Hi I’ll not go into all other symptoms for now. I’m curious I’d people had/have retention? I know people have a lot more but interested if anyone has simular am out iv been measured at 140 and 160 last time Thanks
Hi, that IS a high retention volume to be sure!
I`ve had a supra pubic catheter in for almost 3 years and before that I was wanting to go every hour…severe urgency and retention, with a uti now and then ad lots of accidents. Life was not good!
Are you under a urologist?
What`s your next plan of action?
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Thanks for reply yes I’m under urology, 1st one just said not peeing enough and to fill forms in for 3 days of intake and amount I pee and to go back. 2nd one didn’t really look at sheets he just said it’s a overactive bladder and gave me some more medz to try and go back in 2 months I think I’ll get discharged next time. I don’t really expect anything else. But at least it’s a symptom to help me get diognosed iv had a clear mri but without contrast. And mage it out pins and needles was in my head because I was thinking about it. And everyone never did anything g about peeing all time till one new gp sent me My symptoms are tingling in bed under right shoulder blame tingling left foot stabbing right toe (these now gone) Ichy stabbing feeling on both legs near calf hot aches itchy feeling all over legs but only when walking like where the trousers rub as moving recently vit d deficiency That’s it so not bad symptoms the worst is the peeing but something going off
Not bed meant to say in back under shoulder blade
Hi again. If you`re not happy should you be discharged next time you see the uro…tell him so. See what else he can suggest.
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I’ll see if these meds work first hopefully they will. I don’t know what more can be done. I will push for another mri at some point as the letter sent to me kept saying her and im male also when I had evoke test the guy said there is something but consultant will look at results together. Consultant just said that everything is OK. I’m not pushing yet as if I got a cLear mri this time I’ll never get another test so waiting to see if anything gets worse or dramatic changes. Did it take you lot to get diognosed? Thanks