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Hello, My name is Carrie Manson and I’m the Guelph Walk Coordinator.
Unlike most of the other volunteers who support the mission and vision of the PKD Foundation of Canada, I will never know PKD like them.
My story is not because of my diagnosis, it’s because of a boy I met in 1997, whom I fell in love with and have since became a champion for.
Back in 1997 when John and I first started dating, his dad was diagnosed with PKD. He was considered one of the lucky ones as he went on the transplant list, and within a few years he was matched with his wife, Anne. However before the date was set, he received the gift of life through a cadaver instead. He lived several years with his new kidney, but after getting involved in a vehicle collision - he developed complications and passed in March 2009.
In August of 2010 with our family determined to make a difference, we found the PKD Foundation and agreed to launch a Walk to END PKD event in Guelph. Shortly after that decision, my husband was diagnosed and so was his brother.
Thanks to the PKD community, corporate sponsors, generous donors, and all the volunteers who tirelessly donate their time, money and knowledge to help make medical advancements a reality, both my husband and brother-in-law live in a day and age where treatment exists and they can benefit from it for their diagnoses.
So thank you to all who have made a contribution the Foundation so that my husband has hope and has options that his father didn’t have only ten short years ago.
PKD Foundation of Canada Chapters are led by volunteers who want to make a difference in the fight to end PKD! Contact us today to find out how you can get involved with the Guelph Walk. Stay connected with us on Facebook.
ADPKD is the most common inherited renal disorder worldwide, impacting approximately 1 in every 500 Canadians. An estimated 45% to 70% of patients with ADPKD progress to end-stage renal disease by age 65 years.Read more