Sunday, October 27, 2013

The Need for a Gift of Life Continues

Give the Gift of Life

From ReporterHerald.com, Loveland and Aurora, CO, by Joyce Davis

Phyllis McCormack waits for a life-saving kidney

Loveland woman hopes people will consider kidney donation while she waits on the transplant list

Wherever he goes, as often as possible, Gary McCormack is a walking advertisement for a critical need -- a new kidney for his wife, Phyllis.

"I wear a T-shirt that says 'Kidney Needed -- Save a Life,' along with a phone number to call if you want to be tested as a potential donor," he says. "We've put posters around town and messages in church bulletins -- wherever people might see it."

The McCormacks, both in their early 70s, have lived in Loveland for about 40 years. Phyllis McCormack has hereditary polycystic kidney disease in which dozens of benign cysts form on the kidney, eventually rendering them defunct. Although her doctor has been tracking it for years, he recently advised her to get on the transplant list at the University of Colorado Hospital in Denver. She's now at the lower level of stage 4 kidney failure.

The list is for a kidney from a deceased donor. "We've been told that once you're on the list, it generally takes three to five years to work your way up," says Gary McCormack. But, the optimum plan is to find a living donor... [read more about Phyllis]

Kidney Transplants
Types of kidney transplants
A deceased-donor transplant -- the most common form -- uses the kidney of someone who has recently passed away.

Living donor transplants are from a relative or close friend who is alive and donates a portion of his or her kidney

Benefits of a living donor transplant include no waiting period, convenient scheduling for surgery, simultaneous surgery, decreased risk of rejection and a kidney that typically works sooner, better and longer.

Only one donated kidney is needed to replace two failed kidneys. If a compatible living donor isn't available for a kidney transplant, your name may be placed on a kidney transplant waiting list to receive a kidney from a deceased donor. The wait could be a few years.

Questions and answers
Can I live with only one kidney?

Yes. You can function with only one kidney and your remaining kidney will grow larger and function for both kidneys.

How do I become a donor?

A series of tests will determine if you are an eligible candidate. Your blood type must be known before the testing process.

How long will I be laid up after being a donor?

The hospital stay after donor surgery averages three to five days. If the donor resides outside of the Denver metropolitan area, he/she may be asked to stay in the area for approximately one week after the donor surgery.

Most people can return to work after two to three weeks, depending on their recovery from surgery and the type of job they have. A donor with a physically demanding job may have to wait a little longer.

Will donating a kidney affect my future health? Is there a risk?

Most people live a long and healthy life after donating a kidney. The remaining kidney grows bigger and simply takes over for both kidneys. There is a slightly increased risk of high blood pressure and kidney failure in a small number of donors.

How much will it cost to be a donor?

Treatment related to the donor within the first three months will not cost anything. This includes pre-operative evaluation, surgery, hospital stay, outpatient visits and medical treatment -- all paid by the recipient or his/her insurance company.

Direct costs are related to time off work, transportation and non-hospital lodging related to the evaluation and surgery.


Kidney Donation vs Payment to Donor

From CBC.ca, Canada

Kidney payment ethics questions raised

Woman who waited 9 years for kidney isn't comfortable with payments


Before Canadians consider paying for kidneys, other options for reducing waits should be carefully considered, a transplant recipient and a bioethicist say.

Helen Sklarz, 60, said the nine years she spent on dialysis were bittersweet.

"It filtered and cleansed my blood and it removed toxins so I could stay alive but it took away my quality of life," Sklarz said Friday. She received a kidney 16 months ago.

Sklarz inherited polycystic kidney disease from her father. It left her with fluid-filled cysts that were triple the normal size at times.

Dialysis meant being tethered to a machine for four hours, three weeknights a week, which Sklarz said was exhausting. Dialysis can lead to headaches and severe foot and leg cramps. Sklarz also needed angioplasty to clear clogged vessels so her dialysis access site wouldn't be blocked.

She also had to keep a restricted diet. Even the fluid in a bunch of grapes could be too much on a hot day, she recalled.

In contrast, after the transplant, Sklarz says her life is "incredibly wonderful." She's able to renew old friendships, make new ones, enjoy long weekends away, hike, garden, travel and volunteer — activities she'd severely curtailed before receiving the kidney.

Paying kidney donors could be 'less costly, more effective'

On Thursday, researchers in Calgary published a modelling study that suggested paying $10,000 to living donors would increase the number of transplants performed among wait-listed dialysis patients by five per cent, and would be less costly and more effective than the current organ donation system.

"Our model found that a strategy of paying living donors for their kidneys not only saves money for the health-care system, but that the outcomes including quality of life for patients is improved," said study author Lianne Barnieh of the University of Calgary.

Despite the long wait, Sklarz isn't comfortable with the idea of paying for organs.

"This to me doesn't feel ethically correct," Sklarz said. "There's the potential for so many financially strapped and vulnerable populations to make a rash decision for cash."

Slarz said she'd rather governments ease wait times for people in need of organ transplants by educating Canadians to help overcome fears and encouraging people to register their consent to donate upon death, when organs can potentially save eight lives.

Paying kidney donors is socially divisive and needs to be carefully thought through, said Linda Wright, director of bioethics at Toronto's University Health Network.

"Organ donation has always been routed in voluntarism and altruism and this is changing it in a very fundamental way," Wright said of the proposal.

Iran is the only country where paying for organs is legal.


Citrus Fruits and PKD

From DNAIndia.com

Eating citrus fruits helps prevent formation of kidney cysts

A component of grapefruit and other citrus fruits like naringenin, blocks the formation of kidney cysts, a new study has revealed.

The team of scientists from Royal Holloway University, St George's, University of London and Kingston University London used a simple, single-celled amoeba to identify that naringenin regulates the PKD2 protein responsible for polycystic kidney disease and as a result, blocks formation of cysts.

Professor Robin Williams from the School of Biological Sciences at Royal Holloway said that this discovery provides an important step forward in understanding how polycystic kidney disease may be controlled.

To test how this discovery could apply in treatments, the team used a mammalian kidney cell-line, and triggered the formation of cysts in these cells. They were then able to block the formation of the cysts by adding naringenin and saw that when levels of the PKD2 protein were reduced in the kidney cells, so was the block in cyst formation, confirming that the effect was connected.

Meanwhile, Dr Mark Carew, from the School of Pharmacy and Chemistry at Kingston University, said further investigation is underway to understand the action of naringenin at the molecular level. This work will entail looking at the function of the PKD2 protein as a cell growth regulator.

The study is published in British Journal of Pharmacology.


PKD Disease 

From DNAIndia.com, by Santosh Andhale

Beware! Renal cysts can stay hidden till it's late

Polycystic kidney disease is silent, it's detected in an advanced stage.

Vilas Sawant (name changed) enjoyed a generally healthy life like most other bank employees his age. Last month, the 31-year-old suffered back pain. He consulted a number of doctors in the hope of getting some relief.

Understandably, he underwent numerous tests. A sonography revealed cysts in both the kidneys, an ailment that is described in medical terms as polycystic kidney disease (PKD or PCKD).

PKD is a common life-threatening genetic disease that is usually detected in the advanced stage. It is characterised by multiple cysts typically in both kidneys.

“We call it a silent disease as it is not detected until it has advanced. People with a history of kidney ailments in the family should go for a regular check-up, so early intervention through medication can save the kidney,” said Dr Jatin Kothari, nephrologist at PD Hinduja Hospital.

Sawant is an executive with a multinational bank and lives in Borivli. A general physician referred him to an orthopaedic specialist. He was advised some blood tests.

But it was the kidney function test that reported a high creatinine level of 4.5 milligrams per decilitre. (The normal should be below 1.) Which is when he was checked by a nephrologist and the cysts were detected. [Read more]

Sunday, October 20, 2013

Where is the PKD News?

With the annual fundraising and awareness walks and events behind us, the news globally regarding PKD has just about dried up. Hopefully this is just a temporary slump.  People with PKD and those working hard to find a cure have not gone away.  Stay tuned for more to come.  Thank you for reading the PKD News Blog.

PKD Research

From SBWire.com

"Polycystic Kidney Disease - Pipeline Review, H2 2013" Now Available at Fast Market Research

Boston, MA -- (SBWIRE) -- 10/17/2013 -- Global Markets Direct's, 'Polycystic Kidney Disease - Pipeline Review, H2 2013', provides an overview of the indication's therapeutic pipeline. This report provides information on the therapeutic development for Polycystic Kidney Disease, complete with latest updates, and special features on late-stage and discontinued projects. It also reviews key players involved in the therapeutic development for Polycystic Kidney Disease. Polycystic Kidney Disease - Pipeline Review, Half Year is built using data and information sourced from Global Markets Direct's proprietary databases, Company/University websites, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third party sources, put together by Global Markets Direct's team.

Note*: Certain sections in the report may be removed or altered based on the availability and relevance of data for the indicated disease.

View Full Report Details and Table of Contents

Scope

- A snapshot of the global therapeutic scenario for Polycystic Kidney Disease.
- A review of the Polycystic Kidney Disease products under development by companies and universities/research institutes based on information derived from company and industry-specific sources.
- Coverage of products based on various stages of development ranging from discovery till registration stages.
- A feature on pipeline projects on the basis of monotherapy and combined therapeutics.
- Coverage of the Polycystic Kidney Disease pipeline on the basis of route of administration and molecule type.
- Key discontinued pipeline projects.
- Latest news and deals relating to the products.

Reasons to Get This Report

- Identify and understand important and diverse types of therapeutics under development for Polycystic Kidney Disease.
- Identify emerging players with potentially strong product portfolio and design effective counter-strategies to gain competitive advantage.
- Plan mergers and acquisitions effectively by identifying players of the most promising pipeline.
- Devise corrective measures for pipeline projects by understanding Polycystic Kidney Disease pipeline depth and focus of Indication therapeutics.
- Develop and design in-licensing and out-licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope.
- Modify the therapeutic portfolio by identifying discontinued projects and understanding the factors that drove them from pipeline.

Companies Mentioned in this Report: Emergent BioSolutions Inc., Plexxikon Inc., Pfizer Inc., Synta Pharmaceuticals Corp., Metabolic Solutions Development Co., IC-MedTech, Inc., Endocyte, Inc., ManRos Therapeutics, Napo Pharmaceuticals, Inc., DiscoveryBiomed, Inc.

Sunday, October 13, 2013

New Chair of National Kidney Foundation has Gifted Kidney to His Son

Kidney News

From RenalBusiness.com

GREGORY SCOTT NAMED CHAIRMAN OF THE NKF

NEW YORK— Gregory W. Scott of Newport Beach, CA., has been elected chairman of the National Kidney Foundation, Inc. (NKF). He is currently president of Winfield Management, LLC, an investment management and real estate development company. Previously he served as chairman and CEO of APS Healthcare, Inc. and prior to that as executive vice president and CFO of PacifiCare Health Systems. Scott is a living donor, having gifted a kidney to his son, Steven, who suffered from polycystic kidney disease (PKD).

"One in three Americans is at risk for developing kidney disease and yet so few are aware of it," says Scott. "During my term as chairman, I want all Americans to understand these facts and come to the realization that it is important for everyone to protect our kidney health. Of course, this is absolutely essential for those individuals most at risk due to high blood pressure, diabetes or family history of kidney failure. Left unchecked and therefore untreated, kidney disease can lead to kidney failure requiring dialysis or a transplant. Early detection can prevent further kidney damage and so screening is essential. Our goal is also to generate awareness of healthy lifestyle and risk reduction strategies."

Scott plans to pursue these goals by building on established NKF educational efforts and advancing them. These include NKF's community health programs as well as the nationwide awareness campaign targeted at those at highest risk for developing kidney disease and the primary care providers who diagnose and treat them.

"Our Primary Care Education Initiative is going to have a major impact on awareness by making sure people at risk are tested, understand the basics about kidney function and are having the conversation with their primary care physician about the risks of developing kidney disease," says Scott. "My family has been touched by kidney disease and, the numbers suggest, there is a high likelihood that many others will be touched, also, at some point in time. I ask all Americans to join us at the National Kidney Foundation as we work to reduce the incidence of kidney disease and its impact on families across the country."


Fundraising for PKD

From the PKD Foundation

DIY for PKD

Fundraise Your Way: Take the fight against polycystic kidney disease into your own hands!

Are you passionate about finding treatments and a cure for PKD? Take the fight against this disease into your own hands by organizing a local fundraiser.You can do just about anything to raise dollars for PKD. Sean plunged into freezing waters. Cyrilla hiked 500 miles. Zac threw his daughter Anabel a birthday party.

And you? You can host a lemonade stand, neighborhood garage sale, bowl-a-thon, work jeans day or dinner party for PKD… the sky is the limit!

Get started today with these 3 easy steps:
Create your fundraiser. Begin today by creating your DIY fundraising webpage, customized by you with a photo and story.
Ask for support. Invite your friends, family members and co-workers to make a donation to your fundraiser. Our online tools and tips will help make your fundraising easy and rewarding.
Help end PKD. For every dollar you raise, 79 cents supports our mission-critical work of research, along with education and support services, advocacy and awareness programs.

Create your fundraiser today!

Questions? Email us at fundraisingevents@pkdcure.org.


Walk for PKD

From KSDK.com, Channel 5, St. Louis, MO, by Aja Williams (video clip)

St. Louis Walk for PKD hits Tower Grove Park Sunday

Polycystic Kidney disease is one of the most common genetic diseases worldwide.

PKD affects both children and adults, and often results in a need for dialysis or a kidney transplant. Right now, there's no treatment or cure for PKD, but the PKD Foundation hopes to change that.

Sunday, a nationwide Walk for PKD will be held, and St. Louis is one of a number of cities taking part in it.

Volunteer Traci Short spoke to NewsChannel 5 at Noon about the walk and how people can help.



PKD Research

DeccanChronicle, India

Citrus fruits helps prevent formation of kidney cysts

A component of grapefruit and other citrus fruits like naringenin, blocks the formation of kidney cysts, a new study has revealed.

The team of scientists from Royal Holloway University, St George's, University of London and Kingston University London used a simple, single-celled amoeba to identify that naringenin regulates the PKD2 protein responsible for polycystic kidney disease and as a result, blocks formation of cysts.

Professor Robin Williams from the School of Biological Sciences at Royal Holloway said that this discovery provides an important step forward in understanding how polycystic kidney disease may be controlled.

To test how this discovery could apply in treatments, the team used a mammalian kidney cell-line, and triggered the formation of cysts in these cells. They were then able to block the formation of the cysts by adding naringenin and saw that when levels of the PKD2 protein were reduced in the kidney cells, so was the block in cyst formation, confirming that the effect was connected.

Meanwhile, Dr Mark Carew, from the School of Pharmacy and Chemistry at Kingston University, said further investigation is underway to understand the action of naringenin at the molecular level. This work will entail looking at the function of the PKD2 protein as a cell growth regulator.

The study is published in British Journal of Pharmacology.

Sunday, October 6, 2013

Getting Over the Mountain

Walk for PKD

From Over the Mountain Journal, Birmingham and Northern Alabama

Birmingham Walk for PKD in Hoover

Oct. 12, 9 a.m.-noon
Heardmont Park and Senior Center

The third annual Walk for PKD will be held from 9 a.m. through noon at the Heardmont Park and Senior Center on Oct. 12. The event will raise money for research and treatment of polycystic kidney disease. There will be face painting and a bounce house for children and free health screenings from Samford University and Auburn University pharmacy school students. Winn-Dixie will offer flu shots for $12 at the event. Registration for the free event begins at 9 a.m. and the one-mile walk starts at 10 a.m. Heardmont Park is located at 5452 Cahaba Valley Road. For more information, visit walkforpkd.kintera.org or call 256-318-3868.


Gift of Life

From WTNH.com, Channel 8, Hartford, CT, By Jocelyn Maminta

Kidney donors critical for those with PKD


WHETHERSFIELD, Conn. (WTNH)-- The number one most needed organ is kidneys. More than half on the waiting list are waiting for one. For people with polycystic kidney disease, it's their only lifeline.

Donate Life reminders are most everywhere at the headquarters of the Connecticut Department of Motor Vehicles and its satellite locations.

"The need is so desperate," said Jaime Lazarus, PKD CT Chapter Coordinator.

The need for organ donors is critical for people diagnosed with Polycystic Kidney Disease or PKD.

"It causes cysts to grow over the organ until the healthy tissue starts to deteriorate and the organ begins to fail," said Lazarus.

There is no cure or treatment for PKD, a genetic disorder. The only lifeline is a kidney donation.

Jaime Lazarus's mother had PKD and died waiting for one.

"My mom didn't have to lose her life. And I miss her terribly every minute of every day, so if there's anything we can do to prevent other families from going through this, then I hope people will join me in registering as an organ and tissue donor," said Lazarus. [Read more]
    

From WEAU.com, Eau Claire, WS, By: Megan Lowry 

A look at Polycystic Kidney Disease

EAU CLAIRE When a family member gets sick many times our first instinct is to step in help, but when a family is dealing with a genetic disease many times that's not an option.

One of the most common life-threatening genetic conditions is Polycystic Kidney Disease.

"There are a lot of things in my life that are perfect but then you have this one thing that affects you and you’re in a stalemate," Silas Cole said.

For twenty-two year old Silas twice a week time is kept through an IV.

“I’ve been on dialysis for 3 months now,” said Silas.

He was diagnosed with Polycystic Kidney Disease or PKD at age 15. PKD is a genetic kidney disease that affects more than 600,000 people in the U.S.

The disease causes the kidneys to form cysts. “What happens is when the cysts start growing the normal kidney tissue dies off and you start losing kidney function because of that," Dr. Ibraheem Abbas with Mayo Clinic Health System said.

Doctors say a healthy kidney is about the size of a human fist but a kidney with PKD get a larger than a football and weigh more than 38 pounds.

“It’s a lifelong disease and can have multiple complications and affect multiple generations of a family,” said Abbas.

“It affects the way your family lives and it affects the way your family thinks,” Brenda Cole said.

Brenda has battled PKD for more than a decade. She has undergone two kidney transplants and hit the five year milestone since her last transplant this year.

“I did not know how sick I was until I had the transplant it changed my life,” said Brenda.

Brenda says her health is bitter sweet though as she waits for her son to get the same lifesaving gift...

There is a fund set up with Associated Bank Called ‘The Silas Cole Benefit Fund’ to help with Silas with medical bills. [Read more]



From Northborough Patch, New England,  Posted by Michael Gelbwasser (Editor)

Kidney Transplant Recipient Promotes Awareness

Northborough resident Penny Brown was among the New England Organ Bank volunteers raising awareness of organ and tissue donation during last weekend's festivities.

Penny Brown volunteered during last weekend's Spirit of Shrewsbury to continue repaying an act of kindness 15 years ago.

Brown received a kidney transplant15 years ago.

Brown was among the New England Organ Bank volunteers raising awareness of organ and tissue donation during last weekend's festivities.

"I owe it. I owe my life to transplant," Brown told Northborough Patch this week.

"Someone was kind enough to sign up to be a donor, and I am alive because of it. So, why shouldn't I spread the word and help other people?"

Brown said she had been "sick most of my life" from polycystic kidney disease, or PKD, a genetic disease, before receiving her transplant.

"My mother passed away from (PKD) when I was in my teens," Brown said.

Brown said she ultimately went on dialysis at 39 for 11 months, "a very short time," when her surgeon called to say a kidney was available. [Read more]


From Oldham Evening Chronicle, United Kingdom

Lifesaver Liz changed my world

A PHENOMENAL act of friendship and kindness has given one man and his family new hope of a healthy, happy life together.

Mark Holden, who suffers from the genetic and degenerative disorder Polycystic Kidney Disease, is now well on the road to recovery after a successful kidney transplant.

And the woman who bestowed the lifesaving gift, Liz Whitworth, has been nominated for a Pride in Oldham Award.

Liz (45), from High Crompton, underwent four hours of surgery to pass on her healthy kidney to Mark — the husband of her best friend Ruth — back in April.

Mark’s ailing organs were at a point where he was destined for dialysis if the operation did not go ahead but Liz says when she realised she was a match for Mark it seemed natural to go ahead.

Liz says she can’t believe she’s been nominated for a Pride in Oldham Award. “I’m honoured to be nominated but I feel very humbled by it all,” said the the mum-of-three who is now back at work as a business manager at St Thomas Leesfield CE Primary School in Lees.

“I did think about what I was going to do a lot because I have my own family, but it was something I would have done for anyone close to me.

“I have known Ruth since I was four, she is like another sister to me, and Mark is close to me and my family so doing this seemed an obvious thing to do.”


PKD Research

From MedicalXpress.com

Component of citrus fruits found to block the formation of kidney cysts

A new study published today in British Journal of Pharmacology has identified that a component of grapefruit and other citrus fruits, naringenin, successfully blocks the formation of kidney cysts.



Known as polycystic kidney disease, this is an inherited disorder which leads to the loss of kidney function, high blood pressure and the need for dialysis. Few treatment options are currently available.

The team of scientists from Royal Holloway University, St George's, University of London and Kingston University London used a simple, single-celled amoeba to identify that naringenin regulates the PKD2 protein responsible for polycystic kidney disease and as a result, blocks formation of cysts.

"This discovery provides an important step forward in understanding how polycystic kidney disease may be controlled," said Professor Robin Williams from the School of Biological Sciences at Royal Holloway.

"In the study, we have demonstrated how effective the amoeba Dictyostelium is in the discovery of new treatments and their targets. Having previously applied the same method of testing in our work into epilepsy and bipolar treatments, it is clear that this new approach could help us reduce reliance on animal testing and provide major improvements."

To test how this discovery could apply in treatments, the team used a mammalian kidney cell-line, and triggered the formation of cysts in these cells. They were then able to block the formation of the cysts by adding naringenin and saw that when levels of the PKD2 protein were reduced in the kidney cells, so was the block in cyst formation, confirming that the effect was connected. [Read more]

Tuesday, October 1, 2013

Raising Money for PKD

PKD Fundraising

From BedfordPatch.com, Hudson River Valley, NY, by Tom Auchterlonie

PKD Walk Held in Bedford Hills

The annual Hudson Valley Walk for PKD was held on Saturday morning in Bedford Hills, an occasion to raise awareness of polycystic kidney disease.

Turnout was at least 100, according to Darien DaCosta, an event coordinator and Suffern resident.

DaCosta described PKD as an illness that affects a lot of people but that not a lot of people know about. He was unaware of PKD until his wife, Josie, got it in 2008. The following year she got a kidney transplant.

PKD is a common genetic disease and affects both children and adults, according to the group's website. However, it notes that there is no cure available.

The Bedford Hills walk began in 2004 and was supported by Heidi Camberari, who grew up in Bedford Hills and now lives in Somers. Saturday's walk was a unique Camberari family occasion. Her father, Wayne Grossman, met a cousin named Renee Fishback that he did not know, according to her mother, Sandy Grossman. [Read more]


From the BaltimoreSun.com, Baltimore, Maryland


Sept. 29: The Walk for PKD will begin at 10:15 a.m. with check-in and on-site registration at 9 a.m. at the Hammerman Beach Area of Gunpowder Falls State Park. PKD — polycystic kidney disease — is a common genetic disease that affects children and adults, and often results in a need for dialysis and a kidney transplant. For information, go to walkforpkd.kintera.org or email co-coordinators Carol Mainolfi and Matt Mainolfi at BaltimoreWalk@pkdcure.org.


From YorkPress, York, United Kingdom


A MAN who was given a new lease of life through a kidney transplant is holding a fundraising event in York tonight.

Shaun Johnson, 46, of Darcy Road, Selby, suffered from polycystic kidney disease, and underwent a kidney transplant in 2011, following a year of dialysis.

Tonight he will host the fundraising event at Huntington Working Men’s Club, to raise money for the York Teaching Hospital Charity, to help fund the self-care dialysis unit being set up at Selby’s New War Memorial Hospital.

Mr Johnson said: “Two years ago I was fortunate enough to receive a kidney transplant. However, prior to the transplant I had to have a year of dialysis, and so I know how vital this service is.

“We wanted to think of a way to give back, and to thank the teams at both York and Selby hospital for the support and service they have provided both myself and my family throughout my treatment and ongoing care.

“It would be nice to raise £1,000, but that depends on how generous people are on the night.”

The evening will include live entertainment from The Chicago Blues Brothers Tribute Band, and performances from local acts Jess Simpson and Joe Wilson, with a fundraising raffle. [Read more]


Gift of Life

From Omaha.com, World-Herald, Omaha, Nebraska, by Bob Glissman

Bob Glissmann: Why I decided to donate a kidney to a friend

The 9-year-old girl slept as a machine pumped her blood out of her body, filtered it and pumped it back in.

I was at the Nebraska Medical Center interviewing her mom, who was saying how brave and tough her daughter was. The girl didn't have the option of skipping her kidney dialysis treatment. The treatments kept her alive as she waited for a donor kidney.

After I wrote the story in April 2012, I got tested to see if I could donate one of my kidneys to her. I was a longtime blood donor, and I saw a kidney donation as just a more complicated, painful extension of a blood donation — a donation with an abdominal scar and a recovery period.  [Read more]


FOR KIDNEY DONORS
Risks: Possible long-term risks of kidney donation may include high blood pressure; reduced kidney function; hernia; organ impairment or failure that may lead to the need for dialysis or transplantation; or even death. Negative psychological symptoms are possible during the healing process and years after the donation.

The recipient's insurance may or may not cover follow-up services for the donor if medical problems occur as a result of the donation. A donor's insurance also may not cover those expenses.

-- Source: United Network of Organ Sharing

To become a donor: For more information about becoming a donor, go to
www.organdonor.gov or call the Nebraska Medical Center's transplant office at 800-
401-4444


From DChieftain.com, by Elva Osterreich

Husband donates kidney to wife 

Four years ago Cecilia Robles was diagnosed with polycystic kidney disease.


Traveling three times a week to Las Lunas for dialysis got expensive and was exhausting.

In March, she started dialysis at home, a different system but an effective one. Instead of replacing the blood and cleaning it in a short exhausting space of time, the process was able to happen overnight and more often.

The Robles family already knew the disease as Cecilia’s mother and sister both had gone through the same disease until they died of it.

“My husband didn’t want to see me go through these same things,” she said.

Pedro said as soon as the diagnosis came down, he was thinking about giving his wife a kidney.

“Since the day they diagnosed her, I was thinking about transplant,” he said. “It’s better than being hooked up for life.” [Read more]



From HemelToday, United Kingdom

Hemel taxi driver Andy turned down vital transplant op – because his twin brother needed an organ more urgently

A twin who gave up the chance of a kidney transplant so that his more seriously ill brother could have the surgery is now in desperate need of the life-changing operation.
Taxi driver Andy Twigg, who suffers from polycystic kidney disease, undergoes dialysis to clean his blood at St Albans Hospital three times a week.

He said: “I get there for about 6pm and I probably go home between 10pm and 10.30pm. Without the machine I wouldn’t be here today.”

The disease was discovered almost by accident in the Hemel Hempstead brothers after Lawrence, of Adeyfield, injured himself and was sent for a scan by doctors around 10 years ago.

It set alarm bells ringing and tests on Andy, of Apsley Lock, also revealed he was a sufferer – his two sons, aged 17 and 19, have the condition, too, and they may also need kidney transplants in the future.

Andy said: “It tires you out. It drains you.

“I still do things but I’m not as healthy as I was five years ago.”

Lawrence had a transplant in March 2011 – he was already undergoing regular dialysis while, at that time, Andy did not require the invasive medical treatment.

He said: “I got the phone call for the kidney transplant and I went down there but they didn’t realise there were two of us. I was gutted but it was just one of those things.

“He was dialysing at the time and I wasn’t, so it was better for him to get it.

“I had the choice to have it or to give it to my brother. [Read more]