"It was scary not understanding what was wrong and having little hope. It took years of fighting to be heard and many doctors visits. Fighting is hard when you feel ill. But I know I am not alone.
Viewing entries tagged
Hidden Project
Three years ago, I learned the hard way that blood clots aren’t just a plot device. What started out as a fractured ankle resulted in heart and lung damage, and a very very long recovery time.
As part of our Hidden Project, we're asking people from our community to share stories of their hidden illnesses. We believe that only by sharing our experiences can we begin to understand them – and one another.
People may not understand how invisible illnesses disrupt our everyday lives precisely because they're hidden. Root Experience trustee Tilly Baker tells us how an untimely bout of her condition created a new understanding with her work colleagues.
Our artistic director Simon explores his recent experience of back and hip pain while working on the charity’s project about invisible conditions. He asks whether the medical treatment we receive really gets to the root of the problem...
Our challenging and thought-provoking exploration of what it is to live with a hidden disability is really starting to take some shape – and we're ready to share it with the world, with an exhibition at Brighton Dome next week: The Hubbub.
Do people with hidden disabilities hear differently to others? Composer and sound designer Dougie Evans explores the power of sound through sensitive ears.
You can’t truly understand the scale of obsessive-compulsive disorder (OCD) unless you've experienced it – unless you've been there, done it, and checked multiple times that you do in fact have the T shirt.
I know when I come up against stigma, it’s not because I am not smart or funny or engaging. It’s because people don’t understand dyslexia. They don’t know how limiting it can be and don’t appreciate how a simple change in a process can mean all the difference to me...