As I meet Lizzie Cooper
outside Winchester train station in the April sunshine, she strikes me as
happy, articulate and beams at me as she describes her soon-to-be-husband. But
had you known her at the tender age of 15, by her own admissions she would have
been nearly unrecognisable. She was bitter, angry and withdrawn - a description that could match just about every other teenager in the history of the world. But she perhaps had a better reason than most for feeling so down.
Lizzie as a newborn |
Lizzie was born with a cleft lip and palette, a condition where parts of the
mouth do not form properly in the womb. The result is a facial disfigurement which can, after several rounds of surgery, be rendered completely unnoticeable. She spent
her formative years in and out of surgery and in the waiting rooms of various
consultants. She has had eight operations in total – the first when she was four
months old, the last when she was 22. She hates hospitals but, as a child, accepted that these are the cards she had been dealt. The bullying
and rude comments from strangers, however, were a little bit harder to handle.
She tells me about her first day at school. “I came home and I sat my mum down and I said, “Mummy, what’s wrong with my face? Kids keep asking me what’s wrong with my face.’”
She says that her mum told her that she should go back and tell the other children that she would be able to get a “designer” nose when she grew up, whereas they would be stuck with whatever they had. It didn’t do anything to stop the bullying, she says, but it gave her a mechanism to cope with it; it gave her some hope in the form of thinking that whatever made her stick out could one day be ‘fixed’.
She tells me about her first day at school. “I came home and I sat my mum down and I said, “Mummy, what’s wrong with my face? Kids keep asking me what’s wrong with my face.’”
She says that her mum told her that she should go back and tell the other children that she would be able to get a “designer” nose when she grew up, whereas they would be stuck with whatever they had. It didn’t do anything to stop the bullying, she says, but it gave her a mechanism to cope with it; it gave her some hope in the form of thinking that whatever made her stick out could one day be ‘fixed’.
Four year-old Lizzie |
She hesitates for a bit, and then says that if she has kids,
she would never raise them in such a way. “I’ve been there and I’ve done that
and it’s not a nice thing to be judged on how you look. It’s shallow and it’s
stupid.”
I ask her about family, and she says that they were very
supportive and up front about the kind of challenges that she would have to
face in her life. She feels lucky. “They never made me feel like it was
something wrong with me.”
She tells me a story of a man she knows from CLAPA, the
Cleft Lip and Palette Association, of which she is an active member. She says that this man was not as lucky as her, and that his father never accepted him. The dad apparently had turned round to his mother when has
was born and told the mother that their son must have gotten it from her side of the family. Lizzie
tells me that he had been an extremely bitter man for most of his life, and
that this was the root of it.
Bitterness seems to be a recurring theme. In a previous phone conversation, Lizzie told me that she was absolutely fine about having a cleft but that some people had “real chips on their shoulders” about it. I ask her what she meant by that. “I think some people ask why they were even born like this and why couldn’t their parents have taken the opportunity and just have gotten rid of them before they came in to this world.”
She says it’s definitely a case of “why me”, especially in the situation that occurs when a person with a cleft has reached self-acceptance, but is still being bullied for looking different. Lizzie’s breaking point was the second year of university. She was sick of feeling the way she did and sought some counselling. The first session made her feel much better – she cried, she shouted, but she felt lighter.
Bitterness seems to be a recurring theme. In a previous phone conversation, Lizzie told me that she was absolutely fine about having a cleft but that some people had “real chips on their shoulders” about it. I ask her what she meant by that. “I think some people ask why they were even born like this and why couldn’t their parents have taken the opportunity and just have gotten rid of them before they came in to this world.”
She says it’s definitely a case of “why me”, especially in the situation that occurs when a person with a cleft has reached self-acceptance, but is still being bullied for looking different. Lizzie’s breaking point was the second year of university. She was sick of feeling the way she did and sought some counselling. The first session made her feel much better – she cried, she shouted, but she felt lighter.
Lizzie and husband Chris |
She describes the state that she finds her life in now as a “nice shock.” She tells me that as a 15 year old, she had already resigned herself to a lonely and bleak existence. She believed that she might never go to university, get a job or get married. But she says that despite the heartache, she would not change anything about her life. It has shaped who she is and she is happy with who she has become. “I’m content. I’m quite happy with life in general, you know, it could always be better. But at the end of the day, I feel quite proud of being a ‘clefty ‘, as we know ourselves, and I’m absolutely fine with it. I’m in a job that pays, I’ve got a little flat with my other half and I'm about to get married, so life is good.”
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