Canadian Fabry Association

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News & Events

Important message from our friends at CORD

Please take the time to read CORD’s message: URGENT! Your Voice is Needed to Keep Rare Disease Drugs Coming to Canada Click here for the article You can also visit the Canadian Organization for Rare Disorders (CORD) at their website https://www.raredisorders.ca/

Media

Rare Disease Day 2019 video

Hello everyone, thank you so much for a very successful Rare Disease Day. Below is a collage of the photos from the day!

Event

Webinar Wednesday April 10th 2019

Hello CFA, Below are the details on the upcoming Webinar Wednesday. Join Zoom Meeting https://zoom.us/j/580994594 Meeting ID (if required): 580 994 594

WHO WE ARE

The CFA encourages and supports research into the causes, treatment and management of Fabry disease, but most importantly arranges for, coordinates and increases the facilities available for diagnosis, consultation and treatment of those suffering from Fabry disease.

GET INVOLVED

The CFA is a small group of patients and their families that have gathered together to support and assist others in the community across Canada. If you have Fabry, or know someone affected by the disease, we hope that you will consider getting involved.

LEARN MORE

We are committed to improving the lives of those who live with and are affected by Fabry disease in Canada.

Julia Alton Executive Director

The Canadian Fabry Association (CFA) is committed to improving the lives of those who live with and are affected by Fabry disease in Canada.

Registration number 827560871RR0001

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Contact Us

748 Kelly St
Thunder Bay ON P7E 2A1
Canada

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Be Rare. Be You. Get your tattoo!