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
Webinar: Regulatory Framework on Orphan Medicinal Products for Rare Diseases, May 20th, 2022, at 13.00 CEST
Aniridia-Net and Aniridia Europe are happy to announce this new webinar which will take place on May 20th at 1PM CEST and will talk about orphan medicinal products, recommended to an audience of professionals working in the field of aniridia and the other rare...
Aniridia Europe Webinar: The digital therapeutics value
On April 26th 2022, at 18.00 CEST, Aniridia Europe will present a live webinar hosted by Galina Gening with the presence of Kasperi Kankare to talk about the the measurement of intraocular pressure in patients with congenital aniridia at home. A few years ago, a...
Canary Island holiday raffle, fundraising for the European Aniridia Conference
Help us to finance the 6th European Aniridia Conference by entering a raffle to win 7 days / 6 nights in Fuerteventura with all-inclusive at Hotel Taimar – accessible and inclusive hotel. Do you know the Canary Islands, its incredible…