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# Vision for Tomorrow

Helping those with low vision see a world of potential

## Sitemaps

- [XML Sitemap](https://visionfortomorrow.org/sitemap.xml): Contains all public & indexable URLs for this website.

## Posts

- [VFT Supports 2025 ANA Scientific Symposium](https://visionfortomorrow.org/vft-supports-2025-ana-scientific-symposium/) - The Vision for Tomorrow Foundation is proud to again sponsor and attend the biennial Aniridia North America (ANA) Symposium: Pax6, Aniridia and Beyond. The 2025 meeting offers an environment for leading researchers to network and make connections in emerging science related to aniridia. Sessions will focus on aniridia-related issues including glaucoma, corneal health, and genetics and
- [VFT Announces New Crowdsourced Map of Eye Care Professionals ](https://visionfortomorrow.org/vft-announces-new-crowdsourced-map-of-eye-care-professionals/) - The Vision For Tomorrow Foundation is excited to announce a new crowdsourced map of U.S.-based eye care professionals to empower the aniridia and low vision community. One of the most frequently asked questions from families and patients is where they can find ophthalmologists familiar with treating aniridia and related eye conditions. “We wanted to create
- [Happy Aniridia Day 2025!](https://visionfortomorrow.org/happy-aniridia-day-2025/) - VFT wishes everyone a Happy Aniridia Day! This special day falls on June 21, the Summer Solstice, because the brightness and position of the sun significantly affects the lives of people with aniridia. VFT is thankful for its Patient and Family Advisory Committee (PFAC) because we know we are stronger when we work together .
- [Working to Preserve Long Term Vision for Aniridia - Understanding Why Pax6 Mutations Cause Aniridic Keratopathy](https://visionfortomorrow.org/working-to-preserve-long-term-vision-for-aniridia-understanding-why-pax6-mutations-cause-aniridic-keratopathy/) - The Vision for Tomorrow Foundation continues to fund research to move closer to clinical treatments for aniridic keratopathy (AK). Most recently, VFT awarded a grant to Melinda Duncan, PhD, Trustees Distinguished Professor of Biology, University of Delaware, to better understand the molecular basis of AK while testing potential drugs that could slow or stop it.
- [A Look Back at 2024](https://visionfortomorrow.org/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 that participated in the Chinn Family Campaign, the Chicagoland Cameron Can and VFT Event and
- [Today is Rare Disease Day! 2-28-25](https://visionfortomorrow.org/today-is-rare-disease-day/) - 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 partnerships. We are stronger when we work together to support and fuel the entire Rare
- [VFT Fundraising Efforts Happening Now](https://visionfortomorrow.org/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 is dedicated to making a difference in the lives of families and children with various
- [VFT Named GreatNonProfit Again for 2024](https://visionfortomorrow.org/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, and people served by nonprofits are asked to share stories of inspiration, express their appreciation.
- [Save the Date - Nov. 8 In Chicago](https://visionfortomorrow.org/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 local foundation dedicated to making a difference in the lives of families and children with
- [VFT Launches Patient and Family Advisory Committee](https://visionfortomorrow.org/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 more patient community engagement, as well as provide feedback regarding the organization’s plans, activities, and
- [ANA Symposium – Patient-Focused Summary Now Available](https://visionfortomorrow.org/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 from clinical and research leaders in aniridia related research. VFT sponsored and attended the biennial
- [Candid Conversation on Aniridia](https://visionfortomorrow.org/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 others and share insights and resources – starting with one of our very own VFT
- [VFT Year in Review 2023](https://visionfortomorrow.org/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 to its mission in 2023. In addition to sponsoring the newly formed NOAH research program and the biennial
- [The Vision for Tomorrow Foundation Announces Board of Director Changes](https://visionfortomorrow.org/board-of-director-changes/) - The Vision for Tomorrow Foundation (VFT) announces changes to its Board of Directors as it moves into its 15th year dedicated to helping those with low vision have the confidence and ability to achieve their dreams.
- [VFT to Support New Non-Invasive Imaging for Tracking Retinal Changes in Young Aniridia Patients Eyes](https://visionfortomorrow.org/vft-to-support-new-non-invasive-imaging-for-tracking-retinal-changes-in-young-aniridia-patients-eyes/) - The Vision for Tomorrow Foundation (VFT) is supporting a research project using new technology called visible light optical coherence tomography (vis-OCT) to detect retinal damage in young aniridia patients. Xiaorong Liu, PhD, Associate Professor of Biology and Psychology, University of Virginia, is leading the project. The research team will take retinal pictures of a small
- [VFT Makes GreatNonProfits 2023 Top-Rated List](https://visionfortomorrow.org/vft-makes-greatnonprofits-2023-top-rated-list/) - The Vision for Tomorrow Foundation is proud to have won the 2023 Top-Rated Award from GreatNonprofits for the second year in a row. 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 inspiration, express their appreciation. Thank you to all
- [VFT Sponsors ANA Research Symposium](https://visionfortomorrow.org/vft-sponsors-ana-research-symposium/) - The Vision for Tomorrow Foundation is proud to sponsor and attend the biennial Aniridia North America Symposium: Pax6, Aniridia and Beyond once again. The 2023 event, presented by VFT partner, Aniridia North America, offers an environment for leading researchers to network and make connections in emerging science related to aniridia. This meeting provides a forum
- [VFT and UVA Continue Partnership to Further Understand Early Eye Development in Aniridia and Albinism](https://visionfortomorrow.org/vft-and-uva-continue-partnership-to-further-understand-early-eye-development-in-aniridia-and-albinism/) - The Vision for Tomorrow Foundation (VFT) is excited to support ongoing work and first-of-its-kind research with the University of Virginia (UVA) to understand initial steps in eye formation and the consequences for aniridia and albinism. Previous studies VFT helped to fund led scientists at UVA to develop new genetic technology for their frog model system to
- [New Member Joins VFT Board of Directors](https://visionfortomorrow.org/new-member-joins-vft-board-of-directors/) - September 2023 – The Vision for Tomorrow Foundation (VFT) welcomes new Board of Directors member Chéleah Googe, PhD. An educator and equity advocate, Dr. Googe currently serves as the Director of Leadership & Equity for Breck School in Golden Valley, MN. She values advocating for students to have access to what they need to thrive
- [2022 Year In Review](https://visionfortomorrow.org/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 this past year was no different. Some highlights include: Funded groundbreaking foundational research on PAX-6
- [VFT Lights Up For Rare Disease Day](https://visionfortomorrow.org/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 that cause low vision from birth – aniridia and albinism. Aniridia affects approximately one in
- [Shop and Donate - Sign up for AmazonSmile](https://visionfortomorrow.org/shop-and-donate-sign-up-for-amazonsmile/) - AmazonSmile
- [Aniridia North America Symposium - Scientific Summary and Themes](https://visionfortomorrow.org/aniridia-north-america-symposium-scientific-summary-and-themes/) - Aniridia North America Symposium
- [Giving Tuesday 2022 is Here](https://visionfortomorrow.org/giving-tuesday-2022-is-here/) - Giving Tuesday 2022 is here!
- [VFT Funds Innovative Research to Understand Early Eye Development in Aniridia and Albinism](https://visionfortomorrow.org/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
- [VFT Makes GreatNonProfits 2022 Top-Rated List](https://visionfortomorrow.org/vft-makes-greatnonprofits-2022-top-rated-list/) - VFT makes the GreatNonProfits 2022 top-rated list!
- [VFT Attends Patient Advocacy Summit](https://visionfortomorrow.org/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 organizations and members that believe in the power of collective impact and understand that together,
- [VFT Sponsors International Albinism Conference](https://visionfortomorrow.org/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 of this conference is to improve the lives of those with albinism. This is the
- [VFT Celebrates Aniridia Day](https://visionfortomorrow.org/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 together in-person in honor of the day. Gatherings took place the weekend before and after
- [Join VFT to Meet Up for Aniridia Day](https://visionfortomorrow.org/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 States to bring Aniridia families together in person in honor of the day. Gatherings will
- [2021 Year In Review](https://visionfortomorrow.org/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 and aniridia. We are busy doing the same now for 2022. VFT-YIR-2021-Final-1-1Download
- [VFT Joins Global Genes](https://visionfortomorrow.org/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 the more than 400 million people affected by rare disease around the globe. VFT is
- [VFT and IWSA Join Forces](https://visionfortomorrow.org/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 collaborate and work together for the benefit of individuals with aniridia and WAGR syndrome. IWSA,
- [Giving Tuesday](https://visionfortomorrow.org/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, VFT sponsored an Aniridia conference for researchers, clinicians and patient groups. That conference spawned a
- [VFT Talks to Dr. Ali Djalilian About Latest Cornea Research and What It Means for the Aniridia Community](https://visionfortomorrow.org/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 by the University of Illinois Chicago (UIC) Department of Ophthalmology and Visual Sciences. Ali Djalilian,
- [Cornea Health and Aniridia: Gene dosage manipulation alleviates manifestations of hereditary PAX6 haploinsufficiency in mice](https://visionfortomorrow.org/cornea-health-and-aniridia-gene-dosage-manipulation-alleviates-manifestations-of-hereditary-pax6-haploinsufficiency-in-mice/) - The Vision for Tomorrow Foundation continues to partner with Ali Djalilian, MD, Professor of Ophthalmology on his ongoing investigations to improve cornea health for those with aniridia and other cornea trauma. Dr. Djalilian is the Director, Stem Cell Therapy and Corneal Tissue Engineering Laboratory at the University of Illinois Eye and Ear Infirmary at the
- [VFT Supports PAX6 International Scientific Meeting at University of Virginia](https://visionfortomorrow.org/vft-supports-pax6-international-scientific-meeting-at-university-of-virginia/) - The Vision for Tomorrow Foundation is excited to participate in the 2019 John F. Anderson Symposium, “Aniridia, PAX6 and Beyond…” at the University of Virginia on November 2 and 3. VFT helped to provide financial support of this important meeting of top researchers from around the world studying congenital eye disorders and the PAX6 gene.
- [VFT Celebrates International Aniridia Day 2021](https://visionfortomorrow.org/vft-celebrates-international-aniridia-day-2021/) - In celebrating Aniridia Day on June 21, 2021, Vision For Tomorrow focused on big and small wins by those in our aniridic community. Throughout the day on Instagram, we recognized academic, athletic, and artistic milestones achieved by several adults and children. If you were unable to check out Instagram, read these stories of perseverance and
- [VFT Partners with NOAH to Support Albinism Research](https://visionfortomorrow.org/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 through support of research. NOAH has announced a request for proposals to support research on the
- [New Aniridia Organization Announced](https://visionfortomorrow.org/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 North American aniridia patients and their families, researchers and clinicians, and patient advocacy organizations. ANA
- [Meet the Researcher: Dr. Djalilian](https://visionfortomorrow.org/meet-the-researcher-dr-djalilian/) - We recently sat down with Dr. Ali Djalilian from the University of Illinois at Chicago. With funding provided by Vision For Tomorrow, Djalilian is studying the use of Mesenchymal Stem Cells for Aniridic Keratopathy. The vision for this research is to provide an alternate and less invasive treatment option to preserve corneal health in patients
- [Brotherly Love](https://visionfortomorrow.org/brotherly-love/) - My brother’s eyes looked a little different when he came home from the hospital, but I wasn’t sure why. I quickly found out. My jaw dropped. It stayed in that locked position for quite a while. I had just been told the most unimaginable thing ever. My brother was partially blind in one eye. I
- [Always Learning](https://visionfortomorrow.org/always-learning/) - As a parent of a visually impaired child, I of course want my daughter to have all of the tools, aides, technology and hopefully one day medicine available to improve her vision. I want these things because I think they will provide Tess an easier life and, most importantly, make her a happier child. However,
- [Glossary of Terms](https://visionfortomorrow.org/glossary-of-terms/) - Acuity - Clinical measurement of the ability to see fine visual detail. Albinism - A genetic disorder causing a decrease in melanin, the protein that pigments the eye, hair and skin. Amblyopia - Poor or blurry vision in an eye that is physically normal. Often caused by a sustained period of disuse, such as occurs
- [Advice For A New Mom](https://visionfortomorrow.org/advice-for-a-new-mom/) - Laura Cross and her husband Craig are the busy parents of three – Cameron, 8, Audrey, 3 and 18 month old Lexi. When Audrey was diagnosed with aniridia at two weeks old, Laura found Vision for Tomorrow and with it a network of support and hope for a bright future for her daughter. The Vision
- [VFT and NEI Partner to Identify Potential Treatments for OCA Patients](https://visionfortomorrow.org/vft-nei-partner-identify-potential-treatments-oca-patients/) - Vision for Tomorrow is proud to partner with the National Eye Institute (NEI), a division of the National Institutes of Health (NIH), to fund a study attempting to identify drugs that will improve vision in people with oculocutaneous albinism (OCA). This study is being led by Dr. Brian Brooks of the NEI, a reknowned researcher
- [The Latest Information on the STAR Research](https://visionfortomorrow.org/the-latest-information-on-the-star-research/) - Phase 2 Proof-of-Concept Study for ataluren in Nonsense Mutation Aniridia PTC Therapeutics’ STAR study is a Phase 2 proof-of-concept study of ataluren, an orally administered, first-in-class, protein restoration therapy for the treatment of nonsense mutation aniridia, a rare genetic disorder that results in disruption in the development of the eye. The STAR study is a
- [Anterior chamber angle in aniridia with and without glaucoma](https://visionfortomorrow.org/anterior-chamber-aniridia-glaucoma/) - The Vision for Tomorrow Foundation is proud to support ongoing work with Peter A. Netland, MD, PhD, Vernah Scott Moyston Professor & Chair, Glaucoma Fellowship Program Director and Robert M. Grainger, PhD, Professor of Biology, both at the University of Virginia. They, along with their team, recently performed a retrospective, comparative study to determine if patients with aniridia and glaucoma had open angles on high-resolution
- [PTC Therapeutics Shares Update on STAR Research](https://visionfortomorrow.org/research-in-the-news/) - Phase 2 Proof-of-Concept Study for ataluren in Nonsense Mutation Aniridia PTC Therapeutics’ STAR study is a Phase 2 proof-of-concept study of ataluren, an orally administered, first-in-class, protein restoration therapy for the treatment of nonsense mutation aniridia, a rare genetic disorder that results in disruption in the development of the eye. The STAR study is a
- [VFT and NEI Partner to Identify Potential Treatments for OCA Patients](https://visionfortomorrow.org/research-in-the-news-2/) - Vision for Tomorrow is proud to partner with the National Eye Institute (NEI), a division of the National Institutes of Health (NIH), to fund a study attempting to identify drugs that will improve vision in people with oculocutaneous albinism (OCA). This study is being led by Dr. Brian Brooks of the NEI, a reknowned researcher
- [The Vision for Tomorrow Foundation Announces New Director of Scientific Affairs](https://visionfortomorrow.org/new-director-of-scientific-affairs/) - The Vision for Tomorrow Foundation is pleased to announce that Dr. Bruce Bloom, President and Chief Science Officer of the non-profit Cures Within Reach, has joined the Vision for Tomorrow team as Director of Scientific Affairs. Dr. Bloom brings more than 30 years of medical research, clinical trial and non-profit management experience to the Foundation.

## Pages

- [Vision For Tomorrow Foundation](https://visionfortomorrow.org/) - The Vision for Tomorrow Foundation seeks to empower people with low vision to have the confidence and ability to achieve their dreams.
- [Map of Aniridia Care Providers](https://visionfortomorrow.org/aniridia-care-providers/) - Map of Aniridia Care Providers with contributions from families with Aniridia - Vision for Tomorrow
- [Donate](https://visionfortomorrow.org/donate/) - The Vision for Tomorrow Foundation depends on your generous contributions. Please donate today!
- [Donate By Credit Card](https://visionfortomorrow.org/donate-by-credit-card/) - Supporting the Vision for Tomorrow Foundation is easy when you donate by credit card.
- [Aniridia](https://visionfortomorrow.org/aniridia/) - Aniridia is a genetic condition and eye disorder that affects people at birth and refers to the absence of the iris.
- [Our Partners](https://visionfortomorrow.org/our-partners/) - About Us - Vision for Tomorrow
- [About Us](https://visionfortomorrow.org/about-us/) - About Us - Vision for Tomorrow
- [Newly Diagnosed](https://visionfortomorrow.org/aniridia/newly-diagnosed/) - If you are reading this section of our website, you are most likely the parent of a child who is newly diagnosed with aniridia. Congratulations on the birth of your wonderful child!
- [Aniridia Resources for Patients and Their Families](https://visionfortomorrow.org/aniridia/aniridia-resources-for-patients-and-their-families/) - The resources are intended to help parents/guardians of students with aniridia engage teachers and school staff, and learn about creating an Individual Education Plan (IEP) that provides appropriate accommodations.
- [Albinism](https://visionfortomorrow.org/albinism/) - Albinism is an inherited condition. People with albinism have little or no melanin, which is a chemical that colors our skin, eyes and hair.
- [Albinism Genetics & Impact on Vision](https://visionfortomorrow.org/albinism/genetics-impact-on-vision/) - Albinism Genetics Most forms of albinism are recessive, which means a child inherits one abnormal gene from each parent.
- [Newly Diagnosed](https://visionfortomorrow.org/albinism/newly-diagnosed/) - If you are reading this section of our website, you are most likely the parent of a child who is newly diagnosed with albinism. Congratulations on the birth of your wonderful child!
- [Support Navigating Aniridia](https://visionfortomorrow.org/aniridia/support-navigating-aniridia/) - Get Support Navigating Aniridia
- [Support Navigating Albinism](https://visionfortomorrow.org/albinism/support-navigating-albinism/) - Get Support Navigating Albinism
- [What Is Albinism?](https://visionfortomorrow.org/albinism/what-is-albinism/) - Our Albinism FAQs answer some of your most pressing questions
- [Albinism FAQs](https://visionfortomorrow.org/albinism/albinism-faqs/) - Albinism FAQs
- [What Is Aniridia?](https://visionfortomorrow.org/aniridia/what-is-aniridia/) - Our Aniridia FAQs answer some of your most pressing questions
- [Aniridia Genetics & Impact on Vision](https://visionfortomorrow.org/aniridia/aniridia-genetics-impact-on-vision/) - Aniridia Genetics
- [Aniridia FAQs](https://visionfortomorrow.org/aniridia/aniridia-faqs/) - Our Aniridia FAQs answer some of your most pressing questions
- [Legal and Financial](https://visionfortomorrow.org/legal-and-financial/) - Legal and Financial - Vision for Tomorrow
- [Contact Us](https://visionfortomorrow.org/contact-us/) - Please contact us with questions, to get involved, or connect with a family support liaisons at info@visionfortomorrow.org
- [Join Us](https://visionfortomorrow.org/join-us/) - The Vision for Tomorrow Foundation is here to provide support and information to those affected by albinism and aniridia. We hope you'll join us!
- [Links We Love - Albinism](https://visionfortomorrow.org/links-we-love-albinism/) - Links We Love - Albinism
- [News](https://visionfortomorrow.org/news/) - The Vision for Tomorrow Foundation is excited to share news and updates about research, giving opportunities, and more!
- [Research](https://visionfortomorrow.org/research/) - A focus on funding research is at the heart of The Vision For Tomorrow Foundation.
- [Meet the Researcher](https://visionfortomorrow.org/meet-the-researcher/) - Meet the Researcher
- [How Vision Works](https://visionfortomorrow.org/how-vision-works/) - How Vision Works
- [Legal Information](https://visionfortomorrow.org/legal-information/) - The Vision for Tomorrow Foundation Legal Information
- [PayPal Giving](https://visionfortomorrow.org/paypal-giving/) - Your generous giving is integral to the Vision for Tomorrow Foundation's ability to help families in need of support. Donate with PayPal Giving

## Headers

- [Vision For Tomorrow Foundation Header](https://visionfortomorrow.org/pixheader-item/vision-for-tomorrow-foundation-header/) - Vision For Tomorrow Foundation Header

## Footers

- [Foundation Footer](https://visionfortomorrow.org/pixfooter-item/foundation-footer/) - Foundation Footer

## Popups

- [Cookie policy popup](https://visionfortomorrow.org/pixpopup-item/cookie-policy-popup/) - Cookie policy popup
- [Information popup](https://visionfortomorrow.org/pixpopup-item/information-popup/) - Information popup
- [Donate by Credit Card (PayPal)](https://visionfortomorrow.org/pixpopup-item/donate-by-credit-card-paypal/) - Donate by Credit Card (PayPal)

## Categories

- [Community](https://visionfortomorrow.org/category/community/)
- [Research](https://visionfortomorrow.org/category/research/)
- [Aniridia](https://visionfortomorrow.org/category/research/aniridia/)
- [Albinism](https://visionfortomorrow.org/category/research/albinism/)

## Tags

- [albinism](https://visionfortomorrow.org/tag/albinism/)
- [research](https://visionfortomorrow.org/tag/research/)
- [Vision for Tomorrow](https://visionfortomorrow.org/tag/vision-for-tomorrow/)
- [cornea](https://visionfortomorrow.org/tag/cornea/)
- [PAX6](https://visionfortomorrow.org/tag/pax6/)
- [aniridia](https://visionfortomorrow.org/tag/aniridia/)
- [Ali Djalilian MD](https://visionfortomorrow.org/tag/ali-djalilian-md/)
- [Aniridia Day](https://visionfortomorrow.org/tag/aniridia-day/)
- [adaptive sports](https://visionfortomorrow.org/tag/adaptive-sports/)
- [Aniridia North America](https://visionfortomorrow.org/tag/aniridia-north-america/)
- [International WAGR Syndrom Association](https://visionfortomorrow.org/tag/international-wagr-syndrom-association/)
- [aniridia research](https://visionfortomorrow.org/tag/aniridia-research/)
- [Giving Tuesday](https://visionfortomorrow.org/tag/giving-tuesday/)
- [International WAGR Syndrome Association](https://visionfortomorrow.org/tag/international-wagr-syndrome-association/)
- [IWSA](https://visionfortomorrow.org/tag/iwsa/)
- [WAGR](https://visionfortomorrow.org/tag/wagr/)
- [low vision](https://visionfortomorrow.org/tag/low-vision-2/)
- [no iris](https://visionfortomorrow.org/tag/no-iris/)
- [Global Genes](https://visionfortomorrow.org/tag/global-genes/)
- [rare disease](https://visionfortomorrow.org/tag/rare-disease/)
- [Rare Disease Day](https://visionfortomorrow.org/tag/rare-disease-day/)
- [Global Albinism Alliance](https://visionfortomorrow.org/tag/global-albinism-alliance/)
- [ISCA](https://visionfortomorrow.org/tag/isca/)
- [InternationalScientificAlbinismConference](https://visionfortomorrow.org/tag/internationalscientificalbinismconference/)
- [patient support](https://visionfortomorrow.org/tag/patient-support/)
- [Great Nonprofits](https://visionfortomorrow.org/tag/great-nonprofits/)
- [Pax-6](https://visionfortomorrow.org/tag/pax-6/)
- [Light up for Rare](https://visionfortomorrow.org/tag/light-up-for-rare/)
- [fundraising](https://visionfortomorrow.org/tag/fundraising/)