Спонсоры

 

Firmly committed to curing Vitiligo, the VR Foundation is a non-profit organization funding and fast-tracking medical research globally. We are challenging vitiligo with educational and medicinal enlightenment. We educate; we advance knowledge; we care. We are the VR Foundation

 

 

 

 

 

VITSAF’s mission is to provide Public Awareness and Enlightenment on vitiligo through education, entertainment, dedicated work and counseling. We seek to improve the Quality of Life of people distressed by vitiligo, primarily in West Africa.

 

 


 

National Vitiligo Foundation Inc - National Vitiligo Foundation is a patient oriented site dedicated to information on the cure and treatment of vitiligo.

 

Vitiligo Support International (VSI) is a nonprofit organization providing support, information and educational resources for vitiligo patients, their families, and health professionals. The VSI provides free quarterly newsletters to 50,000 registered members, which include medically reviewed articles on current vitiligo news, the "What's On Your Mind” column answering patient questions, latest research, and clinical trial recruitment announcements. The VSI website includes support group meeting announcements, active message boards for all ages, a physician locator, vitiligo product listing and library.

 

 

The World Health Academy is a foundation established under Swiss law with the objective of providing leadership on global health matters, forming a global health agenda, facilitating a platform for the continuing medical education.

The Jundiaí Medical School was founded in 1968, as an autarchy, located 50km from São Paulo, in one of the most developed regions of Brazil. It is a high-concept School, assembling two reference hospitals. This Medical School has graduated around 2500 doctors. It has also residence in dermatology, which is recognized by the Brazilian Dermatology Society, for over 30 years, being one of the most disputed from Brazil. Professor Paulo R. Cunha MD, PhD is the chairman of the Department of Dermatology in Jundiaí Medical School- São Paulo- Brazil.

We strive to provide everyone with vitiligo, a chance to live a good life. This is why the Swedish Vitiligoförbundet focuses on activities that will lead to increased investment in research, greater opportunities for better care and treatment, and to disseminate information about the complex disease.

Vitiligo Society of Kenya (VISOKE): Beauty Beyond the Skin

Vitiligo Support Group Uganda (VSGU): Together we shall Arise and Shine

Masedi a Botswana - Vitiligo Support in Botswana – let there be light

MBWF - Make a Better World Foundation (Italy), an Italian non-profit Association in memory of Michael Jackson, a long-time vitiligo sufferer, and for the benefit of every vitiligo sufferer in the world.
The MBWF Foundation is committed to various projects to help persons in need, principally sick children based on the same dream that Michael Jackson shared with all his followers: to make the world a better place for everyone.

Russian Society of Dermatovenerologists.

Croatian Dermatovenereological Society organises and supports public health activities (fight against melanoma – EMD, psoriasis, chronic wounds) and cooperates with the Croatian Academy of Sciences and Arts in scientific matters. CDS is also a member of the International League of Dermatological Societies (ILDS).

 


 

Alanic International™ (Australia)

 

Vitiligo Bond Inc - Founded Novemeber 2010 Vitiligo Bond Inc. is an awareness, empowerment and support group in Atlanta Georgia with a worldwide audience.  Vitiligo Bond has established 5 state proclamations in Georgia, North Carolina, South Carolina, Maryland and Colorado with other states to follow.  These proclamations acknowledges June as Vitiligo awareness month as well as a special recognition day on June 25.

 

ПОЧЕМУ ЭТО ВАЖНО

Люди, страдающие витилиго, сталкиваются с большим количеством проблем, которые ограничивают их права на социальные услуги и лечение. Часто от других они могут услышать, что «поскольку витилиго не заразно и не опасно для жизни, вы должны смириться и принять жизнь изгоя, скрывая себя от солнца и от общества».

Витилиго является не до конца изученным и понятным заболеванием. Неоднозначность и сложность этого заболевания кожи требуют международного сотрудничества в исследовании и развитии методов лечения. Важность и необходимость решения социальных проблем, связанных с витилиго, требует планомерной поддержки Национального здравоохранения.

Поэтому - отстаивайте свои права! Подпишите письмо и подтвердите, что Вы нуждаетесь в признании и поддержке. Мы будем признательны, если каждый член Вашей семьи подпишет петицию.

Количество подписей

Мы собрали 502180 из 500 000 подписей (100.44%). Наберем 1 миллион!

VR FOUNDATION

Firmly committed to curing Vitiligo, the VR Foundation is a non-profit organization funding and fast-tracking medical research globally. We challenge the disease of vitiligo with educational and medicinal enlightenment. We care; we educate; we advance knowledge. We are the VR Foundation.

Partners and Sponsors