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The Pelvic Partnership was created by people who have experienced SPD personally and is intended to benefit others who might be affected by the condition now.

We are a national registered charity and offer information to people anywhere in the UK through publications and e-mail contact, the details of which appear on this site.

We would also be interested to know from women with SPD and their families of any areas of concern or difficulty that we should address on this site.

If you would like help or information concerning any aspect of Symphysis Pubis Dysfunction visit our Useful Information and FAQ pages or you can contact us; we will be pleased hear from you.

If you have found our site interesting please let others with SPD know so that they can benefit from the information available.     

Disclaimer:

The content of the pelvicpartnership.org.uk web site is for informational purposes only.  It is not intended to be a substitute for professional medical advice, diagnosis or treatment.  Always seek the advice of your doctor or other qualified health professional with any questions you may have concerning a medical condition.

Site problems? >> webmaster@pelvicpartnership.org.uk