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Drug test shy bladder: I walked out and now I'm waiting

I finally had a job offer that paid properly, and a plastic cup stood between me and it. I couldn't go, I panicked, and now I'm waiting.

I spent most of last year looking for work that paid more than retail. A friend put in a word, I got an offer, and for about a day I felt like my life had turned a corner. The only thing left was a drug test.

I’ve had shy bladder since I was twelve or so. I never told the hiring manager. It’s not something I want to explain to a stranger in HR, and I told myself there must be a workaround for people like me, so I didn’t call ahead or look into it.

The clinic smelled of hand sanitiser and the air conditioning was too cold. I stood in the little restroom with the cup and nothing happened. I can’t pee when someone is waiting outside the door, and this was that times ten. The staff said my only option was to sit in a separate room for three hours and try again. I knew that wouldn’t work, because the more I’m watched and timed, the tighter everything gets. I also had a shift starting soon.

Walking out

So I panicked and left. Apparently that counts as an automatic fail. I sat in my car with the engine off and felt sick. I’ve never taken drugs. I don’t even drink. And I might lose a job worth nearly fifty grand a year over a cup.

I tried to find the urologist who first told me what I had, hoping for a note. He’s retired, and nobody could say where he went.

Since then I’ve heard that I should have disclosed it upfront, and that it may count as a disability I can ask to be accommodated for. Someone from a paruresis organisation even offered to write me a letter of support. I wish I’d known all that before I walked into that clinic.

Now I wait

I’ve asked the company to accommodate me, and they said they’d let me know tomorrow morning. So tonight I’m at the kitchen table, checking my phone more than I need to and trying not to picture the offer disappearing. I honestly don’t know which way it will go.

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.

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