Resources

Vitiligo is an autoimmune disorder that manifests in the progressive destruction of the skin’s pigment-producing cells. This results in white patches on the skin and in some cases white hair. Vitiligo is not contagious. Research suggests that it may be hereditary but here is still a lot to uncover about this disorder. Currently, there is no cure for vitiligo. 1% of the world's population has been diagnosed with vitiligo. That's over 75 million people. 


If you have a medical concern, you should consult with your primary care professional.

The Litty Ligo™ Peer Support Channel

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Please visit our YouTube Channel! Check us out for all kind of videos and event recaps! Hear from the collective and viewers like you!

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Houston Vitiligo Awareness Movement

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Hosting this year's World Vitiligo Day Conference with a focus on mental health, HVAM does amazing work in the vitiligo community! Lead by Diane Wilkes-Tribitt and based in Houston, Texas, the HVAM organization lives up to it's name by raising awareness in a number of ways and WE STAN!!

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The Pigment Painter

Pigment Painter

Lauren Reid is a self taught artist who helps people living with vitiligo share their stories through beautiful watercolor portraits. Check her out on Instagram and Facebook!

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Aarus Foundation

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Based in Mumbai, this non-profit's objective is to develop understanding of people living with vitiligo by sharing experiences and views. Founder Akash Tiwari is very active in his community as people living with vitiligo are treated very poorly in India.

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Living Dappled

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Founded by the amazing Erika Page, Living Dappled is a blog site catered for and by women living with vitiligo. 


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Unite for Vitiligo

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This interactive platform based in India is a new and useful resource for those of us  living with vitlligo! Editor Anshul Singh  gives us new posts every week.

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coming to an event near you!

Litty Ligo offers educational, interactive presentations for all ages, groups and organizations. Let us know what you need!

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