We are in between events, but please continue to check back! You can see our full event schedule for the Foundation here. If you’re looking for local resources, reach out to your chapter coordinator or contact us at firstname.lastname@example.org.
Hello World! My name is Matan and I am the Toronto Chapter Coordinator for the PKD Foundation of Canada. I was diagnosed with PKD 13 years ago, after progressively worse flank pain led me to seek medical attention. Heading up our Toronto Chapter allows me to redirect my energy into helping others affected by PKD. It helps me forget about my challenges and focus on leaving my community a bit better, day by day.
As a PKD patient I feel blessed because some of the world’s top scientists are fighting for our cause. With many studies currently underway, I believe the future of PKD is very promising for patients. Our Toronto Chapter understands the importance of continued research, advocacy and education on PKD and strives to grow our community with the help of dedicated volunteers.
PKD patients can reach out to me at any time and for any reason at email@example.com. Our Toronto Chapter is looking forward to implementing even more educational and social events this year. We aim to consistently improve the help we deliver to our community and the value we deliver to our PKD patients.
I hope you can join us for our next meeting or event!
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 Toronto Chapter. 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