My Third Transplant – Miracles Happen

Thanks for visiting today and I hope you have found the story about my transplants interesting. They happened over an extensive period, beginning in 1986.

My First Transplant – Part One – Link HERE

My First Transplant – Part Two – Link HERE

Early Rescue – My Second Transplant – Link HERE

Today will be the story of my third transplant – Miracles Happen. I love telling this story because it is about Hope.

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My second transplant was in July, 1987 and I really count it as my first one. The first one only lasted a very short period despite desperate attempts to save that nearly cost me my life.

My second transplant came after returning to hemodialysis three times a week from September 1986 to July 1987. That transplant gave us a scare then last a wonderful 31 years. A big success, thirty is a number few transplants succeed to but I hope that improvements in transplant surgery and kidney matching will see transplants last longer and longer.

As the years passed since 1987 my kidney transplant gradually lost its ability to do its job. The numbers slowly went down but there was not much anyone could do to stop it.

As I approached my 60th birthday in 2018 the situation was inevitable. I was struggling and I had gone already past the point of when hemodialysis could/should begin.

Finding it tougher each day, I wrote a post called ” Don’t le me Die, Until I’m Dead” – the link is below in the caption, shortly before resigning myself to begin dialysis again, as a life sentence.

Don’t let me Die, Until I’m dead – Link Here

Looking back I wanted to celebrate one more birthday without relying on a machine’s life saving work. I tried hard but didn’t make it. I was aware that once I began dialysis, my struggling transplant would stop completely. It was like a marathon runner that had gone so far and done it’s best, it finally would take a seat and never rise again.

The day I called the hospital to say I had to come in and begin dialysis was sad but the staff on the ward were great, and that is no surprise. That day I began doing dialysis and feeling better. Tuesdays, Thursdays and Saturdays – even on Christmas Day in 2018. The inability to eat the same or drink the same was super frustrating but important as the days in-between treatment were as important as the days on dialysis in order to stay healthy. I wanted to stay healthy.

In preparation for going on dialysis I had done all the tests, vaccines and appointments to go back on the transplant list. Once I was doing dialysis again, and if my health met standards, then the transplant coordinator would look four times a year NATIONWIDE to try to find me a kidney match.

There was GOOD news and there was BAD news.

The good news was that I have a universal blood type – AB Positive – I can receive a tissue match from anyone. That was a big help.

The bad news was that because of my long transplant I had developed antibodies that would make me a difficult person to match to. My odds of finding a match were told to me to be about 2 in a hundred. As a result the matching process could be eight years or more.

Eight years or more. (sigh) That was demoralizing because that is a long, long, long time on dialysis and dialysis is not without its effects on the body. Perhaps too long to survive or too long to be healthy enough for a transplant.

My wife said to me “Two percent is way more than Zero” – let’s pray and have hope“. Instead of agreeing with my sad perception that it sounded hopeless she focused on the hopeful. I listened, and it helped.

Amazingly I got a call after three months from the transplant coordinator, Andrea. She said “Dave, this has never happened before, and it may never happen again – but we found a match, a close match for you on our first search!”

I was so excited but she said it was a cross country DONOR chain and it would be until April next spring to organize all the different donors and recipients in different hospitals (eight months away).

Since the chain could break any time up to the time of surgery – I was not to talk about it. So I didn’t – at least not for the first 7 months until I had an actual surgery date. Then I was excited, so excited.

A DONOR CHAIN is when each person in a chain is giving their organ to someone they don’t know in order that someone else donates an organ to someone they don’t know. That’s because the person they do know, they aren’t a compatible donor and so cannot donate directly.

These chains match organs to recipients who would otherwise not receive a transplant.

Ten minutes before they wheel me down to the cold operating room in 2019

That was my miracle, an amazing friend of mine had tested to donate to me directly but was not a match. They offered the chain idea as an option and he agreed. As a result of his YES I received my kidney in BC and someone in Ontario received their kidney as well. In fact everyone in the chain got their kidney. ♥ (Thankfully three years later and my friend is doing well! )

My Miracle Happened, I didn’t have to wait and try to survive on dialysis nearly as long as anticipated.

I am and my family are so grateful for a third opportunity to extend my life.

If not for dialysis and transplants I would have died at age 24 – 39 years ago (five years on dialysis and 34 years post transplant.

Thanks for reading. – David

Please take two minutes to become an organ donor. In my province of BC – this is the link here.

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Early Rescue – My 2nd Transplant

Welcome back to Life and Random Thinking.

I feel compelled to talk about my experiences with kidney failure and kidney disease to raise awareness as I celebrate my third anniversary of my kidney transplant on April 24, 2019.

One in 10 people in Canada has kidney disease – that’s FOUR MILLION people. The leading cause is diabetes.

That is someone on every block in Canada, that is someone who lives in the same floor as you in an apartment building.

What about the USA? How many at risk in the United States?

  • More than 1 in 7, that is 15% of US adults or 37 million people, are estimated to have CKD.
  • As many as 9 in 10 adults with CKD do not know they have CKD.
  • About 2 in 5 adults with severe CKD do not know they have CKD
Infographic explaining chronic kidney disease in adults.

Today I will share my second kidney transplant experience. Here is recap of 1986 and my first transplant experience.

I have already shared my experience of dashed hope and a failed kidney transplant in April, 1986. My three hospital roommates, all kidney transplants, all died in the five months I was there in Vancouver General Hospital. I nearly died and am certain I was spared because of prayer.

In mid August, after months of treatments to try to save my transplant, I walked down the hallway one early morning to the nurses station and the nurse there, Grace, was crying. She was looking at my bloodwork results from the previous day – she assumed I had died also. (My roommate Brian, aged 34, had recently passed overnight and we were in shock still.)

What a hug I got, when she looked up, so kind!

Finally in September I went home and returned to thrice weekly five hour hemodialysis treatments and was able to get back on the transplant list again. I felt defeated and worn out, I weighed probably 40 pounds less than when I went in, the battle was over and I had lost. But I hoped to fight again.

I slowly regained strength and went back to work.

That was in September 1986 BUT July 1987 was going to bring a miracle and better days ahead. But I didn’t know it then.

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July 1987

We received the phone call at home in Richmond, BC. It’s the Heather Pavilion at Vancouver General Hospital calling – “Can you come to the hospital right away – we have a kidney for you. The surgery will be after midnight.”

This time the atmosphere is different. Still excited, but it’s tempered because of the internal emotional scars from the previous year’s battle. My wife and I discuss my funeral preferences as she drives me to the hospital. But we hope.

The long spring and summer in these halls in 1986 seemed too fresh as I walked down the hallway again. The phonebooth where I used to make calls. The nurses station. My old room.

Last year I had energy but I dread a repeat of last year – I can recall the horse serum IV that vibrated my body so much that my bed moved across the room. The nurses pushed the heavy bed back against the wall and covered me with heated blankets – over and over again – for two weeks.

But this was 1987 so I prayed it would work and right away. I didn’t say it out loud but I couldn’t handle a long drawn out fight.

Around midnight they rolled me to surgery. It’s colder there and the operating table is less wide, my shoulders stick over the edges. This time I asked the surgeon to pray with me which he was happy to do. The anaesthesia began and my vision disappeared from the edges in and there are never dreams.

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The next day I wake up and the nurses and doctors gather. The surgery went well, the kidney is a match and the transplant is working, … but not well.

I am on a drip for fluids to keep me hydrated and everyone is praying my urine output improves.

Four days later I have a biopsy. Things are moving quickly this time to figure out what’s wrong. That’s good because I am already weary of being here. Thankfully my family doesn’t give up hope, and keeps my spirits up.

Sunday arrives, it’s been another three days and no change. A group of doctors visit my bed and tell me if it doesn’t improve by tomorrow then they will schedule surgery to remove the transplant. Friends gathered to pray, and strangers even.

Sunday night, the floodgates open LOL. It’s a weird happiness when a nurse measures your urine output and has a big smile when she takes a big heavy bag. “Keep it up!” (thumbs up)

That’s it really, I improved and went home in four or five days.

That’s my post – In my second transplant experience the kidney gave us a scare and then began to work. It worked for a long time, 31 years!

AND 31 years is exceptional, I was very, very, very blessed and I am grateful.

But in September of 2018 the transplant had diminished in working to the point where I could no longer function, it had a long downward slide and I was forced to relinquish myself back to hooking up to a dialysis machine again.

I had had a fantastic gift of health and freedom but it would take – a miracle for a third. I love sharing my miracle third transplant, but not in this post today.

FACING THE FACTS


Highlights from the Canadian Organ Replacement Register Annual Statistics 2019 – 2020


• 1 in 10 Canadians has kidney disease; that’s 4 million people.
• The leading cause of kidney failure is diabetes at 38%.
• The number of people living with end-stage kidney disease has grown 35% since 2009.
• 46% of new patients are under the age of 65.
• More than 50,000 Canadians are being treated for kidney failure.
• Treatment for those with end-stage kidney disease:
• 58% are on dialysis, • 42% have a functioning transplant


A person can lose more than 50% of their kidney function before symptoms appear. Symptoms are silent in the early stages.
• There is no cure for end-stage kidney disease.
More than 25% of new end-stage kidney disease patients were late-referrals, which means they started dialysis only 90 days after first seeing a nephrologist.


Organ Donation
• 75% of the 4,300 Canadians on the waiting list for an organ transplant are waiting for a kidney.
• Of the people on dialysis, only 11% are on the waiting list for a transplant.
• The five-year survival rate for adults with transplanted kidneys from living donors is 88% and 81% from deceased donors.
• There were 1,709 kidney transplants performed in 2018.
Median wait time for a deceased-donor kidney transplant is 3 years, 10 months.
• Median wait times for 2018 were:
• longest in Manitoba (6 years, 3 months)
• shortest in BC & Yukon Territory (3 years, 1 month)
• 28% of kidney transplants were made possible by living donors.
• More than 50% of all living donors were unrelated to the recipient.

• Per million population, there were only 21 people who became organ donors and 15 people were living donors.
• Rates per million population for kidney transplants from deceased donors:
• Highest rate BC & Yukon Territory: 24.2
• Lowest rate Saskatchewan: 13.8
• Since 2008, the Kidney Paired Donation Program has completed 721 transplants.

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1986 – My First Kidney Transplant [Part 2]

Welcome back!

This is part two of my post about my transplant in 1986. I decided to break it into two posts for ease of reading. – ♥

Here is the link for My First Kidney Transplant [Part 1] – click here so you can read them in order.

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My story continues from 1984 when I was forced to discontinue one form of dialysis called CAPD and begin another form called hemodialysis. It was a switch from dialysis 4 times a day to 3 times a week.

I still needed dialysis so I had surgery on my left hand to join a vein and artery together to widen the vein on my forearm and that increased its size and blood volume.  That allowed me to have larger diameter needles inserted during treatments.  The surgery left my left forearm with a ropey look to it hence my tendency for many years to wear long sleeves all the time to hide my disfigured arm.  If not for the larger needles though my dialysis would have taken 16 hours instead of five each time.

I have described hemodialysis in other posts but a picture is worth a thousand words. I was videotaped on dialysis in 2019 so I will share that video even though it is many years later when I reverted again to dialysis to live.  – the video is Two minutes in length. 

How dialysis works: (I will keep it short ♥) In the video you can see one needle goes into the bottom of my forearm and is taped still.  Blood rushes up the tube and (with the aid of a pump) is circulated through a filter to remove fluids and toxic things that would otherwise build up and kill me.   The blood filled tube comes back and a second needle is inserted and taped above the first into the enlarged vein above the first needle to return the blood.  You have to stay fairly still for the process and you lose your body heat gradually as your blood returns colder than when it left, that’s why the blanket.  I  had to hook up to a machine for about five hours a day, three times a week – dialysis is not a cure, it’s life support.  If I had not done dialysis I would died quite quickly, about a week or so. 

1984 until April,1986

(Back to the story, sorry for the sidetrack♥) Dialysis continued three times a week until April 1986 when I got the call. – my transplant was scheduled for 1 a.m. the next morning.  I excitedly headed to Vancouver General Hospital for my kidney transplant – our hopes were high. My family was excited.

It was a sunny day and blue skies looked ahead.

We stayed up late that night as the surgery was after midnight and we hoped the dawn would be the beginning of a new life of health and freedom with my young family.

I woke up a few days later in pain, it was 3 in the morning and isolated except for a nurse. It was the beginning of five months in the hospital and a myriad of attempts to save the transplant from rejection.

While the city celebrated Expo 86 just a few miles away I fought to live and enjoy my
life with my family and my young daughter. My fight and hospital “visit” lasted five months from April until September.

In September, I returned home, barely alive and back on hemodialysis. During my time in hospital my three roommates and fellow co-transplant patients had all died. Brian was just 34, he and I had been transplanted 24 hours apart. I was grateful to survive the summer of course but battle worn.

I was sad, much thinner (I had lost a lot of weight, nearly 40 pounds) but I was able to return to work and sleep at home.

It was awesome to be home. I could enjoy that absolutely. My daughter was three and I had lots to live for, special moments to treasure. That’s medicine you can’t prescribe.

Even going to work was better than that hospital ward, small room and the hospital bed.  I was worn out.

I finished 1986 hoping I would get another chance of a transplant if I could find the mental and physical strength AND if a donor match could be found.

My next transplant chapter was in 1987 – although I didn’t know it at the time, which makes waiting harder of course, and it would be a miracle.

Better days lay ahead and I had to keep the faith, and live on dialysis.

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Thanks for reading – David

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1986 – My First Kidney Transplant – [part 1]

Welcome to “Life and Random Thinking” and thank you for visiting.

My next three posts will be a change in topic because my health battles have been a big part of my life.

My next three posts I have decided to write as I celebrate my third anniversary of my third kidney transplant in 2019. I am so grateful to still be around, and it’s due to the generosity and friendship of a kind man.

In each post I will try to keep my comments brief and leave out the countless steps in between. I apologize since the first post is lengthy but the others are not. – David

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In 1980 I became a husband after I found and married my wife in a whirlwind. We had our first date August 6th, 1979 and were married March 8, 1980. When you find someone that special, you want to be with them always. It turned out I would need her strength and love over the years ahead many, many times.

1990s and dressed up

In 1983 we celebrated with the birth of our daughter in October but in July of that year I could no longer manage daily life without life assistance in the form of dialysis due to kidney failure. In July I went to Vancouver General in renal failure. They operated on me to insert a tube into my abdomen – about twelve inches of tube was inserted inside and another foot protruded from my abdomen which I taped there and hid under my shirt. So it began.

That dialysis was four times a day, every day. I did a portable type of dialysis and carried a gym bag to work so I could go to a small room for my 30 minute lunch break daily and carry it out before going back to my desk.

This dialysis is called CAPD (Continuous Ambulatory Peritoneal Dialysis). Continuous because you do it 24 hours a day. Ambulatory which means portable and Peritoneal because that is the name of the abdomen cavity where the fluid sits in a persons body while they do dialysis. The lining of this cavity filters the fluid drawn out from the body.

My routine was to get up early and drain my abdomen using the tube which involved hooking up a tube and an empty bag. Standing I would let the fluid drain out into the empty bag on the floor – usually about 1.5 litres of fluid came out.

Then I would hang a full bag of IV solution, one litre, or just hold it high enough so it would drain into my abdomen. The solution was always cooler than body temperature so it was always chilling the first half hour especially on winter mornings. When the bag was empty. I would cap off the tube into my abdomen and head to the bus stop and go to work. That was bag 1 for the day.

At work with my gym bag I would work until lunch and repeat the drain and refill process in the nurses closet office in the building. That was bag 2 and then back to work for the afternoon.

When I got home from work it was time to repeat the process with bag # 3.

Before I went to bed it was time again for bag #4, had to go to sleep early as I had to get up early and do it all again the next day and the next day. Of course there was restrictions on fluid and diet but I don’t recall those as too difficult and my wife was always so wonderfully supportive.

A short video here is worth a thousand words, about 90 seconds long.

I probably did CAPD for about a year and half. Then some bouts of peritonitis and stays in the hospital lead to the access point being sutured shut so I could recover. I am glossing over the details but they were painful times involving stays in hospital.

End of part 1 of this post (I try to keep them brief).

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Thank you sincerely for reading – David

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Lucille Ball – The Plot Thickens

Welcome Back! I am excited to tell you about a podcast series that I listened to with huge enthusiasm.

I enjoy reading biographies a great deal but it turns out that when the biography is narrated by Ben Mankiewicz (The host of “The Plot Thickens”)THEN I zip through the episodes much as I binge occasionally on an excellent K-drama on Netflix.

You can link up to the podcast here and listen or I use Google Podcasts.

The crew behind Ben must be awesome researchers as each episode of Season Three of “The Plot Thickens” was like a slice of hot apple pie and I devoured each one. I may listen to the whole series again because it was so interesting.

I can totally understand why Lucille Ball was chosen for the focus for an entire season. Lucille started from poverty in Jamestown USA and she failed in her chosen career more than once but never gave up, eventually moving from the Queen of B Movies to the Queen of television.

The podcasts tell her history, her heartbreaks, and much about the behind the scenes happenings of show business life.

I loved how the podcast included live recordings of Lucille, Desi, and their daughter. It also included recordings from others who witnessed their lives up-close.

Lucille went from almost starving on the streets of New York to running a studio and possibly being the reason why Star Trek and Mission Impossible are the legends they are today.

Lucille Ball’s big break began on RKO studios and she eventually bought the studio – but that comes later in the series and I hope you check one or two episodes out yourself using one of the link above.

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I love this quote;

One of the things I learned the hard way was that it doesn’t pay to get discouraged.

Keeping busy and making optimism a way of life can restore faith in yourself.

Lucille Ball

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If you think you knew her story before, listen and learn a little bit more. –

Best wishes – David

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In Two Days – Two Years!

In two days – Third Anniversary 🤗🤗🤗

dfolstad58's avatarLife and Random Thinking

Thank you for visiting today, I am both looking ahead and looking back today.

I know I could write much more about this experience♥♥♥

I hope that this post will refresh your own appreciation for the treasure that being alive and healthy truly is, and learn more about being an Organ Donor.

Sincerely, David

My last dialysis ?

Two years ago today I was at Penticton Hospital, having what I thought would be my last hemodialysis treatment. I was excited and confident, in 48 hours I was going to get my long awaited new kidney transplant !

It turned out that to be extra cautious I did another two hours hooked up for dialysis the night before the surgery in Vancouver Hospital, but my buzz of excitement wasn’t lessened at all.

April 24, 2019 my family gathered around my bed in excitement to wish me success and pray for…

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