What is the PV Network?
The Pemphigus Vulgaris Network is a voluntary, not-for-profit, group started in 1997 to provide information and support for people living with pemphigus and their relatives, friends and carers. We also provide an information resource for doctors and other medical professionals. We are part of the British Association of Dermatologists’ patient support group organisation and are members of the Skin Care Campaign, National Voices (previously called the Long-term Conditions Alliance), and the All Party Parliamentary Group on Skin. We are entirely unfunded and rely on donations. If you find this website useful and would like our work to continue, we would appreciate any donations (howevever small). Cheques should be made out to the Pemphigus Vulgaris Network and sent c/o 26c St Germans Road, London SE23 1RJ. Contact information for the PV Network is given at the end of this page.
