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 all I am thinking of getting my Covid 19 vaccine on the 2nd of September 2021 but I am still not 100% sure if its safe for a person with Vitiligo.Did anyone on the forums took the vaccine already…Continue
Hi AllI want to know if Narrow Band UVB Phototherapy really works in treatment of Vitiligo ?Continue
Do vitiligans seek to have relationships with other vitiligans, because of fear of being accepted by those who dont have vitiligo... Who do you feel comfortable dating and why?Continue
Hi everyone! A few months back I noticed quite a few people on here whowere interested in forging relationships and/or looking for a romanticconnection, so i started a site for vitiligo singles. Come…Continue
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