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. Learn more About us.
Join us to benefit from all our services and to stay in touch.
Events
A chance to hear from and ask questions in person to people interested in aniridia.
Find out about our conferences and meet ups plus the annual Aniridia Day.
Watch the videos of the fascinating sessions at our past events.
Aniridia Network offered us information, support, friendship, understanding and most importantly given us many positive role models for Zoe as she grows older. Thank you”
– Heather, mum to Zoe who has aniridia
Contents
- Blog/News: Read the experiences and opinions of people, who have or are connected to aniridia. Plus Aniridia Network news
- Join our network: to get or give more 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
Aniridia Network 