The 2020 National Report Card

Three years ago our membership filled out our survey that provided data for our National Report Card. It’s time to update this information.

In September, we will email our members links to our survey. Completing this survey will not only provide HAE Canada with important information that will be used to advocate for access to treatments, it will also give members a chance to win a travel grant to attend the next HAEi Global Conference.

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Latest News

May 22nd, 2020|

HAE Canada is excited to announce that our new and improved website officially went live today, May 22, 2020. This project was made possible through our partnership with

Great News!

May 19th, 2020|

HAEGARDA and TAKHZYRO are now available in Canada. Please talk to your HAE specialist about access. Thank you Canadian Blood Services (CBS) for a very collaborative, informative and

HAE Day 2020

May 16th, 2020|

For HAE Day 2020, HAE Canada wants to celebrate! To honour the day we have two BIG announcements: 1) Our website received a facelift! We hope our

Virtual HAE Global Walk

April 1st, 2020|

It’s time, once again, for HAE Canada to please ask you to take out your walking shoes and participate in the virtual HAE Global Walk arranged by HAE

Support Family Testing

Give valuable insights in HAE science

Hereditary Angioedema (HAE) is a hereditary disorder. It is therefore very important to have other family members tested. To help you in this process HAE International has developed two documents for patients. You can download the documents below:

Support Family Testing – Patient Pack 1

Support Family Testing – Patient Pack 2

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