Hi, anyone suffer with UTIs? Or similar symps? Is it endo?
UTI? : Hi, anyone suffer with UTIs? Or... - Endometriosis UK
UTI?
Yes, I frequently get UTI-like symptoms caused by endo. You should get your urine checked though by the GP, just to make sure it’s not an infection. Hope you feel better soon x
Hi there, yes, I do! It’s agony, I get the Endo pain under control and then the UTI feeling comes 😞. I try to put a hot water bottle between my legs to help, not glamorous but helpful xx
Hi, yes all the time. Esp around my period. I can be up 5/6 times a night for a wee & have full aching stabby pains on one side. Would often get wee checked by dr to be told no UTI. I’m now almost 4 weeks post and been diagnosed with endo. So yes it is poss it could be endo definitely. See your GP. All the best. X
Yes unfortunately… Surgeon didn’t find endo on my bladder but said it was inflamed. Most likely interstitial cystitis which is known as a sister disease of endo , it is so so painful. If I could feel my bladder starting to flare I found the best thing was try to rest limit movement and hot water bottle between legs or sometimes even a cold ice pack would bring great relief! Also I would sit in the bath just so I could relax my bladder when feeling like needing to wee constantly.Mine (touch wood) settled since having my little girl but do get checked for UTI just in case - I didn’t bother once, as I was expecting it was my usual flare but turned into a kidney infection from an untreated UTI - whoops!! 🙈
Hi,yes I do! I get UTI symptoms but there is never an infection - I was diagnosed with endometriosis a few weeks ago post laparoscopy. As others have said, interstitial cystitis and endo often go hand in hand!
I’ve been having infections for around 20 years and have only recently been diagnosed with pcos and endo. I never knew the uti symptoms could be the same as endo symptoms!! I’m so glad I saw this post. A few times I thought I had an infection only to be told the urine test was clear. I’ve not once been told it could be endo symptoms. I don’t know about others experiences with doctors and nhs but I haven’t found mine very helpful at all.
I recently had my first experience of this. I’m not sure how long I’ve had endo as only diagnosed from an endometrial cyst about 3 years ago.
Had to go to the toilet every 10 mins or so. Painkillers helped as did plenty of water and also a hot water bottle. I didn’t have burning when I peed but burning afterwards? I’ve not had it since.
I think the anxiety of wondering what it was was worse than the UTI symptoms.