PKD Foundation of Canada | SwitchFrame Media
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PKD Foundation of Canada

Clients

Polycystic Kidney Disease Foundation of Canada

Category
Case Study, Social
About This Project

The Polycystic Kidney Disease Foundation of Canada is the only national organization solely dedicated to fighting Polycystic Kidney Disease through research, education, advocacy, support and awareness. Our goal is simple – to discover treatments and a cure for Polycystic Kidney Disease.

 

Arie was diagnosed with autosomal dominant polycystic kidney disease (ADPKD) when he was 21 years old. He has since received a kidney transplant from a donor match and friend. Arie and his family live in Ontario, Canada.

 

Cheri Barton was diagnosed with autosomal dominant polycystic kidney disease (ADPKD) 13 years ago after mutating the gene. Due to her enlarged liver, she is constantly asked if she is pregnant and can only wear maternity clothing. Cheri and her family live in Ontario, Canada.

 

Luisa Miniaci-Di Leo a été diagnostiquée de la maladie polykystique autosomique dominante (MPRAD) en 1989 après de nombreuses fausses-couches. Elle a depuis dû cesser de travailler et vit avec plusieurs complications causées par le gonflement de son foie qui créé une pression sur son abdomen. Cela a aussi des conséquences sur ses fonctions respiratoires et digestives.