Support Pelvic Dysfunction, Campaign and Charity for SPD and PGP

im looking to make some friends who know how hard life is with the conditions i have. It is such a big life change and people don\'t have to go through it alone, this community is a support group for all those who suffer with SPD, PGP, and/or connective tussue disorders (fibromyalgia, hypermobility etc) or want to know anything about them. About me: it hurts to go through it sometimes its easier to just post my blog if anyone wants to know what i have endured its all there.\r\n\r\nI try and stay strong as i am trying to make a difference, trying to start a community on here so you can all make some friends and gain support from other sufferers, and i am also trying to create a charity which is more of a support system right now, but it is really hard and im hoping someone out there can relate to me.\r\n\r\nI was told i couldnt be a mam so my son is a miracle child and i thank my lucky stars every day.\r\n\r\ an england new charity with aims to: STAMP out PREJUDICE,\r\n\r\nSTAMP out LACK of awareness\r\n\r\nINCREASE the help that SPD sufferers NEED\r\n\r\nHave people realise:\r\n\r\nI may NOT LOOK disabled but my disability is NOT visual and is very much REAL!!\r\n\r\\r\n\r\nSPD is common but not normal during pregnancy.