I have already posted in the Research opportunities page but
wondered if it was ok to post this here as well? If not, then please forgive me.
I’m a 3rd year anthropology student, who also
suffers from a collection of disabling conditions, including fibro, NEAD and arthritis. I’m interested in chatting
to people about their experiences of using disabled loos as part of my
dissertation.
Do you find your body becomes judged by others wondering if
you are ‘allowed’ to be using the disabled toilet? I have so-called ‘invisible’
conditions and I am frequently subjected to looks of distrust when I use a
disabled loo.
I will not use ANY discussions here as part of my project
without express permission from people, but it would be really useful to hear
other people’s experiences.
If people are uncomfortable speaking here I’m more than
happy to chat in private 