Vision for Tomorrow provides fantastic assistance for children with Aniridia and their families. The condition is so unusual that young parents are often at a loss to understand its implications and appropriate treatment. Fortunately, Vision for Tomorrow provides the resources and references to assure them their child will do just fine and grow up happy and healthy.
This nonprofit is doing great work educating the patients and community about aniridia and helping find research.
It is inspiring to read the comments of those that VFT has helped. The commitment to empowering individuals with aniridia and albinism and their families through providing essential resources is laudable. Thank you for being a vital source of support and information for those navigating these conditions. Keep up the fantastic work!
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Excellent foundation serving those with rare ocular conditions. The members of the board are wonderful individuals who are passionate about the cause.
Great organization to support and bring awareness to a segment of the population affected by rare vision deficiencies. Funding goes towards research and support for families affected to hopefully one day find a cure. Great source of information on genetic vision conditions that are not widely known.
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Vision of Tomorrow is a great foundation that spotlights ocular conditions affecting those with albinism and aniridia that most people are unaware of. Supporting Vision for Tomorrow helps fund research and education so that advancements in science can help find a cure and treatments as well as preventions to improve the quality of life for those affected. Helping fund research currently done by some of the best scientific and medical minds allover the world will bring that goal closer to fruition.
Vision for Tomorrow was a critical source for information and hope for my wife and I when our son was diagnosed with aniridia on day four of life. The Foundation serves as a valuable resource for the patient community and also raises money to fund promising research geared toward the low vision community. We strongly support the Foundation's mission.
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I have received wonderful support from Vision for Tomorrow for my family and my son who has aniridia. The Board is extremely dedicated, hard-working and is 100% volunteer. The group is to be commended for its work in advancing medical research for this group of patients affected with aniridia and albinism.
VFT is such a wonderful group. In additional to the extensive research for Aniridia and Albinism, VFT serves as a general educational and networking group for those with Aniridia, Albinism and their families. Our son was born with Aniridia, we are very grateful for finding VFT quickly into his diagnosis and their continued efforts to fund research.
Since I have connected with VFT I am happy to see the transparency through the website and by talking with others. I am hopeful that the research will help my two boys, who inherited the condition from me, to keep the sight that they have.as they grow older..
Vision for Tomorrow has been so helpful for us as we learned to navigate our son's Aniridia diagnosis. We were able to meet others in the community, learn about ongoing research, and see that there was a lot of hope for a great future for our son. I appreciate how they send updates of current research too.
Such an amazing organization doing great things!! Have a nephew they are helping so much!! Thank you!!
What a wonderful organization, so happy to donate to such an amazing cause that is doing the work to help so many people.
This organization is so important to those who live with rare eye disorders. The parents, Board members, researchers, doctors and donors work tirelessly for those individuals. Everyone should consider learning more and supporting this group. It can truly make a difference for those many do not know about.
I am delighted to have the opportunity to write about the Vision for Tomorrow Foundation! Through the leadership of a strong board and a group of dedicated volunteers, VFT carries out its mission to empower those with low vision due to aniridia and albinism to achieve their dreams. This is accomplished by supporting promising research, attending and helping to finance important conferences, and reaching out to families, while constantly searching for new initiatives and ideas. As the mother and grandmother of loved ones with aniridia, I know that VFT has been, and continues to be, a source of strength and a beacon of hope for our family.
I can't say enough about this great organization! Its dedicated volunteer staff devotes countless hours to such a wonderful cause - helping those living with aniridia and, hopefully, finding a cure for aniridia or finding a way to prevent it in the first place. By way of just one concrete example, VFT co-sponsored a symposium bringing together dozens of North American aniridia experts and organizations to share their researchist month. If VFT can achieve its goals, children will be able to know the beautiful gift of unaided reading, participate fully in many of the daily activities we take so much for granted, and achieve their full potential in life. VFT is a group of selfless individuals who deserve our support.
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When I'm deciding whether or not to support a nonprofit, the first thing I look at is how much money the organization pays insiders. VFT passes that test with flying colors. Officers and members of the Board of Directors receive no compensation from VFT. And, as far as the day to day operations, those are handled by a dedicated group of unpaid volunteers. The second thing I look at is the organization's goals. VFT passes this test as well - it is a very worthy cause. So many of us take our vision for granted. What Aniridia does is steal the precious gift of sight from those it afflicts and leaves them, instead, with significant lifelong challenges. VFT's leadership group and volunteers are determined to fight Aniridia and stop it in its tracks. I wholeheartedly endorse Vision for Tomorrow.
VFT is a top notch organization that is leading the way in research. We are grateful for the leadership of VFT and hope the best for the future. Highly encourage supporting this great organization!
The best organization run by the very best people. Thank you for all you're doing! VFT is an outstanding group helping so many people.
Having a nephew with aniridia, I am a proud supporter of VFT. Raising awareness and funding research are just two parts of their mission which I find incredibly important. I know they will continue to help improve the lives of those with low vision, including my nephew.
The Vision For Tomorrow Foundation is an outstanding organization led by outstanding people who demonstrate first hand the virtues of humility, compassion, kindness and empathy. The Foundation is providing vital information and resources to advance research for individuals with low vision. VFT exceeds the standards in so many ways!
So thankful for the Vision for Tomorrow Foundation. My daughter has aniridia, and the research they help fund may save her vision down the road. The board members are professional and dedicated to helping those with aniridia and albinism. I'm thankful for the opportunities I've to collaborate with them to improve outcomes for people with aniridia!
The Vision for Tomorrow Foundation is an exemplary organization with an impressive mission. The support and help they provide is such a gift.
I’m a proud supporter of Vision For Tomorrow. I have family living with aniridia, so VFT’s cause is personal to me. VFT’s commitment to raising awareness and funding research to improve outcomes for people with low vision is admirable and important. The organization has strong leadership and direction for the future, and I look forward to continuing my support in the years to come!
The Vision For Tomorrow Foundation is an effective and successful organization because they are excellent collaborators. VFT works well with other nonprofits, sharing information and resources and helping to build a diverse and global community of stakeholders to improve diagnosis and management of congenital Aniridia. VFT is a critical part of developing and enhancing research on this disorder.
I have witnessed firsthand the love and dedication with which the board members selflessly sacrifice their time and energy to advance the cause and spread awareness on behalf of those afflicted with aniridia. The organization, like it’s board members are first class.
VFT is a wonderful and dedicated group focused on accelerating research to improve understanding of vision issues related to Aniridia in order to help patient care and treatment options. Collaborative relationships and working in tandem with other organizations is a positive goal of VFT. I am honored to work with and for them to further their mission!
My best friend’s husband and precious daughter both have aniridia. They have been through multiple surgeries. Without groups like Vision for Tomorrow, they will likely completely lose their full vision. I donate in hopes of one day restoring both of their vision. And I know they benefit from Vision for Tomorrow.
Vision for Tomorrow is an outstanding organization. My nephew has low vision, and I so appreciate the strides this organization is making through research to improve the life of my nephew and others. I value the awareness efforts from this organization as many people aren’t aware of aniridia and albinism.