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PKD Warrior

Learn about Polycystic Kidney Disease (PKD) and about my journey

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Blog, In the news, My experience of PKD, Organizations, Transplant

Bike to the moon, a chance to stop PKD!

May 1, 2023

Once again this year, I will be participating in the PKD Foundation of Canada bikeathon! Its goal is to raise funds to fund research and finally find a cure for Polycystic Kidney Disease (PKD) that ruins the lives of more than 13 million people worldwide! The Ride to the Moon bikeathon…

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Blog, Organizations

September 4th is National Polycystic Kidney Disease (PKD) Day!

September 3, 2022

September 4 is the National Polycystic Kidney Disease (PKD) Day, recognized by the Government of Canada and 41 cities across the country. We are more than 13 million individuals of all origins who suffer from this hereditary disease, and there is no cure. It is the most common hereditary disease and…

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reins vs covid
Blog, In the news, Organizations

Covid new normal – What the kidney insufficiency/immunosuppressed patients need to know

July 3, 2022

On June 14, 2022, I attended a virtual lecture given by the Kidney Foundation of Canada. Whether you are in end-stage kidney disease, have received a transplant or are immunosuppressed for another reason, we all ask ourselves a question: what do we need to know to protect ourselves in a world…

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Communauté
Blog, My experience of PKD, Organizations

Meeting the Quebec kidney community

April 11, 2022

For the past two months, I have been meeting more and more people related to kidney disease and organ transplantation. I’m trying to get to know my community better, and it means a lot to me to hear other people’s stories. Surprisingly (for me, anyway), everyone’s story with the disease is…

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logo CODA
Blog, Organizations

Canadian Organ & Tissue Donors Association (CODA) volunteers and why they’re important

January 31, 2022

This week, while digging a little into Canadian and Quebec organizations related to organ donation, I discovered the Canadian Organ and Tissue Donors Association (CODA) and its volunteers. According to its website, the CADO has had a mandate to promote organ donation in Quebec and Canada since its creation in 1983.…

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Who is the PKD warrior?

My name is Judith Bélair-Kyle, I am 36 years old, I am from Quebec and I have Polycystic Kidney Disease (PKD). I am writing this blog to inform people about this currently incurable disease, kidney failure and organ transplantation. I want to talk about the impact that this disease has...

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Recent posts

  • My journey to motherhood after a transplant
  • Transplant rejection and my first signs of rejection
  • 10 tips to get back in shape after a kidney transplant
  • Bike to the moon, a chance to stop PKD!
  • Why do we have 3 kidneys after a kidney transplant?

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