Susan Wolfe – Vision for Tomorrow

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 conditions....

November 28, 2022

VFT Makes GreatNonProfits 2022 Top-Rated List

Community

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 are asked to share stories of...

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

Community Research

VFT Joins Global Genes

February 28, 2022 — This year for Rare Disease Day, the Vision for Tomorrow Foundation is grateful for organizations like Global Genes which envisions a globally connected community equipped to eliminate the challenges of rare disease and provides hope for...

February 28, 2022

Aniridia North America Symposium – Scientific Summary and Themes

Community Research

Aniridia North America Symposium – Scientific Summary and Themes

The Vision for Tomorrow Foundation is excited to share a summary from the Aniridia North America Symposium it helped to sponsor late last year. The Symposium was a forum for the scientific community to present current aniridia-related research findings and...

February 7, 2022

Community Research

VFT and IWSA Join Forces

The Vision for Tomorrow Foundation (VFT) and the International WAGR Syndrome Association (IWSA) executed a Memorandum of Understanding (MOU) agreement in November 2021. The IWSA and VFT share common goals and objectives and are pleased to formalize their relationship to...

December 14, 2021

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Author: Susan Wolfe

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

VFT Joins Global Genes

Aniridia North America Symposium – Scientific Summary and Themes

VFT and IWSA Join Forces

Giving Tuesday 2022 is Here

VFT Makes GreatNonProfits 2022 Top-Rated List

VFT Attends Patient Advocacy Summit

About Vision for Tomorrow

Albinism

Aniridia

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