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.
Event
VITFriends Vitiligo support group meeting in New York
Clinton Hill Branch Library. 380 Washington Ave, Brooklyn, NY, USA
Our first meeting in October was a great success. Everyone left with a sense of belonging and peace. Come see what we're all about! Hope all coming from near and far can make it on Saturday, November 22, 2014, between 3:00 PM and 5:00 PM.
If you would like to attend, please contact Pat (mochanet@verizon.net) or Shazaad (vitiligocamo83@gmail.com)
More details at http://www.meetup.com/VitFriends-NYC-Vitiligo-Meetup/events/217343122/
FAQOther Questions
- I have vitiligo: will my children have vitiligo, too?
If you have vitiligo, it’s natural to worry about your children. While there is a genetic component, vitiligo is not a straightforward hereditary disease like eye color or heigh...
- I have a new job - should I tell colleagues about my vitiligo?
Starting a new job can be both exciting and nerve-wracking, — especially if you’re concerned about stares or questions regarding your skin. Taking a proactive approach can help ...
- Which diseases most commonly accompany vitiligo?
Vitiligo is rarely an isolated event. Because it involves an overactive immune system, it often coexists with other autoimmune disorders. According to extensive 10-year clinical...
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 JúliaBy taking a little time to fill in the anonymous questionnaire, you can help researchers better understand and fight vitiligo.