Sunday, August 27, 2017

PKD Research: Reducing Cyst Growth with Cancer Drug, Using PDG to Eradicate PKD

PKD Research

From Science Daily

Cancer drug may benefit patients with inherited form of kidney disease


A cancer drug called bosutinib may inhibit the growth of cysts in patients with autosomal dominant polycystic kidney disease (ADPKD), according to a study appearing in an upcoming issue of the Journal of the American Society of Nephrology (JASN). The findings point to a potential new treatment strategy for affected patients, but the long-term benefits remain to be determined.

ADPKD is an inherited disorder that affects up to 1 in 1000 people and is characterized by cysts in the kidney and other organs. As patients' kidney volume increases due to cyst growth, they gradually lose their kidney function and often develop kidney failure. Current treatments are primarily supportive, such as focusing on hypertension and other secondary complications.

The inherited mutations that cause ADPKD affect a protein involved in various signaling pathways that often involve enzymes called tyrosine kinases. Therefore, a team led by Vladimir Tesar, MD, PhD (Charles University and General University Hospital, in the Czech Republic) tested the potential of an investigational drug called bosutinib that inhibits a particular tyrosine kinase called Src/Bcr-Abl.

The phase 2 study included patients with ADPKD who were randomized 1:1:1 to bosutinib 200 mg/day, bosutinib 400 mg/day, or placebo. Of 172 patients enrolled, 169 received at least one treatment. The higher dose of bosutinib was not well tolerated.

The annual rate of kidney enlargement was reduced by 66% for patients receiving bosutinib 200 mg/day vs. those receiving placebo (1.63% vs. 4.74%, respectively) and by 82% for all patients receiving bosutinib vs. those receiving placebo (0.84% vs. 4.74%, respectively). The study was not powered to demonstrate a treatment effect on kidney function, but there was no evidence of a benefit associated with bosutinib compared with placebo over the 2-year treatment period.

"The reduction in growth of cysts through treatment with bosutinib was confirmed, although gastrointestinal side effects (primarily diarrhea), which were partly dose-dependent, may represent a substantial drawback for the further development of the drug for patients with ADPKD," said Prof. Tesar.



From Rare Disease Report, by James Radke

Can Preimplantation Genetic Diagnosis (PGD) Eradicate Genetic Diseases?

Last week in Nature, an article by David Cyranoski was published regarding the rise of preimplantation genetic diagnosis (PGD) in Chinese fertility clinics with the intention of eradicating genetic diseases.

PGD was first performed in England almost 2 decades ago to preferentially select for female embryos to be implanted in parents at risk for X-linked genetic conditions. Since then, the technique has advanced significantly; while many countries are performing PGD, the article in Nature indicates that China is outperforming all other countries, and furthermore, PGD is not considered to be part of an ethical issue there as it is in other countries.

Using PGD, Chinese clinics have reported being able to avoid producing children with, or at risk for, retinoblastoma, short-rib-polydactyly syndrome, Brittle-bone disease, Huntington’s disease, polycystic kidney disease and deafness.

The eradication of a genetic, chronic condition could have a significant impact on healthcare costs. For example, the cost for a PGD to avoid having a child with cystic fibrosis would be $57,000. While seemingly expensive, a cystic fibrosis patient incurs about $2.3 million in medical costs over his or her lifetime.

Similarly to the way that Iceland’s eradication of Down syndrome has led to concerned tweets like the one below, similar concerns could be justified.




Specifically, PGD raises concerns that it will be used only by the well-off to create an elite genetic class. It is an expensive procedure, likely to be limited to families with better healthcare coverage.

In China, while many parents are concerned about genetic diseases, some parents are trying to weed out genetic anomalies to create a superior child. Sijia Lu, chief technology officer of Yikon Genomics has stated some couples are asking to weed out the mutation that renders many Asians unable to process alcohol. Right now, such selection is not allowed.

While such queries are theoretically a concern, some argue that it shouldn’t be. Joe Leigh Simpson, a medical geneticist at Florida International University in Miami said, “With every reproductive-biology advance, we get the same questions: ‘won’t there be a slippery slope that leads to abuse?’ But it never happens.”

As for using PGD for its intended use – to screen for genetic diseases – its use in the United States remains limited right now, partly because is very expensive and insurance generally does not cover it.

Sunday, August 20, 2017

PKD Foundation News: PKD Awareness Day, CRISPR Research, Toddler Walks 100 KM for PKD, Gift of Life, PKD Real Costs

PKD Foundation News

From PKD Foundation

#PKDAwarenessDay is fast approaching

We need your voice in the weeks leading up to Awareness Day on Monday, September 4. With an estimated 600,000 Americans suffering from the effects of PKD, the Average American is just 1.2 degrees of separation from someone with PKD. Visit our page to download and share #PKDAwarenessDay social resources and spread the word now. Your voice is the most important to finding treatment options for this chronic, genetic disease.


CRISPR Research Update

A recent article in the New York Times announced that scientists have successfully edited genes in a human embryo to repair a mutation. Peter Harris, Ph.D., Mayo Clinic geneticits, director of the ADPKD genetic mutation database and former PKD Foundation Scientific Advisory Committee (SAC) member, has written a piece about this discovery and what its implications are for PKD. You can read his take on the science on our website.



Register today and Walk for PKD

Bring your family and friends and join over 10,000 participants that will be walking for PKD. With 100% of donations funding research your donations have never been more powerful! You can help us accelerate treatments to patients faster: register for your local Walk and start fundraising today.


From Fort Saskatchewan Record, By Leanne Delong

Toddler walking 100 KM’s for kidney foundation

Two and a half year old Sam McKail is 81 kilometres into his 100 kilometre goal and will walk his final kilometre with those partaking in the Calgary Kidney Foundation March Sept. 8-10.


Fort Saskatchewan toddler Sam McKail is on a mission to walk 100 kilometres in 100 days in support of the Calgary Kidney Foundation’s annual kidney walk and as of Aug. 14 he has already reached 81 kilometres.

The kidney walk will take place Sept. 8 - 10 with participants marching 100 kilometres in three days from K-Country to Calgary and Sam will walk his last kilometre down the hill of Calgary’s Olympic Park with family and other marchers.

“I’m kind of amazed because when we first started, pretty much everybody asked if he could actually walk 100 kilometres a day for 100 days and at that point he was only two years and four months old and that is a pretty high expectation, so I was a little nervous,” said his mother Kirstin Lehmann.

What started as a light hearted joke in her family last year has turned into a solid commitment between mother and son.

Lehmann decided to fully commit to the challenge on May 5 and she let the kidney foundation know that Sam, now two and a half years old, would be partaking in the march in his own way.

“They have thrown themselves behind Sam and made him his own mini marcher t-shirt and a little name tag,” she said.

Every time Sam completes ten kilometres Lehmann makes a video, which is posted online.

“He just keeps on going and it’s been a great way to explore Fort Saskatchewan,” she noted.

She said they moved to the Fort in April from Calgary.

Why they support the kidney foundation

Lehmann and her family have been involved with the kidney foundation for many years.

“The story dates back to 2010, long before Sam was even born. My uncle, even though he had been a remarkably healthy active person, couldn’t beat genetics and developed polycystic kidney disease and he needed a kidney transplant or dialysis,” she explained.

Her mother had volunteered to donate a kidney and completed all the prep work but at the last minute another family member stepped in to donate.

Lehmann’s mother felt that donating a kidney was meant to be so she called the Kidney Foundation and asked if they wanted a kidney. Her kidney was donated to the Paired Exchange program and because of that, a new kidney was able to go to someone on the transplant list.

“80 per cent of the people on the organ transplant waiting list are waiting for a kidney, so this was huge for somebody else. The thing was my mom was in her early 60’s at this point and people assumed her lifestyle would be extremely compromised due to only having one kidney,” said Lehmann.

People would worry about her mother every time she got a cold.

“It’s amazing how many people don’t realize you can live with one kidney and still live a very functional life,” she noted.

Her mother decided to prove all these people wrong and walk the kidney march’s 100 kilometres in three days, just to show them that they are wrong.

Her mother will now be marching for her fifth year come September.

“Over the five years she has raised almost $20,000. She is just $700 shy of reaching that goal within the next couple of weeks leading up to this year’s march,” said Lehmann.

She said if that was not enough to get her son involved, Lehmann’s cousin is also marching this year with her parents as well.

For more information on the kidney foundation visit, www.kidney.ca.

To follow Sam’s journey visit Lehmann’s blog, www.greatnorthernfamily.com.




Gift of Life

From New York Post, By Christian Gollayan
World’s best student donates kidney to teacher

Wanna be a teacher’s pet for life? Don’t give an apple — give a kidney.

That’s what Ali Golian, 30, did for his former teacher Sonia Leonardo.

Golian and Leonardo go back to 2010, when he studied radiology under the now-42-year-old at London’s Kings College Hospital. “Sonia was an incredible teacher,” Golian tells South West News Service. He credits her with inspiring his career track (he’s now a radiology-equipment tutor).

After Golian graduated from school, he landed a job at Leonardo’s hospital. The two became fast friends, and worked together for two years. But they fell out of touch after she changed jobs.

Fast forward to five years later, when a Facebook post caught Golian’s eye. Leonardo’s sister was thanking friends for sending get-well flowers on her sister’s behalf. Concerned, Golian texted Leonardo.

His mentor and friend, he learned, was home on sick leave due to complications from polycystic kidney disease. The genetic disorder had caused cysts to grow in her kidneys, and she was in dire condition: Her kidney function had been reduced to 10 percent.

The transplant list, she told Golian, had a projected wait list of three years — and in the meantime, staying alive would mean enduring five half-hour dialysis sessions every single day. [Read more]




From MedicalXpress


A new analysis indicates that few strategies to increase living kidney donation have been evaluated effectively; however, educational strategies targeted to recipients and their family and friends have the best evidence of being successful. The analysis, which appears in an upcoming issue of the Clinical Journal of the American Society of Nephrology (CJASN), also provides possible suggestions that could help investigators, organizations, and policy makers determine which, out of the many strategies that may be used to increase living donation, should be considered.

There is a critical need to increase rates of living kidney donation to address the growing organ shortage; however, it's unclear which strategies are effective. To investigate, Scott Klarenbach, MD, MSc (University of Alberta) and his colleagues summarized the breadth and quality of the evidence on approaches to increase living kidney donation.

When the researchers conducted a search of the medical literature, they found very few high quality studies. The most evidence related to educational strategies: those directed at both the potential recipient and their close social network. Of the 7 studies that focused on educational strategies, 2 studies that targeted the potential recipient's close social network reported significant benefits. Other approaches were also identified, but their impact was assessed through less rigorous study designs.

"Living kidney donation is the optimal treatment for patients with kidney failure, who would otherwise be treated with dialysis. It improves survival and quality of life, and is less resource intensive and can be safely performed with appropriate donor selection," said Dr. Klarenbach. "There are large numbers of patients with kidney failure waiting for a kidney transplant, and increasing living kidney donation would reduce their wait time and improve outcomes."

In an accompanying editorial, Krista Lentine, MD, PhD (Saint Louse University School of Medicine) Didier Mandelbrot, MD (University of Wisconsin School of Medicine) noted that certain steps are needed for practitioners and policymakers to expand living donor kidney transplantation. "We and others believe that the strategies that have the potential to improve informed consent and access to living kidney donor transplantation include: (a) broader and repeated living donor kidney transplantation education beginning at earlier stages of kidney disease and involving the patient's social network, (b) removal of disincentives to donation, (c) optimized efficiency in the evaluation of donor candidates, and (d) improving the safety and defensibility of donor selection," they wrote.




PKD Research

From FigShare


Abstract Background There is limited real-world data on the economic burden of patients with autosomal dominant polycystic kidney disease (ADPKD). The objective of this study was to estimate the annual direct and indirect costs of patients with ADPKD by severity of the disease: chronic kidney disease (CKD) stages 1–3; CKD stages 4–5; transplant recipients; and maintenance dialysis patients. Methods A retrospective study of ADPKD patients was undertaken April–December 2014 in Denmark, Finland, Norway and Sweden. Data on medical resource utilisation were extracted from medical charts and patients were asked to complete a self-administered questionnaire. Results A total of 266 patients were contacted, 243 (91%) of whom provided consent to participate in the study. Results showed that the economic burden of ADPKD was substantial at all levels of the disease. Lost wages due to reduced productivity were large in absolute terms across all disease strata. Mean total annual costs were highest in dialysis patients, driven by maintenance dialysis care, while the use of immunosuppressants was the main cost component for transplant care. Costs were twice as high in patients with CKD stages 4–5 compared to CKD stages 1–3. Conclusions Costs associated with ADPKD are significant and the progression of the disease is associated with an increased frequency and intensity of medical resource utilisation. Interventions that can slow the progression of the disease have the potential to lead to substantial reductions in costs for the treatment of ADPKD.

World’s best student donates kidney to teacher

Sunday, August 13, 2017

Living with PKD: Columbus, IN, New Zealand, Walk for PKD: Milwaukee, Dialysis Membrane Technology

Living with PKD

From The Republic, Columbus, IN, by Brian Blair

Fighting together: Mom, daughter wage battle against disease

photo



Suffering through physical weakness, weariness and memory fog amid an incurable disease is one thing.

But painstakingly waiting is quite another — waiting for news that another person will grant the gift of renewed life with a donated organ.

Or the terrible-news-turned-redeeming-sacrifice that one who has died was altruistic enough to sign up for organ donation.

Columbus resident Debbie Patterson, 57, needs a kidney transplant as soon as possible. Thirty-year-old daughter Casey Durnil, also of Columbus, will need one soon enough.

Both have progressive polycystic kidney disease. It causes numerous fluid-filled cysts to grow in the kidneys, reducing kidney filtering function and eventually leading to organs failure, according to the National Kidney Foundation.

The mother has only 15 percent kidney function. The daughter only 12 percent, although she must make other medical-related adjustments before she can be considered for a transplant.

“There’s got to be at least one person out there who has an O (blood type) kidney for my wife,” said Gerry Jones, Patterson’s husband of seven years. “So I pray that someone else has the heart and soul to care enough to donate a matching one for Debbie. This is my prayer every minute of every day.”

Patterson recently sat in their 31st Street living room with a textbook-thick binder filled with medical background and notes, much of it highlighted in yellow marker, about her and daughter’s condition.

The mother suffered through back pain at work just that day from problems in her left kidney. There’s not much she can do for such obstacles other than taking acetaminophen.

Patterson was diagnosed in March 2010. Doctors diagnosed Durnil a year and a half later.

Durnil could begin daily dialysis within a few weeks as a step to help her. Both still work full-time at Phoenix Quality Management, a supply chain services company in Walesboro.

But Patterson notices regular reminders that her kidneys are struggling. Partly because she is low on absorption of iron and other vitamins, she couldn’t even muster the strength to drive a small yard-sale stake into the soft, rain-soaked ground of her lawn recently. But still, she managed to laugh at her plight.

“What else am I going to do?” Patterson asked. “Sit here and cry?”

She has been on the organ-donor waiting list for a year amid a process that sometimes stretches to five years.

She knows the number of people in the United States waiting for a kidney is more than four times greater than the number of transplants.

The United Network for Organ Sharing shows that in 2016, there were 19,060 kidney transplants nationally. And there are currently 96,966 people in the United States on the waiting list for a kidney.

The network also shows that kidneys rank as the most in-demand organ for transplants, far outpacing the need for other organs such as livers, hearts, and lungs, needed in that order.

Dr. Jennifer Bucki, Patterson’s nephrologist with Indiana Kidney Specialists in Indianapolis, said she has straightforwardly laid out the facts about the average wait for a new kidney, and other factors affecting Patterson’s situation “hopefully without being too blunt.” But the physician also mentioned that her patients also must remember that she has seen firsthand a number of transplant success stories among those she has treated.

Bucki complimented Patterson’s upbeat ways amid substantial challenges.

“She has a good attitude, even though she has experienced her share of ups and downs, including seeing changes in her body, and changes in her endurance as her disease has become symptomatic,” Bucki said.

The specialist supports publicity about cases such as Patterson’s.

“It helps the community become involved not only in thinking about their own health, but also with them thinking about becoming organ donors,” Bucki said.

Jones, a semi-truck driver in Indiana and Kentucky, soon will spread the word about needing a kidney donor by posting a message on his vehicle as he roams the interstates.

“There’s got to be at least one person out there (who’s a donor match),” said Jones, who is the wrong blood type to be a donor.

A number of people have tried to donate. But none who were a blood type O match made it through the initial phone-screening interview as a viable donor candidate.

So they wait. And hope. And pray, along with others. [Read more]




From Stuff, New Zealand

Kiwi basketball great Kenny McFadden diagnosed with serious kidney disease

Kenny McFadden (R) played a huge part in Steven Adams' development.

Kenny McFadden (R) played a huge part in Steven Adams' development.


Kenny McFadden, Kiwi basketball great and mentor to Steven Adams, has been struck down by a serious kidney disease.

The American-born former Wellington Saints player-coach was rushed to hospital several weeks ago with acute respiratory failure.

While he managed to pull through following a night of "extreme medical intervention", McFadden was subsequently diagnosed polycystic kidney disease, a genetic disorder that requires regular dialysis until a suitable kidney donor can be found, his friends say.

For more than 30 years McFadden has made a significant impact on basketball in this country as both a player and coach.

However, a Give A Little page set up by friends and colleagues of his partner, Angelia Beamsley, said the illness has left him unable to work.

"This is placing heavy financial strain on him and his partner which on top of regular visits to the hospital is making a tough time that much harder," a statement on the page said.

"By creating this page we are attempting to raise funds to help with his quality of life and to ease the burden on his partner and family."

After playing for Washington State University in the USA, McFadden moved to Wellington in 1982 where he enjoyed great success with the Saints.

He led the team to seven finals appearances, winning five NBL titles between 1982 to 1988.

Following his retirement in 1996, McFadden became heavily involved with junior player development, founding his own hoops academy in Wellington as well as coaching the Junior Tall Blacks to the under-19 World Championships in 2009.

It was through his coaching work that he met Adams, and he went on to play a key role in the Kiwi's miraculous rise to the top of the basketball world with the NBA's Oklahoma City Thunder.

McFadden first took Adams under his wing as a 14-year-old who had been shifted by an elder sibling to the capital from Rotorua in order to get his life back on track.

He has been the young man's mentor ever since, refining his skills early on at his academy and then later providing the guidance and advice as the young man headed stateside to chase his dreams.





PKD Walk

From Milwaukee Journal Sentinal

Milwaukee Walk for PKD:

Event is 2.5 mile benefit for polycystic kidney disease, 10 a.m. Sept. 10. Registration begins at 8:30 a.m. Bayshore Town Center, 5800 N. Bayshore Drive, Glendale. Registration is free; donation requested. walkforpkd.org/milwaukee




Dialysis Research

From WOW News, Malaysia

UTM researchers develop haemodialysis system using membrane technology



Statistically, it is estimated that one in twelve Malaysians has kidney failure and millions more are at risk. Commonly, these patients need dialysis treatment when they reach the final stage of kidney failure or typically known as the end-stage renal failure (ESRF), where they lose 85% to 90% of their kidney function.

In Malaysia, the number of dialysis patients keeps increasing with the estimation of 5,000 new cases of ESRF being reported each year. The statistics from the National Kidney Foundation Malaysia reveals worrying figures where the total number of haemodialysis patients had increased from 12,182 patients in 2005 to 38,157 patients at the end of 2016. In fact, with he right projection there will be 43,000 haemodialysis patients altogether by the end of 2017.

Every year, the government allocates RM50 million to cater to the cost of treatment of around 38,000 ESRF patients. However, only 35,580 patients from that number undergo haemodialysis treatment. Out of the 35,580 patients, government hospitals are able to cover the expenses for only 8,000 patients. The remaining patients have to solely rely on the subsidy from the Government and NGOs. According to local sources, the amount paid by each patient for every session is RM162 (around USD$38 with government subsidy), and part of the amount comes from the cost of the haemodialyser. It is known that the market price for an imported haemodialyser can be as high as RM125 (US$30) per dialyser depending on the brand and packing size. Therefore, immediate action is needed to compensate and reduce at least the cost of haemodialyser.

To that end, UTM made it a mission to establish its own brand for renal products, starting with the production of a haemodialyser. In order to do that, Prof Dr Ahmad Fauzi Ismail and his team from the Advanced Membrane Technology Research Centre (AMTEC), Universiti Teknologi Malaysia (UTM), began their research into creating a home-grown haemodialysis system for blood purification using membrane technology that would greatly reduce the cost of treatment for Malaysian ESRF patients, and the government and NGOs who are subsidising treatment. This is because at present, hospitals and haemodialysis centres in Malaysia solely depend on imported renal products from modern countries like Japan and Germany.

The project started with the development of a high performance haemodialysis membrane, where prior to membrane fabrication process, a polymer solution was prepared by mixing 18 wt.% polysulfone and 8 wt.% polyvinylpyrrolidone in N-methyl-2-pyrrolidone as the solvent. Both membrane and haemodialyser were produced using in-house equipment and instruments producing a well-optimised membrane specifically designed to remove critical uremic toxins while retaining essential proteins like albumin in blood, resulting in an optimised blood purification process. Further, along with the low production cost and high flux achievement, this home-grown haemodialyser is capable of removing sufficient amounts of uremic toxins from a patient’s blood including a large fraction of recalcitrant middle molecular weight molecules.

It is anticipated that the reduced price of this home-grown haemodialyser, in addition to the product’s trusted performance, will heighten the chances of market penetration in Malaysia, with the potential to greatly reduce costs borne by patients, the government, and NGOs, freeing up valuable resources to be used in other high impact projects that cater to the nation’s needs. With such an impact to Malaysian society as a whole, it is little wonder that UTM’s long-term goals include making Malaysia a regional base for renal products in Southeast Asia, and perhaps one day, the world.

Sunday, August 6, 2017

PKD Chain of Life, Donor Kidneys Rejected, DonateLife Week, PKD Creates Giant Liver

Gift of Life

From US News & World Report, By Dennis Thompson


A donated kidney is turned away for transplant an average of seven times before reaching the patient who finally receives it, a new study shows.

Transplant centers regularly reject kidneys based on a donor's age or perceived quality of the organ, even though these kidneys are eventually accepted and work well for people farther down the waiting list, explained lead researcher Dr. Anne Huml, a nephrologist and health disparities fellow with Case Western Reserve University in Cleveland.

The centers are likely being appropriately picky in selecting organs, to ensure the greatest chance of success by carefully matching each kidney to each recipient, Huml said.

"If someone's been waiting five years, why rush and take the first kidney offered when within a month they'll be offered a better kidney and their outcome will be better?" Huml said.

But such hesitation can mean that patients high on the waiting list remain on dialysis while organs that would have suited them fine pass down to others who've waited less time, said Dr. Sumit Mohan, an associate professor for medicine and epidemiology at Columbia University's Mailman School of Public Health.

"The general sense is that surgeons are less willing to take risks, so what ends up happening is there are a large number of kidneys that people say no to that end up getting transplanted way down the list," said Mohan, who co-authored an editorial accompanying the study. Both appear in the July 27 issue of the Clinical Journal of the American Society of Nephrology.

Worse, patients rarely are told that their transplant center has passed on a donor kidney offered to them, Mohan said.

"If your surgeon says no, I don't want that kidney, you're never informed. You're not even told that's the case," Mohan said. "Patients need to be more engaged in the process and have a better understanding of what's being agreed to on their behalf."

More than 100,000 people currently are waiting for a kidney transplant in the United States, Mohan said.

Despite this, nearly 1 in 5 deceased donor kidneys are discarded annually. Nearly 15 percent of organs are tossed away because no recipient can be located, Mohan said.

Dialysis keeps a delay in receiving a kidney from becoming immediately life-threatening, Huml said. However, there is a high mortality rate associated with dialysis, and people who are on dialysis longer don't do as well once they have received a kidney, Mohan said.

For the study, Huml and her colleagues reviewed more than 7 million organ offers that were made for 31,230 kidneys from deceased donors between 2007 and 2012. All the kidneys were eventually transplanted.

The researchers found that donor kidneys were offered a median of seven times to different patients before being accepted for transplantation.

Centers most often gave a pass to a donated kidney either based on donor-related factors such as age of the person or quality of the organ, or because the minimal acceptable criteria for a transplant center had not been met. Each of those two general reasons accounted for 3.2 million rejected offers, or around 45 percent.

Transplant centers largely pass on kidneys from donors with high blood pressure, a history of diabetes, reduced kidney function or death related to heart problems, the researchers found.

In those cases, centers that want to keep their success rates high are rejecting organs that appear dicey, even though they end up being successfully transplanted into another patient, Mohan said.

The study also found that transplant centers are more picky in choosing kidneys for patients who are male, Hispanic, overweight or obese, or suffering from high blood pressure resulting from kidney failure, Huml said.

Patients with medical problems such as excess weight or high blood pressure likely face more difficult surgeries, and so doctors are more choosy about the kidney that's right for them, Mohan explained. [Read more]




From Hartford Courant, CT

Yale-New Haven Hospital Puts Connections On Display In 18-Patient, 9-Kidney Exchange

Yale Kidney Chain

As Janet Labati, a small, thin woman from Newtown, sat next to her kidney donor Laura Miller, of Old Lyme, the two women whispered and laughed like old friends. However, it was the first time they had ever met.

"She's my angel," Labati said as she rested her hand on Miller's arm. "I'm so grateful just to be able to walk around and feel good again."

Emotions ran high on Thursday at the Yale-New Haven Hospital when nine kidney transplant patients met their donors for the first time. All had been strangers, but they are forever linked in an 18-patient, nine-kidney exchange; the largest exchange ever performed in Connecticut.

When a previous transplant failed, Labati said she thought she was out of options.

"Kidney disease had taken a toll on my body," she said. "I contacted the hospice to discuss end of life care, I never dreamed I would have a third chance."

But her husband, Jim Labati, wouldn't give up on her. He said he donated one of his kidneys through Yale's kidney exchange program in the hopes that his wife would receive a kidney and no longer require the use of a dialysis machine to filter toxins from her bloodstream.

"Being on dialysis is surviving but it's not living," he said. "I donated a kidney so Janet could receive a kidney."

Miller said she had originally wanted to donate to her friend Randy Smith of Old Lyme.

"I feel rewarded and pleased that I saved a life," Miller said. "How many people can say that at the end of the day?"

The mastermind behind the exchange was Dr. Peter Yoo, director of Yale's program in paired organ exchange. He said it started with one altruistic donor, Robin Gilmartin, of West Hartford. Gilmartin and her wife, Diane Mack, both said they decided to donate their kidneys after reading an article in the Hartford Courant about a four-way kidney exchange performed at the hospital. Her only motive was to help others, she said.

"Donating a kidney is an extremely low-risk surgery. It doesn't change your functioning in the least," Gilmartin said. "For relatively little inconvenience, it's a tremendous reward."

Little did Gilmartin know that her decision to donate would set off a chain reaction in which Yoo was able to match 18-patients together. [Read more]




From Bendigo Advertiser, Australia, by Mark Kearney

Bendigo kidney recipients use DonateLife Week to describe how organ donation changed their lives


On meeting Maree Derby, it is impossible to tell that just five weeks ago she was the recipient of a kidney transplant.

Her mood is upbeat, her eyes are bright and 18 months of dialysis at Bendigo Health already feels like a distant memory.

“Sometimes I’ve got to remind myself to slow down, that I’ve had a major operation,” Ms Derby, who suffered from polycystic kidney disease, said.

Speaking during DonateLife Week, an annual initiative encouraging organ and tissue donation, the 52-year-old explained how gifted organs transformed her family’s life.

Not only was Ms Derby an organ recipient, her mother, Gwen, also underwent a kidney transplant for polycystic kidney disease.

Her 25-year-old daughter has also been diagnosed with the hereditary condition.

“It does follow you around a little bit, but you have to get on with it,” she said when asked how it felt knowing this was a process she would eventually endure.

“I also think it gives you time to accept it.”

Peter Van Schajik, another Bendigo kidney recipient, did not have so long to prepare; he was struck down last year with an aggressive case of IgA nephropathy, a build-up of antibodies in the kidneys.

Eight weeks ago, a transplant operation freed him from four days of dialysis every week. It also put to an end a horror three-year period during which time a workplace accident left Mr Van Schajik with burns to 35 per cent of his body.




Living with PKD

The Sydney Morning Herald, Australia, by Rachel Clun

Woman donates 12 kilogram liver to university learning museum

Fiona Murray with her donated liver.



Fiona Murray's liver was large. So large people would often ask her when her baby was due.

A healthy human liver weighs about 1.5 kilograms, but Ms Murray's weighed a massive 12.08 kilograms when it was removed.

"When I actually had the operation I said, 'can somebody take a photo of it for me' but they took one step forward and said,'well actually, the fellow in pathology said could we actually have it for the museum'," she said.

And after receiving a donor liver and kidney herself, Ms Murray said she jumped at the chance to donate her own to science.

"I just said, 'yeah that would be great, I don't mind, I don't need it'."

The Brisbane woman's liver was donated to the University of Queensland's Integrated Pathology Learning centre, where she said students can now use it as a learning tool.

"If someone's donating to me, for me to live and do all the things that I love to do so if someone would like to learn from my donation, then that was pretty much just giving the gift of knowledge," she said during DonateLife Week.

Ms Murray, now 47, was diagnosed with polycystic kidney disease when she was 25 years old. When she was in her 30s the disease spread to her liver, which continued to grow.

"(It was) rather uncomfortable, it's pretty much like being pregnant for years and years," she said.

Strangers would often ask her when she was due, but rather than get annoyed Ms Murray said she would use it as a way of bringing up the topic of organ donation.

"I didn't get sick of that totally; sometimes it was just more of an avenue to tell people, 'oh no that's not a baby bump, it's actually polycystic liver due to polycystic kidneys and I need a donation of a liver and kidney."

While Ms Murray said she didn't feel particularly unwell, she realized her condition was serious when dialysis failed to improve her health.

"It was making it worse: I lost a lot of weight, I was cramping up on the chair, my liver was so big it was encroaching and sitting and suffocating all the other organs when I was sitting on the dialysis chair," she said.

She was on the transplant list for just a couple of weeks before receiving a donor kidney and liver in early 2014.

As well as being able to now bend down and do up her own shoelaces, Ms Murray said she had been enjoying the freedom the transplant had given her.

"Life now is my own journey, I don't have to think about having to go on dialysis, I can do whatever I want now, I can choose," said Ms Murray, who has just completed a course in medical administration and plans on studying to be a radiographer. [Read more]

Sunday, July 30, 2017

PKD Fundraising, CarrierCheck: DNA Testing, Need Kidneys: Georgia, Gift of Life: Hyattsville, MD, PKD Kidney Breaks Guinness Record

PKD Fundraising

From The Post-Journal, Jamestown, NY, by KATRINA FULLER

Change For Chihopi Fundraiser Expands For Second Year

Bemus Point teens Allyssa Seeley, Cameron Rowe and Taylor Samuelson are gearing up for the second annual Change For Chihopi yard sale fundraiser for Camp Chihopi. This year, the event will not only feature a yard sale, but also a pulled pork dinner and a basket auction. 
P-J photo by Katrina Fuller


Bemus Point teens Allyssa Seeley, Cameron Rowe and Taylor Samuelson are gearing up for the second annual Change For Chihopi yard sale fundraiser for Camp Chihopi. This year, the event will not only feature a yard sale, but also a pulled pork dinner and a basket auction. P-J photo by Katrina Fuller


BEMUS POINT — A few area teenagers are bringing together a bigger and better fundraiser for Camp Chihopi this year.

Taylor Samuelson and Allyssa Seeley, along with Cameron Rowe and Madison Russo are continuing their success with last year’s Change For Chihopi yard sale fundraiser by expanding it. The teenagers will be seniors at Maple Grove High School in the upcoming year, and they are excited to help benefit a camp that gives a great summer experience to children who have had liver or intestinal transplants.

Aside from the yard sale, which will offer hundreds of items, the crew has organized a barbecue pulled pork dinner for early August with the help of Farmer Brown’s and a basket auction with items from businesses across the area.

Camp Chihopi is a part of the Childrens Hospital of Pittsburgh of UPMC, and offers a four-day experience of camp life with other children that have had similar medical experiences. The camp is for children ages 7 to 15 that have received liver and/or intestine transplants.

Last year, Samuelson and Seeley created the Change for Chihopi fundraiser by hosting a yard sale and accepting donations that they delivered in person. The pair worked as camp counselors-in-training last year.

For Samuelson, the fundraiser and volunteering opportunity were highly personal because her brother, Ryan, had attended camp there. He was born with a genetic disorder called autosomal recessive polycystic kidney disease.

Ryan has had four transplants in his life.

This year, Farmer Brown’s has partnered with Chihopi to hold a pulled pork dinner, which will include a pulled pork sandwich, coleslaw, baked beans, a brownie and a drink for $10. A basket raffle with baskets from businesses across the area will also be held, including items and certificates from places like Guppy’s, Honeycomb Hair Salon and Lighthouse Market.

Samuelson said the funds raised will go to a good cause. She said she is glad to see the event is expanding to include other things.

“It just helps to keep it fresh and keep the community involved,” Samuelson said. “Just stop by and see what it’s about.”

Seeley said even the smallest donations help the camp.

“It’s definitely going toward a great cause,” she said. “The children appreciate every bit of it.”

The event is scheduled for Aug. 4,5 and 6 from 9 a.m. to 7 p.m. and will be held at 3635 Route 430 in Bemus Point. To donate directly, visit www.givetochildrens.org/changeforchihopi.




PKD Research

From Eureka Alert

Sema4 partners with Helix to launch CarrierCheck™

A new, easy way for consumers to access a genetic screen for 67 hereditary diseases

THE MOUNT SINAI HOSPITAL / MOUNT SINAI SCHOOL OF MEDICINE

Sema4, an interdisciplinary health information company focused on empowering people to take charge of their health and data, today announced the launch of CarrierCheck™, a simple saliva-based test that provides individuals with a snapshot of how their DNA may affect their future children. CarrierCheck, the only carrier test that screens for 67 conditions that can be ordered by consumers online, was developed in collaboration with Helix, a personal genomics company that today launched the first online marketplace for DNA-powered products.

"Sema4 and Helix are perfectly aligned in their missions to help consumers gain greater access and understanding of their personal genomic data," said Sema4 CEO Eric Schadt, PhD. "We are excited to launch CarrierCheck, our first product on the Helix platform, to empower consumers with the understanding of their own DNA and gain insights useful to their future family planning."

While many companies, including Sema4, currently offer physician-ordered carrier screening tests, CarrierCheck stands apart in providing individuals with an online ordering pathway to a genetic test with easy-to-understand results that can reveal an individual's probability of being a carrier for any of the 67 hereditary conditions tested-- including cystic fibrosis, sickle cell disease, and polycystic kidney disease.

The process is simple: A consumer purchases CarrierCheck on helix.com and is then directed to the Sema4 website to create an account and complete a brief health history questionnaire. A physician from Sema4's partner network reviews the health history to ensure CarrierCheck is appropriate for the individual. Once approved, a saliva collection kit is mailed to the consumer. The saliva sample is then sent to Helix's CLIA- and CAP-accredited Next-Generation Sequencing lab, where Helix sequences the DNA and securely stores it for the customer. The portion of genetic data relevant to CarrierCheck is delivered back to Sema4 for analysis. Each customer can track their test and then view their personalized CarrierCheck report via their online Sema4 account, and genetic counseling services are also available to help customers understand their reports.

"We have been working with the Sema4 team since before their spinout from Mount Sinai, and we are proud to be working with a partner that is committed to pairing clinical-grade interpretation with our high-quality sequencing," said Justin Kao, Co-Founder and SVP of Helix. "Carrier screening is one of the most well-known and sought after types of DNA tests, and we are proud to feature CarrierCheck in our marketplace to provide people with an accessible carrier screen that also offers genetic counseling support."

Helix's proprietary technology, called Exome+, reads every letter of all 22,000 protein-coding genes in your body, which produces 100 times more data than most consumer genetics companies. CarrierCheck is available to purchase for $199 plus a one-time cost of $80 for the Helix DNA kit for new customers. With Helix, consumers only need to get sequenced once to access CarrierCheck and other products on the Helix marketplace. CarrierCheck and the Helix DNA kit are now available for purchase on the Helix website.




Gift of Life

From Hyattsville Life, Maryland, BY SANDY LUNDAHL

Chelsea School administrator with PKD receives ‘greatest gift’ from student’s father



Kristal Weems-Bradner, Interim Co-Head and Middle Division Principal at the Chelsea School in Hyattsville, shakes hands with Alec Casey at his graduation recently. In June, Alec's father Chris (not pictured) donated a kidney to Weems-Bradner, who has polycystic kidney disease. Photo courtesy of Pete Broyles, Chelsea School


There are many stories about educators who change students’ lives. But sometimes, it’s a student — or their family — who changes the life of an educator.

Kristal Weems-Bradner was diagnosed with polycystic kidney disease in her late 20s, a genetic disorder that runs in her family and can result in kidney failure. Now 48, Weems-Bradner has been on daily, peritoneal dialysis for more than two years. Weems-Bradner is the Interim Co-Head and Middle Division Principal at the Chelsea School in Hyattsville.

“My mother, some of my aunts and many of my cousins, including male cousins, all have the disease,” Weems-Bradner said. She says her mother received a kidney from a deceased donor that lasted for 6-7 years and then she returned to dialysis for the remainder of her life. Her mother died in January 2016.

“I knew what to expect,” said Weems-Bradner.

Polycystic kidney disease (also called PKD) causes numerous cysts to grow in the kidneys. These cysts are filled with fluid. If too many cysts grow or if they get too big, the kidneys can become damaged. PKD cysts can slowly replace much of the kidneys, reducing kidney function and leading to kidney failure, according to the National Kidney Foundation.

Weems-Bradner was on the transplant list, on dialysis and waiting for a deceased donor while friends and relatives were tested to see if any of them were a match. Her son, the best match, was disqualified when they learned he also has the gene for polycystic kidney disease.

Many people who need organ and tissue transplants cannot get them because of a shortage of donations, according to the National Kidney Foundation. Of the 123,000 Americans currently on the waiting list for a lifesaving organ transplant, more than 101,000 need a kidney, but only 17,000 people receive one each year. Every day 12 people die waiting for a kidney.

Two years ago, Weems-Bradner spoke to a biology class at Chelsea School about how kidneys function and different ways they stop working. After the class, Alexander (Alec) Casey offered her something precious: Alec offered to donate one of his kidneys. Unfortunately, donors must be at least 18 years old.

Fast forward two years.

“I’m 18 now,” said Alec, who recently graduated from Chelsea School. “Do you still need that ‘thing’?” he asked Weems-Bradner. “I want to give you my kidney,” Alec says he told Weems-Bradner the day after his 18th birthday. “She told me that I had to talk with my parents.”

With his parents’ approval, Alec went through the questionnaire process, but stopped when he learned — incorrectly — that people with tattoos could not donate. Rather, prospective donors are advised not to get a tattoo before donating because of the risk of infection.

That’s when Alec’s father, Chris Casey, 66, stepped in and went through the same extensive process and found out that he was a perfect match for Weems-Bradner.

Chris wanted to give back to a school and school official who had given so much for his son.

“It’s because of my affection for Weems-Bradner and the [Chelsea] school,” said Chris. “My son had been in public school and was not receiving the academic support he needed. Within 18 months of attending [Chelsea] he made substantial progress despite his dyslexia and ADHD. He received the highest score in the ACT reading test and was declared ‘college-ready.’”

Chelsea School is a small college-preparatory school for students with learning disabilities or Attention Deficit Disorder or Attention Deficit, Hyperactivity Disorder. Chelsea School serves students in grades 5 through 12.

“We try to build strong relationships with our students and family,” Weems-Bradner said. Each teacher becomes an advisor to two or three students, she explained, and stays in contact weekly with the family initially and then at least monthly to inform parents of their child’s progress and to find out about potential problems as early as possible.

“She [Weems-Bradner] changed my thinking about school and life,” Alec said. “When I first came to [Chelsea], my main purpose was definitely not school. I was fighting a lot. She gave me lots of advice and we had a really good connection. I would call her more than my advisor whenever I needed help.”

Weems-Bradner says she is “blown away” when she thinks about Chris’s donation of his kidney to her. She described her feelings in a Facebook post on June 30, 10 days after surgery:

I am an African American woman and I need to thank a white man for saving my life. In this day and age of such turmoil, especially between the races, … What are the chances of this man being a direct match when I had been waiting on the transplant list for 2 years without any potential matches (living or cadaver). On June 20th, Chris donated a kidney to me. This is one of the greatest gifts anyone has ever given to me. I am eternally grateful to [the Casey] family, for they are truly a blessing to me. … We are surrounded by hate, distrust and malice [and yet] there is truly good in the world, and there is truly hope!

Donation is not risk-free; it carries the same risk profile as having an appendix removed, says Give a Kidney, a charitable organization that promotes altruistic or non-directed living kidney donation. But it’s important to know that it is generally considered very safe to live with one kidney. Most people with one kidney live healthy, normal lives with few problems, says the National Kidney Foundation. In other words, one healthy kidney can work as well as two. [Read more]




Living with PKD

From WJBF, ABC Affiliate, Evans, GA By Samantha Williams

Local family in desperate need of kidneys


Polycystic Kidney Disease runs in the Browning family’s genes and has shown up in three generations so far. This family is heartbroken over recent news. A mother and a daughter are in desperate need for kidney transplants, but since the disease runs in the family, other family members can’t help.

Doctors recently told one of them that it’s crucial to get a transplant by the end of this year.

“I just want to see Jenna Claire grow up. She wants to be a vet, so I want to see that,” Angie Moon said.

She went to the doctor in December and found out her kidney function had dropped to 25 percent. When she went back just three months later, it had dropped rapidly to 18 percent. That’s when doctors told her she needs a kidney transplant by the end of the year or she will be put on dialysis.

“I knew what my long term life would be, would be dialysis, bad kidneys, transplant, but my mom didn’t have those problems until age 65. I figured I had more time. I didn’t think I would be sitting here at 43,” Moon explained.

It all started with Angie’s grandfather. He was 62 years old and at the stage where he needed to be put on dialysis, but he passed away before that was possible.

Angie’s mom, Phyllis Browning, was diagnosed with Polycystic Kidney Disease nearly 30 years ago and has been on MCG’s transplant list for the last four years. Like her father, Phyllis said she never talked much about her need for a kidney.

“That’s kind of been my theory since ’89… to live my life as best as I can, and if it’s God’s will that I get a kidney, I’m all up for is play,” Browning said.

But that all changed when her daughter, Angie, got blood results in March. Angie said she hasn’t fulfilled everything she’s destined for here on earth, yet. She said God isn’t finished using her.

“I know his plan for me would be a living donor because a living donor’s kidney gives me 25 years without dialysis, and if I take a deceased donor, it’s only good for ten years,” Moon said.

And Angie’s daughter, Jenna Claire, said she not only hopes her mom and granny find donors, but she hopes she doesn’t have to deal with the disease and heart ache in her lifetime.

“It kind of made me feel a little worried… yes, technically worried. I want her to be at all of my performances. I would say donate if you can,” Jenna Claire said.

“If this touches your heart, and you feel like you want to donate to my mom or me, don’t hesitate, whether it’s your blood type or not,” Moon said.

Jennifer Browning, Angie’s sister, will also need a kidney at some point in the future. You can be the answer this family is so desperately praying for. Angie said you can contact the transplant locations and request to be a donor.
She explained the process is not difficult and will be completely paid for by their insurance.

If you feel compelled to donate, call the transplant centers: Phyllis is at Augusta University Medical Center: 706-721-2888. Angie is at the Medical College for South Carolina: 843-792-1594.




From The Sun, United Kingdom, By Lizzie Parry, Digital Health Editor

RECORD BREAKING Doctors remove the world’s largest kidney from man – and it weighs MORE than a newborn baby

 Doctors have removed the 'world's largest kidney' from a man at Dubai Hospital

Doctors have removed the 'world's largest kidney' from a man at Dubai Hospital

Ahmad Saeed, 56, from Dubai, suffered polycystic kidney disease causing giant cysts to engulf his kidneys.

DOCTORS have removed the "world's largest" kidney from a man in Dubai.

The organ weighed 9lbs 3oz - more than an average newborn baby.

And the 56-year-old patient also had his second kidney, which was also severely enlarged, removed.

The operation took place at Dubai Hospital, after the man complained he was unable to walk or talk - and he is now living on dialysis while waiting for a kidney transplant.

Surgeons operated on Ahmad Saeed, taking out both of his enlarged kidneys, after diagnosing him with polycystic kidney disease.

It had caused several cysts to form on the man's kidneys.

The larger of the two measured 34cm by 17cm in diameter, and weighed 9lbs 3oz.

In contrast, a normal kidney measures around 12cm by 6cm and weighs 5oz.

Doctors at the hospital said the kidneys are the largest ever reported.

The last world record, they noted, was set at 4lbs 6oz.

Mr Saeed's polycystic kidney disease, caused his kidneys to swell in size.

"Before the surgery, I felt so tired and had an enlarged stomach. I couldn’t walk properly and I just wanted to stay in my room with the door closed." Ahmad Saeed

They grew so big they were soon crushing his internal organs, forcing him to undergo surgery.

Mr Saeed told how his failing health led him to become depressed and withdrawn.

He said: "Before the surgery, I felt so tired and had an enlarged stomach.

"I didn’t feel like talking to friends or going out at all.

"I couldn’t walk properly and I just wanted to stay in my room with the door closed.

"Now, I am back to normal, I can move, I can jump and I can run. No one believes that I have had both kidneys removed."

Sunday, July 16, 2017

PKD Research: Grapefruit Juice Useful Against Cysts; Swimming & Shaving Heads for PKD, Gift of Life: Give Donors a Break, Teen in Helena, MT,

PKD Research

MiceTimes of Asia

The most useful juice for the kidneys

People who have kidney problems, doctors recommended to drink grapefruit juice.

Of course, if it is not contraindicated to you from other diseases.

Scientists at the University of London, found in the grapefruit a substance that can prevent the formation of cysts in the kidneys.

This substance called naringenin and is also present in other citrus fruits. It successfully blocks the formation of cysts in the kidneys, an effect which occurs when polycystic kidney disease, by regulating the PKD2 protein responsible for this.

This study was published on the eve of world kidney day, celebrated globally on 13 March and aims to raise awareness of the importance of kidneys and the risk factors for the development of kidney disease.

Discovery benefits naringenin can be a vital step forward in the future treatment and prevention of kidney disease, say the study authors.

One of them, Professor Robin Williams said: “this discovery is vital in helping us to understand how to control polycystic kidney disease.

Kidney disease are debilitating condition that can lead to death and finding an effective treatment is really urgent priority of scientists.”




PKD Fundraising

From MuskokaRegion.com, Ontario, Canada

Swimming Lake Muskoka from Gravenhurst to Port Carling for organ donations

Organ Transplant Swim



Six swimmers taking a 30-kilometre trek from Gravenhurst Wharf to Hanna Park in Port Carling are raising funds and awareness for those living with organ issues.

Camp Kivita, a summer camp in Muskoka for children with organ difficulties/transplants, will receive 100 per cent of the funds raised.

This is the second year the swimmers, three returning swimmers and three new, are taking to the water. They are set to start at 6 a.m. Saturday, July 29, with Sunday, July 30 reserved if the weather is not co-operating. However, it is unlikely they will postpone.

“The only thing that will stop us is a thunderstorm or a gale,” said organizer and swimmer Ricky Jacobs.

Last year they raised more than $10,000 for Camp Kivita, which allowed 10 kids to attend the camp, and an Ontario award of merit for their efforts, which Jacobs’ said was very unexpected.They will be swimming relay style with each swimmer taking 30-minute legs. They anticipate finishing at Hanna Park between 3 and 6 p.m., although their arrival time at the park is a rough guess. Anyone wishing to see them off or welcome them in will be welcome.

Muskoka cottager Paul Jacobs and his battle with polycystic kidney disease was the catalyst for son Ricky to start the inaugural swim. He is on dialysis and near the top of the waiting list for a transplant.

The family has a longtime connection with and passion for Muskoka, which is why Jacobs’ says he wouldn’t hold the swim anywhere else.

In addition to his dad Ricky also swims for longtime friend Gini Buckman.

According to Ricky’s wife Livy, Buckman has Type 1 diabetes and now, at the age of 43, needs a pancreas.

Another swimmer, Wendy Chong, also has a personal connection. Her father is awaiting a heart transplant.

There are so many connections to the swimmers and the need for donors. Swimmer Nick Knezic will be doing the swim for the first time. It was New Year’s Eve when he mentioned he the idea of doing a long-distance swim. It was a perfect fit. Like the Jacobs’ family, Knezic has a connection with Muskoka as a Cache Lake cottager but he also has a link to the need for organ donor awareness. His father Dario died while on dialysis.

There is also a celebrity in their midst. They are joined by former Olympic swimmer Zsofia Balazs. Balazs was the first Canadian woman to compete in the open water 10-km swim. She placed 18th.

A pontoon boat, on loan from Walker’s Point Marina, will transport the swimmers waiting their turn in the water. There will also be a lead boat and a kayak guiding the swimmers.

A number of local businesses have stepped forward to sponsor event and they welcome more as well as people wishing to sponsor the swim for Camp Kivita.

There will be live updates via social media the day of the swim using the hashtag #organdonorswim, on facebook.com/organdonorswim, or visit kidney.ca/organdonorswim for more information.



From Bridport News, United Kingdom, by Rene Gerryts


COLDER: Laura Lovelace raising money for the PKD kidney charity by having her hair shaved


HER husband thinks she looks like Sinead O'Connor and loves her new look, her mum just thinks she's amazing and Laura Lovelace herself is just feeling the cold.

But the former Beaminster School pupil is also feeling very grateful to everyone who's made her head shave so worthwhile as she's raised more than £1,200 for the Polycystic kidney disease (PKD) charity.

She decided to go bald for the charity as a way of both paying tribute to her mum Sue Andrews whose kidneys failed necessitating a transplant and to the charity which helped her.

Laura, who now works in Waitrose in Bridport, said: "My mum's suffered with polycystic kidney disease for as long as I can remember.

"This year in March she had a kidney transplant because the disease caused kidney failure.

"While she was going through dialysis and everything that else that happened to her during that time she was really just held our family together and remained positive.

"She was just a real inspiration to me so I just wanted to do something to give back to the charity because without that charity coming up with dialysis and supporting all the research behind and things like that my mum wouldn't be here.

"I was inspired to do the head shave by Jo Harp one of my husband's friends who raised a lot of money. I wanted to do something that raised a lot of money and mum wouldn't let me do a sky dive.

"Donations are still coming in but so far we've raised more than £1,200."

Laura's not unused to different hairstyles but grew her hair long for her wedding last year and having decided on the head shave last December kept it growing it so she could also support the Little Princess Trust by donated her 16inch ponytail.

Apart from feeling the cold Laura's quite keen on her new look and husband Sam said he loves it.

She had the shave at Snip Hair and Beauty on the St Michael's trading estate.

Mum Sue, from Broadwindsor said she offered to do the head shave too.

"But Laura said I'd been through enough. I had peritonitis a couple of times too and almost missed her wedding last year through sepsis but was thankfully discharged from hospital less than 24 hours before she got married. It has been a tough time.

"I was waiting for a transplant for more than five years which is longer than average.

"Unfortunately I went into kidney failure because your kidneys deteriorate over time."

She had the operation at Southmead Hospital in Bristol.

She can be supported at justgiving.com/fundraising/Laura-Lovelace

PKD causes numerous cysts to grow in the kidneys which can slowly replace much of the kidneys, reducing kidney function and leading to kidney failure. It is the fourth leading cause of kidney failure.




Gift of Life

From Chicago Tribune, by Paul Basken, Arthur Caplan



At 5 a.m. on the first Friday of April, a perfectly healthy 27-year-old newlywed awoke in a hotel 300 miles from her home and walked into the nearby hospital. There, the modern-day American hero and true Wonder Woman let a team of surgeons cut open her abdomen and take out a vital organ. For the lucky recipient of her right kidney, Brittany Burton's imponderable kindness was an act of lifesaving heroism. And for all her fellow taxpayers, it was a living bequest worth as much as a million dollars.

One of us was the beneficiary of both of those gifts. Both of us badly wish that many more people in dire need could find themselves in the same happy position. And yet — largely because so many Americans don't realize the beneficence shown to them by heroines like Brittany that early spring day — many of those in need probably will die instead.

The math is pretty simple.

For those suffering kidney failure — from inherited conditions or other diseases — the only option for survival other than a transplant is dialysis. That means a laborious and time-consuming mechanical filtering of the blood — usually for many hours, three times a week — to replace the job done by the kidneys. This costs about $90,000 a year and rising. Most of that bill is covered by government insurance through Medicare.

The average five-year survival rate on dialysis is about 35 percent. Otherwise healthy people with an inherited condition such as polycystic kidney disease can fare better. People do find suitable donors after many years on dialysis, but it's not a realistic permanent solution for anyone. Those who survive lengthy periods on dialysis miss lots of work and family life and incur other costs — it's not hard to see that one dialysis patient can cost U.S. taxpayers $1 million or more.

Brittany spent months going through batteries of tests, suffering distractions during her honeymoon to avoid Zika and any other disqualifying bugs, getting holes poked in her arms, and finally undergoing major elective surgery, with no thought of getting any financial reward.

She can't truly explain her generosity. The closest she can manage is to point out a TED talk in which a Georgetown University professor tries to describe that rare breed of person who looks out at the world and doesn't see any one life — including people she has never met on the other side of the planet — as being any less valuable than her own.

For such a person, it simply seems illogical not to give up one kidney to save a fellow human traveler when science says that one remaining kidney is almost always enough to survive a full life.

One major problem for those dying of kidney disease is that not everybody thinks that way. But a second, and far more solvable problem, centers on the fact that Brittany didn't just donate for free. Instead, the government took her altruistic lifesaving donation as an opportunity to make money.

The big medical bills began arriving right after Brittany's beautiful kidney was tucked inside her recipient. Fortunately that recipient has pretty good insurance through his employer, and the out-of-pocket hospital and drug costs were pretty manageable.

The biggest expense, as it turns out, concerns the government. By law, Brittany cannot be paid a dime of compensation for the gift of her kidney. But markets in organs aside, shouldn't heroes be reimbursed for legitimate expenses? These amounted to maybe a few thousand dollars for trips by her and her husband to testing appointments around their home in North Carolina, and to the Baltimore hospital where she underwent additional tests and the transplant surgery.

Even more costly is Medicare. Although some kidney donors don't need any added coverage, some sign up for the government-run health plan — at $3,000 a year — because it is the only way to guarantee coverage in case they have complications related to the donation surgery. Brittany had her own private coverage through her job as a high-school counselor. But having submitted to a "voluntary" medical procedure, she could not expect private insurance to foot the bill in the rare event of a complication.

So the bottom line is that Brittany saved taxpayers hundreds of thousands of dollars a year, and in return the government's "thank you" note is a Medicare bill of $3,000 a year.

Even worse, Medicare only allows that coverage for 36 months, meaning that a hero like Brittany is on her own if she experiences some problem related to her donation after three years. It's a massive disincentive for any well-meaning person who wants to save a life and help cut government spending.

Our government's current ban on any kind of payments, other than the reimbursement of immediately obvious costs such as Brittany's airfare to Baltimore, simply goes too far. Heroes should not have to go broke as the price of their generosity.

Right now, about 100,000 Americans need a kidney. More than 4,000 Americans die every year while waiting for a transplant. There are fewer than 20,000 donor kidneys available for them each year. Transplants increase average survival rates more than tenfold.

If finding a living donor for a kidney patient can save the government tens of thousands of dollars a year, why not allow a small share of that amount to offer the altruistic some help to cover their costs of medical tests and future health insurance?

Brittany's not asking to be paid, and we aren't either. But saving lives and saving money, by encouraging more people to be like her, just seems a matter of common sense and common decency.

Paul Basken is a kidney transplant recipient and a staff writer at The Chronicle of Higher Education . Dr. Arthur Caplan is head of the Division of Bioethics at New York University School of Medicine.




From Independent Record, Helena, MT, by MATT NEUMAN

Helena teen receives life-saving kidney transplant from family friend

Ashley and Ryan



On the second floor of a Primary Children’s hospital in Salt Lake City, doctors wheeled Ashley Lindgren, 19, into the operating room just after 1 p.m., Tuesday, June 20. She was about to get another chance at a normal life.

For the last 10 months, Ashley had undergone near daily dialysis, the exhausting process of removing her blood, filtering it, and returning it to her body.

In early August 2016, Ashley’s single functioning kidney flipped over, twisting the arteries connecting to it, cutting off the flow of blood. She was life-flighted to Salt Lake City, where she underwent emergency surgery to try and save it.

The surgery failed.

Ashley had just graduated from Capital High and was set to begin studying theatrer in Missoula at the University of Montana that fall. She was in the midst of performing in Montana Shakespeare Company’s rendition of “King Lear” when all her plans suddenly came to a halt.

“I lost all of it overnight. All of my plans for the future, all of the people I left behind in Helena, it just all fell apart.”

For 10 months, Ashley’s life revolved not around gaining her education, hanging out with friends or pursuing her passions. It was centered around early morning dialysis, a process that after three hours of filtration, left her so worn out that she slept until 3 p.m. most days. But this summer, Ashley received a glimmer of hope.

Ashley first met Ryan O’Connell at her uncle Jay’s wedding. She was only a toddler, and he was a groomsman.

Ashley had been diagnosed at 6 months old with autosomal recessive polycystic kidney disease, a disease that leads to the growth of cysts on, and eventual failure of, the kidneys.

O’Connell, a friend of the family for about 30 years, said he knew she had kidney problems as a child, but had not heard much about it in years. He came across a GoFund.mepage created for Ashley’s family last September, learned her kidney had failed, and needed a transplant.

“I had just lost my job at New West Health when they closed down. And something just told me I was in the right place in my life to do something that really made a difference. Once we got the process started, I just knew it was going to happen.”

A dancer, golfer and actress at Capital High, Ashley was an outgoing, model student.

Ashley had her first transplant at age 14. Her mother, Tammy Lindgren, was a match and successfully donated one of her kidneys to Ashley. Doctors think that because Ashley was still young at the time, space was made as she grew, and her mother’s donated kidney moved around, and ended up flipping over and failing last year.

Her father, David Lindgren, did not have the same blood type, so could not donate to Ashley. He enrolled in a crossmatch program, where he would donate to someone who he matched in exchange for receiving a donation from someone who matched with Ashley. Unfortunately, the crossmatch never materialized.

In February, O’Connell started the process of becoming a donor for Ashley. He was a match, and passed the extensive exams, questionnaires and interviews.

His family was hesitant at first. O’Connell has two teenage boys of his own, and said his family was concerned about him volunteering to go under the knife.

“They were supportive once we did the research about how safe this process is. I think they also came on board once they saw my passion for doing this.”

On June 19, O’Connell, his girlfriend and sons caravanned with his parents down to Salt Lake City. That night, the night before the transplant surgery, the O’Connells and Lindgrens picked up dinner to-go from Ashley’s favorite restaurant, Olive Garden, and headed back to the hotel to eat.

“They don’t have one in Helena, so it’s really a treat for me. Chicken fettuccine alfredo. You just can’t beat that,” he said.

Ashley said the dinner conversation wasn’t overly emotional, even though it was the culmination of so much struggle and pain.

“The word ‘surreal’ kept coming up,” O’Connell said. “Even now, just thinking we did that, you know the conversation just stops.”

On Tuesday morning, O’Connell went into Utah University Hospital, on the same campus as Primary Children’s. The surgery took less than three hours. O’Connell said he heard some voices as he slipped under the anesthesia, and woke up to his family waiting for him.

Later that night, he found out that Ashley’s surgery was a success.

By 7 p.m., Ashley said she could feel her new kidney working. After almost a year of constant tiredness, she felt alert and focused, even after a four-hour-long surgery.

“I could finally take it all in, like everything had been blurry for so long.”

The surgery left her with 19 staples and a crescent-shaped scar on the left side of her abdomen. She calls it her moon scar.

Ashley will be in and out of Salt Lake City until July 25 for follow-up tests to make sure everything is working properly. After that, she will finally pick up where she left off a year ago, and will be off to the University of Montana for a theater degree.

O’Connell said he never could have imagined the feeling of self-satisfaction he got after the surgery. He asked others to keep the Lindgrens in their thoughts while Ashley heals, and to keep an eye out for all she will be able to accomplish now.

“I’m really just a guy with an extra kidney. Ashley and the Lindgrens are the true heroes with what she has been through. I’d really like to raise the awareness of being an organ donor. Not everyone can donate a kidney or a lung or whatever, but if it is something you are able to do, there are options out there to help offset some of the costs. I would just hope everyone can find something that brings them this level of deep satisfaction that I have.”