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