Make Friends, Share Healing Ideas, Inspire Hope
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!
P.S. Commercial posts, including repeated endorsements of "cures," will be removed.
Hello everyone,I have decided that as soon as I turn 18 I am going to get a tattoo with a design which shows to people that I am completely comfortable with my vitiligo and I have come to accept and…Continue
My name is Dina and from beautiful State of California. Grateful I found this group and found comfort with knowing I am not alone. We know how it is to live with Vitiligo and can relate with one…Continue
I have had vitiligo for 13 years now and I haven't had that many issues when it comes to it spreading as it has only ever caused a new patch once every few years or so. However, in the last year I…Continue
Dear Sir,First of all I want to thank you for creating such a wonderful and unmatched forum for the people suffering from Vitiligo and their relatives. I have used the information available here from…Continue
Disconnected (4 online)
You are disconnected from chat. Connect to join the chat.
Sign up to chat on Vitiligo Friends.