Archive for the ‘SEEKING KIDNEY DONOR’ Category

Boss Gives Employee Kidney

Tuesday, November 17th, 2009

Liquor Store Employee Calls Kidney ‘Gift Of Life’

A liquor store worker in Philadelphia said his boss gave him the “ultimate gift” this spring when he decided to give him a kidney, WFMZ-TV reported.

“He gave me the gift of life,” Rob Fenstermaker said of his boss, Brian DeAngelis.

DeAngelis said he decided to be Fenstermaker’s kidney donor after watching him get worse every day.

“We as a store noticed that he was getting sicker and sicker,” he said.

Other co-workers began talking about how they could help him. They discussed donating sick leave before talking about the possibility of a transplant.

Two co-workers tested but they were not a match.

Then DeAngelis decided to give it a shot.

“I kept passing all the tests,” he said.

Once he found out he was a match for Fenstermaker, he said he never looked back.

The surgery was in May, and both men say they are doing well and have developed a unique bond.

Fenstermaker said he’s grateful.

“He gave me the ultimate gift,” he said.

Kidney Navel Donation

Tuesday, November 17th, 2009

Kidney Failure

The kidneys are a pair of organs in the back of the abdomen. In an average day, about 200 quarts of blood flow through the kidneys, where excess fluid and waste products are filtered out and turned into urine. The kidneys regulate the levels of important minerals, like potassium, sodium and phosphorus, in the blood. In addition, the kidneys release three hormones: erythropoietin (EPO, which causes the bone marrow to make red blood cells), renin (regulates blood pressure) and calcitriol (a form of vitamin D, which maintains calcium for strong bones).

When the kidneys are damaged by disease or injury, they may not be able to function properly. Toxic waste products build up in the blood, the body retains fluid and blood pressure rises. Eventually, patients need dialysis (mechanical filtering of the blood) to stay alive. According to the National Kidney Foundation, more than 485,000 people in the U.S. are currently being treated for kidney failure.

Kidney Transplantation

Another option for kidney failure is a transplant, or removal of diseased kidneys and replacement with a donor kidney. Traditionally, donor kidneys have come from cadavers. But since people can survive with just one kidney, sometimes a living person is willing to donate a kidney. A living donor is typically genetically-related because he/she is more likely to be a tissue match for the recipient. Sometimes, however, a friend, co-worker or stranger can be a good tissue match and donate a kidney.

In addition to being a better match, using kidneys from live donors has other advantages. Recipients don’t have to wait until a cadaver kidney becomes available (most candidates spend one to two years on the waiting list). The transplant surgery can be scheduled at a time that is convenient for both the donor and recipient. A living kidney doesn’t have to be transported very far (usually just to the next surgical suite), so it is fresher and generally in better condition than a kidney from a deceased donor and starts functioning sooner.

According to the United Network for Organ Sharing, as of October 23, 2009, more than 82,220 people were on the waiting list for a kidney transplant. Last year, 16,520 kidney transplants were performed in the U.S. 5,968 (more than 36 percent) of those transplants were from living donors.

Living Kidney Transplants – Surgery for the Donor

The first successful living kidney transplant was done more than 50 years ago. For a long time, the surgery to remove a kidney was done through a large incision. Rolf Barth, M.D., Transplant Surgeon with the University of Maryland Medical Center in Baltimore, says it wasn’t uncommon for the donor to spend more time in the hospital after donating a kidney than the transplant recipient.

Eventually, doctors learned how to remove a donor kidney laparoscopically, by making a few small incisions in the abdomen and using a camera and miniature surgical instruments. For the donor, laparoscopic kidney donation is much easier. Recovery is much faster (one or two days in the hospital versus one or two weeks with open surgery). Patients have less pain and less scarring and are able to get back to work fairly soon.

More recently, a few surgeons have started performing laparoscopic kidney removal through a single incision in the belly button. Barth explains that once the incision is made into the belly button, a small port (open connection) is placed through the incision. Gas can be forced through the port to expand the abdomen and give the surgeon more room and access to the kidneys. The camera and surgical instruments are passed through another slot in the port.

Once inside, the surgeon cuts and seals off the blood vessels and connecting structures to the kidney. Then the port is removed. The opening into the belly button is stretched out, giving the surgeon enough room to pull out the kidney. The organ is then carried to the recipient’s operating room for transplant.

Barth says most people who are candidates for laparoscopic kidney donation are eligible for the single incision surgery. Once the surgery is finished, the incision and eventual scar is hidden inside the belly button. So donors have no visible scars.

http://www.wsoctv.com/health/21640003/detail.html

# For general information on kidney function, donation or transplantation: National Institute of Diabetes and Digestive and Kidney Diseases
# National Kidney Foundation
# United Network for Organ Sharing

“Parishioner’s prayers for kidney answered by her priest”

Thursday, November 12th, 2009

12:00 AM CST on Wednesday, November 11, 2009

By DAVID FLICK / The Dallas Morning News
dflick@dallasnews.com

Even with her puckish sense of humor, no one could doubt that Carrie Gehling has faced serious health issues.

She lost both legs to a 40-year fight with diabetes and suffered four heart attacks, one of which left her clinically dead for 2 ½ minutes.

After years of dialysis, she needed a kidney transplant, but her medical history made her a high-risk candidate. Several hospitals had turned her down until Medical City Dallas Hospital earlier this year agreed to the procedure – with the provision that she find a live donor.

Among those she turned to for help was her pastor at St. Rita Catholic Church. Monsignor Mark Seitz is a popular and energetic priest who, when not tending to his flock, occasionally indulges in inline skating.

One day he was thinking about where Gehling could get a donor.

“And then I thought, why not me?”

He went through testing that proved he was an acceptable match. When he broke the news to Gehling, she responded with her usual wit.

“I said I was going to call it my holy kidney,” she recalled.

The transplant took place Tuesday morning. Later in the day, a spokesman at the northwest Dallas parish said the procedure had gone well. Both patients were conscious and recovering in their respective rooms at Medical City.

Gehling, 45, noted before the procedure that some scientists believe transplant recipients pick up some of the traits of the donors.

“I told people I hope I don’t pick up roller blading,” she said. “And I’m not going to become a nun.”

Seitz, 55, said before the procedure that he intended to set aside his blades for a stack of books during the weeks of recuperation.

He considers organ donation to be an extension of his pastoral duties.

Last summer, when he first heard that Gehling needed a kidney, “it got me thinking about what a priest does,” Seitz said. “We follow the model of one who literally gave his life for us. If he can lay down his life, I can give away a kidney.”

The attitude surprised no one at the church, where Seitz preaches on Sunday and Gehling teaches a catechism class to children.

“He’s always been there to help those who need him the most,” parishioner Michelle Chadwick said of Seitz.

She noted that he worked to establish a sister church in Honduras and, back in Dallas, inaugurated a Spanish-language Mass at the traditionally Anglo congregation.

Susan Scheetz, who worked with Gehling in the parish catechism classes, said she is a favorite among everyone who knows her.

“The kids adore her, and parents will drop by to ask how she’s doing,” Scheetz said. “I’ve never seen her without a smile on her face.”

Gehling said she did not always take life so light-heartedly or have such an easygoing relationship with the church.

“I lost my faith for a while when I was 20 and my father died of a heart attack,” she said.

She was so angry that although she had been a longtime parishioner, she avoided driving past St. Rita’s on her way to work.

“Then one day, I woke up and thought, ‘What in the world is wrong with you?’ ” she recalled. “If my father had lived after that heart attack, he would have been a vegetable. What the Lord did was for the best.

“There’s only one way to put it: Thy will be done.”

Both said they have been overwhelmed by support from the parish – and beyond.

On Monday night, parishioners gathered for a special rosary service, and Seitz said parishioners have spread the word everywhere.

“There are people all over the world praying for us,” he said.

Gehling said before the operation that she was eagerly looking forward to the procedure.

“When you’re high-risk, there are people who don’t think you’re going to make it, but I say, ‘You don’t know me,’ ” she said. “There’s more in life that I want to accomplish.”

http://www.dallasnews.com/sharedcontent/dws/news/localnews/stories/DN-kidneydonor_11met.ART.State.Edition2.4b76347.html

“Kidney swap involves series of selfless acts”

Thursday, November 12th, 2009

baltimoresun.com

By Kelly Brewington | kelly.brewington@baltsun.com

November 11, 2009

When 10-year-old Sean Menard’s battle with kidney disease took a turn for the worse, his former kindergarten teacher’s aide offered him one of her kidneys. When it turned out she was not a good match, her husband volunteered.

His act of kindness not only enabled Sean to get the kidney he desperately needed, but it became a vital link in a chain of four donors who would give their healthy kidneys to four people in need of new organs.

The University of Maryland Medical Center announced the series of donations Tuesday, which marked its first kidney exchange. Known as a four-way swap, the procedure took place at the Baltimore hospital over two days last week among unrelated living donors and recipients from four states, ranging in age from 10 to 74 years old. Surgeons used a single-incision technique in which the organs are removed through a patient’s belly button.

Several of the patients spoke at Tuesday’s news conference, including Emmet Davitt, 50, the husband of Sean’s teacher’s aide.

“I really do view it as an opportunity, not as a great heroic act,” said Davitt. “I wish Sean the best and look forward to seeing him running around.”

Such swaps have taken place for several years at a handful of medical institutions nationwide, including Johns Hopkins Hospital, the first to do the procedure in 2001. They use pairs of donors and recipients who might not be good matches for each other but would match other people.

This one started with Edward Behn, 59, of Westborough, Mass., who had watched a friend die of renal failure last year. He wondered if he could help save someone.

His kidney went to an anonymous man in Maryland. The man’s wife donated her kidney to Sean Menard. Emmet Davitt, the husband of Menard’s former teacher’s aide, donated his kidney to Carl Lichtman, 64, of Lake Worth, Fla., who was facing the grim prospect of lifelong dialysis. Lichtman’s wife, Stacey, 60, donated a kidney to Bob Loudermilk, a 74-year-old Vietnam veteran from Virginia Beach.

Kidney transplants in children are infrequent; the University of Maryland does just three or four a year, said Dr. Matthew Cooper, director of kidney transplantation at the medical center. Last year, of the 16,520 kidney recipients nationwide, 773 were children, according to the United Network for Organ Sharing.

Children are more likely to reject a kidney and suffer infections after transplant, Cooper said. And since the organs last an average of 20 years, children are more likely to need a second transplant later in life.

When Michael and Jeannie Menard of Catonsville adopted Sean at 7 weeks old, he had been diagnosed with polycystic kidney disease. At 6 months, he had one kidney removed, in the hopes that the other would grow and function better. After years of treatment at the University of Maryland, Sean reached a point where he was getting worse. He became lethargic and could play outside for only 10 minutes at a time.

His teacher’s aide, Julie Davitt, had spent hours with him every day in class, helping him use the bathroom and perform other small tasks. She grew attached to Sean, who greeted her with a hug every morning.

When she offered her kidney, the Menards refused, taken aback at the gesture. But Davitt called the Menards back a few days later, saying she had already secured the paperwork to volunteer to be a donor. It turned out that Julie Davitt could not donate, but her husband offered to.

“I was just floored that they wanted to do this, that they wanted the best for my son,” said Jeannie Menard. “I know we will always be close to them. He gave my son life.”

“Kidney transplants at UCLA Medical Center have a domino effect”

Tuesday, October 27th, 2009

Kidney transplants at UCLA Medical Center have a domino effect
The hospital has paired up 18 patients as part of a rare transplant chain.
By Molly Hennessy-Fiske

At 8:25 Thursday morning, Dr. Peter Schulam extracted a healthy kidney from a 60-year-old woman, slipped it into a bowl of sterile ice and wheeled it into the operating room next door. The donor, Nancy Seruto, a San Dimas mother, had never met the recipient, a 67-year-old retired flight attendant from Santa Ana.

Less than two hours later, Seruto’s husband was on the same operating table at Ronald Reagan UCLA Medical Center. Another stranger, a 53-year-old Chatsworth mother of two, was giving him a kidney.

They were among 18 patients paired by surgeons as part of a rare transplant chain, built largely on trust.

Each link in the chain represents a paired donation in which a donor gives a kidney to a stranger, trusting that another stranger will donate a kidney to his or her loved one in return.

Such chains are difficult to build, because of the trust issues involved and medical complications. Donors and recipients must have compatible blood types and antibodies. Surgeons usually have to perform multiple transplants simultaneously in adjacent operating rooms, both to ensure that transplanted kidneys stay healthy and that donors do not get sick or back out, breaking the chain.

After Celia Contreras, 39, volunteered to donate her kidney to help a family friend as part of the UCLA chain, she said her husband pressured her not to, worried that their three children might one day need a kidney.

Contreras, an elementary school teacher, held her ground.

“I truly believe that what you put out there comes back to you,” she said.

For would-be recipients, donor chains can shorten the wait for a transplant by years, experts say. As of this month, 82,061 people nationwide were waiting for a kidney; 16,416 of them in California, according to the United Network for Organ Sharing, based in Richmond, Va.

Network officials are developing a national registry that they plan to launch next year with five pilot sites, including UCLA. That could lead to an additional 1,000 to 2,000 kidney transplants annually, according to Dr. Bryan Becker, president of the New York-based National Kidney Foundation.

“It’s a huge opportunity to expand the donor pool,” said Dr. Jeffrey Veale, director of the UCLA Kidney Transplantation Exchange Program.

For now, donor pairs have to rely on smaller networks, including the National Kidney Registry in Babylon, N.Y., which two years ago started keeping a list of paired donors. UCLA surgeons used the registry to build the latest donor chain, their fifth and one of about a dozen the registry coordinated nationally this year, a spokesman said.

The chain started last year with Harry Damon, a firefighter in Grand Rapids, Mich.

Damon, 55, wanted to donate in memory of his 22-year-old son, who had died in a snowmobile crash. He contacted the registry looking to give his kidney to a young man.

Instead, he was matched with Sheila Whitney, 49, of Compton, a disabled teacher’s aide with lupus who had been waiting on dialysis for more than six years.

“I thought, ‘This is bound to be,’ ” Damon said.

He flew to Los Angeles for the chain’s first transplant June 8.

The same day, Whitney’s 27-year-old son, Reginal Griffin, donated to Keenan Cheung, 44, a USC housing manager and father of three from La Cañada Flintridge. Cheung’s wife, Jeanne, 43, who works at a Burbank production company, donated to Sonia Valencia, 29, a resource teacher in Commerce who is friends with Contreras.

Surgeons then had to coordinate with the California Pacific Medical Center in San Francisco to match Contreras with Priscilla “Pia” Miller, 36, of Fresno, a disabled bank teller, flying Contreras’ kidney to San Francisco for a transplant June 10.

Miller’s roommate’s brother, Anton Goodfriend, 25, of Springfield, Mo., an armored car driver, then flew to San Francisco in July to donate to Ross Bloom, 55, a real estate investor in Chatsworth. Bloom, who was incompatible with 97% of donors on most waiting lists, called the chain a miracle.

On Thursday, his wife of 34 years, Fern Bloom, donated to Joseph Seruto, 64, a business owner from San Dimas. Bloom had never been operated on before, but was giddy as she waited in a gown in the preoperative room. She called the chain “bashert,” Yiddish for “meant to be.”

Down the hall, Seruto’s wife, Nancy, a bookkeeper, was preparing to donate to retired flight attendant Donna Morrison.

The Serutos did not have to join the chain — they were compatible with each other. The couple, who have been married 37 years and have two grown children, chose to participate after their doctor suggested they could help Morrison, a former globe-trotting flight attendant who had been on dialysis for several years.

Late Thursday, Morrison’s fellow Continental flight attendant, Ellen Harmetz, 61, of West Los Angeles, donated to Phyllis Thompson, 54, of Simi Valley, a stay-at-home mom.

Thompson’s husband, Gregory, 56, a project manager at an architectural firm, is scheduled to make the last donation in the chain Tuesday.

Hospitals generally do not allow members of a transplant chain to meet before their operations, wary that they might back out.

UCLA surgeons allowed the first few pairs of the latest chain to meet at the hospital the day after the first batch of surgeries.

Griffin was surprised to discover his kidney had gone to an Asian man. He had assumed the recipient was white.

“I was amazed to see the line-up of the chain — all different ethnicities,” Griffin said.

The mood of the gathering reminded him of the atmosphere after the terrorist attacks of Sept. 11.

“When people are really in need of help, we forget about the class system and race and really reach out,” he said. “It humbles you, the whole situation.”

His mother, who was still recovering, went in pajamas, rail thin, scars snaking down her arms from years of dialysis, determined to meet Damon.

Recalling that meeting this week, Whitney started to cry.

“I had went through so much,” she said, at home and back to her normal weight. “A lot of times I wanted to give up.”

Thursday’s pairs were also curious about each other. They eyed strangers in the hospital waiting room, trying to find their match.

“I would love the opportunity to thank them,” Thompson said.

They were all recovering well late Thursday, and are scheduled to meet for the first time at the hospital today.

National Kidney Foundation seeks to improve transplant process

Thursday, October 22nd, 2009

National Kidney Foundation seeks to improve transplant process

Patti Singer • Staff Writer • October 20, 2009

The number of people waiting for a kidney transplant and the time they must wait has mobilized the National Kidney Foundation to end the wait in the next 10 years.

Representatives of the Kidney Foundation and from Strong Memorial Hospital will discuss End the Wait: Making the Dream a Reality, at 6 tonight in the Flaum Atrium, University of Rochester Medical Center, 415 Elmwood Ave.

John Davis, chief executive officer at the national level, is scheduled to be joined by Dr. Mark Orloff of the University of Rochester Medical Center Transplant Center and Drs. Chris Barry and Carlos Marroquin, the newest members of the kidney transplant surgical team.

The event is significant for Bob Legge, 57, of Lyons. On Wednesday, he will undergo a transplant. His wife’s sister is the donor.

“She’s my hero,” he said.

Diagnosed with kidney disease in 2003, Legge has been on the waiting list for two years. This summer he learned that his sister-in-law is a match.

Legge, also a board member of the National Kidney Foundation Serving Upstate New York, said that 20 percent to 25 percent of people on dialysis, as he is, die each year.

He said it’s important to improve education about living donation and remove barriers for the donors. He said that many people have asked his sister-in-law about her fears. “She said, ‘When you learn about it, it’s not so scary,’” Legge said.

According to the Kidney Foundation, the average wait for a kidney is five years. Nearly 400 local people are waiting for a transplant, and more than 7,000 people in New York and 81,000 nationwide are on the list.

The initiative seeks to improve the outcomes of first transplants, increase living and deceased donations and change public policy.

Currently, living donors can lack protections in the workplace and also for health and life insurance. The foundation also is working with Congress to expand Medicare coverage of immunosuppressant medications beyond the current 36 months.

PSINGER@DemocratandChronicle.com

“A determined mom gets a transplant center to change its rules”

Tuesday, October 13th, 2009

http://www.kansas.com/living/family/story/1003988.html

A determined mom gets a transplant center to change its rules
By JOSEPHINE MARCOTTY

Two years ago Kelly Lawson was living a mother’s nightmare. Her infant son’s kidney transplant had failed, and he was growing up far from home, hooked to a dialysis machine.

She was driven by one thought: “I can’t sit here and watch my son die in front of my eyes.” She became a mom with a mission – finding him a living kidney donor.

Her son, Dominik, is now a thriving 4-year-old, and she is a bit of a legend at the University of Minnesota Medical Center-Fairview.

In a little more than a year, the family’s story, broadcast by e-mail and news reports, inspired about 200 people to call on Dominik’s behalf – far more inquiries than the U has ever received for a kidney patient.

Because of Lawson, the university hospital is now joining the growing number of transplant centers that are changing their rules so that they can provide advice to patients on how to find and approach donors. It is a significant departure from the long-held conviction that providing such information is unethical because it might be perceived as soliciting donors.

Lawson, 39, an emergency room nurse from Taconite, Minn., says it’s about time.

“There was nothing at the hospital,” she said. “It leaves you feeling very, very helpless.”

Hospital officials say that in part they are acting in self-defense. Patients are becoming savvier and more assertive about finding donors. Educating them up front will help reduce the volume of calls and screenings involving volunteers who won’t or couldn’t be donors anyway. But it is also a recognition that patients and would-be donors need help that transplant centers are uniquely able to provide.

“If you are soliciting donors, this is how to do it,” said Cathy Garvey, director of the university hospital’s living donor program. “And tell us before you go on TV, please. It causes havoc on our end.”

Dominik was born without functioning kidneys. Lawson gave him one of hers when he was 20 months old and just big enough to tolerate the surgery. But seven weeks after the transplant, he got an infection and his body rejected the organ.

Doctors told Lawson that only 3 percent of the population would be a match. Dominik was at the top of the list for a deceased-donor kidney, but he would most likely die before he got one. A living donor was his best chance.

Lawson didn’t know where to begin.

“I thought, ‘I need to contact the media,’ ” she said. “If they see my boy’s beautiful face … ”

She began sending e-mail to television stations and newspapers around the Twin Cities and northern Minnesota. She also got some help from the media experts at Fairview Health Services, which owns the university’s Amplatz Children’s Hospital.

She succeeded beyond anyone’s expectations. TV and radio stations in the Twin Cities and northern Minnesota all ran stories about Dominik. At times the university’s transplant office was so overwhelmed they couldn’t return every call.

“I would be livid,” Lawson recalled. “I’d say: ‘You have to call back every single person. They are not going to call a second time.’ ”

Then Lawson got lucky. ABC News wanted a patient to illustrate a national story about living kidney donation. In the fall of 2007, Dominik’s sweet smile and golden curls were all over the national evening news.

In California, 20-year-old Mary Cousineau saw the program. She had met Kelly and Dominik at the university’s Ronald McDonald house while her little brother was getting a bone marrow transplant. He died just two weeks before ABC broadcast Dominik’s story.

As she watched, Cousineau for the first time understood what Kelly Lawson was facing – and what she needed. A kidney donor.

She immediately called Minnesota. At Lawson’s urging, Cousineau waited several months while she grieved the death of her brother. But in early 2008 she saw Dominik again in the dialysis unit at university hospital. She turned around and went straight to the transplant center for testing.

She was among the 3 percent.

Kidneys rocked his world

Tuesday, August 25th, 2009

Charles G. Anderson Sr. Special to the Reporter-News
Monday, August 24, 2009

Chris Komorowski, 27, of Abilene, never dreamed that his whole world would change shortly after Christmas in 2008.

He had not been feeling well, had gained weight, and there was a weird taste in his mouth. Komorowski had always been healthy and active, so he did not think anything was wrong with him.

He had graduated from Abilene High School in 2000 and went to Abilene Christian University for nearly three years. He was active in gymnastics at AHS and at ACU where he was member of the famed Flying Cats gymnastic demonstration team.

After leaving college, he enrolled at Texas State Technical College where he studied digital imaging and then he went to work for a local company.

Chris’s mother, Beth, said that Chris had a sore in his mouth, and a local dentist had said he needed to see a doctor.

“We went to a rural hospital where I grew up,” she said.

“You need to go directly to the hospital, and you will probably start dialysis,” he was told after a series of tests.

He was in the hospital by 5 p.m. that day.

“A nurse came into the room and told us that Chris would start dialysis,” Beth said. “I told her she had the wrong room. I could not believe it.”

He spent four days in the hospital, and he had tests run to see if they could find what had caused his kidney problem.

“My kidneys were barely functioning,” Chris said. “I thought everything was fine, but the kidneys were not filtering the impurities out of my system.”

His dad, Ted, was also at a loss on what was happening to Chris. One day they thought Chris was in good health, and the next day he was taking dialysis.

“No one could tell us why his kidneys were failing,” Ted said.

“I was shocked and scared,” Chris said. “After a while, I decided that this had happened, and I needed to deal with it.”

He spends several hours a week hooked up to dialysis. His left arm has a big blue mark on it where he has been stuck numerous times with a needle.

“I am all tied up for about four hours,” Chris said half jokingly in speaking of his dialysis. “I read, watch TV or take a nap.”

Chris got an appointment at Scott and White hospital in Temple in July, and the doctors urged him to consider a kidney transplant. Other tests were run, and the doctors told Chris they just did not know what caused his condition. The tests showed that he did not have diabetes, and no one in his immediate family had any problem similar to what he had encountered.

“You may be a good candidate for a kidney transplant,” the doctors told him. “We are running more tests to see if you are well enough to take another kidney.”

His mother, father and a brother are the best sources for a match, Chris said. “If I am approved, they will run tests to see if they match.”

All three have agreed to be the donor if they match.

When his friends heard about Chris’s problem, some volunteered to help.

“Hey man, you need a kidney,” a friend told him. “I’ve got two.”

“It would all depend on whether there is a match,” Chris said.

Meanwhile, he is waiting to hear from the doctors in Temple and expects a letter any day.

If he is approved and no matches are found in his family or with his friends, Chris will go on a waiting list.

“If I get a kidney from a live donor, it will last longer,” he said. “If it is from a cadaver, they do not last as long.”

Chris explained that in dialysis, the blood is taken out of the body and cleaned and then put back into his body.

“I get changed out,” he said with big grin.

Chris weighed about 170 pounds when he was in college with the Flying Cats. By the time he started dialysis, he weighed 310 pounds but is back to 270 now.

“I found out a weight gain was one of the symptoms of my kidney problem,” he said.

He has taken some hard knocks because of his illness. Not only has he gained weight, but he no longer has a job.

“I plan to help out more around the house,” Chris said. “I still go out with friends, but even that has changed some.” He said they usually play games on the computer or do something at home as he is tied so closely to the dialysis treatments.

Chris has to be careful with his diet. He said there are some foods that would hinder his condition even now.

“If I get a transplant, I will always be taking certain pills and sticking to a diet,” Chris said.

“I had plans for an apartment of my own,” Chris said. “When this came up, all my plans had to be changed.”

“We are trying to go right on with life,” Ted said.

Chris lacks just a couple of courses at TSTC, and he has nearly three years toward his college degree.

Asked what would happen if the doctors said he is not a candidate for a kidney, Chris said he would just go ahead with life and deal with it.

“I hope to get a new kidney, finish my degree and go back to work,” he said.

Then Chris glanced down at the scars and blue marks running up and down his arm.

“I hope to go back to the same company to work,” he said. “If I can’t go back there, I hope to find another job somewhere in Abilene.”

Meanwhile, Chris is waiting for a letter from Temple.

“Whatever comes, I will face it,” he stated.

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.”

Woman’s illness spawns donation

Sunday, July 26th, 2009

The Anapolis
By SHANTEE WOODARDS, Staff Writer
Published 07/20/09

Laurie Sears Deppa had every intention of undergoing surgery to help an Edgewater woman in poor health.

Laurie Sears Deppa, who lives in Annapolis, decided to become part of Johns Hopkins Hospital’s paired kidney exchange program, which links previously incompatible donors to patients in need.

But after months of testing, the she learned that her kidney would not be a match for Jenny Cisneros, the 24-year-old whose health troubles have been documented in The Capital.

So Deppa, who lives in Annapolis, decided to become part of Johns Hopkins Hospital’s paired kidney exchange program, which links previously incompatible donors to patients in need.

Deppa had surgery last month, and one of her kidneys was donated to a West Virginia woman she’d never met. Deppa is still recovering from the procedure, but is pleased she made a difference for someone, if not for Cisneros.

Once she has fully healed, she plans to pick up her regular exercise regimen and eventually announce her plans to run for mayor of Annapolis.

“I thought I’d have a good kidney. I don’t drink or smoke and I’m pretty healthy,” Deppa said. “Some people think I’m crazy … (but) I just thought I’d help somebody, and what’s more important than giving the gift of someone’s life?”

Nationally, there are more than 300,000 people on the waiting list for a kidney transplant, according to the U.S. Department of Health and Human Services. In Maryland, 9,209 people are on the list, including 259 who have been added this year.

There are nearly 210,000 kidney donors available nationwide through the Organ Procurement and Transplantation Network, and that total includes about 4,300 in Maryland.

Cisneros is still awaiting a kidney, despite coming close to receiving a transplant at least three times before. Last year, a donor was found, but became ill and the transplant was later ruled out. This time, at least two candidates – including Deppa – went through a series of tests only to be ruled out as donors in the end. Her antibodies have been the problem, and now she’s in Minnesota to see if doctors at the Mayo Clinic can help.

“I was so frustrated because all these people called in to get tested and none of them were a match,” said Cisneros, 24. “‘I was like, ‘what’s the problem?’ and they said ‘it’s your antibodies.’ So I Googled how to get rid of them and the Mayo Clinic came up.”

Cisneros’ troubles with her kidneys began in 2003, when she thought she had a touch of the flu. But her doctor ordered a full round of tests and she was eventually diagnosed with Goodpasture’s syndrome, a disorder that weakens the kidneys and lungs. She was told that the disease would run its course through her body and not return.

After a treatment course of chemotherapy and steroids, Cisneros received her mother’s kidney. But that too began to fail, and she also developed congestive heart failure and hypertension.

The Capital published a story about her health challenges in January. At that time, she was fully dependent on dialysis treatment, which is still the case.

“She’ll act like everything is OK, like everything is fine and dandy, but it’s really not,” said Michelle Collett, a friend. “She’s such a tiny little thing, and she’d like everyone to think that she’s the strongest thing out there, but this has got to take a toll on the body. I don’t know how many more years she can handle it.”

Her friends set up a Web site, www.savejenny.com, and used billboards in the area to encourage people to get tested.

Potential donors get a blood test and urine test. If both are matches for someone who needs a kidney, they move on to a CT scan.

Deppa completed her rounds of testing, which included an X-ray, CT scan and blood work, in addition to the initial tests. She took a trip to Europe and believed she’d come back in time for Cisneros’ transplant surgery. Instead, she learned that the donation couldn’t move forward because there was a concern about Cisneros’ antibodies.

But the experience has helped turn Deppa into an advocate for organ donation.

“The sad truth is that there are a lot of people out there who believe that if they become a donor … medical personnel do not do everything they can to save their life; they’d rather harvest the kidney. We know that’s ludicrous, Deppa said. “Maybe this will have good karma. I helped one person and maybe, in response, others will do the same.”

For more information, visit www.savejenny.com. To be tested, call Athalene at Johns Hopkins Hospital at 410-614-6604.