Tell your vitiligo story. Tell us about some of the treatments you have used. What are you doing now with medical students? Your role with this organization. What are your hope and dream for the future for Vitfriends and also for your own vitiligo. Because of your job you are always in the public, how is that for you as your vitiligo continues to progress?
How long has he had vitiligo? How has it been to minister with the condition? What percentage of his body has vitiligo? What has the support been like from spouse, family, friends, church? Would you ever consider re-pigmentation?
Sharing how she lives and deals with Vitiligo. Also, what is her new project and how can it help individuals with Vitiligo? How long has she had Vitiligo?
How long have you had Vitiligo? How do you handle your VIT? What would you like to change right now? Does other family members have VIT? What treatments have you tried if any? Would you ever repigment?
How long have you had Vitiligo? How was your teenage years with VIT? Does other family members have VIT? What medical treatment have you tried? Would you ever repigment? How does your family deal with your VIT? What and how would you encourage someone who was recently diagnosed with Vitiligo? We would love to have our conference 2012 in Hartford, is there a vitiligo community there?
A conversation with a FRIEND about how she handles her Vitiligo? How long has she had Vitiligo? What can she share with others who are battling and struggling emotionally with Vitiligo?
27 min
About VITFriends VITILIGO Support Group
From the publisher's feed
A Vitiligo Support, Education and Awareness Network.