I've just bought some Urostemol tablets for what I assume is an overactive bladder, but haven't taken them yet as I'm having a scan in a few weeks time after having a PMB. Atrophy was diagnosed at the hospital a ffew weeks ago but they want to have a better look. One of my concerns was the number of times I had to go to the loo (especially at night)...but I'm also not going on long walks any more because of the number of times I've had to find a loo (or a bush) at very short notice. It is affecting my life. I have switched to decaff q1tea and coffee and am limiting how much liquid I drink and I have been better recently. I'll take the Urestomol after I've had the scan. My lady doctor didn't mention atrophy when she did my referral which worried me terribly. I've had irritable bowel for most of my adult life which now seems have improved....maybe it would be too unfair to have irritable bowel and nervous bladder!
Disappearing contributors - part 2
Have you stopped buying papers?


. Thankfully I've never lost control (yet). For me, it means not being able to go out without knowing where the toilets are. Long journeys, especially at short notice, don't bear thinking about. 