Kidney Walk: Of grandparents, grandchildren, good friends and transplants

A couple of former sports writers were walking on Rivers Trail, taking part in Kamloops’ 10th annual Kidney Walk on Sunday, when they were joined by Hugh McLennan.

Just minutes earlier, McLennan had been saluted by organizers, participants and volunteers as one of two honourees for this edition of the Kidney Walk. He had undergone a kidney transplant on Nov. 22, 2019, at St. Paul’s Hospital in Vancouver. His long-time friend, Louis (Big Rig) McIvor, the other honouree on Sunday, had given McLennan one of his kidneys.

McLennan, the host of the Spirit of the West radio show, is well-known in the ranching community in B.C. — he and wife Billie run cattle near Pinantan Lake, northeast of Kamloops. He also is easily recognizable, what with the 10-gallon hat, walrus moustache and cowboy boots.

By now, though, the cowboy boots were gone, replaced by a pair of sneakers.

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Tammy Mathieu and Louis (Big Rig) McIvor give grandchildren a ride alongside Hugh McLennan on Sunday during the Kidney Walk along Rivers Trail near McDonald Park. (Photo: Murray Mitchell/Murray Mitchell Photography)

It had been apparent early on that McLennan was thrilled to have been selected as an honouree. While doing hemo-dialysis, he had always been more than willing to help out by taking a turn at the microphone and also supplying musical entertainment at past Kidney Walks. He and McIvor also have been quick to promote organ donation and transplantation when given the opportunity.

As thrilled as McLennan was with that honour, though, he wore an even bigger smile as he told the story of a phone call he and Billie had received the previous day.

Their grandson, Reed, who will turn 16 on Nov. 20, is playing midget hockey in Winfield, B.C., which is located between Vernon and Kelowna on Highway 97.

Hugh’s voice was bursting with pride as he talked about the phone call.

A goaltender, Reed’s junior B rights belong to the Sicamous Eagles of the Kootenay International Junior Hockey League. It seems that the Eagles were scheduled to play the host Spokane Braves on Friday and found themselves short a goaltender, thanks to an issue involving a passport.

So . . . a call went out to Reed, who joined the Eagles in time to ride the bus to Spokane. He was looking forward to what he was looking at as a learning experience and expecting to take in the game from the cozy confines of the bench.

Except that the Eagles found themselves trailing, 3-0, just 3:49 into the game. Shortly after, the call came from head coach Ty Gunn: “McLennan . . . let’s go!”

With Reed in goal, the Braves added two more goals and took a 5-0 lead into the third period. It was 6-1 just 1:02 into the final period.

In the end, I’m sure the Eagles will tell you that they simply ran out of time. They lost the game, 6-5, scoring their fifth goal late in the third period.

Reed more than did his job, though, turning aside 39 of 41 shots in 54 minutes 20 seconds, in his junior B debut.

While Hugh was relating the story of a grandfather and his grandson, McIvor and fiancée Tammy Mathieu also were on Rivers Trail. They weren’t alone as they had two grandchildren in tow — or was it the other way around?

Regardless, with grandchildren in the conversation and on Rivers Trail, I couldn’t help but think about what it must mean to Hugh to be able to be part of his grandson’s life. After all, had Louis not given Hugh a kidney almost two years ago, well, who knows?

My wife, Dorothy, received a kidney six years ago Monday — Sept. 23, 2013. Our only grandchild, Kara, turned three in July. Dorothy had done peritoneal dialysis for almost four years before having her transplant. Again, without that kidney, who knows?

When we got home after Sunday’s Kidney Walk, we spent some time on a video chat with Kara.

Grateful doesn’t begin to explain what that kidney means to our family. You can bet it’s the same with the McLennans and anyone else who has needed a kidney and been fortunate enough to get one.

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If you are thinking about being a donor, feel free to call the donor nurse co-ordinator at St. Paul’s Hospital (604-806-9027 or 1-877-922-9822), or email donornurse@providencehealth.bc.ca.



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2019 Kidney Walk: Wet day can’t douse spirits. . . . Goal surpassed. . . . Stop thief!

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A Kidney Foundation information booth (back left) was set up at Sunday’s Kidney Walk, while beneath the Lordco canopy you were able to find merchandise after first checking in at the registration table. (Photo: Murray Mitchell/Murray Mitchell Photography)

We awoke Sunday to cool weather (12 C) and showers.

The cool wasn’t a problem because warm weather and people with kidney disease aren’t a good match.

But the drizzle . . .

KWlogo2Well, if you have been, or are being, impacted by kidney disease, what’s a little rain? Right?

And so it was that more than 100 people were at McDonald Park on Kamloops’ North Shore on Sunday for the city’s 10th annual Kidney Walk.

Not all of them took part in the walk, which always follows Rivers Trail for more than one kilometre to McArthur Island, but they all were there to show support to people in our community who are dealing with kidney disease or to remember friends and loved ones.

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Larry Read, the Kidney Walk’s emcee, kept folks informed and everything on time. (Photo: Murray Mitchell/Murray Mitchell Photography)

We couldn’t have done it without Larry Read, the sports information guru for the WolfPack at Thompson Rivers U. He is our emcee, and he brought along six athletes from the WolfPack swim team and, oh boy, what a big help they were. This wasn’t the first time Larry brought volunteers from TRU, and it is a tremendously positive feeling to see these young people so eager to help at an event like this one.

With Larry at the controls, we saluted Hugh McLennan and Louis (Big Rig) McIvor as the honourees for the 2019 Walk. Hugh, a rancher, is the host of the Spirit of the West podcast and a familiar figure in the cowboy world in Alberta and B.C. When he needed a kidney almost two years ago, he got

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Hugh McLennan (left) and Louis (Big Rig) McIvor, the honourees of Kamloops’ 2019 Kidney Walk, address the crowd. (Photo: Murray Mitchell/Murray Mitchell Photography)

one from Big Rig, a long-time friend who is a former long-haul driver and radio personality.

They were introduced by Edna Humphreys, the executive director of the Kamloops chapter of the B.C. and Yukon Branch of the Kidney Foundation of Canada. Hey, if there’s a renal-related event in Kamloops, you can bet that Edna is the push behind it.

We went into this walk with a goal of raising $20,000. By the time the counting is done, we will be somewhere around $24,000, which is unbelievable. In all of our pre-walk chatter, I don’t once remember anything close to that figure being mentioned.

In 2018, we raised $21,764, after bringing in $16,736 in 2017.

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Allan Dodds (right) returns money that had been lifted from the Brock Central Lions Club’ breakfast table on Sunday. (Photo: Murray Mitchell/Murray Mitchell Photography)

There was some excitement late in the program, too.

The Brock Central Lions Club was there, again, to provide us with a pancake breakfast, along with sausages and coffee, all by donation.

So with most of the folks already eating and a few in line to fill their plates, a cry went up: “Stop her! Stop her! She took the money box.!!”

It seems that a person had appeared on the scene, got in line for breakfast, then grabbed the cash box and took off on the run.

However, her plan hadn’t accounted for Allan Dodds, who when he isn’t playing Superman works at Lordco in Kamloops. His connection with us? His wife, Julie, has kidney disease and is in need of a transplant.

Anyway . . . Allan took off after the thief, caught up with her and brought back the money.

As Julie wrote on her Facebook page: “My husband not only helped set up . . . and with the delivery of chairs and tables, he helped present a large cheque, and also chased down a would-be thief.”

In the end, the Lions Club raised $326.90, all of which, thanks to Allan, was there to be donated to the Kidney Walk.

If we were to give out an MVP award this year, it would go to Allan. As a member of the Southern Central B.C. branch of the CIM (Canadian Institute of Mining, Metallurgy and Petroleum), he presented the Kidney Walk with a cheque for $5,000 in late August.

Through Lordco, he was able to provide us with a truck with which he picked up tables and chairs from the good folks at TRU. He also supplied, again through Lordco, a large canopy that really came in handy considering the weather.

And, of course, he topped it all off by jumping into a phone booth — OK, there aren’t any of those these days; he just went behind the Lordco truck — where he donned the Superman suit and went on to rescue the money.

Thanks, Allan!

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Dorothy Drinnan (right) and friend Leona Backman enjoy a rainy time during Sunday’s Kidney Walk. (Photo: Murray Mitchell/Murray Mitchell Photography)

Dorothy says: Thank you! Thank you!! Thank you!!!

With help from so many of you, she was able to raise $3,230 for Kamloops’ 10th annual Kidney Walk, which was held on Sunday morning.

With such great support from so many terrific people, she was the leading fund-raiser for a sixth straight year, and she now has raised more than $16,000 in total.


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Julie Dodds (in red jacket) has kidney disease and is in need of a transplant. She poses with friends and family, all of whom were there to support her at Sunday’s Kidney Walk. (Photo: Murray Mitchell/Murray Mitchell Photography)

 

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Not all of the participants in Sunday’s Kidney Walk were of the human variety. This pooch got into the spirit of things by donning a Kidney Walk t-shirt, too. (Photo: Murray Mitchell/Murray Mitchell Photography)

Talking kidneys with Freda, Howard, Dorothy and Jill. . . . Update on Vic Morin’s situation. . . . Kamloops Walk on Sunday

With Kamloops’ 10th annual Kidney Walk set for Sunday, my wife, Dorothy, along with friends Freda and Howard Brown, got together with Jill Sperling of Kamloops TV station CFJC on Thursday. OK, I was there, too.

We met at McDonald Park, the site of the Walk, where we chatted about kidneys, transplantation, dialysis and the Kidney Walk.

Dorothy had her transplant six years ago, after almost four years of peritoneal dialysis. Freda recently began doing hemo-dialysis; she does three runs a week at Royal Inland Hospital. Howard was hoping to donate a kidney to his wife and spent the past nine months undergoing all of the necessary tests. However, one of the tests turned up a kidney stone, so he has been disqualified, at least for now.

There’s all that and more in this piece right here.

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In the TV piece referred to above, Howard Brown points out that if you are considering being a live kidney donor, you shouldn’t wait because the testing process takes some time.

But, at the same time, if the medical team finds any issues with your health, they will be dealt with ASAP. In Howard’s case, he already is being put in touch with a specialist in Kamloops and is hoping to have the kidney stone removed so that he can get back into a process that, hopefully, will end with him being a donor for his wife, Freda.

That brings us to Vic Morin, a friend who lives in the Dallas area of Kamloops and who also is in need of a kidney.

Vic has been a regular at Kamloops Kidney Support Group meetings for a while now, and was preparing to begin peritoneal dialysis (PD) in the near future. That is the same form of dialysis that my wife, Dorothy, did before she was fortunate enough to get a kidney from a live donor.

Because Dorothy had experience with PD, she and Vic have had many conversations over the past months. And we were quite excited to hear last week that he was to have a catheter surgically placed into his peritoneal cavity next week. That meant he was one giant step closer to beginning PD.

(BTW, someone who does PD hooks up to a machine called a cycler and does a fluid exchange seven nights a week while sleeping — toxic fluid out, clean fluid in, to be carried around all day in that cavity.)

Unfortunately, Vic’s kidney function deteriorated so rapidly that he was to begin hemo-dialysis on Friday. However, things now have been moved to Monday. He still is on schedule to have a catheter surgically installed on Wednesday so that he can begin training for peritoneal dialysis.

While all this is happening, the search continues for a live donor.

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One of the reasons that I stopped writing about hockey here and turned mostly to renal-related items is that a lot of education is needed when it comes to kidney disease, dealing with kidney disease, organ donation and transplantation. . . . If I am able to provide enlightening information in this space I will be more than pleased. . . .

A few things you should know . . .

There is no cure for kidney disease. Once you have been diagnosed, that’s it; it doesn’t go away.

A person who has had a kidney transplant isn’t cured. For example, Dorothy takes anti-rejection drugs twice a day in order to keep her system from rejecting the organ that is foreign to her body. Those drugs also suppress her immune system so there are some precautions that have to be taken as she goes through daily life.

Should you choose to be a live donor, you don’t need to be the same blood-type as the person in need of a kidney. Instead, you are able to donate through the Living Donor Paired Exchange Registry. In short, your kidney goes to someone else, but only on the condition that the person you want to help gets one from another live donor. This is how Dorothy got her kidney — her best friend gave a kidney to someone (neither she nor Dorothy have any idea who it went to), and Dorothy got one from someone else. No, we don’t know a name, nor do we have any idea how many donors and recipients were involved in that particular chain.

If you are being tested and an issue with your health is discovered, it will be dealt with ASAP. In Howard’s case, a doctor at the renal clinic at St. Paul’s Hospital in Vancouver got him in touch with a specialist in Kamloops in short order.

A donor will spend a couple of days in hospital — Dorothy’s friend had surgery on a Monday and was released from hospital on Wednesday. It is suggested that a donor take it easy — no heavy lifting, for example — for up to six weeks and then it’s full-speed ahead. I know of one donor who was back to jogging in three weeks.

A donor also will continue to be monitored by the medical community. Should there be serious issues with the remaining kidney, a donor would automatically go to the top of the transplant list.

And, yes, a person is able to live with one kidney.

I would never pressure anyone to be a donor. If you are at least thinking about it, I would only ask that you do some research.

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If you are thinking about being a donor, feel free to call the donor nurse co-ordinator at St. Paul’s Hospital (604-806-9027 or 1-877-922-9822), or email donornurse@providencehealth.bc.ca.

Should you make the call and be asked who will be the recipient, feel free to mention Freda Brown or Louis Victor Morin.

Understand, too, that the people who work in renal clinics are big on privacy — I mean, they are really, really big on privacy. Everything you say or do will be kept confidential.

As well, a donor is able to change his/her mind and walk away at any time during the process.



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Don’t forget that the 10th annual Kidney Walk Kamloops is scheduled for Sunday (Sept. 22) at McDonald Park on the North Shore. . . . We will begin registering folks at 10 a.m.; we will go for a walk at 11.

Larry Read, who is so involved in our community, will be the emcee, again. Hugh KWlogo2McLennan and Louis (Big Rig) McIvor will be in attendance as the honourees for this year’s walk. When Hugh needed a kidney almost two years ago, Louis, his longtime friend, stepped up and gave him one.

As well, the Brock Central Lions Club will be on hand to provide breakfast — pancakes, sausages and coffee — by donation. A year ago, they served more than 100 breakfasts.

The Kidney Walk helps raise awareness about kidney disease and raises funds for important programs and services to help kidney patients in this community and others across BC and the Yukon.

Dorothy will celebrate the sixth anniversary of her transplant on Monday. She will spend part of Sunday taking part in her sixth straight Kidney Walk; she also helps Edna Humphreys and me pull the whole thing together.

If you would like to help out — Vic Morin is part of her support team — you are able to make a donation right here.

More hepatitis C-infected kidneys being transplanted. . . . Disease able to be treated following surgery. . . . Kidney Walk set for Kamloops on Sept. 22

Kidneysign


A study published Thursday in the Journal of the American Society of Nephrology reports that American transplant centres are using three times more hepatitis C-infected kidneys for transplant rather than dispose of them.

There has long been a fear that a transplant receiving a kidney with hepatitis C would become ill. According to this report, medical advancements in treating hepatitis C mean that those recipients won’t become ill.

Jen Christensen of CNN writes:

“Hepatitis C is a viral infection that causes liver inflammation, sometimes leading to serious damage. Prior to 2018, most of the infected organs went to patients who already had hepatitis C. Since 2018, most of these infected kidneys, about 75 per cent, went to patients who did not have the virus.

“Patients who received infected kidneys had nearly the same function as those who received uninfected kidneys, the study said.”

Dr. Vishnu Potluri, the study’s lead author and a nephrology fellow at the U of Pennsylvania, told Christensen:

“The key thing about hepatitis C is that millions of Americans have this infection and most don’t know that they have it, it’s mild and takes many years for it to progress.”

Christensen continued: “Until a few years ago, there weren’t really good options to treat hepatitis C. Now, there are drugs with high cure rates, Potluri said. The transplant community realized that you could transplant a kidney from someone with hepatitis C and start treating them right away, Potluri said, and the early trials found the infection could be cured after the transplant.”

Hopefully, this study will signal a change for the system in the U.S., where nearly 40 per cent of hepatitis C-infected kidneys donated between January 2018 and March 2019 were discarded.

Christensen’s story is right here.





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Don’t forget that Kamloops’ 2019 Kidney Walk is set for Sunday, Sept. 22, at McDonald Park. You are able to register starting at 10 a.m., with the walk to begin at 11.

The Brock Central Lions Club will be on hand to provide breakfast — pancakes, sausages and coffee — by donation.

A few numbers for you: Kidney Walkers in B.C. and Yukon have walked 26 million kilometres over the past 12 years. That is more than 67 return trips to the moon. . . . They have raised more than $2.5 million in support of kidney patients. . . . The Kidney Walk helps the Kidney Foundation raise awareness about kidney disease and raises funds for important programs and services to help kidney patients in this community and others across BC and the Yukon. . . .

As of mid-August, in the region served by Kamloops’ Royal Inland Hospital, there were 1,378 patients with chronic kidney disease being monitored by nephrologists. Of those, 140 had undergone transplants, and 114 were on dialysis. . . . As of Aug. 27, there were 68 people in our area on the pre-transplant list. . . . In 2018, there were 339 kidney transplants performed in B.C., a one-year record.

My wife, Dorothy, will be celebrating the sixth anniversary of her kidney transplant by taking part in her sixth straight Kidney Walk. In her six walks, she has raised more than $15,000. If you would like to support her, you may do so right here.

Cree rapper opens up about kidney situation. . . . Victoria preschool owner donating to stranger

Karmen Omeasoo is known in the music world as Hellnback. He is a Cree rapper who made quite a name for himself as an Indigenous performer. When he was 19, he learned that he had Type 2 diabetes; now he’s nearing 40 and about to go on dialsyis. . . . “My kidney function right now is at seven per cent,” he told Lenard Monkman of CBC News. “Seven per cent out of 100.” . . . Omeasoo is referring to his GFR (glomerular filtration rate). As a point of reference, my wife’s GFR was 11 when she began dialysis; six years after transplant, it’s in the mid-60s. . . . Monkman’s piece on Omeasoo is right here, and it is terrific. It is worth reading as Omeasoo details the symptoms and what he has been through to this point.


Three cheers to Kim Thorsen, the owner of Ross Bay Preschool in Victoria. She is preparing to donate a kidney, and she knows that it will go to a complete stranger. According to a story by CHEK-TV in Victoria: “Altruistic donors are incredibly rare. Of the 335 kidney transplants in B.C. last year, 100 were from living donors. But only four of those donations went to total strangers.” . . . More from this story: “As a living donor, Thorsen would go to the top of the transplant list in the rare event she needed a transplant. And even though she had no doubts before, Kim recently learned her kidney will most likely go to a child.” . . . “I’d be okay helping anyone,” Thorsen said, “but knowing it might help a child is amazing.” . . .

If you are contemplating being a kidney donor, it is important for you to understand that should you have issues with your remaining kidney at any time post-surgery, you would go to the top of the list. That is something is stressed in the preparatory period leading up to surgery.

CHEK-TV’s full story is right here.



Dorothy Drinnan had a kidney transplant on Sept. 23, 2013. Now she is preparing to take part in her sixth straight Kidney Walk. We will walk in Kamloops on Sept. 22 at McDonald Park, with registration at 10 a.m., and the walk at 11. . . . If you would like to be part of Dorothy’s team by supporting her with a donation, you are able to do so right here. She has been Kamloops’ No. 1 individual fundraiser each of the past five years.


Kidney disease hasn’t slowed own our girl Maggie. . . . Take a moment for PKD Awareness Day

Allow me to introduce you to our good friend Margaret (Maggie) Thompson.

She and my wife, Dorothy, have forged quite a friendship, one that began because they have something in common — both have had kidney transplants.

Dorothy had one six years ago; Maggie underwent one more than eight years ago.

A few years ago, they got together, along with Edna Humphreys, and started the Kamloops Kidney Support Group in an attempt to help others who are dealing, directly or indirectly, with kidney disease. To say the KKSG has been a success would be something of an understatement.

Dorothy and Maggie both did peritoneal dialysis before being cleared for transplant, and both are representative of how having kidney disease doesn’t have to slow one down.

Having said that, though, Maggie is in a league of her own.

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Maggie Thompson, with the Blue Bomb before parting with it last week. (Facebook photo)

In brief, here is a definition of peritoneal dialysis from kidneyfund.org: “Peritoneal dialysis (PD) is a treatment that uses the lining of your abdomen (belly area), called your peritoneum, and a cleaning solution called dialysate to clean your blood. Dialysate absorbs waste and fluid from your blood, using your peritoneum as a filter.”

A catheter is surgically implanted into our peritoneum that will allow you to do fluid exchanges. You learn how to do PD manually four times a day before being given a cycler that allows you to do it while sleeping at night. And the only way it limits your ability to travel is if you allow it to, something Maggie wouldn’t do.

A Harley-Davidson rider and owner, Maggie took a lengthy trip with friends into the U.S. a few years back. She drew up a travel schedule and arranged with Baxter, the company that provides PD supplies, to make fluid drops at various stops. Friends constructed a trailer that she towed behind her Harley; it contained other needed supplies.

As the friends travelled, then, they would stop to allow Maggie to do her exchanges.

Since having her transplant in July of 2011, Maggie hasn’t slowed down at all. She moved to Edmonton early in 2018, but makes regular visits to Kamloops, where she had lived for 30 years. Earlier this summer, she took two grandsons to the Calgary Stampede — yes, she also has a car — and then on a tour around Vancouver Island that included a stop in Tofino.

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Maggie Thompson, with her new ride, Sassy Sapphire. (Facebook photo)

Late last week, Maggie rode her Harley — she called it the Blue Bomb — to Kamloops, where she visited the local dealership and traded it in on a Freewheeler Trike that she has dubbed Sassy Sapphire.

After a few days with us, Maggie climbed aboard Sassy Sapphire on Tuesday morning and headed home to Edmonton. She arrived early last evening having been on the road for almost 12 hours.

No, kidney disease hasn’t slowed down Maggie Thompson in the least.


It is National Polycystic Kidney Disease (PKD) Awareness Day in various parts of the world today (Wednesday, Sept. 4).

According to a news release:

“Since 2014, Health Canada has recognized September 4 as National Polycystic Kidney Disease (PKD) Awareness Day – a special day devoted to raising awareness of this life-threatening, genetic disease.

“Polycystic kidney disease (PKD) is a chronic, genetic disease causing uncontrolled growth of fluid-filled cysts in the kidneys, often leading to kidney failure. With 66,000 Canadians and millions worldwide living with PKD today, chances are high that you know someone with the disease.

“The more who know about PKD, the more resources we can dedicate to finding treatments and a cure. PKD Awareness Day is our opportunity to step up our efforts and gives us a platform to widely spread the word, share stories and encourage others to learn more. On PKD Awareness Day, let’s come together as a united front to spread the word about this disease further than we ever have before!

“Since its creation in 1993, the PKD Foundation of Canada has raised more than $1 million towards research, support and help for families living with PKD. From the first research grant awarded in 1999, the PKD Foundation of Canada has set up chapters and support groups across the country, built an expansive and passionate volunteer network, and connected with PKD groups around the world to support our most notable fundraising event – the Walk to END PKD.

“Today, the PKD Foundation of Canada is the only national organization solely dedicated to fighting PKD through research, education, advocacy, support and awareness.”

In Kamloops, locals involved in the PKD Foundation will appear before City Council on Sept. 10 in an attempt to spread awareness.


Here in Kamloops, preparations are well underway for the annual Kidney Walk, which is scheduled for Sept. 22 at McDonald Park. . . . If you would like to take part, we register at 10 a.m., with the walk to follow at 11. Some of us will walk a couple of kilometres, but there isn’t a defined distance. In fact, you don’t need to walk at all. Just come and join us for the breakfast — pancakes, bacon and coffee, by donation — with the Brock Central Lions Club doing the cooking. . . .

My wife, Dorothy, will be celebrating the sixth anniversary of her kidney transplant by taking part in her sixth straight Kidney Walk. In her six walks, she has raised more than $15,000. If you would like to support her, you may do so right here.




Having transplant in Vancouver? Kidney suite might be for you. . . . KKSG gatherings set for September

If you or someone you know is a candidate for a kidney transplant and lives outside of Vancouver, you will learn in the lead-up that a stay of at least a couple of months in the big city will be necessary after surgery.

And with the cost of accommodations being what they are in the big smoke, well, you might have questions.

You should know, then, that there are kidney suites available in Vancouver . . .

The Kidney Foundation of Canada, BC & Yukon Branch offers seven kidney suites within Vancouver. These are for post-kidney-transplant recipients who have come to Vancouver from outside the Lower Mainland and need to stay in town for up to two months after surgery. These suites are fully furnished, and are located near major transit lines.

These suites are free for those who meet our financial criteria (low income) and just $35 per night for those who do not.

There is more right here.


If you happen to live in Kamloops and area, you may be wondering about the next gatherings of the Kamloops Kidney Support Group (KKSG). . . . We get together on the second Wednesday and second Saturday of every month. In September, that will be Sept. 11, 10 a.m., and Sept. 14, 9 a.m. . . . All coffee drinking and eating of eggs takes place at the Barside Lounge and Grill at Chances Casino, 1250 Halston Ave. . . . Believe me when I say that these gatherings are informal.


SOME ODDS AND ENDS . . .

One in 10 Canadians live with kidney disease or are at risk – most are unaware of this. . . .

You can lose up to 80 per cent of your kidney function before experiencing symptoms. . . .

As of mid-August, in the region served by Royal Inland Hospital in Kamloops, there were 1,378 patients with chronic kidney disease (CKD) being monitored by nephrologists. Of those, 140 have undergone transplants, and 114 are on dialysis. . . .

As of December 2018, there were 665 people in B.C. waiting for organ transplants, with 528 of those being kidney patients. In 2018, 335 kidney transplants were performed in B.C.


Some numbers from a piece by the editorial board of The New York Times from earlier this week:

About 20 Americans die each week waiting for organs. . . .

More than 100,000 people in the United States are currently waiting for organs, and only about 35,000 will receive them in 2019. . . .

That piece also included this:

“Far too few people are donating organs to begin with, and far too few of the organs that have been donated are making their way to patients in waiting. Experts say that misconceptions about donor eligibility requirements and, in some states, cumbersome registration processes are preventing nearly half of those who support organ donation from becoming registered donors. Outdated standards are causing transplant surgeons to reject some 75,000 usable organs every year, according to a Washington Post analysis. And an astounding lack of accountability and oversight in the nation’s creaking, monopolistic organ transplant system is allowing hundreds of thousands of potential organ donations to fall through the cracks.”

The complete piece is right here and it’s well worth your time if you are interesting in the American transplantation system.