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Event

CFA Community Open Forum Webinar May 26

Information on our Webinar on May 26

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Event

Chaperone Therapy with Dr. Khan @ Wed Apr 14, 2021

Information on the webinar April 14th

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News

Building a National Strategy for High-Cost Drugs for Rare Disease

The Canadian Government has a website now for working on a national strategy for high cost drugs for rare diseases.

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Event

CFA Virtual Family National Conference: March 7th, 2021

**Updated with Agenda!** A one day virtual conference for the Canadian Fabry community. A chance to connect and talk with others.

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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.

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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.

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

Julia Alton Executive Director
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1964 Hawkridge Dr.
Thunder Bay ON P7J 1H2
Canada

If have any questions or would like to get involved, please fill in the form below.

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