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

News

Are You Interested in Sharing Your Experience with Fabry Disease?

Are You Interested in Sharing Your Experience with Fabry Disease? If so, Fulcrum Research Group, an independent, third-party market research firm, is seeking Fabry patients or their caregivers for a market research study. Specifically, the research will aim to gain a better understanding of individual patients’ experiences and opinions about: Their journey from initial symptoms […]

Event

Webinar Wednesday September 26 2018

Information on the Webinar hosted by Taimi Lynch

Event

Webinar Wednesday September 12 2018

Information on the Webinar hosted by Ryan Deveau

Event

Nova Scotia Patient Empowerment Meeting

Hello Nova Scotia CFA members, A Patient Empowerment Meeting is coming your way! Put October 14th in your calendar and fill out the registration form to join us for an empowering day!   Below is the information and also please click here to register!  

Event

Winnipeg Patient Empowerment Meeting

Please keep reading for details! Registration: Click here

News

Idorsia Pharmaceuticals Announcement

Full Press release link Idorsia Pharmaceuticals (www.idorsia.com), a Swiss biotech company, is developing lucerastat, a new oral therapy for patients with Fabry Disease. The Phase 3 clinical study MODIFY has just enrolled its first patients and will investigate the use of lucerastat monotherapy for the treatment of adult patients with Fabry disease, irrespective of their […]