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, there are a few different options:

Email Us

Liam and Debby

Email Debby Casher at debby@visionfortomorrow.org.
Debby Casher has a child with aniridia and she is happy to share her story
and lend an ear.

Facebook Us

United Families of Aniridia has a Facebook Page called UFA which has 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. You can ‘like’ our Facebook Page by clicking on the link just to the right of this section of the website.

Call Us

Sometimes you need to hear a live voice and just talk. Give us a call at 847.877.9007.
We hope you choose to reach out and get support from a wonderful community of people living with albinism!

Comments are closed.

A Family's Perspective

  • Brotherly Love: My brother’s eyes looked a little different when he came home from the hospital, but I wasn’t sure why. I quickly found out. My jaw dropped. It stayed in that...

Links We Like

  • Useful Links For Aniridia: Where can I buy sunglasses for my child?  Where can I get a hat?  What books do you recommend?  Find links to these and other useful tips here!  To suggest...