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.
Friends,It took me a while to decide to write this post about vitiligo on hands. Although the post is strait forward regarding the very low chances to re-pigment, it also brings good news about…Continue
Because of more and more hot weather, how to prevent the spread of vitiligo.Continue
Vitiligo is an auto-immune disease which is affected by various people of any age, sex, and constitution. There is a loss of normal skin color and the skin turns white when an individual suffers from…Continue
Hi Friends,I recently came across a very interesting article on vitiligo which I feel one must be aware of. This article helps us to understand about vitiligo, causes and role of homeopathy…Continue
Dear all i am suffering from vitiligo from 10 years . My viligo got unstablized after stopping betnosol forte. i am taking PUVB treatment also doesnt help . please suggest me what to do .Continue
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