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At a recent meeting in Vancouver (Canada), leaders of vitiligo support organizations from 5 continents established a World Vitiligo Alliance, and invite leaders of other organizations to join. This is a major development in vitiligo area and more details will be released soon at www.worldvitiligoalliance.org
In the photo, from left to right: Jean-Marie Meurant (AFVitiligo, France), Ogo Maduewesi (VITSAF, Nigeria), Dr. Maya Tulpule (Shweta, India), Dr. Adrian Mar (Vitiligo Association, Australia), Yan Valle (Vitiligo Research Foundation (USA)
FAQOther Questions
- How can I cure vitiligo?
Currently, there is no cure for vitiligo. However, many treatments can help manage the condition by restoring skin pigmentation, halting the progression of depigmentation, and i...
- 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 eas...
- I have vitiligo: will my children have vitiligo, too?
If you have vitiligo, you might wonder about the chances of your children developing the condition. While there is a genetic component, vitiligo is not a straightforward heredit...
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.