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| By Feona MorrisonLiving in a world that is obsessed with your physical appearance, having any deformity is an everyday challenge. Everyone knows that today’s society is very image-conscious and there is pressure on one to look perfect.Shivanie Naryan, as these photos bear out, still requires corrective surgeries.When Pamela Tulshi was pregnant with her second daughter she was overwhelmed with joy. However, the mother was taken aback by the appearance of her newborn after giving birth. Her little bundle of joy had a deformed right side face. The infant had no right ear.That baby was named Shivanie Naryan. She is now 19 years old and is still living with that birth defect. Her mother has grown to accept and love her child that way. The young woman who hails from Grove, East Bank Demerara, is like any other girl her age. She laughs and makes jokes. But unlike other girls she’s had a much more difficult life.Whilst growing up, she always isolated herself from others and didn’t have many friends. Believe it or not, Shivanie cannot even recall playing ‘dolly house’. But despite the fact that she didn’t look like others, this young woman was determined to go to school. She attended the Grove Primary and later gained a spot at Covent Garden Secondary after sitting the Secondary School Entrance Examinations.According to her, she was forced to remain at home on numerous occasions because pain was her constant distraction. So intense were the pains that they sent shockwaves through her body. Shivanie recalled that these pains usually affected her concentration during classes and she had no other alternative but to rest her head on a desk to ease the discomfort. “Like when this thing (pain) start up nobody can’t talk…nobody can’t touch me…” No amount of pain killers made her nightmare disappear.Desperate to put a stop to her daughter’s everyday agony, the mother took her child to see a doctor. However, she was told that no medication could be prescribed for her child. Nevertheless, she completed High School and still stresses over the fact that she was unable to take part in work studies. Shivanie, who has never been employed, hopes to one day become a trained teacher.BEHIND THE HAIRHaving a facial disfigurement can sometimes be a painful psychological problem for those affected. Shivanie is self-conscious about her appearance. She uses her long,Cheap Jerseys From China, silky, black hair to hide that part of her face, particularly when leaving her home. This, she said, was done in an effort to prevent curious stares, strange looks and hurtful remarks from others.Shivanie recalled that one day during high school she was summoned by a teacher over her prohibited hairstyle. A bit hesitant to disclose her reason for disobeying the school rules she eventually explained to the teacher that her face did not look like every other child. Her mother later visited the school and held discussions with the teacher. Shivanie was given permission to continue wearing her hair that way. She anticipates the day when she will have a normal life and be able to go about without having people gazing at her.Her mother disclosed that she was told by doctors that her daughter would need to undergo three steps of surgery to fix her abnormality. She would also need reconstructive surgery on her right ear.PLASTIC SURGERYIn February 2014, Shivanie and her mother traveled to New Delhi, India, for her first plastic surgery. The cost of the operation was funded by a charitable organization. The surgery was a success and they spent one month in the foreign land. Operations lasted for eight hours, but recovery was the hardest part.Shivanie related that after the surgery she felt very drowsy and was unable to do anything without assistance. But her mother was always by her bedside to answer to her daughter’s every call. Tulshi stated that her daughter’s entire body was swollen and discoloured after the operation. The mother said that it was very hurtful to see her child that way and she looks forward to the day when all surgeries will be complete.For now, Pamela Tulshi will continue to teach her daughter to be confident in herself and show her how beautiful and special she is. She is also requesting assistance from the public with funding her daughter’s remaining surgeries. Persons desirous of making contribution can contact Tulshi on (592) 266-3191 or 666-9972 |
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