Tel: 07825 855888
The Birthmark Support Group offers information to anyone affected by a birthmark (including port wine stain, haemangioma and congenital melanocytic naevus). The group produces newsletters, medical information packs and offers contact with others in similar situations. The website is regularly updated with the group's activities and provides links to other relevant organisations. They have separate groups for teenagers and adults.
Last updated on 09/10/2013
Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. Patient Platform Limited has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.