Share Your Vitiligo Story
We would love to hear your thoughts! Do you have a story to tell about your vitiligo? Would you like others to know how your life has been affected? This is your opportunity to let others know what it is like to live with these conditions.

*The negative and the positive effects.
*Patient perspective.
*Share your thoughts and let others see the impact.

It's up to you, if you just want to get something off your chest, here is your chance.

You can submit anonymously or share your name.

We will add stories to this website, future documentaries, and with your help build a picture of the extent these conditions have on real people and their lives.

Please note: We will not publish your name and may edit your story to protect the privacy of others mentioned.

No! It's Called Vitiligo!
VBI Interviews Beautiful MeShona
Vitiligo Selfie Video Clip Upload
If you don't want to share your story you can get involved by doing the following!

Here's a fun selfie one liner you can say and do with your phone's camera.
Email all video clip to info@vitiligobond.org. Your video clip may be chosen to be in a future documentary called, No! It's called Vitiligo.

Here's what to say below:

No! It's called Vitiligo

Your story about vitiligo *
Your answer
Name *
Your answer
Email *
Your answer
Gender *
Country, City, State *
Your answer
Submission
By submitting my story or video clip, Vitiligo Bond and partners, can publish it on this website, social media and use it in other publications.

I agree

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