Whether you are a new parent of a child with aniridia or have aniridia yourself and need to get some answers or just relate to someone, we are here for you.

Debby Casher has a child with aniridia and she is happy to share her story and lend an ear. Reach out to Debby via email at [email protected].

The United Families of Aniridia is subgroup of Vision for Tomorrow.  The group lives online via a Facebook page.  It is an active community of individuals who ask questions and share experiences. In addition, we continuously post any information which may be of interest to individuals living with aniridia.

Also be sure to like the Vision for Tomorrow Facebook page.

We hope you choose to reach out and get support from a wonderful community of people living with aniridia!

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