This survey is for people living with vitiligo and for caregivers of people with vitiligo.
Vitiligo Patient Views: The First Global Vitiligo Patient and Caregiver Exprience Survey
The Vitiligo International Patient Organizations Committee (VIPOC) is conducting this survey to understand the experiences of people with vitiligo and those who care for them.
Survey outputs will be analysed to inform the development a global whitepaper, which will be used to drive policy change for vitiligo.
This survey should take approximately 20-30 minutes to complete.
Click below to access the survey in your language.
VIPOC board members thank you for your participation and for your input into improving the lives of people living with vitiligo, globally.
In collaboration with and with the support of the following scientific societies and organizations:
