Through our volunteer helpline and Facebook support group for women with PGP, we hear directly from women about their experiences of PGP, in engaging with healthcare professionals and accessing treatment. To develop our response to the call for evidence, we surveyed women with PGP to ask their views on access to healthcare to supplement the results of an earlier survey we undertook in June 2018.
You can access short summaries of the results below:
The Pelvic Partnership consists of volunteers who have had pelvic girdle pain (PGP) and wish to support other women. We aim to pass on information based on both research and the experience of other women with PGP. We are not medical professionals and cannot offer medical advice and the information we provide should not take the place of advice and guidance from your own health-care providers. Material on this site is provided for information and support purposes only.