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.
Hi Friends, I'd like to share with you some thoughts.First of all, * from the web*:Functional Medicine addresses the underlying causes of disease, using a systems-oriented approach and engaging both…Continue
Friends,I'm convinced that the only way to counter attack vitiligo is following a Functional Treatment (FT). I haven't seen a case yet that a FT didn't improve vitiligo. Stop spreading is the main…Continue
CLINICAL TRIALNEW CLINICAL TRIAL IS AVAILABLE FOR VITILIGOWe are pleased to share news about a new nationwide clinical trial for vitiligo. The name of the trial is “An Open-Label Pilot Study of the…Continue
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