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  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_024.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_003.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_027.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_002.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_004.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_006.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_007.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_005.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_008.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_009.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_010.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_011.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_013.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_012.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_014.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_017.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_015.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_018.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_016.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_019.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_020.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_021.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_022.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_023.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_026.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_025.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_028.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_030.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_029.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_033.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_031.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_032.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_034.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_035.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_036.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_037.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_038.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_039.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_040.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_041.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_001.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_002.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_006.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_005.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_012.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_011.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_013.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_009.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_015.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_001.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_007.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_004.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_003.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_008.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_010.jpg
  • EXCLUSIVE: A 21-year-old woman delivered a baby with two heads and three hands, sending doctors of the state-run facility into a tizzy in central India. Babita Ahirwar, a resident of Basauda village in Vidisha district of Madhya Pradesh, delivered the baby around 7:30 am on November 23 through C-section. Babita was married to Jaswant Ahirwar around one and a half years ago. The couple which was eagerly waiting to welcome their first baby was devastated after seeing the infant born with a deformity. "It was a mixed feeling when the nurses handed over the baby to me. Initially, I thought it was a twin, but when the nurses removed the towel, I was shocked to see our firstborn with two heads and three hands. All we wanted was a normal and healthy baby, but the almighty wanted to punish us this way. I don't know why," said new mom Babita told Newslions. Dr Surendra Sonkar of Vidisha Sadar hospital said: "On Saturday morning around 7:30 am, we facilitated the delivery of a baby through C-section. The baby had two heads and three hands. The third hand had two palms attached to it. "There is only one heart visible in the newborn. This is a very rare condition and this is the first time. I have come across such a case in my career," he said. "We had initially kept the baby in the ICU, but we thought it was better to refer them to a better-equipped facility in Bhopal," he added. At present, the baby is undergoing treatment at Bhopal's Hamidi Medical College and Hospital. 23 Nov 2019 Pictured: Baby born with two heads and three hands in central India. Photo credit: Newslions Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA555409_014.jpg
  • September 1, 2017 - Leon, Spain - A dog sits next to dry riverbed. Spain is on its way to its worst drought in 20 years. The marshes hold less than half of the water they can store, with 47.93% of reserves. In Leon, in the north of the country, its main reservoir barely reaches 10% on 1st September 2017. (Credit Image: © Alvaro Fuente/NurPhoto via ZUMA Press)
    RTI20170901_zaa_n230_138.jpg
  • September 1, 2017 - Leon, Spain - Spain is on its way to its worst drought in 20 years. The marshes hold less than half of the water they can store, with 47.93 percent of reserves. In Leon, in the north of the country, its main reservoir barely reaches 10 percent. (Credit Image: © Alvaro Fuente/NurPhoto via ZUMA Press)
    RTI20170901_zaa_n230_135.jpg
  • September 1, 2017 - Leon, Spain - Spain is on its way to its worst drought in 20 years. The marshes hold less than half of the water they can store, with 47.93 percent of reserves. In Leon, in the north of the country, its main reservoir barely reaches 10 percent on 1st September 2017. (Credit Image: © Alvaro Fuente/NurPhoto via ZUMA Press)
    RTI20170901_zaa_n230_140.jpg
  • September 1, 2017 - Leon, Spain - Spain is on its way to its worst drought in 20 years. The marshes hold less than half of the water they can store, with 47.93% of reserves. In Leon, in the north of the country, its main reservoir barely reaches 10%. (Credit Image: © Alvaro Fuente/NurPhoto via ZUMA Press)
    RTI20170901_zaa_n230_121.jpg
  • EXCLUSIVE: A UK TEAM OF SATELLITE HISTORIANS CLAIM TO HAVE MADE HISTORY-CHANGING DISCOVERY OF THE LOST CITY OF ATLANTIS WITH PIX AND VIDEO – LINK TO VIDEO TRAILER OF FILM MADE OF DISCOVERY http://ingeniofilms.com/elements/atlantica/ DOWNLOAD LINK TO IMAGES: https://we.tl/t-9t8GLOOvz7 By Magnus News Agency A UK team of satellite historians claim to have discovered the true location of the lost city of ATLANTIS. Ground-breaking antiquity specialists Merlin Burrows believe the ruins of the legendary civilization can be found in modern-day southern Spain. The exact location is somewhere north of the city of Cadiz, Andalucía, centred around the Doñana National Park, which the UK historians believe was once a vast inland sea. And they claim from the park south and north there is further evidence of the ancient civilisation, with 15 other settlements dotted along the coastline. Atlantis was recorded in the writings of Greek philosopher Plato who lived around 400BC. He described an advanced island civilization that ruled a vast maritime empire, some 9,000 years before his own era. The city of Atlantis at the centre of this empire was described as having, among other features, an enormous harbour wall, huge entrance pillars, a temple to the god Poseidon and massive circular pieces of land carved out by the Atlanteans to live on. It is thought a cataclysmic natural disaster, such as a tsunami or volcanic event, eventually wiped out the Atlanteans, consigning their legacy to legend. But now using unique satellite investigation techniques, aerial photography and ground observations of the site, British experts believe they have found all the features of Atlantis Plato described and evidence of how they were destroyed. Although some scholars believe Atlantis to be a myth, Merlin Burrows claim their discoveries will once and for all prove the lost civilization existed. Maritime historian Tim Akers, head of research at Merlin Burrows, said not only had they discovered Atlantis
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  • September 1, 2017 - Leon, Spain - Spain is on its way to its worst drought in 20 years. The marshes hold less than half of the water they can store, with 47.93% of reserves. In Leon, in the north of the country, its main reservoir barely reaches 10% on 1st September 2017. (Credit Image: © Alvaro Fuente/NurPhoto via ZUMA Press)
    RTI20170901_zaa_n230_121.jpg
  • April 28, 2018 - Legnica, Poland - April 28.2018 Legnica Poland Ola Janiszewska was born with a half of her heart. The daughter's parents learned about her daughter's illness during routine tests for pregnant women. Ola has two operations done in a hospital in Poland. Another surgery is needed but none of the hospitals in Poland wants to do it. One chance for Ola who is currently 2 years old is surgery in Germany. Dad Oli is a policeman. They can not afford to pay for the operation. The operation should be done up to 3 years old. The operation at the clinic in Münster in Germany costs 37 000 EURO  ..Ola Janiszewska with her mother Luiza Janiszewska and my dad Krzysztof Janiszewski  (Credit Image: © Piotr Twardysko via ZUMA Wire)
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  • April 28, 2018 - Legnica, Poland - Ola Janiszewska was born with a half of her heart. The daughter's parents learned about her daughter's illness during routine tests for pregnant women. Ola has two operations done in a hospital in Poland. Another surgery is needed but none of the hospitals in Poland wants to do it. One chance for Ola who is currently 2 years old is surgery in Germany. Dad Oli is a policeman. They can not afford to pay for the operation. (Credit Image: © Piotr Twardysko via ZUMA Wire)
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  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
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  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52526_004.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52526_002.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52526_006.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52526_005.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52526_007.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52526_008.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52526_011.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52526_010.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52526_009.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly, Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52526_001.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly and Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52543_002.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly and Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52543_003.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly and Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52543_004.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly and Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52543_005.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly and Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52543_006.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly and Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52543_001.jpg
  • ***PREMIUM EXCLUSIVE. NO WEB UNTIL 4.15 GMT JULY 12 *** These are the exclusive first pictures of Minka Kelly and Jesse Williams stepping out together in public. The rumored new couple were seen leaving a movie theater together in West Hollywood, CA on Friday, July 7. Reports claim the Friday Night Lights star, 37, had been spending time with Williams, 35, since they worked on a video games project together in Paris. An onlooker said: "The pair were trying to not be noticed and were seen leaving the Sunset 5 movie theatre in West Hollywood. They both had baseball caps and looked dressed down and very low-key. They were seen in a car park after watching the movie The Beguiled.” Minka dated baseball player Derek Jeter from 2008 to 2011, reuniting again briefly in 2012. Williams is in the midst of a bitter custody battle for his two children, son Maceo, aged one, and daughter Sadie, who is three, pending his divorce from wife Aryn Drake-Lee. He filed the divorce petition in April after fours and half years’ marriage, although the couple were together for 13 years, long before his acting career took off. The Grey’s Anatomy actor has opened up about the well-publicised divorce in Jay-Z's Footnotes For 4:44 video, in which he makes reference to cheating rumours surrounding his marriage. He says: 'I was in a relationship 13 years, 13 real years, not 5 years, not 7 years, 13 years and all of a sudden mother f***ers are writing think-pieces that I somehow threw a 13-year relationship. Like thee most painful experience I’ve had in my life like with a person I’ve loved with all of my heart, that I threw a person and my family in the trash because a girl I work with is cute.' Neither Kelly or Williams has commented on speculation their relationship has transitioned from professional to personal. 07 Jul 2017 Pictured: Minka Kelly and Jesse Williams. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA52543_007.jpg
  • EXCLUSIVE: A UK TEAM OF SATELLITE HISTORIANS CLAIM TO HAVE MADE HISTORY-CHANGING DISCOVERY OF THE LOST CITY OF ATLANTIS WITH PIX AND VIDEO – LINK TO VIDEO TRAILER OF FILM MADE OF DISCOVERY http://ingeniofilms.com/elements/atlantica/ DOWNLOAD LINK TO IMAGES: https://we.tl/t-9t8GLOOvz7 By Magnus News Agency A UK team of satellite historians claim to have discovered the true location of the lost city of ATLANTIS. Ground-breaking antiquity specialists Merlin Burrows believe the ruins of the legendary civilization can be found in modern-day southern Spain. The exact location is somewhere north of the city of Cadiz, Andalucía, centred around the Doñana National Park, which the UK historians believe was once a vast inland sea. And they claim from the park south and north there is further evidence of the ancient civilisation, with 15 other settlements dotted along the coastline. Atlantis was recorded in the writings of Greek philosopher Plato who lived around 400BC. He described an advanced island civilization that ruled a vast maritime empire, some 9,000 years before his own era. The city of Atlantis at the centre of this empire was described as having, among other features, an enormous harbour wall, huge entrance pillars, a temple to the god Poseidon and massive circular pieces of land carved out by the Atlanteans to live on. It is thought a cataclysmic natural disaster, such as a tsunami or volcanic event, eventually wiped out the Atlanteans, consigning their legacy to legend. But now using unique satellite investigation techniques, aerial photography and ground observations of the site, British experts believe they have found all the features of Atlantis Plato described and evidence of how they were destroyed. Although some scholars believe Atlantis to be a myth, Merlin Burrows claim their discoveries will once and for all prove the lost civilization existed. Maritime historian Tim Akers, head of research at Merlin Burrows, said not only had they discovered Atlantis
    MEGA308562_012.jpg
  • EXCLUSIVE: A UK TEAM OF SATELLITE HISTORIANS CLAIM TO HAVE MADE HISTORY-CHANGING DISCOVERY OF THE LOST CITY OF ATLANTIS WITH PIX AND VIDEO – LINK TO VIDEO TRAILER OF FILM MADE OF DISCOVERY http://ingeniofilms.com/elements/atlantica/ DOWNLOAD LINK TO IMAGES: https://we.tl/t-9t8GLOOvz7 By Magnus News Agency A UK team of satellite historians claim to have discovered the true location of the lost city of ATLANTIS. Ground-breaking antiquity specialists Merlin Burrows believe the ruins of the legendary civilization can be found in modern-day southern Spain. The exact location is somewhere north of the city of Cadiz, Andalucía, centred around the Doñana National Park, which the UK historians believe was once a vast inland sea. And they claim from the park south and north there is further evidence of the ancient civilisation, with 15 other settlements dotted along the coastline. Atlantis was recorded in the writings of Greek philosopher Plato who lived around 400BC. He described an advanced island civilization that ruled a vast maritime empire, some 9,000 years before his own era. The city of Atlantis at the centre of this empire was described as having, among other features, an enormous harbour wall, huge entrance pillars, a temple to the god Poseidon and massive circular pieces of land carved out by the Atlanteans to live on. It is thought a cataclysmic natural disaster, such as a tsunami or volcanic event, eventually wiped out the Atlanteans, consigning their legacy to legend. But now using unique satellite investigation techniques, aerial photography and ground observations of the site, British experts believe they have found all the features of Atlantis Plato described and evidence of how they were destroyed. Although some scholars believe Atlantis to be a myth, Merlin Burrows claim their discoveries will once and for all prove the lost civilization existed. Maritime historian Tim Akers, head of research at Merlin Burrows, said not only had they discovered Atlantis
    MEGA308562_024.jpg
  • EXCLUSIVE: A UK TEAM OF SATELLITE HISTORIANS CLAIM TO HAVE MADE HISTORY-CHANGING DISCOVERY OF THE LOST CITY OF ATLANTIS WITH PIX AND VIDEO – LINK TO VIDEO TRAILER OF FILM MADE OF DISCOVERY http://ingeniofilms.com/elements/atlantica/ DOWNLOAD LINK TO IMAGES: https://we.tl/t-9t8GLOOvz7 By Magnus News Agency A UK team of satellite historians claim to have discovered the true location of the lost city of ATLANTIS. Ground-breaking antiquity specialists Merlin Burrows believe the ruins of the legendary civilization can be found in modern-day southern Spain. The exact location is somewhere north of the city of Cadiz, Andalucía, centred around the Doñana National Park, which the UK historians believe was once a vast inland sea. And they claim from the park south and north there is further evidence of the ancient civilisation, with 15 other settlements dotted along the coastline. Atlantis was recorded in the writings of Greek philosopher Plato who lived around 400BC. He described an advanced island civilization that ruled a vast maritime empire, some 9,000 years before his own era. The city of Atlantis at the centre of this empire was described as having, among other features, an enormous harbour wall, huge entrance pillars, a temple to the god Poseidon and massive circular pieces of land carved out by the Atlanteans to live on. It is thought a cataclysmic natural disaster, such as a tsunami or volcanic event, eventually wiped out the Atlanteans, consigning their legacy to legend. But now using unique satellite investigation techniques, aerial photography and ground observations of the site, British experts believe they have found all the features of Atlantis Plato described and evidence of how they were destroyed. Although some scholars believe Atlantis to be a myth, Merlin Burrows claim their discoveries will once and for all prove the lost civilization existed. Maritime historian Tim Akers, head of research at Merlin Burrows, said not only had they discovered Atlantis
    MEGA308562_010.jpg
  • EXCLUSIVE: A UK TEAM OF SATELLITE HISTORIANS CLAIM TO HAVE MADE HISTORY-CHANGING DISCOVERY OF THE LOST CITY OF ATLANTIS WITH PIX AND VIDEO – LINK TO VIDEO TRAILER OF FILM MADE OF DISCOVERY http://ingeniofilms.com/elements/atlantica/ DOWNLOAD LINK TO IMAGES: https://we.tl/t-9t8GLOOvz7 By Magnus News Agency A UK team of satellite historians claim to have discovered the true location of the lost city of ATLANTIS. Ground-breaking antiquity specialists Merlin Burrows believe the ruins of the legendary civilization can be found in modern-day southern Spain. The exact location is somewhere north of the city of Cadiz, Andalucía, centred around the Doñana National Park, which the UK historians believe was once a vast inland sea. And they claim from the park south and north there is further evidence of the ancient civilisation, with 15 other settlements dotted along the coastline. Atlantis was recorded in the writings of Greek philosopher Plato who lived around 400BC. He described an advanced island civilization that ruled a vast maritime empire, some 9,000 years before his own era. The city of Atlantis at the centre of this empire was described as having, among other features, an enormous harbour wall, huge entrance pillars, a temple to the god Poseidon and massive circular pieces of land carved out by the Atlanteans to live on. It is thought a cataclysmic natural disaster, such as a tsunami or volcanic event, eventually wiped out the Atlanteans, consigning their legacy to legend. But now using unique satellite investigation techniques, aerial photography and ground observations of the site, British experts believe they have found all the features of Atlantis Plato described and evidence of how they were destroyed. Although some scholars believe Atlantis to be a myth, Merlin Burrows claim their discoveries will once and for all prove the lost civilization existed. Maritime historian Tim Akers, head of research at Merlin Burrows, said not only had they discovered Atlantis
    MEGA308562_009.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_008.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_010.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_005.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_011.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_006.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_002.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_003.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_004.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_007.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_001.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_009.jpg
  • EXCLUSIVE: A UK TEAM OF SATELLITE HISTORIANS CLAIM TO HAVE MADE HISTORY-CHANGING DISCOVERY OF THE LOST CITY OF ATLANTIS WITH PIX AND VIDEO – LINK TO VIDEO TRAILER OF FILM MADE OF DISCOVERY http://ingeniofilms.com/elements/atlantica/ DOWNLOAD LINK TO IMAGES: https://we.tl/t-9t8GLOOvz7 By Magnus News Agency A UK team of satellite historians claim to have discovered the true location of the lost city of ATLANTIS. Ground-breaking antiquity specialists Merlin Burrows believe the ruins of the legendary civilization can be found in modern-day southern Spain. The exact location is somewhere north of the city of Cadiz, Andalucía, centred around the Doñana National Park, which the UK historians believe was once a vast inland sea. And they claim from the park south and north there is further evidence of the ancient civilisation, with 15 other settlements dotted along the coastline. Atlantis was recorded in the writings of Greek philosopher Plato who lived around 400BC. He described an advanced island civilization that ruled a vast maritime empire, some 9,000 years before his own era. The city of Atlantis at the centre of this empire was described as having, among other features, an enormous harbour wall, huge entrance pillars, a temple to the god Poseidon and massive circular pieces of land carved out by the Atlanteans to live on. It is thought a cataclysmic natural disaster, such as a tsunami or volcanic event, eventually wiped out the Atlanteans, consigning their legacy to legend. But now using unique satellite investigation techniques, aerial photography and ground observations of the site, British experts believe they have found all the features of Atlantis Plato described and evidence of how they were destroyed. Although some scholars believe Atlantis to be a myth, Merlin Burrows claim their discoveries will once and for all prove the lost civilization existed. Maritime historian Tim Akers, head of research at Merlin Burrows, said not only had they discovered Atlantis
    MEGA308562_006.jpg
  • EXCLUSIVE: A UK TEAM OF SATELLITE HISTORIANS CLAIM TO HAVE MADE HISTORY-CHANGING DISCOVERY OF THE LOST CITY OF ATLANTIS WITH PIX AND VIDEO – LINK TO VIDEO TRAILER OF FILM MADE OF DISCOVERY http://ingeniofilms.com/elements/atlantica/ DOWNLOAD LINK TO IMAGES: https://we.tl/t-9t8GLOOvz7 By Magnus News Agency A UK team of satellite historians claim to have discovered the true location of the lost city of ATLANTIS. Ground-breaking antiquity specialists Merlin Burrows believe the ruins of the legendary civilization can be found in modern-day southern Spain. The exact location is somewhere north of the city of Cadiz, Andalucía, centred around the Doñana National Park, which the UK historians believe was once a vast inland sea. And they claim from the park south and north there is further evidence of the ancient civilisation, with 15 other settlements dotted along the coastline. Atlantis was recorded in the writings of Greek philosopher Plato who lived around 400BC. He described an advanced island civilization that ruled a vast maritime empire, some 9,000 years before his own era. The city of Atlantis at the centre of this empire was described as having, among other features, an enormous harbour wall, huge entrance pillars, a temple to the god Poseidon and massive circular pieces of land carved out by the Atlanteans to live on. It is thought a cataclysmic natural disaster, such as a tsunami or volcanic event, eventually wiped out the Atlanteans, consigning their legacy to legend. But now using unique satellite investigation techniques, aerial photography and ground observations of the site, British experts believe they have found all the features of Atlantis Plato described and evidence of how they were destroyed. Although some scholars believe Atlantis to be a myth, Merlin Burrows claim their discoveries will once and for all prove the lost civilization existed. Maritime historian Tim Akers, head of research at Merlin Burrows, said not only had they discovered Atlantis
    MEGA308562_004.jpg
  • EXCLUSIVE: Talk about a wardrobe malfunction! Jamie Foxx's bizarre fashion looks more like Robin Hoodie than his 'Robin Hood' character Little John as he is spotted wearing a hoodie on his legs instead of pants! Jamie Foxx who plays ‘Little John’ in the new movie ‘Robin Hood’ seems to have been taking the title very seriously as he wears not one, but two matching hoodies.. one on his top half and one on his legs instead of pants, with the hood dangling in between his legs. This strange behaviour comes as rumours surface that he and ‘secret’ girlfriend Katie Holmes are set to get married in Paris, France. In these photos, the Hollywood actor could be seen wearing a ‘Do-rag’ as he left a building before heading to the set of his current movie “Power” being filmed in New Orleans. Katie Holmes sparked rumors of an engagement when she was spotted wearing a diamond ring as she walked from the production office to get a coffee. Filming did not start until the following day. But her publicist later issued a statement, insisting the ring was merely a screen prop. Holmes, who divorced ‘Top Gun’ star Tom Cruise in 2012, is believed to have been secretly dating Foxx for five years. Foxx, 50, and Holmes, 39, went public in April during a PDA-packed beach outing on a Malibu beach after shying away from getting cozy together in public for years. 29 Nov 2018 Pictured: Jamie Foxx. Photo credit: MEGA TheMegaAgency.com +1 888 505 6342
    MEGA315597_002.jpg
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