mums with spd/pgp

Symphisis pubis dysfunction/Pelvic girdle pain

4

Trying to raise awareness of spd/pgp.!

I have had spd for 10 years now..but I only had support the last 2 years.I thought i was on my own.Unfortunetly,I am now permanently disabled because they didnt treat the pgp...

Started by Angie on 03/29/2011 in Mums With Spd/pgp

Last update on 05/08/2011 by Sarah

0

Living with Spd?

Hi just wanted to hear from other mums that cope with having spd.

Started by Angie on 03/23/2011 in Mums With Spd/pgp

Last update on 05/08/2011 by Pauline

0

NEW ENGLAND SPD CHARITY & CAMPAIGN

www.supportpelvicdysfunction.co.uk and help@supportpelvicdysfunction.co.uk Not only a new SPD charity but one that has aims to raise awareness, gain acceptance as a non-visual...

Started by Sarah on 05/08/2011 in Mums With Spd/pgp

Last update on 05/08/2011 by Sarah