Susan Wolfe – Vision for Tomorrow

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

Community Research

Giving Tuesday

Today is Giving Tuesday – a global day of generosity. Please consider a donation to help Vision for Tomorrow in the work we do funding research and supporting families affected by aniridia. Your dollars make an impact: Two years ago,...

November 30, 2021

Community

Shop and Donate – Sign up for AmazonSmile

Have fun shopping on Amazon this season and support VFT while you are at it with no additional cost to you. AmazonSmile makes it easy to support the low vision research VFT does year-round. On the website: Go to...

November 17, 2021

Research

VFT Talks to Dr. Ali Djalilian About Latest Cornea Research and What It Means for the Aniridia Community

The Vision For Tomorrow Foundation is excited to share more details on the VFT funded research published in the medical journal “Science Translational Medicine”. The study, “Gene dosage manipulation alleviates manifestations of hereditary PAX6 haploinsufficiency in mice”, was published primarily...

November 3, 2021

Community Research

New Aniridia Organization Announced

VFT Proud to Help Create New Umbrella Group October 28, 2021 – The recent creation of a new nonprofit organization, Aniridia North America (ANA), has been announced by its founding Board of Directors. This umbrella organization will represent, serve, and support...

October 28, 2021

Research

VFT Partners with NOAH to Support Albinism Research

June 2021 – The Vision for Tomorrow Foundation (VFT) is proud to support the National Organization for Albinism and Hypopigmentation (NOAH) with a grant for its new Research Program dedicated to improving the quality of life for people with albinism...

June 25, 2021

1 2 3

Author: Susan Wolfe

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

Shop and Donate – Sign up for AmazonSmile

VFT Talks to Dr. Ali Djalilian About Latest Cornea Research and What It Means for the Aniridia Community

New Aniridia Organization Announced

VFT Partners with NOAH to Support Albinism Research

Join VFT to Meet Up for Aniridia Day

2021 Year In Review

VFT Joins Global Genes

About Vision for Tomorrow

Albinism

Aniridia

Receive VFT News