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We address every phase in the vitiligo drug discovery process, from basic research all the way to the clinic, in order for new treatments to reach patients. At the Vitiligo Research Foundation, we have only one incentive: to bring a vitiligo treatment to market for nearly a 100 million people worldwide who are affected by this devastating condition.
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FAQOther Questions

I have a new job - should I tell colleagues about my vitiligo?
Starting a new job can be both exciting and nerve-wracking, — especially if you’re concerned about stares or questions regarding your skin. Taking a proactive approach can help ...
Shall I try low-fat diet for my vitiligo?
The link between dietary fat and autoimmune diseases like vitiligo is a compelling yet complex puzzle that continues to intrigue scientists. While the conversation is ongoing, o...
Vitiligo and Pregnancy
VRF Frequently Asked Questions Vitiligo and Pregnancy Pregnancy, treatments, inheritance, fertility and the questions people usually remember to ask five minutes after leaving t...

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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.

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.
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By taking a little time to fill in the anonymous questionnaire, you can help researchers better understand and fight vitiligo.