We are commired to transparency in our financial reporting and the effective stewardship of our assets as mandated by our mission and by our Board of Directors.
How We Spend Your Money
We believe the most efficient way to finding a cure for vitiligo is by directing as much grants funding as possible to the best and most innovative researchers. The VRF Scientific Advisory Board identifies and evaluates evaluates the best targets for our funding, ensuring your donation has the greatest possible impact.
Annual grants awarded by the VRF allow scientists to pursue groundbreaking research leading to new insights into vitiligo origins, triggers and, ultimately, to new treatments. We support investigations with the potential for rapid clinical application and understand the importance of supporting projects in all stages of development. This enables VRF-supported researchers to generate the clinical data and biosamples necessary to leverage and secure additional funds from other foundations and government agencies.
Your Donation Dollars At Work
We have recently awarded these grants to help start or continue promising new vitiligo research projects. Not only do these grants promise to advance the understanding and treatment of vitiligo, but they are also critical to attracting and retaining the interest of top scientists.
Financial and Business Disclosures
If you have been kind enough to donate to us, please remember that we are a 501 (c) (3) not-for-profit organization, your donation is fully deductible as a charitable contribution. Our tax ID # is 45-2498489.
To learn more about tax dedictible contributions see IRS Publication 526.
The IRS Form 990 is the annual tax return that nonprofits in the US submit to the Internal Revenue Service. It provides detailed information about a nonprofit’s income, expenses and operational activities, allowing donors to evaluate how effectively the nonprofit is performing.
- IRS Determination Letter (PDF)
To be part of our campaign to cure vitiligo, please make a donation. No gift is too small and your contribution will directly support vitiligo research and awareness programs.
If you have any questions regarding your donation or our finances, please contact us.
I support the petition to designate June 25 as Vitiligo World Day and save millions of people worldwide from social isolation and persecution.
What is coming?
Expert Answers Most Frequently Asked Questions about Vitiligo
Join us for a Live Facebook event with Erika Page from Living Dappled. We'll bust common myths about vitiligo and answer your most frequently asked questions. Date: J...25 January 2018 12:00, Facebook Live
First NY Vitiligo Community Group meeting of 2018
will be on Thursday, February 8th, from 7PM - 8:30PM on the 11th floor of NYU's Ambulatory Care Center at 240 East 38th Street, between 2nd and 3rd Avenue Since this ...08 February 2018 07:00, NYU's Ambulatory Care Center at 24...
How can I cure vitiligo?
There is no cure for vitiligo, but there are a number of effective treatment options that can be discussed with your GP or dermatologist. The aim of treatment is to st...
Is vitiligo contagious?
Vitiligo is NOT contagious. It cannot be passed on or caught from touching someone with vitiligo, shaking hands, swimming in the same pool, sharing towels, sitting nex...
Can Ginkgo Biloba help with vitiligo?
Ginkgo Biloba extract seems to be a simple, safe and fairly effective therapy for arresting the progression of the vitiligo. Ginkgo Biloba is known to have anti-inflam...