I received my diagnosis at the age of 21. I was diagnosed with Ehlers-Danlos syndrome (EDS) first and a couple of hours later I was diagnosed with mast cell disease. I had no idea what was going on, I just remember feeling very different to the people around me. I remember feeling ill all the time, experiencing a lot of pain, not being able to enjoy eating without being sick.
As I was getting older, it was consuming every part of my life. I lost nearly all my friends, as I was at home 24/7. After going to the doctor’s multiple times, I kept getting turned away. I had to almost prove how poorly I was.
This is the first time I’ve ever been this open and the reason I’m putting myself in this vulnerable position is, so awareness increases about rare conditions.
Day by Day
Sharing my interpretation of the unique experiences an individual with rare diseases is living with, has been a great honour. As my art concerns itself with societal concepts and how art is able to bring these to the viewers attention and possibly reconsider their opinions about them, this was a project congruent with my practice. I hope to deliver a thought provoking and encouraging viewpoint on the life of my paired changemaker.Artist Profile
The imperfections of life are the driving force behind Sara’s art. Depicting life’s rawness is her central aim. Sara specialises in water-based and oil-bar paintings on large scale papers, which allow for the subject matter to mould the fragile paper medium. The wonky and imperfect end product speaks to the perfectly imperfect nature of life. In Sara’s practice, she focuses on societal issues, such as the varying impacts of climate change on different parts of our society.