Reply: I Can't Pee in Public Bathrooms, and it is Actually Ruining My Life

NOTE: You are posting the message as a 'Guest', you can not edit the message or delete it
Please Log in or Register to skip this step.

Attachments

Allowed file extensions : jpg, jpeg, gif, png,

Maximum File Size : 7.8 MB Maximum Image File Size : 0.1 MB

Add Files...

You can drop files here or use the add files button.
X

Topic History of: I Can't Pee in Public Bathrooms, and it is Actually Ruining My Life

Max. showing the last 6 posts - (Last post first)

  • ann
8 years 6 months ago

Yes - the writer clearly sees the need to raise awareness of paruresis, and it's so good to see the female perspective in a mainstream magazine article.

  • Jean
8 years 6 months ago

Hi Ann
As you know, I am a fellow sufferer. I also found this article very interesting. I thought the ripeness of the writer's language was probably a reflection of the magazine she is writing for. I looked her up and she is American and obviously very busy, so may be difficult to contact. Good to know that the condition is being publicised - her experience seems very familiar to me as well.

  • ann
8 years 7 months ago

It's pretty rare to come across articles about paruresis, but particularly unusual to come across articles about women with paruresis. I came across this article in a 2016 edition of Cosmopolitan. Written by Nicole Rupersburg, this really resonated with me - I found myself in similar situations so many times in the past. Nicole - we are indeed kindred spirits. www.cosmopolitan.com/health-fitness/a594...me-public-bathrooms/ .

Time to create page: 0.014 seconds
Find the UK Paruresis Trust on Facebook
Follow the UK Paruresis Trust on YouTube
Follow us on Instagram
Registered with Fundraising Regulator
Community Fund
BMA Patient Information Awards Highly Commended 2019
Trusted Information Creator
Hospital Saturday Fund