What is Aniridia?

Aniridia is a rare genetic eye disorder marked by the partial or complete absence of the iris, leading to visual impairments and associated conditions like glaucoma and cataracts. It requires lifelong monitoring and treatment to manage its complications.

Who are We?

The Canadian Aniridia Foundation provides education, support, awareness, and promotes research for those affected by Aniridia.

Support Our Mission

At Aniridia Canada, our mission is to empower, support, and advocate for individuals and families affected by aniridia. We are dedicated to raising awareness, advancing research, and providing essential resources to improve the quality of life for those living with this rare genetic eye disorder.

Through education, collaboration, and community engagement, we strive to bridge the gap between patients, families, medical professionals, and researchers—ensuring that everyone affected by aniridia has access to the knowledge, care, and support they need. Our commitment extends beyond information-sharing; we actively champion advancements in medical research and standards of care to create a brighter future for those with aniridia.

Together, we stand for hope, inclusivity, and progress, working toward a world where individuals with aniridia can thrive without limitations.

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