidneys can become a commodity,” she said.

There’s already a paired exchange registry that sets up the kind of donations the Wilsons sought on Craigslist.

As for the mysterious kidney donor, he’s asked not to be identified.

“I just think he’s the most wonderful man. He’s my hero, and it’s too bad in a way that he wants to remain anonymous,” Lois said.

5 good Samaritans start chains of life

Tuesday, March 30th, 2010

Chicago-area kidney donors lead to linked transplants across country
Kidney transplants

Would you consider donating one of your kidneys to a stranger?
o Yes
o No
By Judith Graham, Tribune reporter

March 30, 2010

Five Chicago-area adults who have stepped forward to give kidneys to strangers may help save the lives of as many as two dozen people, thanks to transplant chains that will multiply the impact of the donations.

Two of the donors are young women in their early 20s, in perfect health and eager to help others. One is a dad honoring a 17-year-old daughter killed in a car accident. Another is a dental hygienist inspired by her father’s death. The fifth is a woman eager to repay a cousin’s act of kindness.

The transplant chains — a new development in the field of kidney transplantation — begin when someone like these five people offers to give a kidney to a stranger. Often, the designated recipient has a friend or relative who is willing to donate but prevented from doing so by medical circumstances.

If that friend or relative decides to give an organ to a stranger who is a better match and that second recipient has loved ones willing to repeat the favor, the chain adds more links. The goal is to allow the first generous act to help as many people as possible.

No transplant chains had originated in Illinois until Loyola University Medical Center entered the five so-called “good Samaritan” organ donors with the National Kidney Registry, an organization that helps arrange matches between potential kidney donors and recipients.

In doing so, Loyola committed to sending the organs wherever they were needed most. “That’s really unusual,” said Garet Hill, founder of the registry, which is working with about 50 hospitals across the country.

Medical centers tend to hold on to good Samaritan donors, seeking to help their own patients. That practice can make it hard to arrange timely matches, and even when they succeed, only one transplant results.

From Loyola’s perspective, chains have a much bigger impact, justifying a different approach. “We see every good Samaritan donor as a national treasure, not an institutional commodity,” said Dr. John Milner, director of Loyola’s living donor kidney transplant program.

A single large pool of donors and would-be recipients could facilitate more matches and shorten long waiting lists for organs significantly, he predicted. The National Kidney Registry has launched 17 chains resulting in six transplants apiece, on average.

Three chains will emerge from the five Chicago-area donors. The first started on March 18, when Christina Lamb, 45, of Melrose Park, gave a kidney to Robert Rylko, 21, of Rockford, who has Alport syndrome, a degenerative disorder.

Lamb wanted to give something back after her husband, Allen, received a kidney from a cousin in May 2006. “Someone close to us gave my husband the gift of life; I felt it was important to do the same,” she said.

The match was arranged after Loyola entered Lamb’s and Rylko’s information with the National Kidney Registry, along with information about Cynthia Ruiz, another donor.

Ruiz, 22, who lives in La Grange, came forward after her mom, Amy, became friends with Rylko’s dad on the Internet and told Ruiz about Rylko’s illness.

“It was really, really upsetting, and I wanted to do something,” Ruiz said.

Testing revealed that she was a “universal donor” who could be a match with any number of people. Knowing that Rylko could get a kidney from Lamb, she agreed to give to a stranger.

That made all the difference to Melissa Clynes, 19, of St. Louis, who had a heart transplant as a child and a kidney transplant at 16 after anti-rejection drugs wreaked havoc on her body. Her mother, Mary, donated that kidney; it was destroyed last year when Clynes contracted a virus.

With the teenage girl on waiting lists at St. Louis Children’s Hospital and Northwestern Memorial Hospital, her mom distributed 11,000 fliers in St. Louis earlier this year asking potential donors to come forward. Eighteen people did, but none worked out.

This month, in despair, her mom Googled “how to find a live kidney quickly” and found the National Kidney Registry. Hill arranged for the family to register Clynes, and almost immediately a match with Ruiz popped up.

The young women’s operations took place Monday at Loyola. Both are reportedly doing well.

The next link in the chain is Clynes’ 23-year-old sister, Sarah, a senior at the University of Illinois at Chicago who hopes to go to nursing school next year. Sarah Clynes’ kidney is likely to go to New York, Milner said.

A second chain will start when dental hygienist Jodi Tamen, 45, donates a kidney in early April, probably to a patient at Ronald Reagan UCLA Medical Center. Tamen lives in West Frankfort and works at Loyola.

Her motivation springs in part from the memory of her father, who died of a heart attack at 62. “I just feel a strong pull to do this,” she said.

The third chain begins with Tim Joos, 53, of St. Charles, who plans to donate a kidney in mid-April. Joos is honoring his daughter Samantha, who died at 17 in a car crash almost seven years ago. Samantha had signed up as an organ donor when she got her driver’s license.

Joos has spoken often to high school students about the importance of organ donation. Last year, he said, “I began to ask myself why I didn’t do this myself.” His kidney is expected to go to a hospital in Philadelphia.

So far, the National Kidney Registry has arranged 112 transplants. Another 30 donors and recipients have been tentatively matched and are awaiting final medical approval, Hill said.

No center has listed as many donors as Loyola. “I almost fell off my chair,” Hill said. “Nothing like that has happened until now.”

Anthony Atala on growing new organs

Saturday, February 20th, 2010

See webinar link below:

copy and paste to your browser -
http://www.ted.com/talks/anthony_atala_growing_organs_engineering_tissue.html

Very interesting!!!

Number of new donors doesn’t keep pace with those needing organs

Sunday, February 14th, 2010

February 14, 2010

In the summer of 2008, Tanya Conrad sent an e-mail to about 50 relatives and close friends, asking if anyone could do her a favor: give up a kidney.

“It is very hard for me to ask you guys this,” she wrote. “But I am in need of help.”

Nearly two years later, Conrad, 36, of Abrams, has joined 1,500 other Wisconsin residents on a transplant waiting list that organ donation advocates wish did not even exist.

About 3,000 people in the state die every year, providing more than enough kidneys, hearts, livers and other organs for everyone who needs a transplant. However, not enough are donors to fulfill the need.

For Conrad, who was diagnosed with kidney disease 10 years ago, that means a life of agonizing uncertainty, with no assurance that a donor will be found before her health deteriorates even further.

“There’s nothing I can do about it,” she said. “That’s what is frustrating about it. I can’t do anything to help myself.”

To promote organ donation, a number of health organizations and others have designated today as National Donor Day — an occasion for people to consider organ, tissue or blood donation.

In Wisconsin, proponents hope to see a significant increase in donations starting in April, when Wisconsin launches a new online organ donation registry.

Rather than waiting to declare themselves organ donors when their driver’s licenses come up for renewal, people will be able to register online. Wisconsin is one of the last states in the country to provide such an online service.

Trey Schwab, outreach coordinator for the University of Wisconsin Hospital Organ Procurement Organization, said he hopes the registry will boost donations statewide from the current 54 percent of all residents aged 16 or older to more than 70 percent — the level in Oklahoma and other leading states.

“That’ll be a big step,” he said of the registry.

The waiting list for an organ has remained fairly steady in Wisconsin at 1,500 people, Schwab said. Depending on the type of organ, the average wait is two to three years.

Sisters tout need for more organ donations

Sunday, February 7th, 2010

By Kevin Haas
RRSTAR.COM
Posted Feb 05, 2010 @ 12:24 AM
Last update Feb 05, 2010 @ 12:26 AM

MACHESNEY PARK — Denise Snelling works to spread a simple message about organ donation: It’s simple.

Snelling saved her sister Michelle Vronch’s life with a kidney donation July 8.

“I don’t think people realize that after this happens, you’re just the same,” Snelling said. “I do everything that I did before. If I had another one to give, I’d give it away, too.”

Both women are back to their normal lives. Vronch returned to work at the Harlem Community Center in mid-October.

“You could tell before that she was tired and needed the transplant,” said Shannon Scheffel, director of Harlem Community Center. “But ever since, she’s been full of energy and raring to go.”

The sisters promised to spread the word about organ donation.

Snelling, of Lexington, S.C., is outgoing by nature. She has turned to local politicians and those seeking office with her goals to bring a transplant program to South Carolina.

Public speaking never came as easily to Vronch, but she has decided to step out of her shell to spread the message.

She’ll share her story at a Rockford Network of Professional Women luncheon at 11:30 a.m. Feb. 15 at Forest Hills Country Club, 5135 Forest Hills Road, Rockford.

“This is so important to me that I just have to overcome that fear,” Vronch said. “If I can get just one person to sign the back of that driver’s license, then I’ve accomplished something.”

Doctors diagnosed Vronch with polycystic kidney disease in 1992. The disease progresses slowly and is characterized by the growth of cysts, which prevent healthy kidney function and often lead to kidney failure.

Polycystic kidney disease is the most common life-threatening genetic disease, according to the National Kidney Foundation.

The disease affects more than 600,000 Americans and an estimated 12.5 million people around the world.

Vronch said she also hopes to organize an annual program to benefit transplant recipients and their families who may struggle to pay medical costs.

She’ll first be the recipient of such an event. Family and friends have organized a benefit for her Sunday.

“I have to pay it forward. That means a lot,” Vronch said.

Staff writer Kevin Haas can be reached at khaas@rrstar.com or 815-987-1354.

“Why do people choose to become live organ donors?”

Saturday, October 17th, 2009

http://www.timesonline.co.uk/tol/life_and_style/health/article6867112.ece

Christine Toomey

Every time Barbara Ryder lifts the latch on the gate of her terraced cottage deep in the Cornish countryside, she is reminded of the unique gift she made to a complete stranger. Two years ago, Barbara underwent surgery to have her left kidney removed so that it could be implanted in a man nearing death. The person whose life this saved, she later learned, was a retired carpenter; he crafted a wooden picket fence for her in gratitude.

Near Barbara’s front door hangs a black-and-white photograph of her mother as a young woman dressed in military uniform. It provides a clue to the deeply personal reason that Barbara, 60, put herself through major surgery for somebody she didn’t know. Her mother, an army private who served in Palestine during the second world war, suffered from severe mood swings and died when Barbara was in her early twenties. “I could never please my mother and I don’t remember her ever telling me she loved me,” Barbara says in a quiet voice after several hours of conversation. “If I’m honest, maybe this was a way of trying to do something that would finally please her.”

She has another, more straightforward explanation for volunteering to become one of this country’s first “altruistic” kidney donors. To her, there can be nothing more worthwhile as a human being than to save the life of another. “If I had been a man I would have joined the fire brigade. I have always wanted to be able to rush into a fire and pull someone to safety.”

Andy Loudon, 69, received Barbara’s transplanted organ in an operation on the same day she donated it: September 18, 2007. “What Barbara did for me, her kindness, is unbelievable. It has given me a completely new life.”

Barbara, who lives alone with a menagerie of cats and a dog from rescue shelters, has been a nurse since the age of 17, when she joined the Queen Alexandra nursing corps and flew to Singapore at the height of the Vietnam war to treat injured soldiers. She remembers quite clearly the moment she decided to donate a kidney. In 2004 she was listening to a radio programme describing what patients with kidney disease feel about having to undergo regular dialysis — the process by which, three or four times a week, toxins are cleaned from their blood. “When your life is normal, you want it to be more exciting,” one said. “When you’re on dialysis you realise how exciting normal is.”

“That radio programme really brought home to me what they go through,” Barbara explains.

Looking back, Barbara believes she had reached a stage when many middle-aged people start asking questions about the value of their lives. She is also convinced that the hardships she has faced made her more sensitive to the needs of others. When her only son, Jeff, was a small child, his father “did a Reggie Perrin”, leaving his clothes on Brighton beach and disappearing. A later marriage ended in divorce. “Some people are so comfortable in their lives, it never occurs to them to think of giving back,” she says. “But many people in their middle years, perhaps with families grown, do ask themselves, ‘What can I do now to be useful?’ ”

Donating an organ to a stranger has only been made possible in this country by the Human Tissue Acts of 2004 and 2006. Before, there had to be a genetic link or “strong emotional tie” between any organ donor and recipient, to prevent the trafficking and sale of organs and to improve the chances of the transplant being a success. But medical advances and improved drugs that reduce rejection have now made it possible to carry out complicated transplant procedures between those who are not genetically related.

“It was not a question of why do it, but why not?” says Barbara. “I’m the sort of person who makes up my mind and does not change it easily. I don’t go in for a lot of soul-searching.”

But making the decision was just the first step. Initially, Barbara faced reservations from her son, Jeff, a 37-year-old father of two. “My mum has always wanted to make the world a better place,” he says. “I just felt that, as a nurse for 40 years, she had done enough. But I could also see she was determined, and knew it was the sort of thing her father would have done too.”

After registering her interest in becoming a living organ donor at the transplant unit in the hospital where she worked, Barbara was subjected to two years of stringent physical and psychological tests to make sure she could withstand the operation. These included ultrasound and specialised x-rays to determine that both kidneys were functioning normally — doctors had to be sure she could afford to lose one. There were also tests to check the chemistry of her blood and tissue type, and screening to rule out underlying medical problems such as diabetes, anaemia or high cholesterol.

While none of these physical tests bothered Barbara, the psychological vetting did. She had interviews with a clinical psychologist every month to six weeks for almost a year. “I understand they had to be very careful in assessing if the operation posed any risk to my mental health, and to keep checking that I hadn’t changed my mind,” she says. “But when the psychologist kept asking again and again why I wanted to do it, and I kept saying ‘because I can’, in the end she concluded I was ‘stubborn’. I took exception to that. From my point of view, I was just determined to do good.”

Barbara then had to be interviewed by Jon Bush, an independent assessor for the Human Tissue Authority (HTA), whose job was to draw up a report making a judgment about her motivation and ensuring she was both acting of her own free will and stood to gain nothing financially. The sort of person who might be considered “inappropriate” to become a donor, Bush explains, would be someone “with misguided beliefs such as thinking they would receive some sort of special spiritual blessing for what they were doing”.

After she had jumped through so many hoops, Barbara says, the surgery held no fears for her once a recipient matching her blood and tissue type was found (the risk of death to a living kidney donor is about 1 in 3,000). “I’m scared of flying and of going on blind dates. But I can quite clearly remember going into the operation feeling totally calm.”

After three hours of surgery her kidney was couriered by motorbike to Addenbrooke’s hospital in Cambridge, where Andy Loudon was prepped and waiting. “When I came round from my operation I was told, ‘It’s already plumbed in and working,’ medical jargon meaning the transplant had been a success,” Barbara recalls. “I felt a huge sense of relief.”

She then spent four days recovering in hospital “with little pain”, but was restless to return home to look after her animals. The day she was discharged she was out walking her dog and shopping in the supermarket. She was intensely exhausted, but her recovery was swift. She did feel “a few twinges of pain” in the first year, she says. She now swims, takes long hikes, cycles and says she feels “healthier than ever” — no more prone to illness than anyone else. For a year or so she felt “intense euphoria” at having made the donation; now she feels “a more quiet and lasting sense of satisfaction”.

It is unusual for an altruistic donor to learn the identity of the recipient, let alone get to know them well. Such transplants are carried out on a basis of strict anonymity. But recipients are permitted to pass a note of thanks through hospital co-ordinators after the operation has taken place. Contact rarely moves beyond this written exchange. Several days after the transplant took place, Andy and his wife, Hilary, wrote to Barbara to say how their lives had been transformed by the operation. Three months later, a meeting between the three was arranged by the HTA, keen to publicise the change to the law that had made altruistic donation possible. Barbara remembers that Andy was apprehensive when they first met at Brown’s Hotel in central London: “He was worried I would think he was too old and might wish my kidney had gone to someone younger.” (Recipients are chosen on the basis of greatest need and with the best blood and tissue match to the donor.)

Before the operation, Andy was asked how he would feel about receiving a kidney donated by a stranger. “I was absolutely amazed,” he recalls. “I didn’t know it was possible, but said, ‘If it’s all above board, then yes!’ Like everyone else on dialysis, I knew I might die waiting for a transplant.” Andy, who has two grown-up children and three grandchildren, suffered from polycystic kidney disease. His grandfather, father and brother had all died of the condition.

Since their first meeting, Andy and his wife now regularly visit Barbara in Cornwall. They also speak frequently on the phone. “I do worry about Barbara now,” says Andy. “I just want to make sure she’s okay. I have felt some sense of guilt since the transplant that my kidney came from a live donor. I worry that Barbara might get sick and suffer physically because of what she has done. So there is a strong connection between us. I owe her my life.”

Barbara, too, admits there are “complicated emotions” involved in such a transplant; she in turn feels a sense of responsibility towards Andy and worries that her donated kidney might one day fail. “Although I am very happy to have met Andy, I would have been quite content never to have known who had received my kidney,” she says. “I feel a little embarrassed when he keeps thanking me.”

The gap between supply and demand for transplant organs is at an all-time high in the UK, so new ways of encouraging organ donation, from both living and deceased donors, are urgently being sought. Most organs traditionally came from people who died of catastrophic brain injury following accidents or a stroke, but improved road safety and medical treatment mean this source fell by 14% per year between 2000 and 2006. Demand for organs is rising by an estimated 8% a year, a result of increased life expectancy and greater numbers of people suffering from diseases requiring transplant surgery such as type 2 diabetes, which can lead to problems of both the kidney and pancreas.

In 2007-8, the year the change to the law took effect, there were 10 altruistic volunteers; so far, from 2008-9 there have been 17. “We only expected to see one or two cases when we first started approving this type of transplant,” says Vicki Chapman, director of policy and strategy at the HTA. “We have found these numbers coming forward very surprising. It is such an extraordinary thing to do.”

The UK has one of the lowest rates of organ donation in the developed world. Last month there were 8,111 patients waiting for a transplant, 7,016 of them in need of a new kidney. On average, 1,000 people die every year waiting for a transplant. Even though about one in four British adults — just over 16m people — are now signed up to the official donor register, relatives often override this wish and doctors do not challenge such refusals. Perhaps we need to ask ourselves some probing questions about whether we could become a donor, in life as well as in death.

Maggie Harris has not met the person who received the kidney she donated in autumn 2007. All she knows is that it went to “a man who was in a very bad way”. “For me, it is definitely a good thing not to have that sort of emotional baggage,” she says.

The 64-year-old retired schoolteacher from Manchester had already had to deal with some unexpectedly hostile reactions to her decision to become a live organ donor from two of her oldest friends. “They were very tight-lipped and head-shaking,” she says. One said to her: “Aren’t doctors supposed to make people better, not chop them up?” The other wrote to her after the operation saying she might consider herself “a new secular saint — St Margaret of the single kidney” and suggested she sell her house and give all her money away if she really wanted to do good.

Maggie is clearly hurt by these exchanges, but she recognises that her decision may have been viewed by some as a kind of “personal challenge”, making them question whether they could do something similar, and possibly making them feel angry and guilty if they recognised they could not. The reactions also illustrate what the historian Barbara Taylor and the psychoanalyst Adam Phillips concluded in their recently published book On Kindness: that, in today’s cynical climate, kindness is all too often regarded as “a higher form of selfishness” (the kind that is morally triumphant and secretly exploitative), or the lowest form of weakness, “a virtue of losers”.

“This was just an operation,” says Maggie. “I knew I could do it. I’ve had operations before. Both my daughters were born by caesarean.” Maggie felt she had been “undeservedly lucky” in life. “I’ve had marvellous health and have a happy family. I felt in a sense it was payback time,” she says. “I didn’t want to feel I had gone through life as a net taker. I felt a sort of moral disquiet that I have had more than my fair share of good luck. So I felt doing this, just like giving blood, was a moral duty.”

Maggie reached her decision after hearing through friends of the plight of someone who had received a kidney from a brother but who was facing death after the transplant failed. Her husband and adult daughters would have preferred her not to become a live donor, but fully supported her decision. “I would have felt affronted and undermined if anyone had tried to stop me disposing of my blood and kidney as I wished,” she says.

Maggie admits that when she was finally given the date on which her kidney would be removed, she felt “queasy”. “As soon as I knew when the operation would take place, I did begin to feel frightened, in the way I imagine a soldier does when given a date to go to the front.”

Maggie’s recovery from the operation was more prolonged than Barbara’s. It took five weeks before she was able to return to her teaching job; the cost of her sick leave was covered by the NHS. But now she says she feels perfectly fit and has been able to resume her passion for flamenco dancing.

Like Barbara, Maggie found the psychological vetting “intrusive”, though she understands the need to question people’s motives. “There might be people with strange hidden agendas,” she says. “Those who expect it to change their lives — haul them out of depression, for instance.”

Yet this is precisely what another living organ donor from Plymouth found it did for her.

Julie Saunders, 43, knows what it is like to live with a degenerative disease that only transplant surgery can cure. For years she suffered from the eye condition keratoconus, which was making her progressively blind. In 2000 the former postal worker received a cornea transplant that restored her sight. Following the operation she became preoccupied with the idea of making a living organ donation herself. “I didn’t view it as a sacrifice, but as a gift,” she says.

For much of her adult life Julie has also suffered from depression. “I tended to dwell on the negative, seeing a glass as half empty rather than half full,” she says. “In some way I felt if I hadn’t been able to make the most of my life, perhaps through donating my kidney I could help someone else make the most of theirs.”

Early last year she went against the wishes of her parents and some of her siblings and began the vetting process to become an altruistic donor. Her parents were “not overly chuffed” and tried to dissuade her. But when they realised she was determined to see it through, they supported her and are now proud of what she has done.

On October 15, 2008, her right kidney was removed at Plymouth’s Derriford Hospital and transplanted into a woman in the north of England suffering from kidney disease. Julie knows little else about the recipient. The woman later wrote her a note saying: “You have given me my life back.”

“From that moment I felt as if my life turned around,” says Julie. “I didn’t expect it to happen. I didn’t do it for that reason. But I just had this overwhelming sense of self-satisfaction. It made me realise, if you put your mind to it, you can do just about anything you want to in life.” She, too, made a rapid recovery, was out walking her dog within a week, and has now resumed regular aerobics and weight-training.

“Some people accused me of only becoming a donor to make myself feel better,” she concludes. “But there are easier ways of doing that. I realise becoming an altruistic donor is not for everyone. But at the end of the day it is individual action that makes a society, and donating your kidney is really no big deal.”

Just how big a deal it is to those waiting for such a gift of life is instantly apparent on visiting the dialysis ward at Derriford. Above the sound of bleeping lights and whirring motors, the half-dozen patients who are having their blood cleaned by dialysis machines — a temporary lifeline — exchange a stream of friendly banter that belies their plight.

One man, curled on his side, who wants to be known only as Perry, sums up their situation. “We are like drowning men waiting to be thrown a rope to save our lives. Whether that rope is made of silk or hessian makes little difference,” he says, referring to the chance of receiving an organ from a live or deceased donor. Perry, a 67-year-old aristocrat and local landowner, needs a transplant because of kidney damage caused by the drugs he had to take after his lung transplant 12 years ago. After undergoing dialysis for nine months, he has been offered a kidney by a longtime acquaintance and he doesn’t want to jinx the prospect by talking about it too much. But he concedes it can make a significant difference whether the donor is living or deceased — transplants from living donors are generally more successful.

In recent years in the UK, the number of living kidney donors has increased from 589 in 2005-6 to 927 (which includes the altruistic donors) in 2008-9: live donations now represent more than one in three of all kidney transplants.

Still, some in the medical profession have taken a great deal of convincing that altruistic donations are a way of filling the gap between supply and demand for organs.

As Sarah Stacey, the living-donor transplant co-ordinator at Derriford explains, the core precept of the Hippocratic oath is to do no harm. So to perform an operation on someone that will bring them no physical benefit — except for a full medical screening and regular follow-up care — is hard for some to justify.

“In the case of live donors who offer an organ to a loved one, it is easier to see they do directly benefit from what they’re doing,” says Jamie Barwell, consultant vascular and transplant surgeon at Derriford. “But in the case of altruistic donors I find myself hesitating every time.”

He recognises that performing operations on live volunteers “fulfils their human right to give of themselves as they wish”, the same principle that applies to blood donors. “You also have to be very clear,” he says, “that the benefit for such organ donors is the feel-good factor they derive from doing it.”

The government is investing £4.5m in a public-awareness campaign to boost the numbers on the donor register by countering common misperceptions, such as the fear that intensive-care staff will struggle less to save the lives of those who have signed up to the register. The campaign aims to increase the number of people registered to donate organs after death to 20m by 2010 and 25m by 2013, which could increase the overall number of transplants by at least 1,200 a year. Of these, an estimated 700 would be kidney transplants, leading to significant savings for the NHS (transplants are considerably cheaper in the long run than dialysis). A nationally co-ordinated transplantation network matching potential donors to recipients is also being introduced.

If these initiatives fail to increase the number of donors registering and transplants taking place over the next few years, the government has vowed to reconsider introducing presumed consent, the system used in countries such as Spain, where organs are automatically donated unless an individual explicitly opts out. Clearly, there is also a need for more living donors. So, moment of truth: I have to ask myself whether I would be willing to donate one of my vital organs while still alive. If it were for the sake of my daughter, I would not hesitate.

But would I do the same for a stranger? If I’m honest, I don’t think so. Fortunately, there are growing numbers who would.

Lufkin teen needs community support for kidney transplant

Wednesday, August 5th, 2009

By JESSICA COOLEY
The Lufkin Daily News

Sunday, August 02, 2009

A Lufkin boy struggling with kidney disease since birth needs community support for a potentially life-changing operation.

Every Monday, Wednesday and Friday morning for the last seven years 16-year-old Adam McCleskley and one of his parents make a trip to Memorial Hermann Hospital in Houston, where he sits for the next several hours getting dialysis. McCleskey was born with autosomal recessive polycystic kidney disease (ARPKD), a genetic disorder with an incidence rate of one in 10,000, according to yougenesyourhealth.org.

“Because Lufkin has no pedi-nephrologists, pedi-dialysis or pedi-pulmonary, he has to go to Houston,” Kelli McCleskey, Adam’s mother said. “I take him two days a week and his dad one day a week. My dad was helping me by going one day a week, but in October 2008 he became sick and passed away December 28.”

ARPKD has a high mortality rate in infants — something the McCleskey family has experienced first hand. At 16 months McCleskey went into cardiac arrest and recovered but in 1997 the family lost an eight-day-old daughter named Kelson to the disease.

“She was also born with kidney failure and her father and I had to decide to take her off life support,” Kelli McCleskey said. “After her death, life was just too hard to deal with and our marriage ended. We had been married for 10 years, but it was very hard for me to handle her death.”

McCleskey was only two at the time of his sister’s death and doesn’t remember the experience. Although McCleskey’s life has been dependent on dialysis for the last seven years, a successful kidney transplant could change that, his mother, Kelli McCleskey said. Also suffering from cystic fibrosis, the boy has already been through one transplant in his life.

“In 2004 my mom donated her kidney to me and we thought it would work, but unfortunately it didn’t,” Adam McCleskey said.

Kelli McCleskey said that during surgery, doctors damaged her removed kidney before placing it in her son but were still hopeful it would function.

“When they took a biopsy later, they said it had 75 percent damage so it needed to be removed,” Kelli McCleskey said. “It was devastating to go through all that and have it not work. No other family members can donate. He has a cousin that is trying to donate her kidney through a matched donation program.”

Matched donation connects individuals who want to donate but aren’t a match for their own family member. Through a cross-matching system multiple transplants can occur. “We’re really hoping matched donation will work for us, but right now from the transplant and all the blood transfusions over the years, his antibodies are on high alert,” Kelly McCleskey said. “They’ll attack anything we try to do.”

For that reason McCleskey first needs to travel to John Hopkins Hospital in Baltimore, where a doctor has agreed to see him for a procedure that will desensitize his antibodies.

“Desensitization is a process that removes harmful antibodies from the blood stream. These antibodies, which fight foreign tissues like those found on a donated organ, can cause organ rejection. These antibodies are removed through a process called plasmapheresis,” a transplant services Web site stated. “Typically, three or four treatments are required prior to transplant. At the start of the plasmapheresis treatments, the patient receives anti-rejection medications to help prevent the reformation of the harmful antibodies. These anti-rejection medications are the same medications that the patient will continue to use after the transplant.”

“After the transplant” are words the family can’t wait to say, Kelli McCleskey said.

“We’re tired of waiting. We’re not going to wait for him to lose his strength before we start pushing for this,” she said. “We have a big family and he’s seeing everyone else doing all these things while he’s stuck in the dialysis chair.”

“That’s what hurts,” she continued, voice breaking with emotion. “It hurts a lot. When does he get to live his life?”

There will be a fundraiser for McCleskey at 2 p.m. today in the Lufkin Sam’s Club parking lot.

“We will be selling turkey legs, sausage-on-a-stick and Ben and Jerry’s has donated 50 pints of ice cream,” Kelli McCleskey said. “We would be so very grateful of anything the community can help us with.”