Roberts loving her new life after transplant . . . Cypress’ new kidney “doing incredibly well” . . .

Have you ever wondered what life is like for a child before and after a kidney transplant?

Kathleen Roberts knows all about it; she’s 19 now and had a transplant four years ago at BC Children’s Hospital.

“Before the transplant,” she says, “I was going to BC Children’s every few months. I was just sick. I slept 16 to 18 hours a day. I had no appetite. I was 82 pounds and five feet tall. I was severely underweight and severely nauseous. The transplant made a huge difference. I have a normal appetite and I’m not sleeping the day away anymore.”

Take a few minutes and read her story, which is right here.


Cypress Roed, an eight-year-old from Harrison Hot Springs, B.C., continues to make progress after undergoing a kidney transplant on Oct. 24 at BC Children’s Hospital in Vancouver.

Her mother, Chantelle Deley, told me in an email earlier this week that “Cypress is doing well for the most part. She is finally in remission!”

Early on, Cypress had been diagnosed with focal segmental glomerulosclerosis, something that damages the kidneys and prevents the filtering of protein from the urine.

The recovery process hasn’t been without a speed bump or two, the latest of which has been having to deal with migraines. Cypress was back in hospital late last week because the migraines were causing severe nausea.

But, as Chantelle wrote,“she is in remission and that’s a major positive.”

It’s important to note that the new kidney “is doing incredibly well.”

“She is amazingly strong,” Chantelle said of her daughter.

Dorothy, my wife, had some health issues six weeks or so after her transplant and spent most of December 2013 in hospital dealing with them. But, as with Cypress, the new kidney just kept doing its job. Hopefully, that continues with Cypress, who is preparing to spend her third straight Christmas away from home.

Cypress is to turn nine on Jan. 22. Her dream has been to celebrate by going swimming. Here’s hoping she is able to make a big splash.



This was posted on a blog called Andrew Kai’s Adventure in Liverland. It was written by his mother:

“I wrote this in the waiting room after Kai coded. They brought him back 3 times before rushing him to the operating room. The plan was to open him up and remove the bad liver to buy him some time. The new liver was only 4 hours away. He had held on at the top of the list for 2 days. He was first in line for a liver and didn’t get one in time.

“I really believed he would make it. I pushed all the doubts out. I kept saying this over and over to myself, I knew my baby was strong and I had to believe for him.”

The post included a photo of a note on which was written:

“Pieces of me are in you

“Pieces of you are in me

“I am here

“You are here

“Kai will live!!!!”

Below the note was a small stone with a heart etched into it.

Kai’s mother continued:

“The heart stone is what they gave to me, and one to him, so that we would have something to connect us when I had to say goodbye the last time. I placed it over his heart and I haven’t put my stone down since I left him.

“HE WOULD HAVE LIVED IF HE HAD A NEW LIVER. Even if it had been just a few hours earlier.

“DONATE YOUR ORGANS. YOU DON’T NEED THEM AFTER YOU’RE GONE.”

Andrew Kai George was born on April 23, 2019. Without a new liver, he died on Dec. 2, 2019, in Indianapolis, Ind.





What happens when a donor and recipient meet? . . . 2019 World Transplant Games set to open. . . . Interesting project underway in Winnipeg

If you have been impacted by kidney disease, please keep in mind that the Kamloops Kidney Support Group gathers this morning (Wednesday, Aug. 14), 10 o’clock, at the Barside Lounge and Grill inside Chances at 1250 Halston Ave. . . . Feel free to join us. . . .

If you are in the vicinity of downtown Kamloops on Monday (Aug. 19), organizers of the 2019 Kamloops Kidney Walk are holding a news conference, 2 p.m., at St. Andrews on the Square, 159 Seymour St. Join us as we announce particulars of this year’s Walk, and also introduce the event’s honourees.


What’s it like when the recipient of a kidney transplant meets the donor? Well, Chris, 21, a recipient, met his donor, Abraham, 19, on Good Morning America recently and, as you might expect, things got emotional. . . . Abraham, whose mother has started the process of becoming a donor, was asked what he would say to anyone considering it, and he responded: “I would say go for it. Reach out to a hospital and see if you’re eligible and if you are eligible, really consider it. I was in the hospital for two days. I was off painkillers in five days. I feel great.” . . .  The whole story is right here.


A lexophile, thanks to a contest in The New York Times: England has no kidney bank, but it does have a Liverpool.


Kerry Eggers of the Portland Tribune has a story right here about Doug Little, now 68, who was a 6-foot-3 forward on the Oregon Ducks basketball team in the early 1970s. . . . Today, Little is on the list and hoping for a kidney transplant.



The World Transplant Games open Saturday and run through Aug. 24 in NewcastleGateshead in the north-east area of England. . . . “The youngest participant,” reports Catherine Priestley, “is a six-year-old Argentinian girl who will compete in the ball throw, long jump and 50-metre sprint, with the oldest an 84-year-old French man taking part in the cycling, swimming and athletics.” . . . Priestley’s story is right here. . . . The Games’ website is right here. . . . It’s worth noting that the 2020 Canadian Transplant Games are scheduled for Winnipeg, Aug. 10-15.



There is an interesting project underway in Winnipeg with two doctors working to educate health care providers about how “to use a match equation than can pretty accurately predict a person’s risk of kidney failure, according to Michelle Gerwing of CTV News. . . . This all is aimed at early diagnosis of kidney disease. . . . As Dr. Navdeep Tangri, a nephrologist, explains: “If you have diabetes and kidney disease today there is a treatment out there that can delay dialysis by up to two decades and potentially prevent it all together, but all of that is non-applicable, we can’t start people on that treatment once their kidney function drops below 30-per cent.” . . . Gerwing’s story is right here.



Kidney stone saved father’s life. . . . Visit the Kidney Community Kitchen. . . . Stevie Wonder to have transplant

It was a humbling experience to sit in my recliner on Friday evening and again on Saturday and hear from so many people via Twitter, email, text, Messenger, etc. As I sat and pecked away on my laptop all those evenings, it was easy to forget that there actually were folks out there who would be reading whatever it is that I was writing.

Thank you all so much for the kind words. They won’t be forgotten.

But considering the direction that I am taking this site, one note stood out from all the rest. Here is part of it . . .

“Best of luck with the new focus. It does hit a little close to home because three weeks ago my 78-year-old father went to the hospital at my urging to have a kidney stone checked.

“In the process, they found a tumour on one of his kidneys — fortunately, it’s early enough that he’ll be having surgery at the end of this month to have the tumour — and hopefully just a very small portion of the kidney — removed.

“It’s often not a stroke of luck to have a kidney stone, but in this case it was because, if not for that, the tumour wouldn’t have been found until it was too late.

“As the doctor told him, the kidney stone saved his life.”

And then there was the email from a WHL insider that included this:

“I am excited to continue to read your work as a kidney patient who is beginning kidney failure.”


Some food for thought from the Kidney Foundation of Canada/B.C. & Yukon Branch. . . .

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


It stands to reason that diet is of utmost importance to folks who deal with kidney disease of one type or another. . . . With that in mind, you should be aware of the Kidney Community Kitchen, a creation of the Kidney Foundation of Canada. The tweet below highlights Classic Hamburgers and the recipe is available by following the link. . . . At the site, there also is an areas that allows you to browse recipes by meal type. Check it out.





It was over a month ago when Stevie Wonder informed concert-goers in London, England, that he is scheduled to undergo a kidney transplant late in September. Yes, he said, a donor has been found.

——

Little is know about what got Stevie Wonder to the point where he needs a kidney transplant. He made the announcement in London to quell rumours about his health, but there don’t appear to have been any statements made since then.

Nina Shapiro, who writes about health-related issues, has more right here.


If you’re new here, Dorothy, my wife of more than 47 years, has had a kidney transplant and her immune system now is compromised. There are a lot of people walking around out there who are just like her, which is just one more reason why immunization is so important.