It's what you don't see
On World Diabetes Day, I thought it would be appropriate to share this piece of my heart with you. In collaboration with fellow type 1 diabetics, I finally finished the post I've been working on since 2016. 14 November 2018 The hardest part about having an invisible illness is that it’s invisible. From the outside, nothing seems to be wrong. Being able to see and visualize something makes it so much easier to understand. Don’t get me wrong, I don’t want your pitty or sorry’s. Explaining an invisible chronic illness to someone is similar to explaining colour to a colourblind person. In a way, you can image or guess what it’s like, but you can’t possibly fully comprehend it. The reality is that an invisible illness is something you don’t “get”, until you get it. What you see, is an ordinary woman or man, girl or boy, living alongside you. Doing what you do, liking what you like and talking like you talk. What you see, are tired eyes and some bruises; which go by