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.
Our Supporters
The Board of Directors expresses gratitude to the following individuals and organizations for their support of the VRF mission.
- Lifetime BenefactorsAksenov Family Foundation

- Distinguished Benefactors

Google Inc. - Distinguished SponsorsIncyte

- Distinguished Patrons
- <Anonymous>
- Anna Altukhova
- Audrey VanStockum
- Dutchphone Holdings Inc.
- Jose Luis Manzanares
- Rajanikanth Kanakameda
- Sean O'Donnel
- Shannon McIntush
- Steve Klein
- Teleup LLC.
- TVOE Inc.
FAQOther Questions
- What joining a clinical trial actually looks like?
Pediatric vitiligo trials · Taking part Cream twice a day, scheduled visits and the practical questions every mother asks before committing the family calendar. The studies disc...
- I have vitiligo: will my children have vitiligo, too?
If you have vitiligo, it’s natural to worry about your children. While there is a genetic component, vitiligo is not a straightforward hereditary disease like eye color or heigh...
- Is there a special diet for vitiligo?
Recent research highlights the potential of diet and nutrition in managing vitiligo, offering an alternative where traditional therapies may be lacking. However, the relationshi...
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.