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,The following is the most comprehensive video (by Dr. John Bergman) about vitiligo that I have seen. It explains the likely causes and solution.I hope you are patient enough to watch it…Continue
Hello Friends! I was recently un-diagnosed with Vitiligo (which explains why the expensive lotions/creams I bought weren't helping) but I have some products I'd like to give away to someone who will…Continue
Had a doctor visit and he was suggesting me to do punch grafts on the hands. Wondering if anyone tried it ad what is the success ratio ?Plan is to do the grafts and continue with the laser…Continue
I am trying to figure out how to manage to go to the grocery store, hair salon, dentist, etc. Does anyone have any advice or suggestions? Some of my thoughts have been along the lines of trying to…Continue
Has anyone had luck taking "Callumae" tablets and seeing repigmentation?? I do UVB, sun exposure, protopic, sterroid cream (rotate the two) and wonder if I should take something internally. Was…Continue
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