Polycystic Kidney Disease

Aldo’s Army

Posted on Jul 28, 2021 in Polycystic Kidney Disease | 0 comments

https://gofund.me/5f4f9e90Aldo has been on dialysis for 21 years! That is truly difficult and a testament to his self-discipline and will to live. Aldo has worked full time while raising a family. Doctors have told him he is failing, Our church has united to help him find a kidney and to raise funds to support him and his family. Life . . . helping one another, loving one another.

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Trust in the Lord

Posted on Apr 17, 2021 in Polycystic Kidney Disease | 0 comments

Often when I worry, worry, worry as I am prone to do, my mother would say to me, “trust in the Lord.” Growing up in a religious family , I’ve heard that a million times. It sure is hard to do when times are tough.  It’s lovely and almost easy to do when things are going smoothly, the day is beautiful, and life is good.  It brings to mind the story of Thomas, the apostle who did not believe it when the other apostles told them, “We have seen the Lord!” Thomas had witnessed the death of Jesus on the cross and refused to believe them, saying, “Unless I see the nail marks in His hands and put my finger where his nail marks have been, and put my hands into His side, I will never believe.” That is one of my favorite stories, because as it is written, Jesus did appear later to Thomas – coming into a locked room no less! Thomas was able to see His nail marks and put his hand in the  wound in the Lord’s  side. I love that story. Thomas was so happy to see Jesus! Jesus even gave me a message that day: “Blessed are they who have not seen and yet believe.”  I need to stop whining and worrying and just trust.                 Trust in the...

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26 Years Post Transplant

Posted on Jan 21, 2021 in Polycystic Kidney Disease | 0 comments

My sister Janice wasn’t even forty-years old when she suffered renal failure. She knew it was coming . . . the end of life as she knew it. That’s what happens when you have a genetic disease in the family – you know what you’re in for . . . As she became sicker, she added her name to the transplant waiting list. Her kidney function had declined to dangerous levels. Back then – in 1995, there weren’t as many people’s names on the waiting list compared to today. There were not quite 37,000 names on the list compared to over 110,000 today.   Hope was wearing thin. The doctors scheduled Janice to start dialysis on Wednesday, January 11, 1995.  Somewhere a terrible tragedy occurred resulting in the death of a child the day before Janice was due to start dialysis. A child saved my sister – a child whose parents donated the child’s organs. I think of the child and the family often. Sorrow and our Joy intertwined. I will be forever...

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Living Organ Donation Reimbursement Program

Posted on Jan 6, 2021 in Polycystic Kidney Disease | 0 comments

Living Organ Donation Reimbursement Program

by Suzanne Ruff, AAKP Board of Directors Member Within families who battle kidney disease as my family does, there is a time for sorrow and a time for joy, a time for weeping and a time for dancing. For many of my family members with complete renal failure, organ donation is their only hope. Some because they had been on dialysis for many years, others because they did not want to be on dialysis. Pre-emptive transplantation (receiving a kidney transplant before dialysis) is recommended more and more. Finding a living donor is strongly encouraged, but it is not easy thing to ask of someone. On July 10, 2019, President Donald J. Trump signed an Executive Order on Advancing American Kidney Health. The American Association of Kidney Patients (AAKP) has also designated that this is the Decade of the KidneyTM. It is encouraging to know that kidney disease is being actively addressed and innovative solutions are implemented, including the elimination of roadblocks that might make finding a living donor easier. Hope is the quintessential weapon to battle kidney disease. As I read the Executive Order, it gives hope. One part of the order refers to the issues that greatly concern a potential living donor as they contemplate their decision to donate. Section 8 of the Executive Order reads as follows: Sec. 8. Supporting Living Organ Donors. Within 90 days of the date of this order, the Secretary shall propose a regulation to remove financial barriers to living organ donation. The regulation should expand the definition of allowable costs that can be reimbursed under the Reimbursement of Travel and Subsistence Expenses Incurred Toward Living Organ Donation program, raise the limit on the income of donors eligible for reimbursement under the program, allow reimbursement for lost-wage expenses, and provide for reimbursement of child-care and elder-care expenses.     As of September 2020, the Living Organ Reimbursement Program is to expand the scope of qualified reimbursable expenses incurred by living organ donors to include lost wages, child-care, and elder- care expenses. We have had five living donors within our family of nine transplants (eight kidney transplants and one liver transplant) among eight different people. I am one of the five living kidney donors. I did not even consider the costs and hardships that a living donor incurs when my sister collapsed in critical condition from renal failure–a time for weeping. I am from a family that supports one another, both physically, emotionally, and financially when one of us is down and out. In 2004, there were no resources anyway. It’s been sixteen years since I became a living donor and my sister is healthy, happy, and thriving–a time for dancing. Fast forward to 2020. Six very short days ago, as I began to assemble information to write this article, my cousin’s son received a kidney from his cousin, a single mother with a ten-year-old child. Both are recovering and I asked them for their thoughts about the Living Organ Donation Reimbursement Program. Neither one of them had a clue that there was a program to help living donors! When I sent the information to my cousin’s son, the recipient, Christopher Burgess, his comment (succinctly given while recuperating) is as follows: “I think there is a flaw still in the law since it takes into account the income of the recipients. Donors can feel guilty asking for reimbursement for some costs from a person that is sick so that caveat probably limits possible donors who need support. That said, I think it’s great to expand the law to care for donors who sacrifice so...

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A Valentine for Organ Donors and My Baby Sisters

Posted on Feb 14, 2019 in Polycystic Kidney Disease | 0 comments

A Valentine for Organ Donors and My Baby Sisters

I have two baby sisters. They’re both taller than me.  Plus we are not babies . . . far from it.  We are in our “golden years” now.  No matter, they’re always my baby sisters. I’m blessed they’re here. Both of my sisters are transplant recipients. Life!  The precious of all gifts.  My youngest sister, Janice, the baby of the family has had a really, really, really tough time in the past year.  Lots of suffering, pain, mountains to climb. Hospitals, rehab, doctors, outrageous ambulance bills, and insurance nightmares. (“‘If you like your doctor, you can keep your doctor” did not apply to her.) She made it through and is home now.  It’s what Polycystic Kidney Disease (PKD) does . . . and seems to never stop doing. My baby sister Janice never complains and I mean never.  Proof? She has said through gritted teeth, writhing in discomfort, a hospital gown tied around her pallid and gray skin, her long thin fingers grasping the bucket close . . . “better me than you.”  Who does that?  Who has the fortitude, love for another, and guts to say such things?  Well . . .my other sister, JoAnn, the middle child, does that, too.  Two women who have battled this disease with tremendous spunk, courage and are shining examples of grit and determination.   The thing about Polycystic Kidney Disease (PKD) is that although both have received kidney transplants, they still have the disease. The transplant does not cure the disease. Which is why I write stuff like this . . . to push for a cure, to ask for prayers and love, and to educate.  I’m not ungrateful!  I do give thanks every day for the gifts of those transplants that give my ‘baby’ sisters life. But, now Janice’s name has been added to ‘the list’ – the waiting list – for a liver transplant – polycystic liver disease.  It just makes me cry what this disease does to families.   Many of you know that our three cousins – great guys- are also battling Polycystic Kidney Disease. Over 100,000 names on the list! Valentine’s Day is all about love. An organ donor is all about love.  Love for your fellow...

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Did you step on your mama’s heart?

Posted on May 13, 2018 in Polycystic Kidney Disease | 0 comments

Did you step on your mama’s heart?

Did you step on your mama’s heart? I was a young mother.  I didn’t know much.  But, I knew the minute I held each of my children I was in love for life.  When my youngest child was about a year old, a birdlike old woman, stooped and hunched over with a twisted wood cane approached us at church.  With a dour look on her face, she pointed her ugly stick at my angelic looking baby girl and said in an unfriendly voice, “When they are little like her, they step on your toes; when they are older, they step on your hearts.” I remember I didn’t say anything, just sort of nodded and hurried away thinking.   Hmmmph! Not this baby girl, she’s a little ray of sunshine. She’s cuddly and I love her so much and she’s a mama’s girl who will love me forever. Fifteen years later, I was at a restaurant with that same daughter who was then sixteen years old.  At another table in the restaurant was an older friend of mine named Peggy.  She introduced us to her ninety-year-old mother. Her mother had a head of white perfectly coiffed hair, a beautiful smile and a friendly face.  We joked about it being Mother/Daughter Day. Peggy’s mother motioned me over with a twinkle in her eye and whispered, “When your children are little, they step on your toes, when they grow up, they step on your heart.  Grow roses. Roses teach you the lesson:  beautiful despite the thorns . . .like our children.” I grow roses.  When I tend my roses, I often think about those two completely different ladies saying the same thing about children stepping on toes and hearts.  The thorns on roses hurt! I shudder to think of the crown of thorns. Thorns make my arm and fingers bleed, but I can forgive the thorn when that fragrant, breathtakingly beautiful blossom blooms.  The way God forgives us. Most everyone has stepped on their mama’s heart.  Some children only tiptoe on their mother’s heart; others have not only stepped, but they have trampled on their mother’s heart.  You’ve gotta have a really strong heart to be a mama. I often wonder about how many times I stepped on my mother’s heart.  She’s in heaven now.  Thankfully, she died knowing how much I loved her.  I knew how much she loved me. Mom had saved my letters and cards, all tied together in a blue ribbon in her underwear drawer. In the margins of my letters, she wrote happy comments to me . . . knowing I wouldn’t see the comments until she died. She loved me despite the times I had stepped on her heart. My youngest child – who happened to be with me each time I had heard that expression – didn’t like me much when she was sixteen years old.  When she was twenty-one years old, though, she wrote me a beautiful letter saying how glad she is that I’m her mother. What a gift! She’s my baby girl. Mothers know a lot . . . they love you unconditionally . . .and forgive you when you step on their heart.  The same way God does.  Happy Mother’s Day! by Suzanne Ruff  ...

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