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.





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