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Welcome to the VPS website. Here you will find advice and information on all vulval pain matters. You can read detailed information about Vulvodynia, Vestibulodynia, Lichen Sclerosus, and other conditions. We offer advice on sex, pregnancy, surgery and other good advice.
The Vulval Pain Society (VPS) is a confidential service for women who suffer from vulval pain due to vestibulodynia and vulvodynia. The Society was set up in 1996 by a doctor and a nursing sister. The VPS is not externally funded or attached to any health service organisation.
The Aims of the Charity as set out in the Governing Document are:
- To promote and protect the physical and mental health of sufferers of vulval pain through the provision of support, education and practical advice
- To advance the education of the general public in all areas relating to vulval pain.
Please bear in mind that this is a UK charity and is aimed specifically at those seeking solutions mainly within the UK nationalised health system. It may therefore not be so relevant to US readers, who might prefer to check the Help on the Web and Links to other organisations sections.
The VPS question
Please participate in our poll question below. Your answer is completely anonymous.How long have you had your condition?