Aniridia Europe gathers people all over the continent
We want to support people with aniridia in all countries and help them to share information and build useful networks in their own countries and abroad.
What is Aniridia?
Aniridia is a very rare disease and every family affected is often alone to face the diagnosis. Even nationally, there’s often only a small group of individuals. Get to know aniridia.
Aniridia Europe, the federation of European aniridia associations and representatives, has been founded to change this situation. Read our mission objectives.
As of September 2021, the federation includes 13 national associations, as well as support groups and contact persons in 20 other European countries.
Get in touch with someone in your country.
News & Events
Registration for EAC 7 is now open!
It is a great pleasure to announce that the 7th European Aniridia Conference, that will be held in Stockholm, Sweden, on 31st May-2nd June 2023, has opened its registration platform. . The preliminary scientific programme is already defined and the list of speakers...
EALA is looking for you! If you are 18 to 30, find out why
We are thrilled to introduce the European Aniridia Leadership Academy (EALA), a groundbreaking initiative brought to you by Aniridia Europe in collaboration with Aniridia Sweden. Our aim is to empower and equip young individuals with aniridia, aged 18 to 30, with the...
“Seeing the invisible” presented at the University of Padua, Italy
The Italian presentation of the Erasmus+ project “Seeing the invisible” took place on 25th October 2023 at the University of Padua, in the framework of the Master Degrees in Sociology and Sciences of Primary Education, in front of more than one hundred students....