We support people in the UK affected by aniridia: those who have it plus their family, carers, doctors, educators and others. We want all these people to be hopeful, confident, supported and well informed regarding aniridia. For them we: organise conferences, meetups and befriending, provide access to professionals and distriubute or signpost to useful information.
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We are a charity that supports people with rare genetic condition aniridia in UK and Ireland. Aniridia causes a lack of irises (the coloured ring) in the eyes and poor vision from birth.
Since 2000 Aniridia Network has been helping people with aniridia as well as their families, doctors and teachers to be: hopeful, confident, supported and well informed about aniridia and related issues.