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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

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Event

Webinar Wednesday February 27 2019

Information on the Webinar hosted by the CFA

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News

AVROBIO announces updated clinical data for Fabry disease

Posted from https://www.businesswire.com

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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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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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748 Kelly St
Thunder Bay ON P7E 2A1
Canada

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

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