Cherubism is a relatively rare genetic condition that Victoria Wright inherited at birth. The first indications of an abnormal bony overgrowth in the lower portion of her face appeared when she was four years old.
Doctors were initially unsure of the underlying cause of the problem.
Wright’s face has been compared by doctors to the weight of a bowling ball. She experienced bullying as she grew older, both at school and on the bus. Victoria was adamant that she would live her life to the fullest and steadfastly refused to let the bullies win. Her current status as a spokesperson and role model is excellent. Here is a look into her life and current appearance.
We all have unique looks, which sets us apart from one another and intrigues us. Some people are born tall, some people are born short, some people gain weight easily, while others don’t gain any weight despite having bad eating habits. We all have various color hair, if we have any at all. Everyone has characteristics that set them apart.
Every year, infants are born with distinct facial characteristics, medical conditions, or syndromes. In spite of the fact that having these distinctive facial characteristics can make life more difficult, those who have them are actually the bravest and strongest of us all. Unquestionably, Victoria Wright is one person to whom this applies. She had cherubism, a rare genetic condition characterized by varying degrees of abnormal bone outgrowth on the lower face, at birth.
She was bullied as a result, called many crude nicknames, and even as an adult, she still gets rude comments. The bullies, however, would not prevail against Victoria. Instead, she became well-known as a role model for all people and decided to use humor to illustrate what it’s like to live with a facial deformity.
If you think her inspirational story is worth sharing, kindly forward this article to your loved ones.
However, Victoria would never allow the bullies to triumph.
Instead, she became well-known as a role model for everyone and decided to use humor to illustrate what it’s like to live with a facial deformity. Please share this article with your friends and family so they can read Victoria Wright’s motivational story.
Her parents were overjoyed for their cherished daughter because everything seemed to be going well. But once she turned four, everything changed. According to Victoria Wright, my mother noticed that my teeth weren’t in the right position as she was brushing them. Cherubism, a rare hereditary condition characterized by varying degrees of abnormal bone outgrowth of the lower half of the face, had become obvious. It was given that name because angelic representations in Renaissance art frequently featured round cheeks.
Facebook/Changingfaces Victoria and her family sought the advice of medical professionals, who in fact confirmed the existence of cherubism. They told the Wrights that after Victoria entered puberty, her condition would get worse. As far as we can tell right now, that didn’t happen. Instead, Victoria Wright’s jaw grew larger, and soon it was having an effect on her eyes as well. She could feel pressure building in her eyes. There was a point when something needed to be done. Following pressure-relieving surgery, her sight was preserved. She still has headaches though, probably from her poor vision.
Cherubism is an uncomfortable condition.
“I experience pain.
It hurts in my head.
Doctors claim it’s the bowling ball’s weight, according to Wright”.
“I have the option of having surgery to shrink my jaw, but I don’t believe it would improve my appearance. I’m at ease with how I look. ”.
As soon as Victoria Wright started school, her life started to become difficult. She detailed how she experienced verbal abuse, intimidation, threats of violence, and other forms of harassment while walking down the street and using public transportation. Buzz Lightyear (the astronaut from Toy Story), Desperate Dan (the wild west character from the Scottish comic magazine The Dandy), and Fat Chin (the nickname given to Victoria at school) are some of the other nicknames she was given. Victoria remembered that “a girl in class used to draw pictures of me and circulate them.”. People would ogle Victoria wherever she went, whether she was at school, on the bus, or just strolling down the street. Despite the fact that she never got used to the looks, she understood it was normal.
“I make a conscious effort not to take it personally. Wright declared, “Even I’m looking”.
“Anger doesn’t help you or the person staring; I used to get angry when I was a teenager. It merely reinforces the idea that those who have physical deformities are hostile, tragic, or terrifying. It can be unsettling to get a hostile glare. But I don’t mind it. She explained, “If someone is curious about me, I simply smile and nod to let them know I’m a normal person with nothing to be afraid of. Most people will smile right back at you. That makes me happy because I know I’ve forged a shaky connection with them”.
Twitter When Victoria Wright entered adolescence, her life changed. She came across Changing Faces, the UK’s top charity for those with physical flaws, scars, or marks on their faces or bodies. They provide “life-altering mental health, wellbeing, and skin camouflage services,” according to their website. They also “work to transform understanding and acceptance of visible difference, as well as campaign to reduce prejudice and discrimination”.
“Changing Faces gave Victoria a lot of assistance. The foundation, in addition to her family, friends, and teachers at school, played a crucial role in helping her understand that despite having a facial impairment, she was just as valuable as everyone else. When I first met them as a teen, I remember thinking, “Wow, you can have a career and be happy and confident with a disfigurement,” she told NHS. It’s common to experience occasional feelings of isolation, particularly if you have a rare condition. It can be challenging when no one else on the street resembles you. Look for support from your peers. One hundred people don’t look, but for every person who does, there are 100 more who will value and respect you for who you are.
Wright’s perspective on life changed as a result of seeing Changing Faces. She began to see the benefits, and even developed a lighthearted attitude toward her appearance. In an interview with 60 Minutes Australia, she admitted to “adoring” Buzz Lightyear from the Toy Story and treating him like a sibling.
Victoria’s decision to forego plastic surgery in order to “do something” about her features has been questioned by many people. Because of this, she has been incorrectly portrayed in the media as being against cosmetic surgery. Victoria Wright is not opposed to cosmetic surgery, in actuality. It’s crucial to be satisfied with how one looks in one’s own eyes, and she is. “I like the way I look, but I don’t mind if people with deformities have surgery. Victoria Wright questioned, “Why should I have the surgery for the benefit of others? I usually feel good about my face.”.
I should be aware since I am a woman that no woman is ever wholly satisfied with how she looks. To please others, though, I won’t change who I am. I don’t want to be scared to go outside and afraid of people, so I don’t want to stay inside,” she continued. It’s their issue, not mine, if they don’t like the way I look. The comedy-drama mockumentary Cast Offs, which was nominated for a BAFTA, where Victoria Wright starred, helped Victoria Wright gain more fans in 2016. Follow-up was done with six disabled people. There was Victoria, who has cherubism, as well as a blind and a paraplegic man.
According to The Guardian, a disabled actor who shared the same disability performed each part. One actor went so far as to criticize the large number of actors who weren’t disabled but played disabled characters: “There will almost certainly be a flood of comments regarding Cast Offs from both disabled and non-disabled people. The portrayal of disabled people as adults who swear, drink, and engage in sexual activity will amuse and seem realistic to some disabled people. a welcome change from either covering disability with child’s play or not at all. Liz Sayce, CEO of the Royal Association for Disability Rights, told the newspaper that some people might find it disrespectful. It was nothing short of amazing for Victoria to play the part.
When she facilitated a Q&A with the directors Miranda Bowen and Amanda Boyle, they recalled a brief but revealing story about her that she once again chose to make humorous. “Victoria, I remember you having to invent a secret during your casting. “You said that you had plastic surgery so that you would look funny.
I can still visualize the expression you were acting with on the other person’s face. It was a funny, brave, and bold moment—everything we wanted, said Boyle.
In the movie, Victoria’s co-stars were Peter Michell and Victoria.
I frequently forgot that neither of you were actors before, Miranda continued. Working with such a talented cast was enjoyable, and you both performed with amazing professionalism and competence. The course of Victoria Wright’s life was filled with joy; she is now a loving mother and a fervent supporter of the rights of people with disabilities.
She has additionally represented the UK in Jeans for Genes, an annual fundraising occasion for the group of people with genetic disorders. “Throughout my life, I’ve come across people who assume that, based on the way I appear, I must lead a lonely, depressing life, but I actually lead a happy life. “Charity activist and public relations expert with a young daughter who makes me laugh every day,” was how she introduced herself.
No matter their skill level, Victoria Wright inspires a lot of people. She cultivates in us the humility and assurance we should all have.
