Ashley (18)
was born with Treacher Collins syndrome, a condition that affects his face.
After being bullied most of his life, he has become an anti-bullying campaigner
and shares his experiences in the hope of raising awareness.
The
syndrome affects my face: I was born with no ears, no cheekbones and a receding
jaw. I have had over thirty operations including three jaw distractions and
cochlear implants. When I was a baby, I had to have a tracheostomy fitted as I
swallowed my tongue and went blue, this was the only way the doctors could save
me.

Growing
up was amazing because I had my family. However, this changed when I started primary
school. It was the toughest and most emotional part of my life. I
ended up attending two different primary schools as a result. Within a week or
two of starting the second school, the bullying began. It started with things getting
thrown at me (bottle lids, food, etc.) but it got worse as the months went on,
to the point where they would physically pin me up against the wall. They also
tripped me up in corridors and in the playground, which upset me a lot.
I
remember cycling to a friend’s house that was about five minutes away, as soon
as I entered my friend’s street the two bullies saw me and started to chase me
home. This chase led to me nearly getting run over and I put myself in danger
multiple times to escape them. They took over my life and I didn't fully open up
to anyone until much later on, with it affecting both my confidence and mental
health. I used to come home every day from school crying to my parents and seeing
my mum get upset and tearful about the situation only made it worse. The school
did nothing to begin with, their solution was to move me into another class. Why
should I be moved and not them? This was the question my family and I couldn’t
help but ask. I started to enjoy it in the other class, but when I went out
into the playground I still was faced with the bullies. They still had control
over certain elements of my life.
Secondary
school was not as bad. I still had the stares, points, and things thrown at me,
but it was better. In 2016, I became a volunteer at a local charity shop which
I loved, and then I became a waiter at a pub. People allowed me to join their
team and I got to show them what I could do. I didn't want my syndrome to be
the front of me, I wanted them to look past the condition and see the abilities
and skills I had.
Then
there was an exciting change. In early 2017, I contacted a charity called
Fixers who work with young people aged between sixteen and twenty-five who want
to use their past to fix the future. This allowed me to share my personal
experience of being bullied as someone with a facial disfigurement. It was
amazing to finally be able to feel brave and open up about this as I was really
shy before sharing my story. My campaign video was aired on ITV News, I was
invited to do some press work and I took part in multiple radio interviews. The
feedback and response from this have been fantastic!
My
future goals are to continue to share my story and raise awareness. I want to
write a book, and perhaps work within the TV industry. Since doing my campaign,
my life has changed for the better. We are all different, but we should be
treated the same and be given the chance to celebrate those differences. I hope
together we can stop bullying!
You
can follow Ashley’s journey on Twitter at Carterashley13
Have you ever
experienced something negative because of your disability? What awareness do
you believe would eliminate bullying?