Susan Wolfe - Vision for Tomorrow

2022 Year In Review

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...

March 6, 2023

Albinism Aniridia Community Research

VFT Lights Up For Rare Disease Day

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...

February 28, 2023

Research

VFT Funds Innovative Research to Understand Early Eye Development in Aniridia and Albinism

VFT Funds Innovative Research to Understand Early Eye Development in Aniridia and Albinism The Vision for Tomorrow Foundation is excited to support first-of-its-kind research with the University of Virginia (UVA) to understand initial steps in eye formation and the consequences...

December 23, 2022

Community Research

Giving Tuesday 2022 is Here

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...

November 28, 2022

VFT Makes GreatNonProfits 2022 Top-Rated List

Community

VFT Makes GreatNonProfits 2022 Top-Rated List

VFT Makes GreatNonProfits 2022 Top-Rated List The Vision for Tomorrow Foundation is proud to have won a 2022 Top-Rated Award from GreatNonprofits. The GreatNonprofits Top-Rated Awards is the one and only people’s choice award where volunteers, donors, and people served by nonprofits...

November 9, 2022

Community

VFT Attends Patient Advocacy Summit

Last month, Vision for Tomorrow Foundation Board Members virtually attended the Global Genes (GG) Patient Advocacy Summit as part of VFT’s new membership of the Global Genes RARE Foundation Alliance. The Alliance is a coalition of more than 750 rare disease...

October 26, 2022

VFT Sponsors International Albinism Conference

Community Research

VFT Sponsors International Albinism Conference

The Vision for Tomorrow Foundation is proud to sponsor the International Scientific Conference on Albinism (ISCA). This unique conference, sponsored by the Global Albinism Alliance, includes researchers, health care providers and albinism organization leaders from around the globe. The goal...

October 26, 2022

Community

VFT Celebrates Aniridia Day

For many of us, summertime means connecting with friends outside. For our aniridic community, it also means time to celebrate International Aniridia Day! This year, Vision for Tomorrow hosted a few meet-ups across the United States to bring Aniridia families...

July 15, 2022

Community

Join VFT to Meet Up for Aniridia Day

Summer is almost here and with that so is Aniridia Day! June 21st is International Aniridia Day which was created to celebrate those living with Aniridia. This year Vision for Tomorrow is planning a few meet-ups across the United...

May 11, 2022

Community Research

2021 Year In Review

Thank you so much for your ongoing support for the Vision for Tomorrow Foundation in 2021. The VFT Year in Review report recaps the 15th Anniversary year including new research projects and expanded networking to support families affected by albinism...

March 24, 2022

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Author: Susan Wolfe

2022 Year In Review

VFT Lights Up For Rare Disease Day

VFT Funds Innovative Research to Understand Early Eye Development in Aniridia and Albinism

Giving Tuesday 2022 is Here

VFT Makes GreatNonProfits 2022 Top-Rated List

VFT Attends Patient Advocacy Summit

VFT Sponsors International Albinism Conference

VFT Celebrates Aniridia Day

Join VFT to Meet Up for Aniridia Day

2021 Year In Review

2022 Year In Review

VFT Lights Up For Rare Disease Day

VFT Funds Innovative Research to Understand Early Eye Development in Aniridia and Albinism

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