Were winding down our scientific programs to focus on policy-making and education.
This is a unanimous decision made by the VR Foundation Board of Directors, after careful deliberation about how best to serve the vitiligo community. In a way, we are a victim of our own success in transforming the landscape of vitiligo research, awareness and funding.
Our work has profoundly changed the lives of nearly 100 million vitiligo sufferers and their families. But this comes at a cost - in time, money and effort. The increasing range and volume of global activities is overwhelming our small non-profit organization. Something had to give, which is a major reason for withdrawing the scientific programs.
We have achieved far more in the scientific field than we thought possible, but now its time to draw back. We must consider what remaining elements of our scientific program should continue, and how to facilitate free access to our data.
You deserve a full explanation. Check out your mailbox for our newsletter this weekend and you will learn where do we go from here.
This is in no way an epilogue for the VRF. Its simply an announcement of a new chapter in our story.
CEO VR Foundation
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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.Copyright (C) Bodolóczki Júlia
By taking a little time to fill in the anonymous questionnaire, you can help researchers better understand and fight vitiligo.