Help us provide a bright future for children with long-term medical conditions.

Vision for Tomorrow Foundation
The Cameron Can Foundation is honored to introduce you to the Vision For Tomorrow Foundation. VFT’s roots began in Riverside when Edward Wolfe was born with a rare genetic eye disease called Aniridia. Edward’s family was drawn to the organization helping other children and families cope with a rare vision diagnosis. Susan and Matt Wolfe now lead the Foundation’s Board. Cameron Can is excited to shine its light on the great work VFT is doing to improve the lives of those with blindness and low vision due to an irreversible birth defect. Each dollar the Foundation raises goes towards funding research (more than 25 studies worldwide to date) and family support for those affected by aniridia, albinism, and other rare genetic eye diseases.
Family

Foundation Video

"Friends of Cameron" Grant

If your family (or a family you know) has a child living at home with Hydrocephalus, Spina Bifida or another life long neurological medical condition please apply for a Friends of Cameron grant from the Cameron Can Foundation.