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  • I am interested.  But don't refer to us as u people.  We are people period.  Just like everyone else.  We just happen to be members of The Vitiligio Support Group.  Do you have a web site?  What is your approach?  What results are you looking for.  How will you use this information?  How do we contact you?  Have you ever done a research project before?
    • Thanx for ur positive response..sorry if u have minded my word "u people".As by using this word i didn't mean some thing wrong but just were taking as community. but i will care and will not use this word. No i don't have website. I want to check psychological effects like depression, stress, self-esteem, fear of negative evaluation and perceived social support. Information of every person will be confidential and i will just use total scores in my results. No personal information will be used. If i may get positive responses here then i will upload my questionnaires and will appreciate evrey one's participation. Yeh i have done some researches on small level but havn't published yet. But this one is my main project.
      • Cool.  I will be more than happy to participate.  Information like this can be helpful in dealing with insurance carriers.
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