Vitiligo Friends

Make Friends, Share Healing Ideas, Inspire Hope

Welcome!

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!

--Steve

P.S. Commercial posts, including repeated endorsements of "cures," will be removed.

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Want to be my friend

Started by Harshal. Last reply by Monika Chauhan 22 hours ago. 1 Reply

I am from Mumbai looking for new friends with same condition. Thanks.

Most comprehensive video about vitiligo (causes and solution)

Started by Robot. Last reply by Robot yesterday. 20 Replies

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

Would you like my products? Misdiagnosed and no longer need them. FREE!

Started by Melissa Freeman. Last reply by Melissa Freeman on Tuesday. 2 Replies

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

punch grafts for vitiligo on fingers

Started by navin. Last reply by navin on Tuesday. 2 Replies

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

How do I . . . ?

Started by Marilyn Washington. Last reply by JD CLARENCE on Tuesday. 3 Replies

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

Rituxan as a treatment option

Started by Ann Jul 8. 0 Replies

Was wondering if anyone heard of or discussed with their doctor trying Rituxan as a treatment option. It is an intravenous infusion. Studies were done several years ago and it did show some promise.

Callumae supplement - anyone have any luck??

Started by Kevin. Last reply by Robot Jul 5. 3 Replies

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

What to use with UVB?

Started by Kevin. Last reply by Robot Jul 5. 12 Replies

I have an at home UVB wand that i use 2-3x per week, along with protopic and sterroid cream rotated. I have been using the UVB with some oil bought from the Merri Clinic that doesnt seem to be doing…Continue

Don't worry

Started by titu. Last reply by titu Jul 4. 5 Replies

Everyone my vitaligo friends Do you konw about the (clovate 0.5mg/g cream) ..... Many of my friends told me it's very usefull...its uk or germane brand and available in india..I v given this cream…Continue

sunscreen...for kids..

Started by babu. Last reply by Robot Jun 30. 2 Replies

pls suggest me a good sunscreen/sunblock wich can be safely used on kids..and also if anything u know abt chemicals in sunscreens that would aggrevate vitiligo...pls share..Continue

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    Send Your Photo to Our "Uniquely Beautiful" Site!

    Uniquely Beautiful showcases the unique beauty of those with Vitiligo--both for others to see, and for those of us with Vitiligo to appreciate our own beauty. While our VitiligoFriends.org is a private network, Uniquely Beautiful is a separate site for public view in order to encourage others with Vitiligo. However, there are no names or contact information, just photos of faces.

    To have your photo be part of Uniquely Beautiful send a face shot or a photo that has your face in it (without makeup, and whether or not you have Vitiligo on your face). We'll add it to the wall of beautiful Vitiligo faces. Someone with Vitiligo coming to this site might feel instantly better about him or herself, knowing the rest of us exist. Someone who doesn't have it would hopefully begin to recognize the diversity and beauty of who we are.

    UniquelyBeautiful.net

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