Help us tell the story of HAE in Canada!

By August 2, 2017Events, News

Hereditary Angioedema (HAE) Canada is gathering information from Canadians living with HAE to better understand what it is like to live with HAE in Canada. Data will be collected from adults 18yrs and older, caregivers of children/youth, and caregivers of adult dependents.

The information gathered will be used for research and advocacy purposes only. It is very important for HAE Canada to understand patient product use, symptoms and needs so we may continue to advocate for improved access to safe and effective therapies and treatments for Canadians living with HAE, as well as retain access to current treatments.

Adults 18yrs and older please click here to access your survey.

Caregiver of child/youth please click here to access your survey.

Caregivers of adult dependents please click here to access your survey.

Please complete the survey before August 16, 2017.
A French version of this survey will be available at a later date.

Feel free to share with friends, family and colleagues who are affected by HAE. HAE Canada thanks you for your interest in our research and for your continued support.

The HAE Canada Team

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