We are a support group and charity concerned with the rare genetic condition aniridia – which causes a lack of irises (the coloured ring) in the eyes and poor vision from birth.
For over 10 years Aniridia Network UK 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. For more details read about us.
Our last conference was in Bristol on 7 June 2014. There were presentations, questions and answers, trustee reports and elections plus a social activity. It was a chance to hear from and ask questions in person to people interested in aniridia – such as Harry featured in this video:
If only we’d known…
A parent says what they wish they’d known when they found out their baby had aniridia:
“If only I’d known what a happy, NORMAL child he would be, with such a love for life, and absolutely no idea he has any limitations at all.” – Laura, mum to Josh
- Blog / News: Read the experiences and opinions of people in the UK, who have or are connected to aniridia. Plus Aniridia Network UK news
- Membership: Join our network to get or give a higher level of support.
- Support us: Your help is vital so we can make a difference: volunteer, donate or fundraise.
- About aniridia: Details of the causes and consequences of aniridia and the related medical conditions.
- Contact us