Comments

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  valarie July 3, 2013 at 3:41am

  my name is Valarie and I am the president of VITFriends VITILIGO Support Group in Boston, MA. www.vitfriends.com We were honored on June 26 to share with the Boston City Council at City Hall all about vitiligo and our support group. Our conference in July 27 at Phillip Old Colony near UMASS - Boston and so we hope that you can come. Our guest this year are from: RI, TX, NC, SC, NH, MA, NY, so we invite you.  https://www.youtube.com/watch?v=lbsmUfx6S0ADelete Comment
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  Marty BlackEagle-Carl June 2, 2011 at 2:42pm

  hey, Hope the tornado didnt cause any damage to you or yours.

   
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  Keigan Williams October 20, 2010 at 3:08am

  Hi Kim- I was diagnosed with Vit in about Nov 2008. Started as speckles on my left side forehead and quickly turned into a large patch. I did lots of research and found a derm in my area that did treatments. He started me on Xtrac (which tends to work really well on facial vit) and I have since seen great results. What started as a large white patch is now down to a small nickle sized white patch. So needless to say, I am finding success. Not sure what the future will hold, but I am trying to stay positive! Also, insurance does not cover said treatments so, they do get expensive, but soo worth it in the end. I still need to post pix of my progress (before and after). Good Luck! :) Im soo glad we have this site to share success stories!!