BE RARE BE YOU
toques and mittens!

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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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Rare Disease Day: Be Rare Be You

Rare Disease Day is just around the corner! On February 28th 2021 Rare Disease Day is recognized worldwide to bring awareness to all those living with Rare Diseases. This year the CFA is keeping theme with our “Be Rare Be You” message by bringing you our exciting new  winter toques and mittens. ORDER TODAY at fabrycanada.com Winter […]

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CFA’s newest launch!

Information on the newest addition to the clothing line!

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Zoeinsights information Webinar December 2

Information on the webinar December 2nd

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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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Contact Us

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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