News - Vision for Tomorrow

A Look Back at 2024

VFT continued to work its mission in 2024 with new research, international networking and launching the Patient and Family Advisory Committee (PFAC). None of this work would be possible without YOUR SUPPORT. This year we give special thanks to those...

February 28, 2025

Albinism Aniridia Community Research

Today is Rare Disease Day! 2-28-25

We are rare but we are not alone – more than 300 million people worldwide live with a rare disease. VFT stands with other Rare patient advocates to raise awareness, support families and help to drive solutions through research and...

February 28, 2025

Community Research

VFT Fundraising Efforts Happening Now

The Vision for Tomorrow Foundation is proud to partner with Cameron Can, a local foundation in the Chicagoland area, to host the Cameron Can Rocks On with Special Guest Vision for Tomorrow, on Friday, November 8th. Like VFT, Cameron Can...

November 7, 2024

Community

VFT Named GreatNonProfit Again for 2024

The Vision for Tomorrow Foundation is one of the first winners of a 2024 Top-Rated Award from GreatNonprofits! Read inspiring stories about VFT and add your own! https://greatnonprofits.org/org/vision-for-tomorrow-foundation The GreatNonprofits Top-Rated Awards is the one and only people’s choice award where volunteers, donors,...

November 7, 2024

Community

Save the Date – Nov. 8 In Chicago

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...

July 22, 2024

VFT Launches Patient and Family Advisory Committee

Community

VFT Launches Patient and Family Advisory Committee

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...

May 30, 2024

ANA Symposium – Patient-Focused Summary Now Available

Aniridia Community Research

ANA Symposium – Patient-Focused Summary Now Available

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...

May 16, 2024

Albinism Aniridia Community Research

VFT Year in Review 2023

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...

March 21, 2024

Community

Candid Conversation on Aniridia

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...

February 27, 2024

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Donate to the Vision for Tomorrow Foundation

A Look Back at 2024

Today is Rare Disease Day! 2-28-25

VFT Fundraising Efforts Happening Now

VFT Named GreatNonProfit Again for 2024

Save the Date – Nov. 8 In Chicago

VFT Launches Patient and Family Advisory Committee

ANA Symposium – Patient-Focused Summary Now Available

VFT Year in Review 2023

Candid Conversation on Aniridia

About Vision for Tomorrow

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