


About Us
We fund research for better treatments or prevention of conditions associated with aniridia and albinism by:
- creating a research strategy that prioritizes projects
- establishing relationships with the leading researchers in the field
- identifying treatments or preventions with the greatest impact on quality of life
- actively fundraising to fund research
We provide support to families affected by aniridia or albinism by:
- offering immediate family support for newly diagnosed families
- empowering affected families with a platform to receive information and fundraise for their cause
- providing access to information on aniridia and albinism in an open, free environment.

Board of Directors
Susan Wolfe, President
Grayson Chinn, Vice President and Secretary
Matt Wolfe, Treasurer
Emeritus Board
Susan Ballis, MD
Wendy Baum, CPA, JD
Volunteer Leads
Debby Casher – Family Outreach
Susie Chinn – Family Support and Fundraising

We’d love to hear from you. Please reach out to us with your questions, to get involved, or to connect with one of our family support liaisons at info@visionfortomorrow.org
Please note our new address:
The Vision for Tomorrow Foundation
106 W. Calendar Avenue
Suite 177
LaGrange, Illinois 60525

Our mission is to create a fun event to raise awareness about low vision, while generating funds for eye-related research. The Vision For Tomorrow Junior Board is comprised of high school students from Deerfield High School in Deerfield, Illinois.

