Saturday, November 16, 2013

KIDNEY STORIES: NEW BLOG

HAS THE ACA EXPANDED MEDICARE’S IMMUNOSUPPRESSIVE DRUG COVERAGE FOR KIDNEY TRANSPLANT RECIPIENTS?
          I had a conversation with my doctor last week. (My nephrologist, Dr. Vavilala, we call him Dr. V).  He asked me if I had heard anything during my last trip to Washington, D.C. about an extension of coverage through the ACA to kidney transplant patients of the immunosuppressive drug coverage beyond the 36 month period that currently exists.  This rang a bell in the back of my brain, so I decided to check it out.
          Every transplant patient or transplant candidate knows the current status of the law.  If you are a kidney transplant recipient, you must take medications the rest of your life to prevent rejection of your transplanted kidney.[i]  Medicare pays for the transplant and immunosuppressive drugs for 36 months post-transplant, but coverage of these critical medications stops unless the beneficiary is Medicare-aged or Medicare-disabled.[ii] Here is where the gap in coverage comes in; if you’re under 65 and you have received a transplant, you are not age-eligible, nor are you considered disabled because after you have a transplant, you are no longer Medicare-disabled.[iii] Coverage for anti-rejection drugs for those patients that fall into the gap is limited to 36 months.[iv] The catch is that anti-rejection meds are very expensive.  One newspaper article I read reports that one patient was paying as much as $1,750 a month,[v] and the National Kidney Foundation estimates that Medicare pays $124,643 for a first year transplant patient, and then pays $24,612 a year primarily for anti-rejection meds thereafter.[vi]
          So what happens to the transplant patient who has to make the choice between heating, eating & driving or taking his immunosuppressive medications?  An all too common scenario for those that fall into the gap is they skip their meds, their newly implanted kidneys fail, and they end up back on dialysis.[vii]
          This is particularly maddening when you consider that your life expectancy on dialysis is about 5 years and your life expectancy from a live transplant can be 12-20 years, with a much better quality of life.[viii] This is particularly striking when you consider that some transplants have lasted as long as 40 years.[ix]
          Another big factor to consider is costs.  The National Kidney Foundation makes the following comparison between the cost of a transplant and the costs of dialysis,
“Medicare spends an average of $86,316 per year for an individual who is on dialysis and $124,643 during the first year of a kidney transplant.  However, after the year of transplant, the cost is much lower at $24,612 for an individual with a functioning kidney transplant.  If the transplant fails, the patient returns to dialysis or receives another transplant, each covered again by Medicare.[x]
          Think about that for a minute; almost a $60,000/year savings by simply preserving and protecting a transplanted kidney! The NKF has proposed legislation for years to plug this gap, but despite wide-spread acceptance, the bill has yet to become law.[xi]
          To answer the doctor’s question, we look to the NKF blog on the subject: 
“We are confident that the declining cost of the drugs, coupled with the fact that many currently uninsured transplant recipients will be able to purchase insurance under the Affordable Care Act (ACA), will make H.R. 1428 / S. 323 very cost effective and increases the possibility of congressional approval.  The CRS study reviewed preliminary information on the ACA’s essential health benefits (EHB) benchmark plan in multiple states, and found that the plans will typically require health plans to cover these immuno drugs.  Thus, since more people will have insurance coverage, fewer will need the extended Medicare benefit, lowering the cost of H.R. 1428 / S. 323.”(emphasis added).  [xii]
          In other words, in the opinion of the National Kidney Foundation, the ACA may now cover that gap in coverage for the immunosuppressant drugs, extending the 36 months in coverage to coverage for a lifetime.  The NKF has made clear that they are still pursuing a bill to extend this coverage and preventing insurance carriers from cancelling you once you have coverage.[xiii]
          I then located the study referred to in the NKF blog.[xiv] The article notes that in 2007, the Government Accountability Office (GOA) found the percentage of kidney transplant failures had nearly doubled when examining the results after a 7 year period, post-transplant.[xv]  The study attributed at least part of this failure to patients not taking anti-rejection meds due to prohibitive costs after the 36 month period had run.[xvi] The article notes that beginning in 2014, patients with a kidney transplant who are no longer entitled to Medicare payments for their anti-rejection meds may have access to extended coverage under the ACA.[xvii] The CRS paper went on to note that a random sampling of plans covered prescription drugs, presumably including immunosuppression drugs used by ESRD patients to prevent transplanted kidney rejection.[xviii] More to the point, the ACA beginning in 2014 requires private health plans offered through exchanges to cover essential health benefits (EHB).[xix] The 2012 benchmark standards require all plans available in exchanges to cover drugs in the immunosuppressive class.[xx] What this means in plain English is that somewhere between 3-24 anti-rejection drugs and roughly 20 products must be covered by state exchanges including common immunosuppressive drugs used by kidney transplant recipients.[xxi] This comes as potentially good news for kidney transplant patients!



[i] Flyer from the National Kidney Foundation entitled “Immunosuppressive Drug Coverage” distributed on March 13, 2013.  See Also: www.kidney.org/…/ImmunosuppressiveDrugCoverage113thCongress.pdf (Accessed 2013).
 
[ii] Id. 
[iii] http://ssa-custhelp.ssa.gov/app/answers/detail/a_id/168 (Accessed 2013)(Age limit is 65); http://www.cpmc.org/advanced/kidney/patients/topics/kidney_eval_disability.html (Accessed 2013)(“ Social Security benefits continue for 12 months following transplant surgery. At that point, Social Security re-evaluates each case, but unless you have another disabling condition (blindness, stroke or severe amputation) or are over 65, your Social Security benefits end.”); www.medicare.gov/Pubs/pdf/11360.pdf‎; (Medicare coverage ends 12 months after you stop dialysis); http://www.dallasnews.com/investigations/problem-solver/20121122-kidney-transplant-recipient-approaching-anti-rejection-drug-deadline.ece (2012)(“ Medicare covers kidney patients under the age of 65 for only 36 months after the transplant surgery, a limit written into the statute under the Social Security Act. The rationale for the ruling is that younger patients will recover from end-stage renal disease following the transplant, get a job and buy private insurance through their employer. But Dawson — like many other transplant recipients — is unlikely to be hired.”)
[iv] Flyer from the National Kidney Foundation entitled “Immunosuppressive Drug Coverage” distributed on March 13, 2013.  See Also: www.kidney.org/…/ImmunosuppressiveDrugCoverage113thCongress.pdf (Accessed 2013).
 
[vi] Flyer from the National Kidney Foundation entitled “Immunosuppressive Drug Coverage” distributed on March 13, 2013.  See Also: www.kidney.org/…/ImmunosuppressiveDrugCoverage113thCongress.pdf (Accessed 2013).
 
[vii] Id.  (“Transplant recipients often have difficulty finding other coverage for their immunosuppressive drugs after Medicare coverage ends… Extending immunosuppressive coverage beyond the 36-month post-transplant limit would improve outcomes and enable more kidney patients who lack adequate insurance to consider transplantation.  Most transplant recipients also have a higher quality of life, and are more likely to return to work than dialysis patients.”).
 
[viii] http://www.kidneyfund.org/kidney-health/kidney-basics/common-questions.html#How_long_can_a_person_live_on_dialysis (Accessed in 2013)(“… the average life expectancy for all dialysis patients is currently between five and six years.”); http://www.bidmc.org/Centers-and-Departments/Departments/Transplant-Institute/Kidney/The-Benefits-of-Transplant-versus-Dialysis.aspx (Accessed in 2013)(“ A living donor kidney functions, on average, 12 to 20 years, and a deceased donor kidney from 8 to 12 years. Patients who get a kidney transplant before dialysis live an average of 10 to 15 years longer than if they stayed on dialysis. Younger adults benefit the most from a kidney transplant, but even adults as old as 75 gain an average of four more years after a transplant than if they had stayed on dialysis. - See more at: http://www.bidmc.org/Centers-and-Departments/Departments/Transplant-Institute/Kidney/The-Benefits-of-Transplant-versus-Dialysis.aspx#sthash.HSuqLkEr.dpuf”).
[x] Flyer from the National Kidney Foundation entitled “Immunosuppressive Drug Coverage” distributed on March 13, 2013.  See Also: www.kidney.org/…/ImmunosuppressiveDrugCoverage113thCongress.pdf (Accessed 2013).
 
[xi] https://nkfadvocacy.wordpress.com/immunosuppressive-drug-coverage/ (2013)(“ Sens. Richard Durbin (D-IL) and Thad Cochran (R-MS) introduced S. 323 on February 13, 2013, to extend Medicare coverage of immunosuppressive drugs for kidney transplant recipients.  Medicare covers dialysis for most Americans, regardless of their age, with no time limit. However, if they are under age 65 or are not Medicare-disabled (receiving Social Security Disability Income), their eligibility ends 36 months after receiving a transplant.  S. 323 eliminates the 36 month time limit to provide continued Medicare coverage for life-saving immunosuppressive medications. All other Medicare would end after three years for kidney recipients, as under current law.
Please contact your Senators and urge them to cosponsor S. 323 to help transplant recipients access the medications they need to maintain their new kidney.
Senate Co-sponsors:
Rep. Michael Burgess (TX) and Rep. Ron Kind (WI) introduced H.R. 1428to amend title XVIII of the Social Security Act to provide Medicare entitlement to immunosuppressive drugs for kidney transplant recipients. This bill would extend Medicare’s coverage of anti-rejection drugs for kidney transplant recipients (who are not Medicare-aged or Medicare-disabled) for the life of the transplant, versus the 36 months post-transplant that Medicare currently covers.
Please contact your Representative and urge them to cosponsor H.R.1428 to help transplant recipients access the medications they need to maintain their new kidney.
House co-sponsors:
[xiv] Talaga, Medicare Immunosuppressive Drug Coverage for Kidney Transplant Recipients (2013).
 
[xv] Id.,  United States Government Accountability Office, End-Stage Renal Disease: Characteristics of Kidney Transplant Recipients, Frequency of Transplant Failures, and Cost to Medicare, September 2007, p.16, http://www.goa.gov/assets/270/267345.pdf.
 
[xvi] Id.
 
[xvii] Talaga, Medicare Immunosuppressive Drug Coverage for Kidney Transplant Recipients, July 16, 2013, p. 5, www.law.umaryland.edu/…/crsreports/crsdocuments/R43154_07162013.
[xviii] Id.
 
[xix] Id.
 
[xx] Id.  See Also:  CRS Report R42663, Health Insurance Exchanges under the Patient Protection and Affordable Care Act(ACA), by Benadette Fernandez and Annie L. Mach.
[xxi] http://www.cms.gov/CCIIO/Resources/Data-Resources/ehb-rx-crosswalk.pdf; Talaga, Medicare Immunosuppressive Drug Coverage for Kidney Transplant Recipients, July 16, 2013, p. 6, www.law.umaryland.edu/…/crsreports/crsdocuments/R43154_07162013.

Thursday, November 14, 2013

KIDNEY STORIES: ROBIN COHEN NEEDS A KIDNEY

I have Polycystic liver and kidney disease. I had a liver transplant in 2008. Now my kidneys are failing, and I am in end-stage renal failure.
Description
Hi,

My name is Robyn Cohen and I have Polycystic liver and Kidney disease. In July 2008 I had a successful liver transplant. But, now my kidney function has gone down dramatically and I am in end stage renal disease and am in desperate need of a kidney… I have been on dialysis since February 2013 when my kidney function fell to 9%. No one in my family can offer me their kidney as they have th...e disease, too. I watched my mother suffer and die from the same disease 18 years ago… and, tragically, one year ago my precious brother Mark died from it also after suffering terribly for many years, as well.
I know for sure I can’t wait much longer for a kidney. I’m hoping that there is someone, anyone, out there that is willing to offer me the precious gift of becoming my donor, and saving my life. I know it’s a huge request, and I’m not comfortable asking but as I said before I’m desperate. My blood type is A+, however I am also compatible with O blood type as well. If you would like more information you may also call the Living Donor Line which is located in the transplant center at UCLA in Los Angeles, California (866) 672-5333 or my transplant coordinator Prest Oshodi at (310) 267-6902.

My life is very full with love and responsibility as I am raising two beautiful grandsons who are 13 and 14 years old. They are the light of my life and give me great joy and purpose. I need to be here and be healthy for them most of all.
If you are reading this, and God lays it on your heart to respond, know that you will not only be helping me but helping me show the rest of my family how to live victoriously through this horrible disease.

Please contact me at robyncohen@roadrunner.com.
 
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Monday, November 11, 2013

KIDNEY STORIES: TRISHA NEEDS A KIDNEY


Hi, my name is Trisha and I am wishing for a kidney, my blood type is O and I live in Amherst, NY
Description
I am in search of a kidney....Hello and welcome to our page ! My name is Trisha, I am 48, married and have three children Ashlee who is 23, Tyler who is 19 and Joe who is 17. I live in Amherst, NY which is about 15 minutes from Canada. I also have my 3 babies, my dogs, Daisy, Mollie and Cricket who are all Shih Tzus.I am surrounded by lots of support & love from my mom and sister and brother. My d...ad died last year and we became involved in UNYTS and through my dad's donation we passed on the gift of life to 7 people. My kidney's started to fail in 1997 with the pregnancy of our last child, I developed HELLP Syndrome which you can read about here http://www.nlm.nih.gov/medlineplus/ency/article/000890.htm
I spent about 6 months on dialysis and was blessed to have my kidneys rebound. Fast forward to 2011 and I got a cold, my boss wanting to be sure I wasn't passing anything on asked me to be checked at my doctor, to our shock, the results showed my kidneys were already in stage 4 renal failure.With the help of my Nephrologist we were able to hold off kidney dialysis for 3 years. I started kidney dialysis on August 16,2013, and I go 3 times a week for 3 hours. I am in the process of being listed at 3 hospitals 's  ECMC in Buffalo, NY, The Cleveland Center in Ohio, and Allegheny General Hospital in Pennsylvania , to learn more on how to become a kidney donor for anyone this link will help you decide, as it is a personal decision http://www.kidney.org/transplantation/livingDonors/infoQA.cfm?id=3
Thank you for visiting our page, if you would like to ask us anything you can email us at d_t_leo@roadrunner.com and as soon as my transplant team is in place we will have the information posted !!
 
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KIDNEY STORIES: A KIDNEY FOR MY MOM


My Mom was diagnosed with CKD (Chronic Kidney Disease) in 2009. This page is being created to be shared and hopefully find its way to someone who can help save her life, and be her donor.
 
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KIDNEY STORIES: A KIDNEY FOR SARAH


We are three friends helping to find a kidney for our friend Sarah. And along the lines do our share in spreading awareness and education for the community
Description
Our friend Sarah is a friendly, happy and highly driven young woman. In 2010, while in grad school, she was diagnosed with kidney failure. The doctors stated that both kidneys had failed, and because of the state of the kidneys, it was too late to determine the exact cause of the failure.  However,  Sarah also has Sickle-Cell Anemia, a  blood disease that also has been having a devastating effect ...on her condition. She has been on hemo-dialysis and is in dire need of a kidney donor. She goes to dialysis 3x a week for about 4hrs, is on 10 different medications at the moment, and has unfortunately, had to stop working in order to be able to continue under her plan of care. She is currently listed on the national organ-sharing waiting list; however that can take up to 10yrs in the state of California, depending on the patient. Being the oldest of six children (therefore, making her siblings too young to donate), and not having enough family members here in the US, she has found herself with no donors. In order to help save her life, we are starting an effort using social-media to aid the search for a donor, as well as starting a fundraiser to help with the medical costs.
She has a blood-type of A+, and can receive from anyone with an A, O, or AB blood type. We are pleading for the public to please help get her off dialysis in order to get her life back. Only one kidney is needed, and a normal, healthy person only requires one kidney to live a long healthy life.
  "A good living donor candidate is someone who is healthy, well-informed and makes a voluntary decision to donate one of their kidneys. Living donors must be over 18 and usually under 70 years of age. They must be in good general health, a non-smoker, with no evidence of significant high blood pressure, diabetes, cancer, kidney disease, heart disease or hepatitis. Living donors can live in any state, and it is important to know that all medicals costs are covered by the recipient's health insurance." And there are programs that will help cover travel costs associated with the transplant. If interested in testing to see if you could possibly be a match, pls inbox or contact:
  Sandra Heisterkamp/ Alejandra Munoz - UCSD Center for Transplantation 619-574-8612 Patient: Sarah O. Umarhabib
If you do not meet the criteria for a donor, you can still help by kindly donating whatever you can afford to:
http://patients.transplants.org/saraho
  Thank you all, and may God bless you...Feel free to hit the "Like" and "Share" button! The more people we reach, the better our chances of helping Sarah.
"An average of 18 people die each day from the lack of available organs for transplant."- DonateLife America
 
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Sunday, November 10, 2013

KIDNEY STORIES: SOCTT'S KIDNEY SEARCH




I am searching for a live kidney donor. I don't  smoke or drink and I have no other illnesses other than PKD which caused me to loose one kidney when I was born and the other three years ago. I had one transplant, but there were surgery complications which caused me to loose it within 48 hours. I have faith that God will touch someones heart and lead them to contact me to help me live a longer life. I have good insurance which will help the donor's expenses. Thank you for your time.
https://www.facebook.com/pages/Scotts-Kidney-Search/217813671726421
WWW.FACEBOOK.COM/KIDNEYSTORIES

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KIDNEY STORIES: FIND A KIDNEY FOR CARRIE


Carrie is a 36 year old single mother.  She needs a kidney from someone with blood type O.  Her transplant center is in Wisconsin.  Dialysis since 7/5/10.
Description
I'm a 36 year old single mother of a wonderful and amazing 14 year old son. I have been a single parent since he was 5.  I need a kidney from someone with blood type O.   If you want to be tested to see if you are a match for me, please call donor team member Stephanie at Froedtert Medical Center at 1-414-805-0310. Tell them you wish to be tested for Carrie Webster.
My story: My mother found out ...while taking me to my well baby checks that I had blood in my urine.  I saw a lot of doctors growing up, but I never understood my situation.  
After having my son in 2001, I became ill.  In 2002, I needed to start dialysis. I was so sick I didn't remember even seeing doctor and having surgery to have my dialysis access created.  All the while on dialysis I was sick, had many infections and surgeries. My surgeon had only a few areas left to work with.
In 2005, I got my call on a Friday night for a deceased donor kidney.  I was so happy but devastated that another family was grieving over the loss of their loved one.  With my newly transplanted kidney I was sick often and rejected a few times.   The doctors were able to bring my kidney back several times.  They were amazed that I fought that long trying to keep it going.  They said I was a fighter.
  In 2010, they couldn't save it anymore.   I had to begin dialysis again in July 2010. I have so many things going on that I hurt every day.  I have appointments all the time with different doctors.  I just recently got out of the hospital with a staph infection ended up going home with a hole in my arm that needed daily dressing and a vacuuming for healing.  I had numerous surgeries I lost count. When I walk into the doors at the hospital they all know me they say, “Hi Carrie.”  
I fight every day for my son.  All my son knows is his mommy being sick and in and out of hospitals.  I live with my mother and she is my rock. Without her I don't know what I would do.  She is always by my side thru all this and I love her very much.  
I have a big family and most support me and wish they could donate but can't due to something wrong with them.  That is why I am reaching out to the public asking for help.  Are you blood type O?   If you find it in your heart to test for me, please call Froedtert Medical Center at 1-414-805-0310.  The donor coordinator's name is Stephanie.  Tell them you wish to be tested for Carrie Webster.  My insurance covers the cost of all pre-op testing and the transplant surgery.
Thank you for taking time to read my story.  If you do not feel that living kidney donation is right for you, then I ask that you please share my page.  You never know who will end up seeing it.  It might just reach that special person…my future donor.
Thank you, Carrie Webster
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Basic Info

LaunchedOctober 23, 2013

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KIDNEY STORIES: HELP ROBBIE FIND A KIDNEY


This page is intended to help me (Robbie) to find a kidney for a transplant!
Description
I would like to just tell a little bit about myself and my kidney disease. I first learned of my Chronic Kidney disease (ckd) when i was just six years old. I was dressed as spider-man and had just got home from a Halloween party, which we were having at my school in Philadelphia. Whenever I went to the bathroom to void (pee) my urine came out red. I thought nothing of it; to be honest I simply th...ought I had been drinking too much fruit punch lol. One day I forgot to flush the toilet and my mom saw the red urine and asked me how long I had been "peeing red". I told her that it had been going on for a while. It turned out to be much worse than fruit punch, it was obviously blood. My mom immediately rushed me to St. Christopher’s hospital. When we arrived at the emergency room, the doctors were extremely worried and ran many tests. The doctors were not sure how this could have happened. They decided on strep throat infection that settled in my kidneys and caused ckd. This didn’t make sense to me or anybody else. I had never been sick up to this point. I couldn't understand how this could have happened; I was a very active little boy who enjoyed ninjas and baseball lol. . From then on the hospital was my second home.
My kidneys failed six years later when I was twelve. I remember the room would spin and I would have aw full nightmares. The doctors had to put me on emergency dialysis to keep me alive at this point. They gave me medicine through my IV that would help me "forget". I never forgot the pain. A dialysis catheter was placed at tip of my inner thigh and it was the first of many brutally painful procedures that no twelve years old should have to go through. This was only a temporary solution. A few weeks later the catheter was removed and a new more accessible dialysis catheter was inserted into my neck. This was still only temporary and i remained in the hospital. In order for me to go home they wanted to place me on a dialysis plan, which would allow me to go home and try to live a normal life.
A peritoneal dialysis catheter was inserted into my stomach, so that I could hook myself up to a machine at home and receive dialysis over night. The procedure to insert the catheter was supposed to be simple. When I woke up, I was in so much pain that i couldn't sit up or move without extreme pain in my stomach. My mom took me to the Ronald McDonald house to get more rest. Something was wrong. I felt very light headed and it kept getting worse. I told my mom that something was wrong. I had never been so scared in my entire life. I thought I was going to die. I passed out and woke up in a stretcher racing down the hallway of the hospital. I saw my mother, crying uncontrollably while being restrained by medical staff. I asked the nurse what had happened and she told me not to worry and that I was going to be ok. I then asked her; “am I going to die". She said; "what’s that honey"? I said;"Nothing". I accepted my fate.
The reason why I went unconscious, and thought I was done for was because when they inserted the catheter into my stomach the catheter nicked an artery the size of a pin head. Fortunately they sewed me back up. I was finally stable enough to go home. I felt tired most of the time and things had changed for me. I had to endure disgusting nutrition shakes that tasted so horrible, every time I took a sip I wanted to vomit. Three time a week i had to inject myself with steroid shots into my stomach. The steroids burned so bad it felt like i was injecting acid into my stomach. I had no choice but to hold an ice pack on my belly for thirty minutes, to numb the area and reduce the pain and burning sensation. One night my parents were awoken by my dialysis machine's alarm. They found me face down in my pillow. I was having seizures, and another fight for my life had already started this time without my protectors. I remember almost nothing. The only thing I remember was my mom trying to hold me up and I heard her yelling; "Robbie please open your eyes!" I couldn't talk and I couldn't open my eyes all the way. When I would try to open my eyes, I couldn't straighten them; they would roll in the back of my head. I woke up in the hospital the next morning and I had no idea what happened until they explained it to me.
At last I received a kidney transplant on feb 18 1999. I was twelve. The kidney did not work at first. They put me to sleep for a procedure that was supposed to last only 45 minutes. I looked at the clock before I went under. The clock read 9:45 am. I woke up at about 7pm. I knew something was wrong again! The ureter was damaged so they had to "piggy back" the original ureter from one of my native kidneys and saved the transplanted kidney. The transplant allowed me to live a better life and at-least I was off dialysis, but it never worked properly.
Ten years later the transplanted kidney failed and I was placed back on dialysis. I was on dialysis for 3 1/2 years before my left native kidney started to self destruct. The kidney was bleeding and it had a blood clot the size of an orange sitting on top of it. The blood clots were being voided through my urine; this is as painful as passing a kidney stone except it was happening all day for about 5 weeks. They were forced to remove the kidney. I had been on the list for about 3 1/2 years and was very close to finding a match. However, when they removed the damaged kidney, a small amount of cancer on the left native kidney was discovered when they removed the kidney. Yet another setback. Because I there was cancer in my body, I was placed as "inactive" on the list! I had dodged a third bullet. If i had received a transplant with cancer in my body, it would have spread like wild fire!
I have been cancer free for almost 3 years now and I am now active on the kidney transplant list. I haven't had any major problems since and I feel better than I ever have. I try to stay as active as possible and maintain a healthy life style! When I get a transplant I plan on going back to school so I can finally start my life...
A living donor is my absolute best Chance for a normal life. Please if anyone is interested in helping me find a living donor, or is interested in learning more, contact Gesinger wyoming valley. @ (570) 808-7300 ask for the transplant department. Give them my name (Robbie Fatzinger)   More info on the pay it forward program http://www.matchingdonors.com/life/index.cfm?page=p030
My blood type is "O". If you are intrested in getting tested you can call Geisinger in wyoming valley,pa The number is (670) 808-5590 Everything including tested is paid by my medical insurance
.
 
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KIDNEY STORIES: HELP BECKY FIND A KIDNEY


Becky Dossett is a 59 year old wife, mother of of 2 and grandmother of 1.  She needs a kidney from someone with blood type A or O.  Call IU Health (Indiana) at 1-800-382-4602 to see if you are a match today!
Description
Becky Dossett is a 59 year old wife, mother of two daughters and grandmother of a six year old grandson.  Becky’s journey with kidney failure all started in March 2005 when she went in to have her gallbladder x-rayed.  The technician asked her how long she had had issues with her kidneys.  That was the first she ever heard of having kidney issues.  
Becky was then diagnosed with Polycystic Kidne...y Disease (PKD).  “PKD is a disorder in which clusters of cysts develop primarily within your kidneys. Cysts are noncancerous round sacs containing water-like fluid. Polycystic kidney disease causes your kidneys to gradually lose their ability to eliminate wastes from your blood and maintain your body's balance of fluids and chemicals. As the cysts enlarge, they produce pressure and promote scarring in the normal, unaffected areas of your kidneys. These effects result in high blood pressure and interfere with the ability of your kidneys to keep wastes from building to toxic levels, a condition called uremia. As the disease worsens, end-stage kidney (renal) failure may result. When end-stage renal failure occurs, you'll need ongoing kidney dialysis or a transplant to prolong your life.”   (Information via Mayo Clinic)
PKD is an inherited disease.  Becky is not sure whether she got it from her mother or father’s side.  Since it is an inherited disease, no one in her family can donate.  She had a potential donor lined up.  Unfortunately, although her donor was a match, during the pre-op testing in August 2013 they found medical issues that made her ineligible to donate.  That is why this page was created.  The hope is that this page will reach Becky’s donor.
Becky is not yet on dialysis, but that time is getting nearer.  Day by day she grows more tired.  Her doctors have started to prepare her for the idea of dialysis.  She attended her educational classes on dialysis in October 2013 to better prepare her for the long road ahead of her.  She is hoping to find her donor before dialysis has to begin.
If you are blood type A or O, you could be a match! To find out, call IU Health (Indiana) at 1-800-382-4602. Tell them you wish to be tested for Becky Dossett.  All pre-op testing and the surgery will be paid for by Becky’s insurance.
If you cannot share your spare with Becky, perhaps you can find the time to at least share her page so that it might reach her future hero.
 
TAGS: help becky find a kidney, Ning, Live Journal, Tumblr, Weebly, WordPress, Facebook, Kidney Stories, Jim Myers, kidney, dialysis, blood, transfusion, donor, recipient, seeking, awareness, National Kidney Foundation, Indiana University, sharing, kidney disease, End Stage Renal Failure, polycystic kidney disease, chronic kidney disease, kidney for, diabetic, save my life, living kidney donor, organ donation, find a kidney for, NCS, share a spare, transplant list, fundraiser, donate life,

KIDNEY STORIES: GIVE A BEAN FOR GREG

KIDNEY STORIES: GIVE A BEAN FOR GREG
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Follow Greg Conners journey for a Kidney Transplant.
Description
Greg is the Executive Pastor of Faith Church. Greg is married to the beautiful Candice Conner. He has two amazing children Sawyer and Lucy. Greg is full of love, kindness, laughter and God. We can’t think of a more deserving person than Greg to receive a kidney. Be Lucy’s & Sawyer’s Hero and give a Bean!
Greg’s treatments are in Oklahoma. He does nocturnal dialysis 3 nights a week. His blood type is O positive.

https://www.facebook.com/pages/Give-a-Bean/475928152506273
WWW.FACEBOOK.COM/KIDNEYSTORIES

TAGS: give a bean, Ning, Live Journal, Tumblr, Weebly, WordPress, Facebook, Kidney Stories, Jim Myers, kidney, dialysis, blood, transfusion, donor, recipient, seeking, awareness, National Kidney Foundation, Indiana University, sharing, kidney disease, End Stage Renal Failure, polycystic kidney disease, chronic kidney disease, kidney for, diabetic, save my life, living kidney donor, organ donation, find a kidney for, NCS, share a spare, transplant list, fundraiser, donate life,

KIDNEY STORIES: VICKY'S TRANSPLANT ASSISTANCE PAGE


This page is about Linda Victoria [Vicky] Wright Terrell. She needs a kidney or donations to help her receive a Transplant. Vickie is the loving mother of 3 and grandmother of 4. She worked as a Registered Nurse for more than 20 years.
https://www.facebook.com/pages/Vicky-Terrell-Kidney-Transplant-Assistance-Page/451164001668497
WWW.FACEBOOK.COM/KIDNEYSTORIES

TAGS: vicky's transplant assistance page, Ning, Live Journal, Tumblr, Weebly, WordPress, Facebook, Kidney Stories, Jim Myers, kidney, dialysis, blood, transfusion, donor, recipient, seeking, awareness, National Kidney Foundation, Indiana University, sharing, kidney disease, End Stage Renal Failure, polycystic kidney disease, chronic kidney disease, kidney for, diabetic, save my life, living kidney donor, organ donation, find a kidney for, NCS, share a spare, transplant list, fundraiser, donate life,

KIDNEY STORIES: KIDNEY FOR ALLEN


Saturday, November 9, 2013

KIDNEY STORIES: PRAYERS AND SUPPORT FOR JACKIE

KIDNEY STORIES: PRAYERS AND SUPPORT FOR JACKIE
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Hello, my name is Jackie, and I need another kidney transplant. I am current doing Peritoneal Dialysis treatments at home to sustain my life.
Description
I am a 40 yr old single female who has been suffering with kidney disease the majority of my life. I was initially diagnosed with Membranous Glomuro Neprhitis at the age of 12, and received my first kidney transplant 9 months later at the age of 13. Because of this disease,  I’ve never been able to have any  children. I got my first Cadaver kidney transplant on Nov. 11, 1986. That kidney only last…ed a year, from Nov. 86’-Nov. 87’, and I had to go back on Dialysis.I spent the next 14 yrs of my life surviving on Dialysis. I received my next Cadaver kidney transplant on Dec. 25, 2001. That kidney was a very good match for me and lasted 12 yrs. In July of 2013, I began Peritoneal Dialysis treatments at home. I have to do 4 treatments a day, with 4-6 hours in between 7 days a week. The Peritoneal Dialysis only cleanse 10-15% of what a real kidney would  do. I have gone through all the Pre-transplant testing required to receive another kidney back in 2012. I’m still waiting to be placed on the transplant list. I must come up with a financial plan to stay in Houston, Texas for 4 weeks, along with my major support person. So I have to raise $3000-$6000 to cover various expenses such as Lodging, Food, Transportation, Medicine and also be able to take care of my bills at home. I have created a fundraising page through Giveforward.com. If you would like to be tested to see if you are a match for me, please contact The Methodist J.C. Walter Referral Line @ 1(713) 441-8900.
https://www.facebook.com/jackiea
WWW.FACEBOOK.COM/KIDNEYSTORIES

TAGS:  prayers and support for jackie, Ning, Live Journal, Tumblr, Weebly, WordPress, Facebook, Kidney Stories, Jim Myers, kidney, dialysis, blood, transfusion, donor, recipient, seeking, awareness, National Kidney Foundation, Indiana University, sharing, kidney disease, End Stage Renal Failure, polycystic kidney disease, chronic kidney disease, kidney for, diabetic, save my life, living kidney donor, organ donation, find a kidney for, NCS, share a spare, transplant list, fundraiser, donate life,

KIDNEY STORIES: FIND A KIDNEY FOR MY MOM

KIDNEY STORIES: FIND A KIDNEY FOR OUR MOM

Paula, our mom, has only 1 kidney and it’s failing her. She desperately needs another one.  Please share this page!
Description
8 years ago, my mom was diagnosed with Chronic Kidney Disease. One kidney was removed, and the other has been sustaining her. She was maintaining a level of function for a while, but recently her numbers are plummeting and dialysis is imminent.
My brother and I have been tested to be donors for her, but we were saddened to find out we were not matches. My dad is willing to donate his kidney as p…art of a paired donation kidney program at Mayo Clinic in Rochester, Minnesota. We have been told by Mayo Clinic that she may be hard to match, and in order to give her the best chance of survival, we need more people to be tested to increase the odds of finding her a match.
Next year, my mom will hopefully be celebrating her 70th birthday, and my parents will hopefully be celebrating their 50th wedding anniversary.
https://www.facebook.com/pages/Find-a-Kidney-for-our-Mom/671467386226446
www.facebook.com/kidneystories TAGS:  find a kidney for my mom, Ning, Live Journal, Tumblr, Weebly, WordPress, Facebook, Kidney Stories, Jim Myers, kidney, dialysis, blood, transfusion, donor, recipient, seeking, awareness, National Kidney Foundation, Indiana University, sharing, kidney disease, End Stage Renal Failure, polycystic kidney disease, chronic kidney disease, kidney for, diabetic, save my life, living kidney donor, organ donation, find a kidney for, NCS, share a spare, transplant list, fundraiser, donate life, image

KIDNEY STORIES: KIDNEY FOR TINA


KIDNEY STORIES: AMY'S QUEST FOR A KIDNEY TRANSPLANT

KIDNEY STORIES: AMY’S QUEST FOR A KIDNEY TRANSPLANT


Lupus Nephritis *Listed in San Antonio, TX at University Health System. *Blood type: A+ *Contact to get tested: Louisa.Gonzalez@uhs-sa
Description
ABOUT AMY:
I am 36 yrs old, I grew up in the best small town, Madill,OK. I played basketball and ran track in high school. I was even a cheerleader during my Freshman and Junior year. My college years, I attended Murray State Junior College and South Eastern State University. Moved to San Antonio in 2001. Received MBA from Webster University. Diagnosed with Lupus in October 2003, End Stage Renal Disease April 2013. I enjoy all types of music, I like going to watch outdoor movies in the summer. I like hanging out with friends, I consider my friends to be my family. I am involved with the Lupus Foundation of America and I work for Choctaw Global Staffing. I enjoy going to outdoor events, Hondo Corn Maize in November and Holiday in the Park are two of my favorite events. I don’t know what I would do without my family (here and Oklahome). They take very good care of me. *+*+*+*+*+*+*+*+*+*+*+*+*+*+*+*+*+*+*+*+*+*+*+ Kidney Program Overview: http://bit.ly/1fbozAJ Kidney Referral Criteria:http://bit.ly/1bOpioR Becoming a Living Donor: http://bit.ly/16XlsXR Living Kidney Donation: http://bit.ly/1gkdi3Y Questions?  Contact: Louisa.Gonzalez@uhs-sa
 
KEY WORDS: amy's quest for a kidney transplant, Ning, Live Journal, Tumblr, Weebly, WordPress, Facebook, Kidney Stories, Jim Myers, kidney, dialysis, blood, transfusion, donor, recipient, seeking, awareness, National Kidney Foundation, Indiana University, sharing, kidney disease, End Stage Renal Failure, polycystic kidney disease, chronic kidney disease, kidney for, diabetic, save my life, living kidney donor, organ donation, find a kidney for, NCS, share a spare, transplant list, fundraiser, donate life,