VIPOC

Why does this survey matter?

We know that vitiligo affects people beyond their appearance, but we need to know more to truly make a difference

If you are a person living with vitiligo, or a caregiver of a child with vitiligo, take our survey now: https://bit.ly/4etDKLW

Make your voice heard!

The first-of-its-kind global vitiligo survey is coming!

Vitiligo Patient Views is the first-of-its-kind global patient and caregiver experience survey, led by VIPOC and globally available in 16 languages. Its goal is simple: to capture the real, lived experiences of people with vitiligo and those who care for them, and transform that evidence into meaningful change

Vitiligo Patient Views: The First Global Vitiligo Patient and Caregiver Experience Survey launches on 15th May.

Help us capture the whole vitiligo picture.

Read more: https://bit.ly/4ncEO99

Without formal membership, your local vitiligo organisation could be missing global strategy, credibility, and advocacy power.

VIPOC now offers a structured membership system tailored for vitiligo leaders because unity isn’t automatic, it’s chosen. Whether you're an emerging group or an established network, joining offers alignment with a global advocacy community.

• Affiliate Membership: For organisations testing VIPOC’s benefits
• Associate Membership: For established advocates needing guidance & shared resources
• Active Membership: For leaders ready to represent vitiligo on the world stage
Membership ensures your organisation gains credibility, access to training, collaboration tools, and advocacy support

Convert your leadership into a global impact officially.

Swipe for membership tiers info, then tap the link in our bio to register your organisation as an Affiliate, Associate, or Active Member of VIPOC, and unlock global advocacy support today.