Looking to hear other people's experience... - Endometriosis UK

Endometriosis UK

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Looking to hear other people's experiences...

AG22 profile image
AG22
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So it's been a while since I posted on here, 2 years infact. My health problems started over 5 years ago with my symptoms including abdominal pain, kidney pains, pelvic/groin pains, nausea, painful sexusl intercourse (during and after) and fatigue. I went through years of going to the doctors and the hospital every month to try and get some answers with no prevail, I've had every test I can imagine which resulted in barely any answers. The only two things that were found was a mass in one of my kidneys which seemed to miraculously disappear when I have a cystoscopy and the second was adhesions around my pelvic area when I had a laparoscopy; I also had a mirena coil put in at the time of the laparoscopy as my periods had also been so bad and I couldn't deal with them anymore. After having no answers and no end in sight I kind of gave up all hope and decided that the doctors couldn't help me so I've just been living through the pain but 2 years down the line I'm now ready to start a family with my partner and I really want some kind of answers. So what I'm wondering really is, although I've had a laparoscopy and endometriosis was not found could endometriosis still be a possibility?

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