Our work is entirely funded by private donations – we receive no money from government. Your money will help us continue funding research into vitiligo and supporting people affected by the condition.
Results To Date
Since 2010, VRF has helped move vitiligo from the margins into a more connected world of research, patient advocacy, medical education and global collaboration.
Some of our work is easy to count: countries reached, doctors trained, tools built and people connected. Other results took years to become visible. Here are a few milestones we are especially proud of.
Since 2010, VRF has helped move vitiligo from the margins into a more connected world of research, patient advocacy, medical education and global collaboration.
Some of our work is easy to count: countries reached, doctors trained, tools built and people connected. Other results took years to become visible. Here are a few milestones we are especially proud of.
Established World Vitiligo Day on June 25. It is now reaching over 120 million people worldwide.
Built the first of its kind AI-Guide On Vitiligo with interactive avatars answering questions in over 50 languages.
Built the Vitiligo Patient Journey Map, a guide through the maze of diagnostic decisions, treatment options, non-treatment paths, and the lifestyle decisions in between.
Organized international Master-Classes on Vitiligo in 11 countries, educating over 3,000 medical professionals, including collaborations with two Nobel Laureates.
Created an open-access World Vitiligo Map, a global directory to connect vitiligo researchers, patient support groups, and activists around the world.
Successfully brought skilled researchers and practitioners into the field, expanding the expertise and innovation dedicated to vitiligo.
Published extensive literature on vitiligo, including over 50 articles, four books, and numerous reviews in prestigious scientific journals.
Established and supported vitiligo support groups and clinics across four continents, providing crucial resources and care for affected individuals.
Launched a networked Vitiligo BioBank across 9 locations, supplying initial funding and biosamples for local researchers, all linked by the Vitiligo CloudBank—the first electronic health record system for vitiligo.
Accelerated first drug development for vitiligo by providing critical insights to regulatory bodies and pharmaceutical companies, contributing to recent breakthroughs in vitiligo treatment.
We are mostly funded by donations, so without your support we would simply cease to exist. To ensure we continue the fight against vitiligo, please donate today.
We are mostly funded by donations, so without your support we would simply cease to exist. To ensure we continue the fight against vitiligo, please donate today.
FAQOther Questions
- Shall I take vitamin D for my vitiligo?
Vitamin D plays a central role in the prevention of different inflammatory and chronic diseases. Consuming 1,000–4,000 IU (25–100 mcg) of vitamin D3 daily should be ideal for mo...
- PTSD in Vitiligo?
Living with vitiligo often involves more than managing visible skin changes. Many individuals face discrimination, social stigma, and feelings of isolation, leading to emotional...
- Is there a traditional medicine to treat vitiligo?
Traditional remedies can be helpful for managing stress or general metabolic health, but when it comes to vitiligo, the evidence is limited. While some natural supplements provi...
Though it is not always easy to treat vitiligo, there is much to be gained by clearly understanding the diagnosis, the future implications, treatment options and their outcomes.
Many people deal with vitiligo while remaining in the public eye, maintaining a positive outlook, and having a successful career.
Copyright (C) Bodolóczki JúliaBy taking a little time to fill in the anonymous questionnaire, you can help researchers better understand and fight vitiligo.