Sunday, July 28, 2013

Fiscal Cliff Cuts to Dialysis, Public Objections Due by August 30

Fiscal Cliff Cuts to Dialysis

From KidneyStoriesBlog
KIDNEY STORIES: DINNER WITH MY SON AND CMS CUTS TO DIALYSIS

This is my son Jim and I having dinner earlier this week. He lives in Phoenix now so I value the time I get to spend with him. As many of you know, I am a ESRD/PKD/dialysis patient that relies on dialysis to stay alive.  Polycystic Kidney Disease is an hereditary disease. In my family, I have lost a cousin, an uncle, 2 aunts and my father to PKD. PKD is the most life threatening of all of the most common life threatening genetic diseases. 600,000 of us in America are effected. There are 12.5 million children and adults world-wide affected with cysts on their kidneys that inevitably lead to kidney failure. The number of people who have PKD is greater that the combined number of people with cystic fibrosis, muscular dystrophy, hemophilia, sickle cell anemia, Down’s Syndrome and Huntington’s Disease. It is twice as common as MS and 20 times more common than CF.

When your kidneys fail because of PKD, you have 3 choices: dialysis, transplant or death. Transplants are hard to come by and take time. I am on 3 waiting lists and the shortest time I have been quoted is 3 years and the longest is 6+. Death is what I am trying to avoid. I want to see my son grow up, progress in his career, (he works for the AZ Diamond backs in their PR department) get married, have children. I’d like to meet my grandchildren. I have to take dialysis 3x/week 4 hours a shot. I have to do this just to live. Without dialysis, I could die in as short as 3-5 days; at the outside maybe a month or two.

Recently, the Center for Medical Services that runs Medicare and Medicaid in response to the cuts passed during the Fiscal Cliff, proposed cuts to dialysis centers, their services and to Medicare patients who rely on dialysis just like me to live. A 2% cut was expected. A 9.4% cut was proposed, amounting to a $970 million dollar cut. The Dialysis Patient Citizens, The National Kidney Foundation and the PKD Foundation all strongly objected. These devastating cuts would have a drastic effect on the medical care we receive at dialysis centers. These effects could include a loss of access to quality care, lead to lowering of the standard of care provided, layoffs of vital dialysis personnel like techs and nurses, cause of closure and consolidation of dialysis centers, and worse yet the rejection of Medicare dialysis patients, who make up 82% of all dialysis patients. Imagine driving several hundred miles a week to obtain life saving dialysis because the center 5 minutes from your home closed.

The CMS knows these cuts are radical and dangerous. They have given members of the public until August 30th to object. All of the organizations that I belong to are urging you to contact your Congresspersons and Senators to register your objections. If we don’t object the CMS will assume we don’t care or the cuts are not harmful and after January 1, 2014, they will be implemented. You can use this link to send a letter: http://tinyurl.com/qet4zj2 . You can use this link to make a phone call: http://tinyurl.com/n46cfrp. You can write a letter. You can sign a petition: https://www.change.org/petitions/center-for-medicaid-and-medicare-services-cms-withdraw-the-proposed-cuts-to-dialysis-centers-and-esrd-patients. I am personally meeting with my local reps of my pols on this issue in the next two weeks. I have written a letter to the editor to my local and most large national newspapers and TV stations. I’m hitting the bloggers next (Daily Kos, Salon, Politico). I do this for my clinic mates that come in and leave everyday by ambulance, have diabetes, have lost mental acuity, are amputees, walk with walkers and canes, and just are not able to fight back or truly understand what is occurring. I do this for my son, my father, and my unborn grandchildren. Please use the links, write a letter, make a call or sign the petition. My son and I would like to keep having dinner together.


Diet Guidelines 

From PKDHealthNotes.org, The PKD Foundation
General Diet Guidelines for the Peritoneal Dialysis Patient
For the most part, extensive dietary restrictions are not necessary for people on peritoneal dialysis. It generally depends upon, how often you do exchanges, volume of exchanges and type of solution used. Your peritoneal dialysis diet will most likely consist of: [Read more]



Living With PKD

From PKDWillNotBeatMe, a blog by Valen Keefer
I hopped in the car, turned the key, and the radio blared with the sound of Bruce Springsteen. “Born in the U.S.A.” I quickly looked over to the passenger seat at Dennis McCloskey, my now biographer, in complete astonishment. [Read more]


From AllAboutKidneys.com
A video presentation by Ronald D Perrone, MD – Professor of Medicine at Tufts Medical Center.


From CBC Hamilton, Canada
Arie and Joy Pekar are like any young couple with a new baby.

They've spent the last few months thinking of names. They read and learned about parenthood. They have no plans for their new son, who arrived June 23, other than for him to be “happy and healthy.”

There's only one difference — little Benjamin's father is in desperate need of a kidney.

For the Dundas couple, life has reached a perfect storm of sorts. Two weeks before Joy gave birth to their first child, Arie, 35, began dialysis for a genetic kidney disease. [Read more]


From Lansing State Journal, Lansing, Michigan
Just a few days out of kidney transplant surgery, Roxanne Frith was feeling stronger than either she or her doctors could have expected.

“My kidney functions are normal,” Frith said Friday on the phone from Mercy Health St. Mary’s in Grand Rapids. “The doctors are using words like ‘amazing’ and ‘spectacular.’”

But things didn’t go exactly as planned for the Lansing photographer and teacher, who has polycystic kidney disease and was scheduled to receive a kidney from her brother on Aug. 12.

During his final pre-surgery tests on Thursday, her brother learned he has late onset PKD and was not a suitable donor, meaning she would have to wait for a kidney.

Then, through a friend, [Read more]



PKD Treatments

From PKD Clinic blog
Chinese Herbs Medicine Help To Polycystic Kidney Disease
I. What is Polycystic Kidney Disease?
Polycystic Kidney Disease, namely fluid-filled cysts, develop in the kidneys, making the kidneysa honeycomb appearance. Gradually these cysts replace the normal kidney tissue, enlarging the kidneys and making them less and less able to function normally. Eventually, the kidneys fail completely.
II. How to treat PKD?
There is no such a therapy which can cure the disease totally at present, all the therapies are trying to control the disease and help the patients to live a longer life with a higher quality. [Read more]


From BeatKidneyDisease.com
Book Offer from Duncan Capicchiano, N.D.
Naturopath, Author, Researcher
Upwey, Melbourne,
Victoria, 3158, Australia



PKD Research

From Renal and Urology News.com
RCC Prevalence 'Surprisingly High' in ADPKD Patients

Patients with autosomal dominant polycystic kidney disease (ADPKD) have a “surprisingly high” prevalence of renal cell carcinoma (RCC), researchers reported online in Nephron Clinical Practice.

Cordula Jilg, MD, of Albert Ludwigs University in Freiburg, Germany, and colleagues conducted a retrospective analysis of patients diagnosed with renal neoplasias from 1988 to 2011 using the Else Kröner-Fresenius registry. They identified 240 ADPKD patients who had undergone 301 renal surgeries. They found malignant or benign lesions in 17 patients, of whom 10 had dialysis over a mean 43 months prior to surgery. Sixteen malignant renal lesions (15 RCCs) were found in 12 of these patients. Of the 12s, eight had undergone dialysis prior to surgery. [Read more]

Sunday, July 21, 2013

Treatments for PKD

Treatments for PKD, Tell Your Story

From PKDCure.org, The PKD Foundation
Written Testimonies Needed for FDA Advisory Committee Review of Tolvaptan

On August 5, the Food and Drug Administration (FDA) Advisory Committee for Cardiovascular and Renal Drugs will be holding a special meeting to discuss the new drug application for tolvaptan as a potential treatment for ADPKD. At this meeting, in addition to testimony from researchers and clinicians, the committee will also hear presentations from the public. The PKD Foundation has submitted the names of several individuals who can speak about the burden of having PKD and the impact on generation after generation of families. They will also be testifying that a pharmaceutical treatment option is long overdue, and that dialysis and transplantation shouldn’t be the only options for people with ADPKD.

You too can make an impact by submitting your story in writing! The FDA will be accepting written testimonies through Monday, July 22. To testify to the committee in writing, please send your submission describing the burden PKD has placed on you and your family to the contact below. If you’ve had a difficult experience with dialysis or transplantation, please share your story to help reinforce the point that PKD patients need treatment options to prevent dialysis and transplantation.


Contact Information:
Kristina A. Toliver, PharmD
Center for Drug Evaluation and Research
Food and Drug Administration
10903 New Hampshire Avenue
WO31-2417
Silver Spring, Maryland 20993-0002
Telephone: (301) 796-9001
Fax: (301) 847-8533
Email: CRDAC@fda.hhs.gov

This committee will review all testimonies and make a recommendation to the FDA, who will make a final decision about tolvaptan. The FDA’s goal is to have a decision by September 1. [Read more]


PKD Foundation Looking for CEO

Chief Executive Officer - Polycystic Kidney Disease Foundation
The Polycystic Kidney Disease Foundation (PKD Foundation) is seeking a dynamic Chief Executive Officer to build on our exceptional record of over 30 years of quality and committed service in promoting research, advocacy, education, support and awareness to discover treatments and a cure for polycystic kidney disease. [Read more]



Making the Gift of Life

From Ipswich Advertiser, Queensland Australia
Dad donates kidney to his baby girl

WHEN Judy Lonie fell pregnant, she and her husband James Lonie were excited by the thought of welcoming their first child.

But the first 18 months of their daughter Heidi's life have not played out as they expected, with a serious kidney condition keeping her in hospital more than she's been home.

Now James is preparing to make the ultimate act of love - donating a kidney to his baby girl.

Heidi was born four weeks' premature and diagnosed with polycystic kidney disease, autosomal recessive.

Her enlarged kidneys were covered in microscopic cysts. The kidneys were getting bigger every day and eventually grew to be larger than a normal adult kidney.

Heidi had both her kidneys removed six weeks ago and the family is waiting for life-changing surgery when James donates one of his kidneys to his baby girl.

The youngster has spent only three weeks at home this year and five months in total since she was born. [Read more]


From Tulsa World, Oklahoma
Wilma Mankiller taught her daughter that being angry about a health problem won't fix it.

Now Gina Olaya, who has the same hereditary kidney disease as her mother, a former Cherokee Nation principal chief, is determined to move on and work to be as healthy as possible.

She had dramatic help in the form of a donor kidney from her sister, Felicia Olaya.

Felicia Olaya never second-guessed her decision to donate a kidney, so long as she was able.

"I just made up my mind," she said. "If I'm healthy and it's God's will, I will be the donor."

Gina Olaya was diagnosed with polycystic kidney disease in 2006. She knew it well. In addition to her mother, several of her mother's 11 siblings had the disease.

It has affected some of her cousins and at least one child in the generation below her.

She tried to do peritoneal dialysis, which is done at home, but had continuous problems with her port and was never able to complete a cycle.  [Read more]


Living With PKD

From Recombine.com
Polycystic Kidney Disease Awareness

Polycystic Kidney Disease (PKD) is a serious genetic condition that affects millions of people worldwide, and yet many people have never heard of this disease. June 17th through June 23rd marked PKD Awareness Week. Although this week has passed, many events are still going on nationwide to help raise awareness about PKD.

What is Polycystic Kidney Disease?

Polycystic Kidney Disease (PKD) is a genetic disorder that causes affected individuals to have clusters of cysts (fluid-filled sacs) in the kidneys. These cysts can also develop in other parts of the body, particularly the liver. The accumulation of these cysts interferes with the kidneys’ ability to function and affected individuals can eventually develop kidney failure...

Where can PKD patients find support?

Check out PKDCure, which offers support groups; has information about current research for curing PKD, political advocacy, and treatments and trials available for PKD patients; and hosts marathons, concerts, picnics, and fundraisers for raising awareness about and finding a cure for the disease.

Share your story at PDK Will Not Beat Me. Created by a PKD patient, Valen Keefer, the website provides a virtual support network for PKD patients–“to share stories, to ask questions and to make life-long friendships.”

What PKD events are in my area?

Each year, PKDCure hosts 2 national events around the United States: Walk for PKD and Run for PKD–each hosted by local chapters of the organization. [Read more]



From Senojeiram.wordpress.com, a blog
... Here’s another one that you should probably get all the facts on, first. PKD causes high blood pressure. I’ll say that again – PKD causes high blood pressure. Severity varies from case to case, but the very simple answer is our bodies are producing renin at a higher rate, and because function is impaired, it’s not getting flushed out. Renin is a hormone that is involved in controlling blood pressure and sodium and water in the body. Too much renin in the system will lead to hypertension. Untreated, mine is stroke-risk high. {Read more]



From ExperienceProject.com, by Megan85
I Have Polycystic Kidney Disease - Ticking Time-Bombs
I was diagnosed six years ago at age 22, completely by accident. My father passed away at age 43 from ADPKD, three weeks before I left for basic training. Since MEPS did not find anything and I had never experienced any medical issues, I mistakenly thought that I must not have inherited the condition. Wrong. Since then, I have track marks in my inner-elbow from IV's, blood draws, ect. I experience low-level flank pain most days, and I've had my share of kidney stones, UTI's, blood in my urine, etc. [Read more]
When the cysts enlarge to a certain size, they become very likely to rupture.What are the cyst rupture symptoms in PKD?

Blood in urine

Blood in urine is commonly seen in cyst rupture in PKD.It can be microscopic or gross hematuria. Microscopic hematuria can not be detected with naked eyes, but gross hematuria can. The blood in urine usually lasts for about a week or several days.

Back pain

Patients with PKD can usually can experience mild back pain.However,if cysts rupture,the pain will become extremely intense. Usually, painkillers are prescribed to control the pain. However, if the patients have serious kidney damage, pain killers should be avoided.

Serious signs

Cyst rupture in PKD may cause very serious signs and symptoms which would need immediate medical attention.Sepsis and hemorrhage are very serious and even life-threatening conditions.If sepsis is not controlled,it may cause failure of other organs. [Read more]



From KidneyServiceChina.com
Polycystic Kidneys: Causes of Blood in Urine

About 50% of sufferers have symptom of blood in urine (hematuria). What are the causes of this problem?

* Rupture of kidney cyst

Blood in urine is the most commonly reported sign of ruptured cysts within the kidney. In case of PKD, the kidneys cysts will become enlarged in size gradually, causing suppression to the kidney and surrounding organs. This may lead to big cyst bursting. Since there are lots of capillaries on the cyst wall, when the cyst ruptures, the red blood cells will enter into the urinary tract and eventually be removed into urine.

* Damage of the kidneys' filtering function

With gradually enlarged cysts in the kidneys, the healthy renal tissues will be damaged, and kidney function may deteriorate. When the filtering units of the kidneys (glomeruli) are impaired, red blood cells will get leaked into the urine, causing Hematuria.

* Kidney stone or UTIs

Both of kidney stone and UTIs are common complications of Polycystic Kidneys. These complications can result in blood in the urine. [Read more]



From DailyStrength.org, 
Polycystic Kidney Disease (PKD) Support Group
Hello everyone!
I'm new to this group, but I was diagnosed with PKD at age 24, almost 5 years ago. It was found by accident after a UTI turned into a bladder infection and was misdiagnosed as a UTI. I was prescribed the wrong antibiotics and the bladder infection went to my kidneys and into my bloodstream, which nearly killed me. I had a fever of 107 for three days. [Read more]



From AllAboutKidneys.com, 

This is a review of polycystic kidney disease for medical students in their clinical years and others learning clinical medicine.



From Mayo Clinic Discussions
Drinking [alcohol] with pkd
Question posted.  No response as of this date.


Traditional Chinese Medicine and PKD

From eshine-Kidney.blogspot.com
Polycystic kidney health rehabilitation exercise can help
... Life is movement, polycystic kidney disease patients and healthy people are different, exercise should note the following:
1, daily activities, work for polycystic kidney disease patients is concerned, how can we not affect the body, which, experts suggest that the patient's condition according to the specific circumstances to develop, vary.
2, a single cyst size of 40 mm or less in patients generally do not have any major disruption, this time most of the patients with cystic although there have been slight mutual pressure, but the pressure between the cyst is not particularly large, relatively high for some security the movement is still possible, but can not participate in some of the collision of sports, such as playing basketball. Some of the usual gentle exercise will not affect the kidneys.
This way, sport health attention, treatment and care can really play a positive role. Therefore, in patients with polycystic kidney disease everyday life must be more movement, with medical treatment, to let the disease faster and better recovery. [Read more]



From SparkPeople.com
Polycystic Kidney Disease And Lose Weight
Variety of treatment of renal cysts,renal cysts how to treat usually practice traditional Chinese medicine approach, the effect issignificant. When the micro-based medicine to penetrate the treatment of single renal cysts,belong to the disease outside the rule. The therapeutic mechanism of this renal cysts treatment:the expansion on the wall of blood vessels, accelerating the wall of blood circulation, renal cystHow therapy to promote the increase in wall permeability, prompting the pressure drop in thewall of blood vessels, reversed due to vascular internal pressure higher than the intracapsular pressure, differential pressure, and accelerate the cyst fluid of water to the blood vessels back to the absorption system in the continued secretion of the cyst wall epithelial cells, renal cystshow treatment to prevent the continuation of the wall of blood vessels and cysts increases.  [Read more dialog between patient and expert]



PKD Research

From Fox Chase Cancer Center, PHILADELPHIA, PA

(July 15, 2013)—Results from the Fox Chase study could eventually lead to the first treatment for autosomal dominant polycystic kidney disease (ADPKD)—a life-threatening and debilitating condition, and the most common inherited kidney disease. A new compound reduces the symptoms of ADPKD in a mouse model, according to research from Fox Chase Cancer Center that will appear in the July 15, 2013 issue of the Proceedings of the National Academy of Sciences.

ADPKD affects between one in 400-1,000 people, making it one of the most commonly inherited life-threatening diseases. Along with cysts, ADPKD can cause the kidneys to swell to the point where they become visible to others, and patients experience abdominal or flank pain. Other complications include blood in the urine and infections of the cysts.
Half of patients develop kidney failure, typically around their fifth or sixth decade, requiring a transplant or dialysis for the rest of their lives. Many also are at increased risk of additional problems, such as high blood pressure, cardiac disease or brain vessel abnormalities.

After administering a new experimental compound once weekly for 10 weeks to mice bred to develop ADPKD, the researchers saw fewer signs of disease, including the tell-tale kidney cysts and enlarged kidneys. In mice with previously established ADPKD, the cysts progressed more slowly during the treatment. Importantly, kidney function also appeared to improve. [Read more]


From ScienceCodex.com
... Xiaogang Li and colleagues at the University of Kansas Medical Centr used a mouse model of ADPKD to explore the role of the protein sirtuin 1 in cyst formation.

They found that inhibition of sirtuin 1 activity using vitamin B3 can reduced cyst formation in the kidneys of ADPKD mice. These findings suggest that therapeutics targeting sirtuin 1 could potentially be used to treat ADPKD. [Read more]



From Journal of Lipid Research
MALDI imaging MS reveals candidate lipid markers of polycystic kidney disease

ABSTRACT

Autosomal recessive polycystic kidney disease is a severe, monogenetically inherited kidney and liver disease. PCK rats carrying the orthologous mutant gene serve as a model of human disease, and alterations in lipid profiles in PCK rats suggest that defined subsets of lipids may be useful as molecular disease markers. Whereas MALDI protein imaging mass spectrometry has become a promising tool for disease classification, widely applicable workflows that link MALDI lipid imaging and identification as well as structural characterization of candidate disease-classifying marker lipids are lacking. Here, we combine selective MALDI imaging of sulfated kidney lipids and Fisher discriminant analysis of imaging data sets for identification of candidate markers of progressive disease in PCK rats. Our study highlights strong increases in lower mass lipids as main classifiers of cystic disease. Structure determination by high resolution mass spectrometry identifies these altered lipids as taurine-conjugated bile acids. These sulfated lipids are selectively elevated in the PCK rat model but not in models of related hepatorenal fibrocystic diseases suggesting that they be molecular markers of the disease and that a combination of MALDI imaging with high resolution MS methods and Fisher discriminant data analysis may be applicable for lipid marker discovery.

Sunday, July 14, 2013

PKD Fundraising

PKD Fundraising To Help Find A Cure

From EventsPE.com, Lakewood, California

PKD Fundraiser for NYC Marathon - Special Concert & Wine Event

PKD Fundraiser will be held on July 28, 2013 at 5 PM at a residence located at 4145 Ann Arbor Road, Lakewood, CA 90712.  Buy tickets to attend.


From MySanAntonio.com San Antonio, Texas
Annual San Antonio Walk for PKD
takes place Sept. 21 at O.P. Schnabel Park (Graff Pavilion), 9600 Bandera Road, starting at 9:15 a.m. Registration begins at 7:30 a.m. There'll be pre- and post-walk activities for the whole family. Contact Patti Ruffin at 210-414-6614 or sanantoniowalk@pkdcure.org.


From Darlington & Stockton Times, United Kingdom
Riders from Darlington, Northallerton and Bishop Auckland tackle seven mountain bike trails in seven days for charity
THREE plucky cyclists are halfway through their epic fundraising mission to tackle some of the world’s toughest mountain bike tracks in seven days.

After months of preparation Peter Wilson, 41, from Darlington, 32-year-old Paul Simpson, from Northallerton, and 42-year-old Robert Bell, from Bishop Auckland are riding Scotland’s world-famous 7stanes mountain bike network in seven days to raise money for the Polycystic Kidney Disease Charity and TFM’s Cash for Kids.

The 7stanes feature some of the most gruelling mountain bike tracks in the country and take in hundreds of miles of the Scottish Borders and Dumfries and Galloway.


The ride, which began on Friday (July 5) at Newcastleton in the Scottish Borders, will end on Sunday at Glentress, near Edinburgh, to coincide with National Transplant Week after Mr Wilson, who suffers from polycystic kidney disease, underwent a kidney transplant in January 2011. [Read more]


From ThisIsLeicestershire.co.uk, United Kingdom
Pete's on fast track to boost organ donation
A bike enthusiast whose life was saved by a kidney transplant has joined forces with a top motorcycle racer to get more people to become organ donors.

Farmer Pete Elliott, from Donington le Heath, knows he owes his new lease of life to a donor...

...The 40-year-old wanted to promote the need for organ donation and after his operation enlisted the help of a young racer from the MotoGP series, Danny Webb.

Pete said: "I have an absolute passion for motorbikes, so it seemed a good way of combining a personal passion with promoting organ donation.

"I had met Danny a few years before and liked him and got on with hid dad and manager Steve Burgess, so thought I could help him out a little bit and help raise awareness of organ donation at the same time.

"I wanted the biking industry to be a bit more aware of the importance of donation.

"I will always be grateful to my donor and it is nice to be able to do something to help out the thousands of others who are in the situation I was in before I got my transplant."

Pete, who farms in Ibstock, has sponsored the rider to wear the national organ donation logo on his leathers.

It carries the web address of NHS Blood and Transplant's donation website and is being seen potentially by millions of people around the world. [Read more]


From The Weston Mercury, United Kingdom
TWO postmen from Weston have donated £1,260 to Southmead Hospital’s renal unit after undergoing kidney operations.

The Weston Mercury reported in April how Chalkie (Charles Czajkowski) donated his kidney to friend and colleague Ian Shillcock who was diagnosed with polycystic kidney disease.

The pair went under the knife at Southmead Hospital and after a successful recovery, the friends have now returned to work at Royal Mail in Weston.

Postman Chalkie, aged 44, and Ian, who works in the company’s sorting office in Warne Road, also started an appeal to raise money for the renal unit at Southmead Hospital.

They put a collection box at the sorting office and sold wristbands for the cause and were overwhelmed with the response.

Thanks to generous well-wishers, the pair have handed over £1,260 to the Richard Bright Renal Unit. [Read more]


Living With PKD

From ScienceDaily.com
Promising Treatment for Inherited Form of Kidney Disease
A drug therapy shows promise for treating an inherited form of kidney disease called autosomal dominant polycystic kidney disease (ADPKD), Mayo Clinic researchers say. The medication, tolvaptan, slowed the pace of kidney cyst growth over the three years of the study. [Read more]


From The DailyRecord.com, Washington State
Madeline (Maddie) Schlesinger has long had a passion for film and television, intrigued, she says, by their potential to inspire.

When she graduated from high school in the Shoreline area near Seattle, she headed to Central Washington University to study filmmaking. This March, her documentary production instructor gave a final assignment: to make a documentary that was compelling.

Schlesinger delivered, producing a film that both she and the subject of her documentary, Claudia Osmonovich, hope will help save Osmonovich’s life as well as the lives of others like her.

Kidney disease

Osmonovich, married and the mother of two teenage children, was 7-years-old and living in California when she was diagnosed with Polycystic Kidney Disease (PKD), a condition that causes cysts to grow on the kidneys. Over time, kidney function declines, eventually forcing patients to seek transplants or go on to dialysis. Osmonovich, 41, who owns the Cle Elum Bakery with her husband, Ivan, hopes for a kidney from a living donor in part because kidneys from living donors tend to begin functioning more quickly and last longer than cadaver kidneys.

Last fall, Osmonovich, whose two children also have been diagnosed with PKD, learned her kidney function had declined to a point where she needed to consider dialysis or a transplant. {Read more]


From Boards.ie
I was recently diagnosed with this disease. It came to light after I got really sick 6 weeks after having my baby. I had a REALLY bad kidney infection so was in hospital for a week and went for a number of scans.

The first consultant basically said I was doomed and would have kidney failure by the time I reach middle age (am 23). The second consultant said there's nothing to worry about, that I'll just need to keep an eye out for infections.

I really haven't a clue what to think? Am waiting to see kidney dr.

Does anyone have any experience with PKD? I suppose I'm just wondering how it might restrict my life down d line. For eg. I heard you shouldn't have anymore kids?! Should limit salt and alcohol etc [Read more]


From the Island Packet.com, Hilton Head
There seems to be an overabundance of "awareness" efforts out there. You see it on Facebook. On Twitter. You see it in the newspaper, on TV and in your mailbox. "Help us raise money for this." "Come walk with us to raise awareness of that."

Before my daughter was diagnosed with two life-threatening diseases, I don't think I paid much attention to all the different days and months set aside for "awareness." Now that my life revolves around tuberous sclerosis complex and polycystic kidney disease, [Read more]


From PKDWIllNotBeatMe.com, a blog by Vallen Keefer
Out of the corner of my eye, I saw my father walking towards me. I turned my head to the right as I sat in my dialysis chair, and we both gave each other a happy and excited smile. That hopeful day of August 12, 2002 was the last dialysis treatment that I had. He stood by my side as he always has in life, and handed me a present. I excitedly opened it to find a beautiful charm bracelet; the one I am wearing on the cover of my biography, “My Favorite American.” Whenever I wear that special bracelet, it takes me back to that exciting day when I could taste the freedom of no more dialysis.  [Read more]


From Montgomery Advertiser, Montgomery, Alabama
The Extra Mile column: Fitness key to woman's recovery following kidney transplant
A ruptured brain aneurysm woke up Rhea Hibbert.

Diagnosed with polycystic kidney disease at age 30, she knew it was a possibility. So was needing a kidney transplant, and going on dialysis. The now 53-year-old lost her father when he was 53. He, too, had been diagnosed with PKD, a kidney disorder passed down through families in which cysts form in the kidneys, causing them to become enlarged.

Hibbert’s father never was a candidate for a kidney transplant.

“Of course, I prayed I could live my whole life without ever needing a transplant or going on dialysis,” she said. “Chances of that were slim.”

The transplant happened on March 8.  

Staying fit, preparing for a transplant

Hibbert, of Montgomery, has always been physically active. A personal trainer, she was involved in cheerleading and twirling while growing up, and plays tennis, attends Box Mania classes, and runs.

After the brain aneurysm 10 years ago, though, she started taking things more seriously. [Read more]


Read more here: http://www.islandpacket.com/2013/07/08/2570912/parents-get-sense-of-control-over.html#storylink=cpy


Read more here: http://www.islandpacket.com/2013/07/08/2570912/parents-get-sense-of-control-over.html#storylink=cpy


Gifts of Life

From WXYZ.com, ABC News Southfield, Michigan
SOUTHFIELD, Mich. (WXYZ) - Sue Jarbo was blessed with four gifts; sons who she calls her bodyguards. But she's facing a battle her young men can't fight alone. It's a kidney disease that will put her on dialysis in the coming weeks.

“She has a disease called PKD. Polycystic kidney disease," said Sue's son Brandon, "It's transferred down from generation to generation. It's a genetic disease which unfortunately means me and my three younger siblings cannot give her a kidney."

In dire need of a transplant, Brandon, 21, her oldest son, searched for donors. He even put out a Twitter message re-tweeted five thousand times.

"We've just been trying so hard and hard," said Brandon, "And it's just been up and down."

"I'm a tough woman," said Sue, "And I always try to keep looking forward. And everybody knows me as Super Sue."

And even with that positive attitude, Brandon knows his mother's life may be on borrowed time until a donor steps forward.

“I’m not going stop doing what I could to get her a kidney." said Brandon, "She is our everything. She raised all four of us. Any Type-B or Type-O blood, whether it's negative or positive could donate." [Read more]
From The Portsmouth News, United Kingdom
IT MAY not be a traditional birthday present, but it’s one that has saved Bridget Malcolm’s life.

Her sister Claire Sharp, 49, donated her left kidney to Bridget, on the day she turned 51.

Bridget, of Gosport, was diagnosed with acute polycystic kidney disease around 18 years ago.

Although it was being managed through medicine, in February last year, part-time care worker Bridget was told she needed a kidney transplant.

Today is the start of National Transplant Week, and the sisters want to share their emotional story, so more people will sign the organ donor register. [Read more]


From LosBanosEnterprise, California
Boyfriend prepares to donate kidney to his true love
LOS BANOS The ticking time bomb in Lindsey Miller hit hard recently, sending her to the hospital and putting her on kidney dialysis.

The 23-year-old Los Banos woman was diagnosed with polycystic kidney disease at age 10. The hereditary disease took her grandfather at 52, her uncle at 34 and her aunt at 27. Lindsey's mother, Tammie Miller, has been on dialysis since 2010 and needs a kidney as well.

The chances of finding a donor are slim — statistically speaking, one person in Los Banos is a match for Miller. In a fortunate twist of fate, that one person just happens to sit across the dinner table from her every night.

Miller's boyfriend, Brandon Kelley, is an almost perfect match. Kidney transplant surgery is scheduled for July 19 at California Pacific Medical Center in San Francisco.  [Read more]


From HaverhillEcho, United Kingdom
A woman who benefitted from a kidney transplant and her husband are seeking to raise awareness of the need for organ donations during National Transplant Week next week (July 8 to 14).

Mandy Smith, 46, from Broadcroft Crescent, Haverhill, had polycystickidney disease which caused fatigue and would have led to her going on dialysis, yet that was avoided as she received a kidney transplant at Addenbrooke’s Hospital in May 2012.

Now her and husband Paul, 46, will have a stall at Tesco, where Mandy works, next week to raise awareness of the need for more people to agree to have their organs donated after death. [Read more]


Natural Remedies

From Kidney Service China.com
Natural Remedies for Enlarged Kidneys due to PKD
1. Renal diet - the best natural treatment for PKD: Drinking water and eat a diet low in protein and sodium.
2. Herbs: Some herbs can help to relieve some symptoms of the disease. The herbs include the following:

Dandelion root - help the kidneys excrete wastes; cranberry - helps to acidify urine; celery and parsley - decrease uric acid; hydrangea and uva ursi - cleanse the urinary tract; buchu and barberry - improve immune function when drunk as a tea and prevent inflammation in the kidneys. [Read more]


Cats Can Get PKD Too

From Catster.com
9 Things You Should Know About Feline Chronic Kidney Disease
A diagnosis of kidney disease can be overwhelming. Here are basics about your cat's illness and treatment, and how to find support.  [Read more]

Sunday, July 7, 2013

Walk For PKD, Help Find A Cure

Walk For PKD, Help Find A Cure

From WalkForPKD.org
Why I Walk...

Traci Short and Team Short
Traci Short's Team Short was the largest team in the Walk for PKD in 2012 with nearly 200 walkers. Traci's husband, Kevin, and 14-year-old daughter Bailey have PKD. "I have two family members with confirmed PKD, and participating in the Walk is my way to make a difference,” Traci said. "My daughter Bailey is only 14. The funds we raise now for research can make a really big difference in her life."

... Traci and Team Short's efforts worked, raising $22,000 for the PKD Foundation through the Walk for PKD.  [Read more]


PKD Will Not Beat Me

From PKD Will Not Beat Me, a blog by Valen Keefer
Snippets of Inspiration
We naturally possess fear of the unknown. We who have PKD know we have it, but some of us choose to live in denial with blinders on our eyes. Others muster the guts to face it head on. Those of us with PKD, or any other illness, have the choice and freedom of how we cope with our battles. I choose optimism. I live wide-eyed, seeking answers to my questions.

This week, my mind needed a break from looking at blood work labs, talking with doctors, and thinking of my endoscopy procedure this Friday. I sat on my living room floor looking at a blank corkboard in front of me, trimmed with a pretty turquoise boarder. I held scissors in my right hand and began turning the pages of several magazines. One by one I started snipping thoughts and phrases that inspired me. [Read more]


Save A Life

From GoFundMe.com
Help Andrea's Fight Against PKD
Hi, my name is Andrea Cooper and I was diagnosed with a life threatening Kidney disease, in June 2007, (Polycystic Kidney Disease). Over the last few years it has spread to my Uterus and Liver. Undergoing multiple operations, and removing over 400 cyst like tumors on both kidney's in November 2007, January 2008, and April 2011.


Living With PKD

From DailyStrength.org
I've been diagnosed with ADPKD for nearly five years and I'm only 18. I didn't think too much of it, until today. I received a text message from my mom (she also has ADPKD) telling me she was coming home from work and to do research on ruptured cysts. Through that research, I found this website and I'm glad I did.

I have a few questions:

What does a ruptured cyst feel like? How long does the pain last? [Read more]


From PKDBattle.blogspot.com

What Age does Polycystic Kidney Disease Set in


... ADPKD patients often have no symptoms until they reach between age of 30~40. The most common symptoms include high blood pressure, hematuria (blood in the urine) and/or pain in the back, sides and belly.

While, ARPKD is usually diagnosed very early on. An ultrasound can reveal cysts in a fetus's kidneys, while it is still in the womb. This disease can also affects other areas of the body such as the liver, pancreas, and spleen, causing low blood cell counts, varicose veins and hemorrhoids.
By age of 60, about 50% of PKD patients will need dialysis or a kidney transplant to replace the kidneys' function. Of children with ARPKD, about 1/3 will need dialysis or a transplant by the time of 10-years old.


From KidneyFailureWeb.com

How Long Can PKD Patients Live On Dialysis

Dialysis is required when PKD develops to kidney failure and according to clinical statistic, about 50% of the patients develop ESRD finally. For PKD patients with dialysis, they have different life span. Some statistics reveal that the dialysis survival rate at close to 80% through one year, 64% through two years, 33% after five years and 10% through 10 years.

For PKD patients who are on dialysis, their life span is affectable by many factors like their age, control condition of the complications, diet arrangement, treatment and living style and so on. All these factors affect their life span seriously, so to live a longer time, it is necessary for PKD patients to take effective treatment, arrange scientific diet, have a tight control about PKD complications and develop good living habits.


From KidneyServiceChina.com
Polycystic Kidney Disease Herbal Medicine Treatment

Herbs for PKD

▪ Uva ursi. It is frequently recommended as a good herb for the kidneys. This herbal remedy has been used to help treat urinary tract infections and acts as a diuretic. Typically, 10g of uva ursi leaf is used to treat urinary tract infection. Check with your doctor before using this plant.

▪ Dandelion. Acting as a diuretic, this herb can promote the excretion of wastes from the kidneys. This herb can be consumed as a decoction, tincture or powdered extract.

▪ Cranberry. It has antibiotic properties and helps to acidify urine.

▪ Celery. This herb works as a diuretic to reduce uric acid level.

▪ Parsley, which works as a diuretic to decrease uric acid; Hydrangea, which cleanse the urinary tract.


From NursingTimes.net, United Kingdom

Live kidney transplant from an unrelated donor

A kidney donor describes and reflects on her experience, from her partner’s diagnosis with kidney failure, through assessment to transplantation and recovery [full article requires subscription]

Sunday, June 30, 2013

Find A Cure for PKD

From NeighborNewspapers.com, Atlanta, Georgia
Cocktails for a Cure to raise funds for kidney disease

In a news release, the Atlanta chapter of the PKD Foundation announced it will host its second Cocktails for a Cure event Saturday from 7 to 10 p.m. at Tongue & Groove in Lindbergh City Center in Buckhead

Participants will be part of an evening to help raise money to find a cure for polycystic kidney disease, which is one of the most common, life-threatening genetic diseases affecting thousands in the U.S. and millions worldwide. The event will include music, catering by Chef Drew Ihrig at Endive, a silent auction and an opportunity to win a raffle prize.

“We are thrilled to host the [fundraiser] again this year,” said Marlene Stewart, PKD Atlanta chapter coordinator. “We invite the metro Atlanta community to help support this important cause by purchasing a ticket to attend or by making a monetary donation online, which will help fund vital research to find a treatment and cure for polycystic kidney disease.”

Tickets purchased online are $25 for single admission (one drink ticket) or $40 per couple (two drink tickets) and $30 for single admission (one drink ticket) or $45 per couple (two drink tickets) the night of the event.


Save A Life

From WCVB.com, the Boston Channel
New Hampshire woman makes public plea for her life
A Londonderry woman is hoping someone will be able to help her live a longer life.

Rosemarie Meuse has polycystic kidney disease. Over time, her kidney function is failing.

Her husband planned to donate one of his kidneys, but he died suddenly days before going to the hospital for a series of tests to see if he was a match.

Now Meuse, grieving the loss of her husband, hopes a stranger will come to the rescue.

"He was the love of my life and he was very selfless and kind," Meuse said of her late husband Philip, who went into cardiac arrest and passed away in March. [Read more]

How to help

To be a living donor, you can be a man or woman in general good health.

For more information on how you may be able to help, contact the following person:

Kristen Pelletier, RN
Living Donor Transplant Coordinator
Brigham and Women's Hospital
617-732-8683


From BCRNews, Bureau County Republican, Illinois
ANNAWAN — Like many other girls, 5-year-old Katelyn DeRycke loves to play outside, to swing on her swingset, to go fishing and swim. She loves playing with her Barbie dolls and with her 8-year-old sister Kyla and the family puppy. She likes playing with the IPAD.


But unlike most other little girls, Katelyn has some special medical challenges. As a newborn, Katelyn was diagnosed with Autosomal Recessive Polycystic Kidney Disease, a disease which claimed the life of her brother Noah in September 2003 when Noah was just 5 hours old....



Living With PKD

From PKDCure.org, The PKD Foundation

Voices of PKD, Stories: 

A Curvy Road to Diagnosis

LeeAnn Hujanen went through a dramatic turn of events that led to her PKD diagnosis on April 11, 2013. Adopted as a child, LeeAnn was unsure of her biological medical history, and didn't know PKD ran in her biological family. In 1999, while she was pregnant with her oldest daughter, the ultrasound tech noticed spots on her kidney. Her obstetrician said not to worry about it, and that they would keep an eye on it. So LeeAnn put the kidney spots out of her mind. [Read LeeAnn's story and many more]


From PKD Foundation, YouTube.com (note: these presentations are each about 45 minutes or longer)


From KidneyServiceChina.com
Exercises and Polycystic Kidney Disease (PKD)
Recommended types of exercises for people with PKD

1. Running, walking, swimming, biking, golfing and rowing are recommended to help you stay as healthy as possible.

2. Mind-body workouts including Tai Chi, yoga, and stretching are also beneficial. These types of physical activities can help relieve stress and control blood pressure due largely to their emphasis on concentrated breathing and relaxation. Add 2-3 sessions of mind-body workouts to your fitness routine.

Types of exercises that should be avoided

a. Avoid contact sports like football, basketball, as a blow to the enlarged kidneys may lead to further impairment, including burst or rupture of cysts.

b. Repetitive impacts sports like cross-country biking and horseshoe riding are suggested to avoided.

Cautions

Always stay well hydrated and drink lots of water while exercising, as PKD have trouble retaining water. Drinks that contain caffeine should be avoided, because they may increase the size of kidney cysts. Avoid high salt content drinks


From FuNeng Kidney Disease Hospital

What causes Polycystic Kidney Disease in Children?

What are the causes of Polycystic Kidney Disease in Children? Polycystic Kidney Disease in Children is a genetic disease, which can do harm to the children. Therefore, if you want to treat your child’s kidney disease, you should know what causes of Polycystic Kidney Disease in Children.
1. Gene deletion: Polycystic kidney disease in children is autosomal recessive inheritance, both parents have a genetic changes to make their children suffer from this disease, the morbidity is 25%.
2. Pathogenesis: Renal cyst is derived in renal epithelial structure, primary in renal tubule and pao capsule. All renal cysts have certain common structural components, including the cortex, the intumescent the cyst containing glomerular filtrate.
(1) ADPKD: more than 95% of polycystic kidney disease in children is caused by abnormal genes on the short arm of chromosome 16. Besides, infection and poisoning effect on tubular, stimulate the cyst genes changed the tubular cell metabolism, which directly cause epithelial cell necrosis and obstruction also promoting cell proliferation to make the cyst formation.
(2) ARPKD: The children’s parents don’t suffer from this disease, but they all carry the disease gene to make the children disease. It is a rare in polycystic kidney disease.


From GoBookee.net, Free eBooks download

Sunday, June 23, 2013

PKD Awareness Day, September 2013

From Congressional Record, 113th Congress, Library of Congress
SENATE RESOLUTION 172--DESIGNATING THE FIRST WEDNESDAY IN SEPTEMBER 2013 AS ``NATIONAL POLYCYSTIC KIDNEY DISEASE AWARENESS DAY'' AND RAISING AWARENESS AND UNDERSTANDING OF POLYCYSTIC KIDNEY DISEASE


Life with PKD

From PKDBattle.blogspot.com
Principles of Daily Life for PKD Patients
Ⅰ. Life care:

Firstly, patients should improve their both mental and physical rest. For example, Nephrotic Hypertension patients should check blood pressure regularly and adjust their bed rest time according to their blood pressure change. [Read more...]


From DailyStrength.org


From PKDWillNotBeatMe, a blog by Valen Keefer
“I think it actually takes a lot of guts for us to come to terms with this that we are not super heroines and it is not about limitations, but preservation to what we have here and now and going into the future.”

This powerful statement came from my dear friend and two-time kidney transplant recipient, Mary Wu. This really spoke to me. I am learning a lot with age and through my health issues this year. Instead of focusing on things that others can do that may not be a practical life path for myself, I am focusing on the beautiful things that I can do and the opportunities that surround me. While these opportunities might be a lot simpler than some folks, they bring me great joy. I think that is what we are all striving for in life: happiness. [Read more]


From KMTV, Omaha, Nebraska

PKD (Polycystic Kidney Disease) Walk for the cure

Join us for a great time celebrating our fundraising efforts throughout the year. We will have music and activities featuring the Penny Kids Dash starting at 8 am. There will be a small raffle, including a chance to win a pair of Husker Tickets! If you wish to join please visit walkforpkd.org and register today!

Occurs once: Oct 12, 2013 (8:00 AM to 12:00 PM)
Contact Name: Jennifer Russell
Contact Email: nebraskawalk@pkd.org
Contact Phone: 402-714-3036
Location:  Walnut Creek Recreational Area
370 and 96th 9902 Schram Rd, Papillion, NE 68046


From KidneyServiceChina.com
Is Seafood Diet Ok for Polycystic Kidney Disease
Polycystic Kidney Disease, or PKD, refers to a condition that fluid-filled cysts invade the kidneys. These cysts wreak havoc on the kidneys, which effect the rest of the body. Common symptoms of this disorder include pain especially in the lower abdomen or back, blood during urination, etc. A healthy diet can help slow down the progression of kidney damage and guard against potential complications. Is seafood diet Ok for PKD patients?

Actually, seafoods should be limited for people with PKD, as they are a rich source of protein. In generally, low protein diet is suggested in case of polycystic kidneys. Here is the reason:

When protein is metabolized by the liver, it leaves a waste product called urea. Normally, urea is expelled by kidneys, in PKD, the kidney function is damaged and urea starts building up which is harmful to the body. A low protein diet will put less strain on the diseased kidneys.


From KUMC News, University of Kansas Medical Center

Vitamin B3 holds promise for treating polycystic kidney disease, research suggests

Despite decades of research, treatments for polycystic kidney disease remain elusive. Now a new study by KU Medical Center researchers suggests that one mechanism for controlling the ravages of the disease might be found in vitamin B3.

Polycystic kidney disease is one of the most common life-threatening genetic diseases, affecting 600,000 Americans and 12.5 million people worldwide. People who inherit PKD develop kidney cysts that grow and multiply slowly over time — patients in their 20s might have few symptoms, but by the time they are into their 40s or 50s, normally fist-sized kidneys containing these fluid-filled sacs can grow to the size of a football, causing pain and destroying kidney function. With a research program dating back to the 1950s, KU Medical Center scientists are internationally recognized experts on the disease — and acutely aware that there is still no cure.

Recently, however, Xiaogang Li, Ph.D., an associate professor of Nephrology and Hypertension and a member of the KU Kidney Institute, found that vitamin B3 helped naturally inhibited the activity of a protein called Sirt1 that influences the formation and growth of cysts. Li and colleagues were able to show that vitamin B3 slowed the creation of cysts and restored kidney function in mice with PKD. The results were published in the June 17, 2013 Journal of Clinical Investigation.  [Read more]


From KidneyFailureWeb.com
From KidneyFailureWeb.com


From Genetics Home Reference, National Institutes of Health
Medullary cystic kidney disease type 1
Medullary cystic kidney disease type 1 (MCKD1) is an inherited condition that affects the kidneys. It leads to scarring (fibrosis) and impaired function of the kidneys, usually beginning in adulthood. The kidneys filter fluid and waste products from the body. They also reabsorb needed nutrients and release them back into the blood. As MCKD1 progresses, the kidneys are less able to function, resulting in kidney failure.

Declining kidney function in people with MCKD1 leads to the signs and symptoms of the condition. The features are variable, even among members of the same family. Many individuals with MCKD1 develop high blood pressure (hypertension), especially as kidney function worsens. Some develop high levels of a waste product called uric acid in the blood (hyperuricemia) because the damaged kidneys are unable to remove uric acid effectively. In a small number of affected individuals, the buildup of this waste product can cause gout, which is a form of arthritis resulting from uric acid crystals in the joints. [Read more]


From StemCell-Kidney.com
The Symptoms of Polycystic Kidney Disease
Symptoms of polycystic kidney disease:

1, urinary abnormality

Main show of Polycystic Kidney Disease is proteinuria and hematuria. It is one of the symptoms at the early stage. Proteinuria is the most often symptoms. It is related to glomerular barrier function. Hematuria is the main factors in check that make polycystic kidney disease patient find themselves suffering from polycystic kidney. [Read more]


From AdverseEvents.com, (note: the web page for this story will not open)
FDA Advisory Committe to Evaluate Samsca for Treating PKD

Sunday, June 16, 2013

Living with PKD

From DailyStrength.org, The PKD Support Group
Really Need Help and Input
Most of you probably won't remember my sister, but she has PKD, has survived peritoneal cancer as Helen has done, survived lung cancer, you name it, she has survived it. NOW, she has fallen and broken her wrist, naturally the arm where her fistula is located and it wasn't a clean break either, a nasty one! 


From WBOC.com, Channel 16 serving Delaware, Maryland and Virginia

Kent Co. Woman Getting New Kidney Through Swapping Process

MILFORD, Del. (WBOC)- For people who need an organ transplant, time on the waiting list is often measured in years. But a Kent County woman is getting off the list much quicker, thanks to a unique process.



From RenalDietGuides.com

[Drink water, do not smoke, keep ideal body weight, watch potassium intake, minimize protein intake, follow an alkaline diet by eating lots of fruits and vegetables, maintain vitamin D levels... read more]


From Beaver Dam Daily Citizen, Beaver Dam, Wisconsin
WAUPUN — When Dominique Oppermann was told she had a kidney disease it was a shock to the whole family.

“We weren’t exactly planning for it,” said her husband Dave, who works at Mercury Marine in Fond du Lac.  “It was a blow to us,” her son Travis, 26, said.  “It was unsettling,” said her son Jeremy, 22.

That’s because although her disease, polycystic kidney disease, is hereditary, she never knew she was prone to have it because she was adopted in Greece when she was 11 months old.



From Lansing State Journal, Lansing, Michigan
For more than 20 years, Roxanne Frith has lived with the knowledge that she drew the short straw in a genetic game of chance.

In line with the probabilities, about half of those in her family — Frith among them — have inherited polycystic kidney disease (PKD). And she’s now reached the point where she needs a kidney transplant.

But the longtime Lansing photographer and teacher views herself as fortunate in many respects.

Medical treatment has come a long way since Frith’s father died of the disease, she said. Her only sibling, who does not have PKD, is donating a kidney. And Frith’s colleagues in the Lansing arts community are pulling together to support her through the surgery and recovery process.

“I am overwhelmed. It has brought me to tears more than once,” Frith said.


From PKD Will Not Beat Me.com, a blog by Valen Keefer
During my recent eight-day stay at Sutter Auburn Faith Hospital, I liked to keep the curtain by my hospital room door partially closed. The first thing I would see were the person’s shoes walking into my room. I loved when I would see Noah’s shoes enter my room. I would yell, “Noah!” Then see his handsome face.

I had been in the hospital almost a week when I started my liquid/soft diet. One particular evening, my dinner consisted of puree soup, jello, mint tea and ice cream. Noah was sitting next to my bed as I slowly started to eat my dinner. The door to my room opened and we both looked down at the shoes entering the room. There was something else entering my room. It looked like the person was pushing a dolly. Noah and I looked at each other with puzzled expressions when all of a sudden a woman and a harp on wheels entered my room. I felt confused and excited. I wondered if someone ordered this and why there was a woman, with a warm smile on her face, and a harp now in my room.



Chinese Treatment of PKD

From PKDClinic.Blogspot.com

Can a Brother of a PKD Patient Give a Kidney Transplant

Patient: Hello, doctor, my younger brother is a PKD patient, and he is waiting for a kidney transplant while undergoing dialysis. I am his older brother, it seems that I am the only one who can help him. Here I want to know whether kidney transplant is the only way and how long can he live if receiving the kidney transplant. Many thanks.
Doctor: I can understanding your current feeling. It seems that dialysis or kidney transplant is the only way to treat kidney diseases in most countries. However, in China, there has no kidney transplant. That is to say, it is such a hospital that helps kidney disease patients avoid kidney transplant and dialysis or get rid of dialysis.
The therapy used in China is Micro-Chinese Medicine Osmotherapy+Immunotherapy... [this proves you can learn something new everyday.  In this case that China does not perform kidney transplants...]



From KindeyCaresCN.Blogspot.com
Chinese herb is special Chinese medicines and it has thousands of years’ history in China. Nowadays more and more westerners are becoming interested in Chinese herbs and they are wandering how these herbs can shrink the multiple cysts in the kidneys and why it can repair kidney damages and improve kidney functions.
One of the merits of Chinese medicine is that it can solve the root cause of the disease and does not cause any side effects or pains to the patients. The Chinese medicine emphasizes the concept of overall treatment. Though it takes effects more slowly compared with the Western therapies, its curative effects can last for a long time. And as we all know that the PKD is a chronically progressive kidney disease so that it needs continuous treatment and there is no instant way to cure it. The Chinese medicines can not only treat the multiple cysts in the kidneys, it can also improve kidney functions and enhance the patients’ immunity and help build up the patients’ physical health. [Now I understand why China puts emphasis on its traditional and holistic medicine if the policy is to minimize dialysis and completely avoid kidney transplants.]

From YouTube.com, posted by KidneyServiceChina.com

The Best Treatment for PKD without Dialysis or Kidney Transplant

Before he came here, his creatinine level was 4.25 umol/L. After one and a half months later with Micro-Chinese Medicine treatment, now, his creatinine level has been reduced to 3.4 umol/L.

"The doctors here treat me the best way I can imagine. It was different than I used to be treated in Greece. And I am satisfied for my treatment. I will continue Micro-Chinese Medicine for my better health."

From Fu Neng Kidney Disease Hospital

How to treat High Blood Pressure Caused by Polycystic Kidney Disease (PKD)?

Renal hypertension caused by PKD is different from primary high blood pressure. For high blood pressure caused by PKD, the key point of high blood pressure treatment is to treat polycystic kidney and reduce the pressure of cyst oppressing kidney.
People with Polycystic Kidney Disease and high blood pressure need to treat Polycystic Kidney Disease, which is the root cause of high blood pressure. PKD can be treated by Funeng Therapy.
Funeng Therapy develops from traditional Chinese medicine (TCM). The huge pharmacopeia of Chinese medicine contains plant, animal, mineral origin, most of them herbs, some of which have good effects on treating Polycystic Kidney Disease. These herbs, which are bitter if you take them orally, can be micronized and osmosed into kidney lesions with the help of osmosis devices. It has been practiced in clinic for more than 20 years and proved great effects on treating PKD.




Research
From PKDCure.org, The PKD Foundation
Two Top Doctors Dedicated to Ending PKD Honored

KANSAS CITY, Mo. – Dr. Vincent Gattone and Dr. Dorien Peters have been awarded the Lillian Jean Kaplan International Prize for Advancement in the Understanding of Polycystic Kidney Disease (PKD). The award is a partnership between the PKD Foundation and International Society of Nephrology (ISN) and recognizes a medical professional or researcher exhibiting excellence and leadership in PKD research and whose work demonstrates tangible achievement toward improving knowledge and treatment of PKD.



From Proceedings, National Academy of Sciences, USA
Polycystic kidney disease (PKD), the most common genetic cause of chronic kidney failure, is characterized by the presence of numerous, progressively enlarging fluid-filled cysts in the renal parenchyma. The cysts arise from renal tubules and are lined by abnormally functioning and hyperproliferative epithelial cells. Despite recent progress, no Food and Drug Administration-approved therapy is available to retard cyst growth. MicroRNAs (miRNAs) are short noncoding RNAs that inhibit posttranscriptional gene expression. Dysregulated miRNA expression is observed in PKD, but whether miRNAs are directly involved in kidney cyst formation and growth is not known. Here, we show that miR-17∼92, an oncogenic miRNA cluster, is up-regulated in mouse models of PKD. Kidney-specific transgenic overexpression of miR-17∼92 produces kidney cysts in mice. Conversely, kidney-specific inactivation of miR-17∼92 in a mouse model of PKD retards kidney cyst growth, improves renal function, and prolongs survival. miR-17∼92 may mediate these effects by promoting proliferation and through posttranscriptional repression of PKD genes Pkd1, Pkd2, and hepatocyte nuclear factor-1β. These studies demonstrate a pathogenic role of miRNAs in mouse models of PKD and identify miR-17∼92 as a therapeutic target in PKD. Our results also provide a unique hypothesis for disease progression in PKD involving miRNAs and regulation of PKD gene dosage.


From Hindawi.com, Case Reports in Medicine