Welcome to the Vitiligo friends network. This is a place where those with Vitiligo, their family, and their friends can share information and stay in touch. Started in 2007, we are now over 7,000 members!

Please consider going to the forum and posting a welcome message. Be sure to let us know what part of the world you are from. You can also use the search box at the top right to look for topics that are already in discussion!

To avoid spammers on the network, we have to approve your membership after you sign up to join (filling out the profile questions helps us a lot). If you send spam or inappropriate messages you will be banned from the network. If you receive unsolicited off-topic messages, or see any inappropriate material here, please report it. We have a no-tolerance policy for those who claim a "cure" or use this space to advertise.

So glad you are here!

--Steve

P.S. Commercial posts, including repeated endorsements of "cures," will be removed.

Research:

• National Vitiligo Foundation, Inc. (NVFI)

Support:

• Vitiligo Support International (VSI)
• Vitiligo Support and Awareness Foundation (VITSAF)
• Vitiligo Bond
• VITFriends Facebook
• VITFriends Website

Children:

• American Vitiligo Research Foundation (AVRF)

International:

• AFB Association Francaise du Vitiligo
• AriV - Associazione Ricerca Informazione per la Vitiligine
• ASPAVIT asociacion de pacientes de Vitiligo
• Deutscher Vitiligo-Bund e.V. (Germany)
• DVV Deutscher Vitiligo Verein e.V.
• Italian Vitiligo Society
• Korean Vitiligo Association
• Spanish Association of Vitiligo Patients
• SSPV+ La Societe Suisse du Psoriasis et du Vitiligo
• Vitiligo Society UK
• Vitiligo Hungary (Hungarian)

Resources:

• Dr. Boissy Basic Vitiligo Information Paper