How can the Society support people who become members?
• By providing personal information by letter, telephone or email. • By putting questions to qualified medical professionals with an interest in vitiligo on a member’s behalf. • By keeping members in touch with the latest research and treatments through our newsletter Dispatches. • By supplying information through our website. • By informing members when researchers are looking for volunteers to take part in clinical trials. • By putting members in personal contact with each other. • By providing information to schools about Vitiligo so that they can recognised problems that may arise for children who have vitiligo or who look different • By our links with other groups working to help people with skin problems.
