About Us


We are loving parents, insatiable researchers, and active members of both our communities and schools. Some of us also have children with low vision.Familes of children with albinism and aniridia at 2008 Event

 

Through our shared experiences, we have learned that information is a source of comfort and power.  Knowledge and awareness leads to support from educators and others in the world of low vision. We have learned that research costs money — lots of it.  Best of all, we have learned that we are not alone.

 

 

We created The Vision for Tomorrow Foundation to:

  • Help families, educators and medical professionals recognize and learn more about low vision impairments(with a focus on albinism and aniridia) in order to provide better support for the people who have them
  • Provide a place where doctors can share their knowledge
  • Raise funds to support research and education, and
  • Generate awareness, so that our children, and others affected by these disorders, are able to lead a rich and fulfilling life.

 

By staying in touch with each other and the issues that affect our world, you can make your home, your school and your community a better place for children with low vision.  By funding research, you can make it possible for every person to see the world in a better light.Girl with albinism on horse

 

Jon Ballis, J.D.
Susan Ballis, M.D.
Richard Baum
Wendy Baum, C.P.A., J.D.
Beth Kaufmann, C.P.A.
Board of Directors


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