News

Evelyn Williamson – Thank you

On behalf of the Canadian Fabry Association we want to thank Evelyn Williamson for her years of dedication to our organization. Evelyn was instrumental participating in our push for the government to fund enzyme replacement therapy for patients in the province of Nova Scotia. She was always a ray of sunshine to the patients she […]

Media

Webinar Wednesday – June 12 – Dr. West

Webinar Wednesday Hosted by Ryan Deveau

Media

Webinar Thursday – May 30th – Dr. Banikazemi

Webinar Thursday Hosted by Ryan Deveau

News

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

News

Rare Diseases allocated funds in the 2019 Federal Budget

The rare Disease Foundation has posted a great article on this: Click here to view their article

Event

Webinar Wednesday February 27 2019

Information on the Webinar hosted by the CFA

News

AVROBIO announces updated clinical data for Fabry disease

Posted from https://www.businesswire.com

Event

Webinar Wednesday November 21 2018

Information on the Webinar hosted by the CFA