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Shy bladder at a festival: the toilet queue that made me act
The bass was thumping, the queue was shuffling, and nothing would come. That was the moment I decided I was done hiding it.
The festival was meant to be the best weekend of my summer. Instead I spent part of it in a plastic cubicle that smelled of chemicals and warm sun, needing to pee and completely unable to.
I’ve had shy bladder for as long as I can remember, and I’m 26 now. A closed cubicle is normally fine for me, but that day the bass was thumping, a queue was shuffling outside, and someone coughed right by the door. Nothing came. I got so angry at myself that I gave up, then tried again an hour later and managed it. By then I wasn’t myself, and my friends could tell.
The planning is the worst part
Every trip, weeks ahead, I’m already wondering where I’ll be able to go. I fly next week and my head is full of airport toilets and plane cubicles. That’s the bathroom anxiety I carry around.
I barely drink either. Once I break the seal I need the loo every ten minutes, and if I can’t go, that’s a recipe for a horrible night. So I stay sober and watch everyone else enjoy themselves.
Finally doing something
After the festival I went looking for answers and found people describing exactly what I go through. Some had it much worse than me, which strangely made me feel I could beat it.
Only my fiancée knows. I trust her completely, and she’s going to be my practice partner. I also picked up a simple idea: write a list of situations from easiest to hardest, work up it slowly, and cross each one off. A man who’s fully recovered says he now drinks coffee on an eight hour drive without a worry, and wishes he’d started at my age.
Next I’m booking a doctor’s appointment and looking at a free online support meeting. Until then I’m trying not to think about toilets until I actually need one.
The biggest reason is simple. If I ever have a son, I want to stand at a urinal next to him and show him it’s completely normal.
Stories come from experiences people shared openly in online paruresis communities. We retell them in our own words and change names and details so nobody can be identified. They are personal experiences, not medical advice.