"Thirty-seven years ago, I received the diagnosis that I had polycystic kidney disease, and my life changed instantly that day. I had no idea that I was ill, let alone had a chronic kidney disease. I did not know anything about PKD, nor anyone that was affected by it."
The fourth and final article in our National Post PKD series features Jan Robertson, a woman who is seeing new hope after years of living with polycystic kidney disease. Doctors discovered Jan had PKD more than 35 years ago, and she hasn’t stopped fighting since. Read more about Jan’s story, and...
Part three of our four-part National Post PKD series features a Nova Scotian woman, now living in Toronto, ON. Jil Eisnor was 20 years old when she discovered she had polycystic kidney disease, but she hasn’t let it stop her from living a normal life. Jil has the mutated gene, meaning...
Part two of our four-part National Post PKD series features the entire Pekar family from Hamilton, ON. Arie Pekar received a kidney transplant from a close friend shortly after Arie’s son was born. Unfortunately his mother, Ilana, who has been on dialysis for PKD for 23 years, has yet to find a...
Our four-part PKD series launched today in the National Post, featuring one of our youngest PKD heroes, Harrison Osborne! Harrison loves superheroes and in fact, is one himself. He was diagnosed with autosomal recessive polycystic kidney disease (ARPKD) before he was even born and is overcoming the odds, living his life...
"I'm 47 years old and people are still asking me if I am pregnant. I try to take it as a compliment about how young I must look, but when people first started asking me, I would turn very red and uncomfortable. Then they would also turn red and it...