Help us tell the story of HAE in Canada! Member Action Required!

By May 10, 2018News

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 caregivers of children/youth.

If you already completed the survey regarding caregivers of children/youth in August 2017, please do not fill it out again.

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.

Please contact office of HAE Canada to become a member and participate in member surveys. office@haecanada.org

This survey is open until June 4 only.

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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