Canada

News from Canada

2020-01-03T13:09:33+01:00December 30, 2019|Canada|

From Executive Director Peter Waite, Canadian Hereditary Angioedema Network: The Canadian Hereditary Angioedema Network has updated its 2014 Canadian Hereditary Angioedema Guideline with an expanded scope to include the management of HAE patients worldwide. It is a collaboration of Canadian and international HAE experts and patient groups led by the Canadian Hereditary Angioedema Network. The objective of this guideline is to provide evidence-based recommendations, [...]

News from Canada

2019-10-11T22:56:14+01:00October 11, 2019|Canada|

From President Jacquie Badiou and Daphne Dumbrille from the HAE Canada office Summers are always too short and 2019 was no exception. July was particularly eventful for two HAE Canada Youth members, Paige and Makayla, who were fortunate to attend HAEi’s Youngsters Summer Camp in Atlanta. Their experience is best heard from their perspectives: Paige: This July I attended a Youth [...]

News from Canada

2019-07-16T16:00:52+01:00July 16, 2019|Canada|

From Daphne Dumbrille, HAE Canada Volunteer Coordinator: HAE Canada has had a busy spring. Things kicked off with the HAE Canada Director at Large, Anne Rowe and Ontario Regional Director, Tina McGrath, attending the Network of Rare Blood Disorder  Organizations (NRBDO) Spring Forum in Toronto in April. It was an informative and busy weekend discussing many issues, particularly around the importance of [...]

Canada

2019-10-21T08:11:24+01:00February 11, 2019|

HAE CANADA Hereditary Angioedema (HAE) Canada / Angioédème Héréditaire (AOH) Canada Canada ·  North America On this page we have pulled together presently available information relevant for HAE patients and caregivers in Canada. HAE online in Canada [...]