Do you want to share your #Vitiligo story?
Whether you have been personally affected by this skin condition or have had a close experience with someone who has, now is your chance to submit a 500-word essay about how Vitiligo (or the Vitiligo Pride Community) impacts you.
The first place winner will be awarded $100, and two second place winners will be awarded $75. Five participants will also be awarded a copy of Yan Valle’s “A Nonsense Guide to Vitiligo.”
Submit by May 20th through the Google form and good luck to all!
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- Who is prone to vitiligo?
Scientists know that some people are genetically predisposed to a specific group of autoimmune diseases – including generalized vitiligo – but do not know who and why.It doesn’t...
- Is it Bitiligo? Vitaligo? Veteligo?
There are so many different ways that people try and spell or even pronounce Vitiligo. Here are some common mis-spellings: bitiligo, vitigo, vitaligo, vitilago, vitiglio, vita...
Our work is entirely funded by private donations – we receive no money from government. Your money will help us continue funding research into vitiligo and supporting people affected by the condition.
Though it is not always easy to treat vitiligo, there is much to be gained by clearly understanding the diagnosis, the future implications, treatment options and their outcomes.
Many people deal with vitiligo while remaining in the public eye, maintaining a positive outlook, and having a successful career.Copyright (C) Bodolóczki Júlia
By taking a little time to fill in the anonymous questionnaire, you can help researchers better understand and fight vitiligo.