For those in the Chicagoland area, we hope you can join us on November 8th in Oak Brook for an exciting evening to raise funds for VFT research and family support. VFT is proud to partner with Cameron Can, a...
The Vision For Tomorrow Foundation is excited to announce its new Patient and Family Advisory Committee (PFAC). The PFAC was created to engage with more persons with aniridia and their family members. The group will help VFT identify opportunities for...
VFT is pleased to share the Aniridia North America Working to Solve the Aniridia Puzzle, A Patient-Focused Summary of Presentations from the 2023 ANA Symposium: PAX6, Aniridia, and Beyond. This summary helps to breakdown the information shared at the meeting...
Thank you for your ongoing support of VFT in 2023. It was a dynamic year for research and partner outreach. VFT is committed to funding promising research to understand and better treat aniridia and albinism and the Foundation remained true...
VFT is celebrating 2024 World Rare Disease Day (February 29) by releasing the first videos in our new series “Candid Conversation on Aniridia.” Listen to patients and families in the aniridia community tell their stories as a way to inspire...
The Vision for Tomorrow Foundation is proud to have won the 2023 Top-Rated Award from GreatNonprofits for the second year in a row. The GreatNonprofits Top-Rated Awards is the one and only people’s choice award where volunteers, donors, and people served by...
September 2023 – The Vision for Tomorrow Foundation (VFT) welcomes new Board of Directors member Chéleah Googe, PhD. An educator and equity advocate, Dr. Googe currently serves as the Director of Leadership & Equity for Breck School in Golden Valley,...
We are excited to share the 2022 Vision for Tomorrow Foundation Year in Review report. The VFT team can’t thank you enough for your support and donations this past year. We remain committed to advancing research and supporting families and...
The Vision for Tomorrow Foundation (VFT) celebrates Rare Disease Day – a globally-coordinated movement working towards equity in social opportunity, healthcare and access to diagnosis and therapies for people living with a rare disease. VFT focuses on two rare diseases...
Giving Tuesday 2022 is Here Vision for Tomorrow is participating in Giving Tuesday on November 29th. There are so many ways to support VFT’s pillars of 1) funding research for aniridia and albinism and 2) providing free support to families affected by these eye...