Aniridia Lithuania has ended this year by launching the official website of the association, where a lot of information about aniridia can be found in Lithuanian language, as well as what to do first when you are diagnosed with aniridia.
It is very important for people who don’t speak any other language.
The association offers guidance and support for all aniridia patients through the new website.
You can find it at .

We are also very proud that our association is a partner of a newly granted international project by European Joint Programme on Rare Diseases, which will start next year.




“AniridijaLT” had its annual national meeting and greeted new members of the association on 11th December 2021. This was a great opportunity to share our experience with a new members, answer questions and talk about the future plans for the association.