Welcome to the Vulval Pain Society, a UK registered charity supporting vulval pain sufferers.
Our aims 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
We offer advice and information on all vulval pain matters. You can read detailed information about vulvodynia, vestibulodynia (previously known as vulval vestibulitis), lichen sclerosus, and other vulval pain conditions. We also have information on sex and vulval pain, pregnancy and vulval pain, and other general good advice.
Petition launched to get pelvic pain included in UK medical student curriculum
The VPS has been asked to pass on details of an online petition to get pelvic pain included in the UK university curriculum for all medical students. You can read more about the petition here:
The VPS is a charity aiming to educate the public about vulval pain as well as provide help and advice to sufferers. We therefore support any initiatives to help increase the knowledge, skills and competencies of all health professionals, including medical students, in improving the assessment and management of chronic pelvic (including vulval) pain. Pelvic pain conditions are poorly managed and have a major impact on patients' quality of life, everyday functioning and reproductive health. It is vital that we invest in the education of our future workforce in the field of pelvic pain if we are to improve treatment and support available to all those living with pelvic pain conditions.
New Facebook group for male partners of vulvodynia sufferers
Partners of Vulvodynia is a new Facebook group for men whose partners suffer from vulval pain. They say 'This group has been set up for men whose partners are suffering from vulvodynia. It's important that we offer support and help raise awareness around this rare condition'.
To join the group, sign up with Facebook if you need to, then just follow the above link to the group page and follow the instructions on the page.
New vulval pain support group on Facebook
Pudendal Neuralgia and Vulvodynia UK have asked us to post a link to a transitional Facebook group which allows ladies to join their full secret Facebook group once the administrator of the group has had contact with them. As the official group's members want it to remain secret, we can't provide details here, but if you follow the above link to the group and (if necessary) sign up with Facebook, you can contact the administrator for details on how to join the group itself.
Manchester Vulval Support Network: meeting on Thursday 15 September 2016, 7.00 pm
Participate in an online study for women with symptoms of vulval pain (Queen's University, Canada)
The Sexual Health Research Laboratory at Queen's University in Canada are looking for women aged between 40 and 55 to take part in an online study on vulval pain. The study will involve completing online questionnaires to assess symptoms, psychological and social wellbeing, healthcare experiences and sexual and relationship functioning.
You can access the study directly at violet.sexlab.ca.
NEW - Transcript and references now available for VPS Podcast 4 - Physiotherapy treatment for vulval pain
You can now read the transcript for VPS Podcast 4, which is Women's Health physiotherapist Helen Forth's podcast on physiotherapy for vulval pain, at Transcript of VPS Podcast 4 - Physiotherapy treatment for vulval pain: a presentation given by Helen Forth.
We've also posted a full list of the references Helen uses in her presentation at References for VPS Podcast 4 - Physiotherapy for vulval pain: a presentation given by Helen Forth. The original video presentation itself and MP3 audio recording are of course still available on our Listen and watch page.