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PKD Warrior

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

Month: July 2022

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Blog, My experience of PKD

Living my best life (it’s the only one I have, anyway)

July 20, 2022

A few weeks ago, I saw several of my friends after a few years without seeing them. The pandemic has obviously complicated things, but I also left the Montreal area in 2019 to start a new career. So it’s been a long time since I’ve seen them, and I couldn’t wait…

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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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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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