Je vis avec le vitiligo

je vis avec le vitiligo mais dieu merci j'ai une bonne formation et je suis juriste malgré les tracasseries que je rencontre ma pensée va droit aux autres personnes vivant avec le vitiligo et qui vivent pire que ce que je vis j'ai ouvert un interface vitiligomondial facebook et je souhaiterait faire parti des acteurs du combat pour une meilleure prise en charge de nos frères merci

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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.

Take part in survey

Quality Of Life Study (10 questions)

Vitiligo Study (49 questions)

Signatures count

We have collected 15326 signatures of 500 000 (3.07%)

VR FOUNDATION: SPONSOR OF THE DAY

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.