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 6,000 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.
After seeing the link to the telegraph article on these very forums, I decided to follow the google trail and came across the case study for anyone interested.Published in JAMA Dermatology - Yale…Continue
I am thinking about trying pseudocatalase cream. If any of you have tried it please let me know if it worked for you. I am currently using uv treatment and it is working but I want to try something…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
Hi everyone,I've previously posted on Clinuvel's clinical study program, evaluating the safety and efficacy of our drug SCENESSE (afamelanotide 16mg) in generalised vitiligo. The company has just…Continue
Check it out:…Continue
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