This past year I interviewed five different people with a visible (or hidden) difference whilst I 'get to know' them a bit better. The purpose of this series was for the readers to have a better insight into their lives/how they would like to be treated whilst hopefully, being just as informative and helpful.😁☀
Meet amazingly awesome Ariel Henley🍂
I first discovered Ariel Henley by reading an article she did for the New York Times about the importance of facial equality. I was so completely moved by her raw, honest and true words, that I just had to include her in this series! Her honesty about the life of a person who is visibly different really spoke to me and so I believed it would be very beneficial for you guys to get to know her. <3
About
Name: Ariel Henley
Age: 28 years old
What do you do? (Work/school/uni etc) I am a writer, focusing primarily on issues related to disfigurement and craniofacial disorders.
What's one thing you want people to know about you?
I'm an identical twin. We both have Crouzon syndrome. Though growing up my sister and I had each other, I know what it's like to feel isolated in your experiences. This is why I love connecting with other people with facial differences and their families. It's easy to feel alone and like nobody understands what you're going through, but there's a whole community of people ready to support you and welcome you.
What's your #visibledifference ?
I have Crouzon syndrome, a craniofacial condition where the bones in the head fuse prematurely.
What's one thing you want people to know about your #visibledifference ?
My appearance does not define me, nor does it limit me in any way. I'm just like everyone else. I just look a little different, and there's nothing wrong with that. (yes!🎉)