Evening everyone. I'm new to the group so I thought I would say hello before I started reading your experiences and stories about life as an endometriosis warrior. I have been on the pathway for five years as a confirmed endo warrior but I have had ovarian cysts for over ten years. Anyway before I bore you all to sleep.... I really wanted to read about your experiences, coping strategies etc. About my pathway..... Numerous laparoscopies, various attempts at prostrap injections (which to be honest I think I hate equally as much as the endometriosis) and two failed attempts at pain blockers in the pelvis. Anyway this is my pathway. Thank you for forming this group. Considering it is affecting one in ten women now it's still so difficult to get good information about it. Have a good evening 😌
Hello. I'm new to the group.... - Endometriosis UK
Hello. I'm new to the group....
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Emmalou80
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