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.
Good News for Vitilego Patients Hi, All, Hope you guys doing well, My name is Mosh, and I have vitilego since years.. maybe more than 14 years. i was worried about my skin a lot, and came here on…Continue
I started this network because I have vitiligo. My vitiligo is very moderate, and I am light-skinned, so may not be too noticeable. But I've always wanted some more immediate forum for those with…Continue
I started PC-KUS combined with narrowband UVB in October 2014. I went to Jordan in 2015 to take part in the Dead Sea treatment (an amazing and fun experience) as well.But, I've seen only very minor…Continue
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