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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_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_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_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_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_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_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_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_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_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_001.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_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_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_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_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_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_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_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_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_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_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_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_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_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_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_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_038.jpg
  • A 75-year-old man suffering from a rare disease has grown a Hellboy-like horn on his head. Shyamal Lal Yadav, hailing from Sagar district of Madhya Pradesh in central India, suffered an injury on his head five years ago. Yadav claims that a horn-like structure started developing in the middle of his head after that. Yadav saw several doctors, but ‘all of them looked clueless’. He finally got the horn sliced with the help of a barber. “I thought to myself finally I had got good riddance from the devil’s horn. But my happiness was short-lived,” said Yadav. As feared, the horn started to grow back on his head and he was completely clueless about his next course of action Fortunately, the growth did not cause any physical discomfort or snowball into a medical issue. But, it had certainly made him a laughing stock. He was embarrassed to roam around in public with the unnatural growth on his head. “I kept doing the rounds of hospitals, but nothing happened. Then I asked my barber to cut the horn with the shaving blade. He did manage to cut it off, but the horn grew back in some time at the same spot,” said the ‘real-life Hellboy’. According to Yadav, he travelled to Bhopal (around 170km from Sagar) and Nagpur (around 388km from his home) to consult senior experts, however, had to come back as he could not afford the cost of the operation. The medical fraternity was in a tizzy as they hadn’t witnessed anything like that. His quest finally ended at a private clinic run by Dr. Vishal Gajbhiye in his home town Sagar. Dr. Gajbhiye said,” “The four-inch horn was solid and had sizable thickness.” The physician carried out a CT scan to ensure that the horn wasn’t deep enough to require the intervention of a neurosurgeon. The physician went ahead with the head surgery to remove the horn. After the horn was removed, the surgeons used the skin of Yadav’s forehead to fill up the gap through plastic surgery. Dr. Gajbhiye calls it a rare case and claimed t
    MEGA503504_002.jpg
  • A 75-year-old man suffering from a rare disease has grown a Hellboy-like horn on his head. Shyamal Lal Yadav, hailing from Sagar district of Madhya Pradesh in central India, suffered an injury on his head five years ago. Yadav claims that a horn-like structure started developing in the middle of his head after that. Yadav saw several doctors, but ‘all of them looked clueless’. He finally got the horn sliced with the help of a barber. “I thought to myself finally I had got good riddance from the devil’s horn. But my happiness was short-lived,” said Yadav. As feared, the horn started to grow back on his head and he was completely clueless about his next course of action Fortunately, the growth did not cause any physical discomfort or snowball into a medical issue. But, it had certainly made him a laughing stock. He was embarrassed to roam around in public with the unnatural growth on his head. “I kept doing the rounds of hospitals, but nothing happened. Then I asked my barber to cut the horn with the shaving blade. He did manage to cut it off, but the horn grew back in some time at the same spot,” said the ‘real-life Hellboy’. According to Yadav, he travelled to Bhopal (around 170km from Sagar) and Nagpur (around 388km from his home) to consult senior experts, however, had to come back as he could not afford the cost of the operation. The medical fraternity was in a tizzy as they hadn’t witnessed anything like that. His quest finally ended at a private clinic run by Dr. Vishal Gajbhiye in his home town Sagar. Dr. Gajbhiye said,” “The four-inch horn was solid and had sizable thickness.” The physician carried out a CT scan to ensure that the horn wasn’t deep enough to require the intervention of a neurosurgeon. The physician went ahead with the head surgery to remove the horn. After the horn was removed, the surgeons used the skin of Yadav’s forehead to fill up the gap through plastic surgery. Dr. Gajbhiye calls it a rare case and claimed t
    MEGA503504_001.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_006.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_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_005.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_008.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_002.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_007.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_003.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_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_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_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_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_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: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_004.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_008.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_006.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_005.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_011.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_002.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_007.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_003.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_004.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_009.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_010.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_001.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_010.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_006.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_002.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_020.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_009.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_005.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_008.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_012.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_007.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_024.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_017.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_021.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_013.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_028.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_023.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_016.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_025.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_019.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_018.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_022.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_029.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_030.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_040.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_032.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_042.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_047.jpg
  • *PREMIUM EXCLUSIVE * Rihanna’s dad Ronald Fenty has told how he thought he was going to die after being stricken with Covid-19 - weeks after the superstar donated $5 million to fight the killer virus. The desperately worried singer and fashion mogul called every day to check on her father’s condition as he spent 14 days fighting for life in a Barbados hospital. Three people on the holiday, island, a favorite of celebrities including Simon Cowell and Mark Wahlberg, have so far died of the virus. “My daughter Robyn (Rihanna’s real name) was checking in on me every day,” said Ronald. “I thought I was going to die to be honest. I have to say ‘I love you so much Robyn.’ She did so much for me. I appreciate everything she had done.” Somehow Rihanna even managed to have a potentially life-saving ventilator for her father shipped from the States to the Caribbean island. Ronald is now recovering at the luxury home the singer brought for him in the parish of St James. Ronald was twice tested and declared virus free before being allowed to go home. Rihanna, born and raised on Barbados, made her huge donation to help fight the pandemic in the U.S. and across the globe through her Clara Lionel Foundation - named after her beloved he’s mother. Rihanna’s massive donation is earmarked for local food banks serving at-risk communities and the elderly and to promote acceleration of coronavirus testing and care in countries like Haiti and Malawi, as well as the mobilization of resources and additional capacity and support for Native communities. Rihanna’s funds are also being used to buy protective equipment for frontline health workers and diagnostic labs, to establish and maintain intensive care units, to accelerate the development of vaccines and other therapies across the globe, to train healthcare workers, and to distribute critical respiratory supplies. Ronald spoke of his terrifying life or death battle aftwr spending the last two weeks at the island’s
    MEGA643414_045.jpg
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