Has anyone got this, or suffered from it in the past? I have had ' suspected ' endromitriosis for just over a year, the abdominal pains just came out of nowhere and I have suffered ever since. I am still awaiting an appointment to see the gynacologist though.
I have read that they have to do a Laparoscopy (sp) to confirm this, and that there is no cure, and treatment has bad side affects
All I know is I have a real good pain barrier, but this pain makes me cry hard, work suffers, my sleep suffers and it's a really miserable time. Pain killers (if real strong) help a little, as does a hot water bottle, but don't think I can live with this for the rest of my life! although I may not have a choice with that!
So I just wondered if anyone here, or you know has suffered the same and if you can offer me any advice?
I have read that they have to do a Laparoscopy (sp) to confirm this, and that there is no cure, and treatment has bad side affects
All I know is I have a real good pain barrier, but this pain makes me cry hard, work suffers, my sleep suffers and it's a really miserable time. Pain killers (if real strong) help a little, as does a hot water bottle, but don't think I can live with this for the rest of my life! although I may not have a choice with that!
So I just wondered if anyone here, or you know has suffered the same and if you can offer me any advice?