Live, enjoy and dare..... also with vitiligo!

Contact with fellow sufferers

Are you young, do you have vitiligo and would you like to talk to fellow sufferers? Good idea, because it helps!
You'll see that you're not alone, and that can help you come out of the wings.

Fellow sufferers can support and cheer each other up. You can find fellow sufferers of your own age by becoming a member of the association. This costs 28 euros per year (from 2022) and you will then receive the glossy magazine four times a year. Spotlight!, in which you read stories of fellow sufferers of all ages. So also children, young people and young adults. Plus the latest news about treatment options and research. With your annual contribution you also support much-needed research into vitiligo.

Meetings and exchanging experiences
The association also organizes a meeting day at least once a year, where you can speak to fellow sufferers.
The association also maintains a private membership Facebook groep in which fellow sufferers exchange experiences.

As a member of you will quickly find fellow sufferers. Register quickly!