Archive WVD 2014

This year, the campaign headquarters moved to Chandigarh, India, under the presidency of Prof. Davinder Parsad. World Vitiligo Day'14 was the biggest yet, with a vast array of awareness and support events spanning the globe. Celebrations run the entire week, to accommodate multiple presentations, speeches and other events aimed at the patients and healthcare community. We have already set up two new 'world records' with 225 vitiligo patients seen by dermatologists at PGIMER in the morning, and 800+ doctors attending events in the afternoon. Forty WVD-branded rickshaws paraded the city all day long.  Read more

Why Is It Important

There are a lot of people who don't want you to stand up for your rights and demand a cure. They say vitiligo is not life threatening and not contagious, and you must embrace a life of a pariah, hiding yourself from sunlight and from the society.

Vitiligo is an under-researched disease resulting in milky white skin patches on the skin. The breadth and complexity of the disease require international collaboration in therapy development. The severity of the disease calls for national healthcare support.

So, speak up for your condition and your rights. Sign the letter to tell the UN Secretary-General that you want recognition and support. It would be appreciated if you could give every member of your family or group an opportunity for signing.

Signatures count

We have collected 502815 signatures of the target 500000 (100.56%). Now let’s get 1 million signatures!


Firmly committed to curing Vitiligo, the VR Foundation is a non-profit organization funding and fast-tracking medical research globally. We challenge the disease of vitiligo with educational and medicinal enlightenment. We care; we educate; we advance knowledge. We are the VR Foundation.

Partners and Sponsors