The Pelvic Pain Support Network has developed from the local independent endometriosis support group based in Poole, Dorset. It is a patient led organization with a board of trustees who are all patients or carers, and is run entirely by volunteers. We have an advisory panel of clinicians, researchers and health professionals who have an interest in pelvic pain from many areas of expertise and countries including the USA, France, Germany and the UK. Our aims are: to provide support, information and advocacy for those with pelvic pain, their families and carers, to promote the education of the public and the medical profession by raising awareness in all matters relating to pelvic pain and its treatments, the advancement of research to increase knowledge and understanding of the impact of pelvic pain.

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