Endo on the bladder: Anyone else have the... - Endometriosis UK

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Endo on the bladder

Country-Girl100 profile image
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Anyone else have the bladder and bowel endo?

Willing to try anything, for any kind of relief.

I have endo on and going into my bladder and now also effecting my bowel. It's triggered normally about day 3 of my period and last for a good 3 weeks. The first few days I just have to be near a toilet, when I need to go... I have to go, there is no holding it in. The pain is just awful, my bladder feels like it's contrating, my eyes are watering with the pain. No pain killers even take the edge off, i've tried a TENS machine, that doesn't help too much either. The pain just drags me down and stops me doing day to day things. Luckly I work with my dad and husband, so they understand when it's the bad times.

I had two ultra sounds, which shown nothing. I had an MRI scan finally which shows I have an endometrioma on my right ovary, endo around the outside and going into my bladder.

Currently waiting on my first laparoscopy which should have been in September, but it was cancelled as I had a missed miscarriage which ended in an operation.

Fortunately, I don't suffer with heavy or painful periods. Just my bladder and bowel.

It would be nice to know others experiences.

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