Hi I'm suffering with water infections quite often I've got pbc but am post liver transplant any one else suffer since diagnosis
Water infection : Hi I'm suffering with... - PBC Foundation
Water infection
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Hi,
I get uti every 4/6 weeks, they have put the camera everywhere and cant see anything that would cause it. Being sent back to see urologist again. Not sure if pbc related or due to the fact of being on immune suppressants, i just know its a pain 😊 x
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I've had a pelvic scan and a transvaginal probe, see my gynaecologists every 4 months I'm going through the change too ,no periods for 6 months I bath and shower regularly its getting me down
I just had another pelvic scan 2 weeks ago and that camera up the pee pee hole was stingy as hell. Im not menopausal yet, they reckon perimenopausal. I see gynaconcologist every 6 months but not for urine infections, i have lychen sclerosus which they say wouldn't cause the uti's.
I know it does get you down,i think some of us are just prone to them.
I get Cystitis around every 6 weeks and need antibiotics I get Leucocyte, protein and white blood cells in my wee. The antibiotics clear it up but it’s just so uncomfortable and no warnings when it will hit. I now have a standby prescription in case i get another bought. Just had ultrasound on bladder and kidneys and all clear results. I drink loads of water daily and do all the right things, but not sure if it’s PBC related or age related. I also have Lichen Sclerosis. Any preventative ideas would be helpful