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aHUS Canada Golf Tournament
On Sunday, June 4, 2023, a special event will take place – the very first aHUS Canada Golf Fundraiser. Join us for an enjoyable day in an effort to raise awareness of aHUS and funds for aHUS Canada, enabling us to continue supporting those with this ultra-rare genetic disease.
For more information, registration, and ordering... » Read More
Click here to email your Premier and Health Minister and ask them to fund treatment for aHUS.
Click here to use our petition to call on the government to fund eculizumab for aHUS (ONTARIO, ALBERTA & B.C. ONLY)
Get Involved!
Our goal is to serve as a resource for all Canadians affected by aHUS, and form a nationwide community of aHUS patients.
Meet the Community
Although aHUS is an ultra-rare condition, there are others just like you across Canada who are fighting this disease. aHUS Canada wants you to know that you are not alone. aHUS patients and families in Canada share their stories… »Read more
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Stay connected with the aHUS community in Canada! To receive info and updates from aHUS Canada, sign up here:
ABOUT US
In addition to providing support to patients and caregivers, aHUS Canada strives to connect those affected by the condition to establish a Canadian aHUS community, build public awareness and understanding of this very rare and potentially fatal disease and advocate for the best possible care and treatment for patients.