Useful Links

For more information about hereditary angioedema (HAE), discussion boards, and support groups for people living with the condition, visit the Web sites of the organizations below. CSL Behring Canada cannot be held responsible for the information/ content/ recommendations of these resources; which are provided for complementary information only.

HAE community

Links to discussion boards:

HAE physician networks

Patient organizations — North America

Patient organizations — international

Other resources for information about HAE

Disease Web sites

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Treating acute attacks

In Canada, there is one option for treating an acute attack of HAE. Find out more.

Canadian Hereditary Angioedema Patient Association (HAE Canada)

Learn more about HAE Canada, a network where patients with HAE, physicians and the Canadian health care system become partners. Visit haecanada.org.