Lee Thomas

Posted on December 19, 2007

Lee Thomas

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    1. C. Battise on 7-4-2008   edit

      Mr. Lee Thomas,

      Thank you for writing the book about your experience with vitiligo. I plan to meet you at the conference in San Antonio. The public need to know that vitiligo is not contagious. It makes me self conscious to look different at this time in my life. But, I take it in stride and thankful that it is not something worst. I have done my own research over the last few years. I have had light treatments,skin creams,change of diet, pills which guaranteed pigmentation,and many dermatologists. I think the B-vitamins helped tremendously through my own research. I am now using x2o,and see positive changes daily.
      Thank you so much for sharing your story. When people talked about Michael Jackson, when he was on the daily news and comments that he wanted to be white was not true. One would have to be cognizant of what is really happening with this skin disorder, and everything that looks like vitiligo is not. The disorder has to be diagnosed by the dermatologist with a Wood’s lamp examination.

      I see commercials for skin disorders, but VITILIGO is never mentioned. Therefore, this skin disorder is not exposed to pulic awareness.
      Beneath the outer skin,we are really alike some were kissed by the sun a little longer that’s all. A great lesson in life. I’m just glad to still be here.
      C.B.

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